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Original Research ARTICLE

Front. Oncol., 04 July 2019 | https://doi.org/10.3389/fonc.2019.00602

Folic Acid Receptor-Mediated Targeting Enhances the Cytotoxicity, Efficacy, and Selectivity of Withania somnifera Leaf Extract: In vitro and in vivo Evidence

Yue Yu1, Jia Wang2,3, Sunil C. Kaul2, Renu Wadhwa2* and Eijiro Miyako1*
  • 1Department of Materials and Chemistry, Nanomaterials Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba, Japan
  • 2DAILAB, DBT-AIST International Center for Translational and Environmental Research (DAICENTER), AIST, Tsukuba, Japan
  • 3Graduate School of Life and Environmental Sciences, University of Tsukuba, Ibaraki, Japan

Nanomedicine holds great potential for drug delivery to achieve more effective and safer cancer treatment. Earlier, we reported that the alcoholic extract of Withania somnifera leaves (i-Extract) has selective cancer cell killing activity. Herein, we developed a folate receptor-targeting i-Extract nanocomplex (FRi-ExNC) that suspends well in water and possesses enhanced selective anticancer activity in both in vitro and in vivo assays. Comparative analyses of folate receptor (FR)-positive and -negative cells revealed that FRi-ExNC caused a stronger decrease in Cyclin D/Cdk4 and anti-apoptotic protein Bcl-2, as well as a higher increase in the growth arrest regulating protein p21WAF1 and pro-apoptotic protein PARP-1, in FR-enriched cancer cells. Our results demonstrate that FRi-ExNC could be a natural source-based nanomedicine for targeted cancer therapy.

Introduction

Withania somnifera is a popular herb (also called Indian ginseng) used in Indian traditional Ayurvedic medicine and health tonics. Although it is known for a variety of health-promoting effects and possesses high therapeutic potential, its mechanisms of action are only beginning to be addressed in laboratories. We reported earlier that the i-Extract possesses potent anti-tumor activity that was assigned to its active components, withanolides. Among them, Withaferin-A and Withanone were found to possess anticancer activity; whereas i-Extract and Withanone have been shown to be selectively cytotoxic to cancer cells, Withaferin-A causes toxicity to normal cells as well (15). Both bioinformatics and wet lab studies have demonstrated that both Withaferin-A and Withanone cause death of cancer cells through multi-target mechanisms (611). Interestingly, the water extract of Withania somnifera leaves was also shown to possess anticancer activity that functions through bioactives and mechanisms that are different to that of the i-Extract (12, 13). Of note, we found that Withaferin-A has the capability to kill telomerase-negative ALT (Alternative Lengthening of Telomeres) cancer cells (14) suggesting that a formulation containing Withaferin-A will be useful for the treatment of complex and aggressive cancers. With this view, a combination of Withanone and Withaferin-A in a 20:1 ratio was generated. This combination of Withanone and Withaferin-A was demonstrated to retain selective toxicity to cancer cells and anti-metastasis potential (15). Most recently, we found that although the methoxy derivative of Withaferin-A lacks anticancer activity, it protects normal cells against a variety of stresses (16). In view of the above information, i-Extract containing a variety of bioactives is considered to be more potent than the individual compounds and warrants further studies on its composition and delivery.

Clinical use of Withania somnifera has not been approved as of yet, due to the difficulty in identifying the real active formula in the mixture. In addition, insufficient targeting effects and the poor water solubility of i-Extract are also challenging issues. Nanomedicine offers a highly potential merger of medicine and nanotechnology for diagnostic as well as therapeutic purposes (17). Through targeted and efficient delivery, the engineered molecules and their derivatives have been seen to offer better therapeutic potential. For example, use of polyethylene glycol (PEG)-coated polymer nanocarriers (1822) has been shown to enhance the action of drugs. Furthermore, the nanocarriers can effectively encapsulate various types of small molecules with different physicochemical features including hydrophilicity (23), hydrophobicity (24), electrical charge (25), and size (26). Enhanced permeability and a retention (EPR) effect has also been reported and serves as a key rationale for using nanocarriers to treat solid tumors (2729). However, the targeted and uniform delivery of the nanocarriers to tumors in sufficient quantities requires optimization. An ideal nanocarrier should be equipped with selective ligands that are highly or exclusively expressed on target tumor cells, and thus endow the carriers with specific targeting capabilities.

Folate receptor alpha (FR-α) is a glycosylphosphatidylinositol cell surface-anchored glycoprotein, overexpressed in 90% ovarian carcinomas and many types of epithelial cancers (3033). It binds to folic acid, mediates its intracellular transport via receptor-mediated endocytosis, and is essential for proliferation of these cancer cell types (34, 35). On the other hand, normal cells and tissues have limited FR-α expression that is restricted largely to the apical surface of the epithelial tissue, where it is inaccessible to the circulating drugs (3639). Due to such limited expression in normal tissues, FR-α has been considered as a candidate for targeted delivery of anticancer drugs (4042).

In the present study, we developed a folate receptor-targeting i-Extract nanocomplex that possesses enhanced selective cancer cell killing activity. We provide evidence that in contrast to i-Ex, FRi-ExNC is water soluble and shows a 3-fold higher cellular uptake by FR-enriched cancer cells in vitro. In vivo tumor assays also supported stronger tumor suppression capability of FRi-ExNC suggesting that may serve as an efficient and safe natural drug candidate for cancer treatment.

Materials and Methods

Preparation of FRi-ExNC

Withania somnifera leaf extracts (i-Extract; i-Ex) were prepared as described earlier (1). Ten mg i-Ex, 5 mg DSPE-PEG-Folate (1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[folate(polyethylene glycol)]) (Nanosoft Polymers, Lewisville, NC, USA) and 10 mg DSPE-PEG-NH2 (N-(aminopropyl polyoxyethylene oxycarbonyl)-1,2-distearoyl-sn-glycero-3-phosphoethanolamine) (SUNBRIGHT DSPE-020PA; Yuka Sangyo, Tokyo, Japan) were briefly dissolved in 10 ml of double distilled Milli-Q water by bath sonication (power output, 80 W; oscillation frequency, 40 kHz) (Branson 2800; Branson Ultrasonics, Kanagawa, Japan). After gentle stirring for 1 h at room temperature, the mixture was subjected to pulse-type sonication (VCX-600; Sonics, Danbury, CT, USA) for 10 min, followed by centrifugation at 1,000 rpm for 10 min at 20°C (model no. 3740; Kubota, Tokyo, Japan). The FRi-ExNC in the supernatant was collected and used for subsequent experiments. The same protocol was applied for i-ExNC preparation except that the DSPE-PEG-Folate was replaced with an equal mass of DSPE-PEG. Fluorescent nanocomplexes were prepared a the similar way with an additional 1 mg of Nile Red (Wako) in the mixture.

Characterization of FRi-ExNC

The spectral profiles and concentrations of loaded i-Extract in nanocomplexes were measured with a UV-Vis-NIR spectrophotometer (V-730 BIO; Jasco, Tokyo, Japan). The structure and morphology of prepared FRi-ExNCs were visualized by high-resolution transmission electron microscope (TEM) (EM-002B; Topcon, Tokyo, Japan), an established and suitable method for the investigation of structural aspects of nanomaterials, at an accelerating voltage of 120 kV. Before the TEM experiments, a nanocomplex solution was deposited on a carbon-coated support and negatively stained using a 1% phosphotungstic acid solution. The size distribution was analyzed using Image-J from TEM images (≥200 particles were measured).

Encapsulation Efficiency of i-Ex

The encapsulation efficiency of i-Ex into FRi-ExNC was calculated using the following equation: encapsulation efficiency = (Wseed-Wnonencapsulated)/Wseed ×100%, where Wseed is the total amount (weight) of i-Ex initially used for FRi-ExNC preparation, and Wnonencapsulated represents the amount of i-Ex that was precipitated after centrifugation during the preparation. Briefly, FRi-ExNC was prepared starting with different weight ratios of crude i-Ex powder and DSPE-PEG polymer as indicated. The amount of i-Ex used in this step was recorded as Wseed. After normal preparation processes, the FRi-ExNCs were subjected to centrifugation at 1,000 rpm for 30 min. The precipitated pellets were then dissolved in 200 μl of dimethyl sulfoxide (Wako) and i-Ex was measured by UV-Vis-NIR spectrophotometer. The amount of i-Ex in pellets (Wnonencapsulated) was determined based on the absorption at 660 nm by reference to its calibration curve.

Cell Culture

All cell lines were obtained from the Japanese Collection of Research Bioresources Cell Bank (Tokyo, Japan) or DS Pharma Biomedical (Tokyo, Japan) and cultured in Dulbecco's Modified Eagle's Medium (Gibco, Grand Island, NY, USA) containing 10% fetal bovine serum, 2 mM l-glutamine, 1 mM sodium pyruvate, gentamycin, penicillin-streptomycin (100 IU ml−1), and Hank's balanced salt solution (Life Technologies, Carlsbad, CA, USA). Cells were kept in folate-free medium for at least 3 days before and during all the treatments.

Cytotoxicity Evaluation

Cell viability was assessed with a Cell Counting Kit (CCK)-8 (Dojindo Laboratories, Kumamoto, Japan) following the manufacturer's instructions. Cells (5 ×103 cells well−1) were seeded in a 96-well plate and allowed to adhere to the substratum overnight. They were then exposed to i-Ex loaded nanocomplexes as indicated. After washing with a fresh medium, the cells were incubated with CCK-8 solution for 2 h at 37°C. Absorbance at 450/690 nm was read on a microplate reader (Infinite M200 PRO; Tecan, Männedorf, Switzerland). A colony-forming assay was performed to evaluate long-term cytotoxicity of FRi-ExNC. Cells were seeded in a 12-well plate at a density of 200 cells well−1. After attachment, they were subjected to treatments for 6 h and allowed to foster in fresh medium for ≥10 days. The forming colonies were washed in cold PBS and fixed with a pre-chilled methanol/acetone (v/v, 1:1) mixture for 10 min. The fixed cells were stained overnight with a 0.1% crystal violet solution (Wako, Osaka, Japan). The colony-forming number was calculated as the mean number of colonies from three independent experiments.

Immunoblotting

Cells were harvested in radioimmunoprecipitation assay buffer (Thermo Fisher Scientific, Waltham, MA, USA) supplemented with a protease inhibitor cocktail (Roche Applied Science, Mannheim, Germany). The protein concentration was determined using a Pierce BCA Protein Assay kit (Thermo Fisher Scientific). Protein lysate (20 μg) was resolved in SDS-polyacrylamide gels, transferred to PVDF membrane and then probed with antibodies specific to: folate receptor alpha (FR-α) (ab125030; Abcam, Cambridge, MA, USA); Cyclin D1 (72-13G), CDK4 (C-22), and PARP-1 (H-250) (all from Santa Cruz Biotechnology, Santa Cruz, CA, USA); p21WAF−1 (12D1) and Bcl-2 (2876S) (both from Cell Signaling Technologies, Danvers, MA, USA); and Caspase-3 (610322; BD Transduction Laboratories, San Diego, CA, USA). The membranes were next incubated with the respective secondary antibodies (Thermo Fisher Scientific). Anti-β-actin (AC-15; Abcam) and anti-β-tubulin (T5293; Sigma-Aldrich, St. Louis, MO, USA) antibodies were used as internal loading controls. The protein bands were quantitated using ImageJ software.

Fluorescence Microscopy Imaging

Cells (1 ×105 cells well−1) were plated on glass coverslips placed in 12-well culture dishes. Nile Red-labeled nanocomplexes were added with or without free folic acid (10 μM) (Wako) when cells had attached to the substratum. After 6 h incubation, cells were washed 2–3 times with cold PBS and fixed in 4% formaldehyde for 10 min. Fixed cells were washed thrice with PBS, followed by nuclear staining with Hoechst 33342 (1 μg ml−1; Thermo Fisher Scientific) for 10 min. After serial washings with PBS, coverslips were mounted and visualized under a microscope (Axiovert 200 M; Carl Zeiss, Tokyo, Japan). For immunostaining of FR-α, the fixed cells were permeabilized using 0.5% Triton X-100 in PBS for 10 min and blocked using 2% BSA in PBS for 15 min. Coverslips containing cells were then incubated with anti-FR-α monoclonal antibody (548908; Thermo Scientific) overnight at 4°C, washed thrice with 0.2% Triton X-100 in PBS (PBS-T) and incubated with Alexa Fluor-conjugated secondary antibodies (Thermo Fisher Scientific). After three to six washings with PBS-T, the coverslips were mounted for microscopy imaging.

Quantification of Cellular Uptake

Quantification of cellular uptake was as described elsewhere (43). Briefly, the calibration curve of i-Ex amount was first established by measuring the absorbance at 660 nm of i-ExNC dispersions at various known concentrations. Cells (2 ×105 well−1) were seeded in 6-well plates and incubated overnight to allow attachment followed by treatment with i-ExNC- or FRi-ExNC-supplemented (i-Ex: 20 μg ml−1) folate-free medium for 6 h. After several (three to six) washings with PBS, cell pellets were collected and resuspended in RIPA buffer, followed by 30 min sonication. One portion of the cell lysate was used for protein estimation (Pierce BCA Protein Assay kit; Thermo Fisher Scientific). The absorbance at 660 nm of the remaining cell lysates was measured on a microplate reader (TACAN) in triplicate. The concentration of i-Ex in cell lysates (i-Ex/protein) was estimated based on the corresponding calibration curves.

Flow Cytometry

Cells were seeded at a density of 2 ×105 cells well−1 in 6-well plates and harvested by trypsin after treatments as indicated. The cell pellets were fixed with ice-cold 70% ethanol overnight at −20°C. To avoid false DNA-PI staining, RNA was removed by incubation with RNase A (20 μg/mL; Thermo Fisher Scientific) at 37°C for 1 h followed by centrifugation (500 g) for 5 min. _The supernatant was then replaced with 200 μl of Guava Cell Cycle reagent (Millipore, Billerica, MA, USA) and incubated in the dark for 30 min. The stained cells were subjected to cell cycle analysis using Guava PCA flow cytometer (Millipore). Apoptotic cells were detected by Annexin-V and 7-aminoactinomycin (7-AAD) double staining: after treatments, attached and resuspended cells were harvested and apoptosis was analyzed with a Guava PCA flow cytometer (Millipore) using Guava Nexin Reagent (Millipore), a pre-made cocktail containing phycoerythrin-conjugated Annexin V and 7-AAD following the manufacturer's protocol. TdT-mediated dUTP-biotin nick end labeling (TUNEL) assay was performed using a Guava® TUNEL Kit (Millipore) following the manufacturer's instructions. In brief, control and treated cells (1 ×105) were fixed with 4% paraformaldehyde at 4°C for 1 h, and then permeabilized using 70% (v/v) ice-cold ethanol overnight at −20°C. The cells were incubated with TdT reaction mixture containing TdT enzyme and Brd-UTP for 1 h, followed by immunostaining with anti-Brd-UTP antibody (37°C for 30 min). The stained cells were recorded on the Guava system. Positive and negative controls supplied in the kit were used in each assay. The cell cycle distribution and fraction of apoptotic cells were determined using FlowJo v.7.6 software (Tree Star, Ashland, OR, USA).

In vivo Anti-tumor Assay

BALB/c nude mice (4 weeks old, female) were obtained from Charles River Laboratories (Yokohama, Japan). Mice bearing HeLa and HT-29 cell-derived tumors were generated by subcutaneously injecting 1 ×106 cells in 100 μl mixture of culture medium and Matrigel (Dow Corning, Corning, NY, USA) mixture (v/v, 1:1) into the flanks of the mice. Intraperitoneal injections of nanocomplexes containing an equivalent dose of i-Extract (50 mg Kg−1) were started when small tumor buds were formed at about 10 days. Saline and free i-Extract (50 mg Kg−1) in 10% Cremophor EL (Sigma-Aldrich) were used as the negative and positive controls, respectively. Injections were continued every alternate day, and the mice were monitored for tumor size and overall health (body weight) until 3 weeks. Tumor volume was calculated as V = L × W2/2, where L and W are the length and width of the tumor, respectively. All procedures were carried out in accordance with the Animal Experiment and Ethics Committee, Safety and Environment Management Division, National Institute of Advanced Industrial Science & Technology (AIST), Tsukuba, Japan.

Statistical Analysis

Results are presented as mean ± standard deviation of at least three independent experiments. The numbers of samples per group in each experiment are indicated in the corresponding figure legends as “n.” Differences between groups were evaluated with the Student's t-test for two groups and two-way analysis of variance (ANOVA) followed by Tukey test for multiple groups. *, **, and *** denote the p-values <0.05, 0.01, and 0.001, respectively.

Results and Discussion

Formation and Characterization of FRi-ExNC for Targeted Drug Delivery

Polymeric micelles modified by FR-PEG-lipid have been shown to be effective for targeted drug delivery to cancer cells (4446). Thus, we designed the encapsulation of i-EX in FR-PEG-lipid using the polymeric micelle system, examined its characteristics as well as anticancer effects in in vitro and in vivo assays. The schematic diagram of FRi-ExNC is shown in Figure 1A. The polymeric micelles containing FRi-ExNC can be easily synthesized through a simple self-assembly technique without any complicated multistep processes. i-Ex was encapsulated in the inner core of micelles that were composed of phospholipid-PEG (DSPE-PEG) (for more details, please see Materials and Methods). The folate derivative of DSPE-PEG formed an outer monolayer shell. Such amphiphilic assembly of DSPE-PEG and DSPE-PEG-folate was expected to be capable of encapsulating hydrophobic i-Ex with high loading capacity, and to generate a uniform polymer micelle structure that could target cancer cells selectively (Figures 1B,C). Ultraviolet-visible-near infrared (UV-Vis-NIR) spectroscopy of FRi-ExNC showed a characteristic peak of i-Ex at ~660 nm, confirming the successful encapsulation of i-Ex in the DSPE-PEG and DSPE-PEG-folate micelles (Figure 1D). Of note, the encapsulated i-Ex showed dramatic improvement. As shown in Figure S1, the FRi-ExNC solution was clear and transparent even after storing for 1 week at room temperature; i-Ex solution showed aggregates/precipitates and became turbid (Figure S1). Encapsulation efficiency of i-Ex was increased and reached ~ 87% when i-Ex and DSPE-PEG were used at a 1:3 ratio (Table 1). These data strongly suggested that DSPE-PEG is very useful for solubilizing i-Ex in water. Although scanning electron microscopy (SEM) can provide detailed information about surface structures, it is generally difficult to observe fragile organic samples in high magnification. Furthermore, SEM requires a multistep process for biological samples. On these premises, we opted to do analysis of FRi-ExNC by transmission electron microscopy (TEM). TEM observations revealed that FRi-ExNC contained particles of homogeneous shape and size ranging from 6 to 15 nm (Figures 1E,F). Through repeated experiments, we confirmed that the shape and size of FRi-ExNC particles were constant, stable and highly reproducible. In view of these criteria and ease of preparation of FRi-ExNC, we next investigated its anticancer efficacy in in vitro and in vivo assays.

FIGURE 1
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Figure 1. Formation and characteristics of FRi-ExNC for targeted drug delivery. (A) An illustration of folate receptor-targeted i-Extract nanocomplex (FRi-ExNC) formed from self-assembly of amphiphilic block copolymers (DSPE-PEG) with folate ligands. (B) Sequence of events leading to tumor regression after FRi-ExNC administration: long circulating nanocomplexes were accumulated in the tumor site by EPR effect and (C) internalized into cells via folate receptor-mediated endocytosis. The low pH environment of the endo/lysosomes decomposed micelles to release i-Extract into the cytoplasm, resulting in cell cycle arrest and apoptosis. (D) UV-Vis-NIR absorption spectra of i-Ex, folate, i-ExNC, and FRi-ExNC showing successful encapsulation of i-Ex in the fabricated micelles. Characteristic peaks of folate at 281 nm (left panel) and i-Extract at 660 nm (right panel) were simultaneously observed in the FRi-ExNC nanocomplex. (E) Representative TEM image (a magnified image is shown in the top right corner) and (F) quantitative size distribution of FRi-ExNC showing homogeneous shape with size ranging from 6 to 15 nm.

TABLE 1
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Table 1. Encapsulation efficiency of FRi-ExNC prepared with different weight ratios of crude i-Extract powder and DSPE-PEG polymers.

Selective Cancer Killing Activity of FRi-ExNC in vitro

In order to compare the biological activity of i-Ex and FRi-Ex nanocomplexes, we first examined the level of FR-α expression in a variety of cells. As shown in Figures 2A,B, Western blotting with a specific anti-FR-α antibody revealed its enrichment in cancer cells, including U2OS, HeLa, and SKOV3. On the other hand, MCF7, HT-29 and A549 showed expression levels similar to the normal cells (MRC5 and TIG3). Based on the expression data, we selected HeLa (FR-α positive, FR+), and MCF7 (FR-α negative, FR-) cancer cells for further analysis.

FIGURE 2
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Figure 2. Selective cancer killing activity of FRi-ExNC in vitro. (A) Western blotting of folate receptor α (FR-α) expression in various cancer and normal cells. (B) Quantitation of western blotting for FR-α from three independent experiments is shown on the right (mean ± s.e.m., n = 3), *P <0.05 (Student's t-test to HeLa). Cell viability assay showing dose- and time-dependent cytotoxicity of FRi-ExNC in (C) HeLa and (D) MCF7 cancer cells, but not in (E) MRC5 normal cells. Folate-conjugated nanocomplexes enhanced selective anticancer activity of i-Ex in FR-α-positive HeLa cells (mean ± s.e.m., n = 5), *P <0.05, **P <0.01 (two-way ANOVA test). (F) Crystal violet staining in control and nanocomplex-treated cells show that FRi-ExNC caused a stronger reduction of the colony-forming ability in HeLa cells. i-Ex concentration: 5 μg ml−1. (G) Quantitation from three independent experiments is shown on the right (mean ± s.e.m., n = 3), ***P <0.001 (Student's t-test). (H) Cell viability of HeLa cells treated with i-ExNC and FRi-ExNC for 4 h in the culture medium with or without folic acid (mean ± s.e.m., n = 5), *P <0.05, **P <0.01 (Student's t-test). Stronger cytotoxicity of FRi-ExNC in folate-free medium indicates its favorable tumor-targeting ability toward folic acid receptor-positive cancer cells. i-Ex concentration: 5 μg ml−1.

In vitro cytotoxicity of i-Ex and FRi-Ex nanocomplexes was evaluated with a water-soluble tetrazolium (WST)-based assay after 4 and 24 h treatments. A dose- and time-dependent cytotoxic response to i-ExNC and FRi-ExNC was observed in HeLa (FR+) cells (Figure 2C). Of note, FRi-ExNC showed greater toxicity at all doses as compared to i-ExNC, indicating a favorable folate targeting efficiency. In contrast, MCF7 (FR-) did not show any significant difference in viability in response to either i-ExNC or FRi-ExNC treatment (Figure 2D). Most importantly, the designed FRi-ExNC exhibited only negligible toxicity to normal fibroblasts, MRC5 (Figure 2E). We next performed long term viability (clonogenicity) assays following 6 h of treatment with either i-ExNC or FRi-ExNC. As shown in Figures 2F,G, FRi-ExNC caused a stronger decrease in colony-forming ability in HeLa cells. As folate is required for cell proliferation (47, 48), FRi-ExNC with the folate ligands on the outer surface would theoretically exhibit a higher affinity to the cells undergoing folate starvation. To test this, we incubated HeLa cells with i-ExNC/FRi-ExNC in a culture medium with or without folate for 4 h. As shown in Figure 2H, in the folate-rich medium, neither i-ExNC nor FRi-ExNC showed noticeable toxicity after 4 h of treatment. However, FRi-ExNC cytotoxicity was detected upon a subsequent culture in the folate-free medium; i-ExNC effect remained unchanged (Figure 2H). A conspicuous difference was observed when incubation time was prolonged to 24 h (Figure S2). These results demonstrated that FRi-ExNC could effectively kill FR-α positive cancer cells in vitro and was safe to normal cells.

Selective Cellular Uptake of FRi-ExNC by FR-α Positive Cancer Cells

In order to investigate whether such selective anticancer activity was mediated by folate receptor-mediated selective internalization, a hydrophobic fluorescein molecule (Nile Red) was co-assembled with i-Ex into the nanocomplexes and thus, fluorescent nanocomplexes could be used for bioimaging.

We first confirmed the expression of FR-α and its localization by immunostaining. As expected, HeLa cells showed higher levels of expression of FR-α, which was mostly expressed on the plasma membrane, compared with MCF7 cells (Figure 3A). We next incubated the cells with Nile Red-labeled i-ExNC (i-ExNCNR) and FRi-ExNC (FRi-ExNCNR) for 6 h to observe cellular uptake behavior. Fluorescence microscopy imaging revealed that as compared to i-ExNCNR, the folate-conjugated composite (FRi-ExNCNR) was more efficiently internalized by HeLa (FR+) cells (Figure 3B). Furthermore, we noticed nuclear staining of FRi-ExNCNR that overlapped with Hoechst staining (blue) suggesting that the small size of FRi-ExNC (diameter ≈10 nm) (Figure 1F) is suitable for its internalization into the nucleus. On the other hand, and as expected, MCF7 (FR-) cells did not show any difference in the uptake of nanocomplexes with or without folate (Figure 3B). We also performed an antagonist experiment by co-incubating the cells with an excess of folate (10 μm) and found a decrease in the cellular uptake of FRi-ExNC (Figure S3).

FIGURE 3
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Figure 3. Selective cellular uptake of FRi-ExNC by FR-α-positive cancer cells. (A) Immunostaining for FR-α shows cellular membrane and cytoplasm distribution of FR-α, and higher expression in HeLa cells. Nucleus was stained with Hoechst. (B) Fluorescence microscopy imaging of HeLa and MCF7 cells incubated with i-ExNC and FRi-ExNC (labeled with Nile Red) for 6 h. FRi-ExNC was more efficiently internalized by HeLa (FR+) cells. (C) Quantitative cellular uptake amount of i-ExNC and FRi-ExNC in HeLa and MCF7 cells after 6 h incubation (mean ± s.e.m., n = 3), **P <0.01 (Student's t-test). FRi-ExNC incubation showed increase in i-Ex uptake by HeLa (FR+) cells, but not MCF7 (FR-) cells.

Making use of the unique optical absorption peak of i-Ex (660 nm) at NIR region (Figure 1D), FRi-ExNC could be detected by UV-Vis-NIR spectroscopy with low noise background despite its presence in the cell lysate. We next determined the relative uptake efficiency of i-ExNC and FRi-ExNC by cells; cells treated with either of these compositions were subjected to lysis and spectrophotometric measurement of i-Ex. The quantitative results revealed that i-Ex uptake efficiency was increased ~2.5 times (from 0.76 of i-ExNC to 1.89 of FRi-ExNC) in HeLa (FR+) cells but remained unchanged in MCF7 (FR-) cells (Figure 3C). These data were consistent with fluorescence imaging results and demonstrated that FRi-ExNC could penetrate into cells via folate receptor-mediated endocytosis, which offer enhanced targeting of cancer cells.

FRi-ExNC Caused Stronger G2/M Arrest and Apoptosis in FR-α-Positive Cancer Cells

In order to obtain molecular insights into the anticancer activity of FRi-ExNC, we performed a cell cycle analysis and found a significant increase in the number of HeLa cells in the G2/M phase after FRi-ExNC treatment (Figure 4A). The growth arrest caused by FRi-ExNC (28% of cells in G2/M phase) was stronger than that caused by i-ExNC (20% of cells in G2/M phase), suggesting that the folate conjugate improved the potency of i-Ex (Figure 4B). The suppression of cell proliferation after nanocomplex treatment was also investigated by Ki-67 immunostaining, an established marker of cell proliferation. As shown in Figure S4A, FRi-ExNC-treated cells showed the strongest decrease in the number of Ki-67-positive cells. Quantitation of the results in the control, i-ExNC and FRi-ExNC groups showed 94.9, 49.0, and 23.6% Ki-67 positivity, respectively (Figure S4B). In order to test this further, we next examined the expression of Cyclin D1, Cyclin-dependent kinase 4 (CDK4), and p21WAF1, key regulators of cell cycle progression (49). Western blot analysis showed a stronger decrease in Cyclin D1 and CDK4 in FRi-ExNC- treated, as compared to i-ExNC-treated, cells (Figures 4C,D). Furthermore, the level of p21WAF1 was significantly upregulated in response to FRi-ExNC treatment (Figures 4C,D), further confirming the occurrence of growth arrest.

FIGURE 4
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Figure 4. FRi-ExNC caused stronger G2/M arrest and apoptosis in FR-α-positive HeLa cells. (A) Cell cycle analysis showing increase in cell population at G2/M arrest by FRi-ExNC treatment. Cells treated with i-ExNC do not show a similar increase at the equivalent dose. (B) Quantitation of cell cycle distribution from three independent experiments. (C) Western blotting for molecular markers of G2/M transition showing a stronger decrease in the expression of Cyclin D1 and CDK4 in FRi-ExNC-treated cells. p21WAF1 was up-regulated after FRi-ExNC treatment. (D) Quantitation from three independent experiments is shown below (mean ± s.e.m., n = 3), *P <0.05, **P <0.01, ***P <0.001 (Student's t-test to Control). (E) Flow cytometric analysis showing a greater increase in apoptotic cell numbers with FRi-ExNC treatment. (F) Quantitation of apoptotic cells from three independent experiments (mean ± s.e.m., n = 3), *P <0.05, **P <0.01 (Student's t-test). (G) Representative blots of apoptotic proteins. Treatment with FRi-ExNC shows a stronger decline in the levels of Bcl-2 and pro-caspase 3. A higher expression level of cleaved PARP-1 was observed in FRi-ExNC-treated cells. Quantitation (mean ± s.e.m., n = 3) is shown in (H). *P <0.05, **P <0.01, ***P <0.001 (Student's t-test to Control). HeLa cells for all the experiments were treated with equivalent dose of i-Ex (5 μg ml−1) for 24 h.

Since i-Ex has been shown to instigate apoptosis at high doses in cancer cells (1), we next examined apoptosis in the control and nanocomplex-treated cells by Annexin V/7-AAD double staining. As shown in Figure 4E, a higher extent of apoptosis was observed in FRi-ExNC-treated, as compared to i-ExNC-treated, cells (Figure 4E). Notably, with the aid of a folate ligand, the proportion of apoptotic cells was elevated from 4.3% (i-ExNC) to 13.5% (FRi-ExNC) (Figure 4F). Similarly, the amount of late apoptotic cells, as examined by TUNEL assay, was 54.4% in the FRi-ExNC-treated cells which was higher than 38.3% for the i-ExNC-treated cells (Figure S4C). Western blotting of proteins critical for apoptosis (50) also revealed that anti-apoptosis factors, B cell lymphoma 2 (Bcl-2), and pro-caspase 3, were downregulated in the FRi-ExNC-treated cells (Figures 4G,H). Immunostaining with a specific anti-cleaved caspase 3 antibody confirmed its upregulation in FRi-ExNC-treated cells (Figure S4D). Consistent with this, cleaved poly-ADP ribose polymerase (PARP)-1 (pro-apoptosis marker) also showed an increase (Figures 4G,H). Altogether, these results demonstrated that FRi-ExNC exerts anticancer activity by inducing cell cycle arrest and apoptosis, and folate conjugates enhanced its potency in FR-α-positive cancer cells.

In vivo Anticancer Effect of FRi-ExNC on Enhancing Selective Targeting of FR-α-expressing Tumors

We next performed in vivo assays to evaluate the anti-tumor effect of FRi-ExNC using a subcutaneous xenograft nude mouse model. As expected, MCF7 cells did not yield solid tumors. On the other hand, HT-29 cells formed tumors with a growth similar to HeLa cells. Due to these technical reasons and to compare the effect of FRi-ExNC on tumors with a similar growth rate, HT-29 and HeLa cells were used in vivo. HeLa (FR+) and HT-29 (FR-) tumor-bearing nude mice with an initial tumor volume of ~100 mm3 were randomly assigned to one of four groups that were administered an equivalent dose (50 mg Kg−1 Body Weight) of i-Ex alone or encapsulated in nanocomplexes (i-ExNC and FRi-ExNC) through intraperitoneal injections. Saline was used as a blank control. For both cell lines, tumors showed progressive growth and reached 1.1–1.4 cm (diameter) and a tumor volume of ~1,200 mm3 in about 22 days. i-Ex, i-ExNC, and FRi-ExNC treated mice showed delayed tumor growth as compared to the control group (Figure 5A). Furthermore, HeLa (FR+) tumors showed strong suppression in the FRi-ExNC treatment group as compared to the saline, i-Ex, and i-ExNC groups (Figure 5A). This could be attributed to selective targeting of HeLa (FR+) cells by FRi-ExNC. On the other hand, HT-29 (FR-) tumors also showed growth suppression in the FRi-ExNC group as compared to the saline control. However, the effect was comparable to i-Ex- and i-ExNC-treated groups (Figure 5B). The tumor inhibition rate in response to FRi-ExNC treatment reached 63.1% in the HeLa xenografts, which was much higher than those treated with i-Ex (18.4%) and i-ExNC (31.2%), whereas there was no significant difference between i-ExNC and FRi-ExNC treatments in the HT-29 xenografts (Figure 5C). These results clearly indicated that FRi-ExNC has the selectivity to impede FR-α-positive tumor progression in vivo. The significantly enhanced therapeutic efficacy of FRi-ExNC was highly consistent with the in vitro observations. In addition, there was no significant loss of body weight in the mice among all treatments (Figure 5D), demonstrating that FRi-ExNC has low systemic toxicity.

FIGURE 5
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Figure 5. In vivo anticancer effect of FRi-ExNC on enhancing selective targeting of FR-α-expressing tumors. Relative HeLa (A) and HT-29 (B) tumor volumes in different groups of mice during the course of treatment (mean ± s.e.m., n = 5), ***P <0.001 (two-way ANOVA test). Subcutaneous xenografts of HeLa (FR+) cells in nude mice treated with FRi-ExNC showed low tumor-forming capacity as compared to HT-29 (FR-) cells. (C) Inhibition rate of HeLa and HT-29 xenografts in nude mice with different treatments at the end of the experiment (mean ± s.e.m., n = 5), *P <0.05 (Student's t-test). The data indicates that FRi-ExNC has the selectivity to impede HeLa (FR+) tumor progression. (D) The average body weight of mice did not show any loss during treatments. All the treatments were performed with an equivalent dose of i-Ex (50 mg/Kg/2 days).

In summary, we have prepared a folate receptor-targeting nanocomplex loaded with i-Extract for enhancing its selective toxicity to cancer cells. The functionalized FRi-ExNC spontaneously assembled under physiological condition by simple sonication and was easily resuspended in water with sizes of ~10 nm. With the aid of folate ligands, FRi-ExNC showed a 3-fold higher cellular uptake and induced stronger cytotoxicity to FR-α-enriched cancer cells in vitro. In vivo anti-tumor assays showed that FRi-ExNC caused stronger tumor suppression of FR-α-positive xenografts. We propose FRi-ExNC as a suitable nanomedicine and platform to facilitate the use of Withania somnifera bioactives for cancer treatment and hence warrant further studies and clinical trials.

Data Availability

The raw data supporting the conclusions of this manuscript will be made available by the authors, without undue reservation, to any qualified researcher.

Ethics Statement

All animal experiments were performed in strict accordance with protocols approved by the Institutional Animal Care and Use Committee of AIST.

Author Contributions

RW and EM conceived and designed the experiments. YY and JW performed the experiments and collected and analyzed the data. YY, RW, SK, and EM prepared the manuscript. All authors discussed the results and contributed in writing the manuscript.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

This work was supported by the Japan Society for the Promotion of Science (JSPS) KAKENHI Grant-in-Aid for Scientific Research (B) (16H03834) & (A) (19H00857), the JSPS KAKENHI Grant-in-Aid for Challenging Exploratory Research (16K13632), and the JSPS KAKENHI Fund for the Promotion of Joint International Research (Fostering Joint International Research) (16KK0117). DAILAB is funded by the DBT (Government of India) and AIST (Japan).

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fonc.2019.00602/full#supplementary-material

References

1. Widodo N, Kaur K, Shrestha BG, Takagi Y, Ishii T, Wadhwa R, et al. Selective killing of cancer cells by leaf extract of Ashwagandha: identification of a tumor-inhibitory factor and the first molecular insights to its effect. Clin Cancer Res. (2007) 13:2298–306. doi: 10.1158/1078-0432.CCR-06-0948

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Widodo N, Priyandoko D, Shah N, Wadhwa R, Kaul SC. Selective killing of cancer cells by Ashwagandha leaf extract and its component Withanone involves ROS signaling. PLoS ONE. (2010) 5:e13536. doi: 10.1371/journal.pone.0013536

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Widodo N, Takagi Y, Shrestha BG, Ishii T, Kaul SC, Wadhwa R. Selective killing of cancer cells by leaf extract of Ashwagandha: components, activity and pathway analyses. Cancer Lett. (2008) 262:37–47. doi: 10.1016/j.canlet.2007.11.037

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Shah N, Kataria H, Kaul SC, Ishii T, Kaur G, Wadhwa R. Effect of the alcoholic extract of Ashwagandha leaves and its components on proliferation, migration, and differentiation of glioblastoma cells: combinational approach for enhanced differentiation. Cancer Sci. (2009) 100:1740–7. doi: 10.1111/j.1349-7006.2009.01236.x

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Vaishnavi K, Saxena N, Shah N, Singh R, Manjunath K, Uthayakumar M, et al. Differential activities of the two closely related withanolides, Withaferin A and Withanone: bioinformatics and experimental evidences. PLoS ONE. (2012) 7:e44419. doi: 10.1371/journal.pone.0044419

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Grover A, Singh R, Shandilya A, Priyandoko D, Agrawal V, Bisaria VS, et al. Ashwagandha derived withanone targets TPX2-Aurora A complex: computational and experimental evidence to its anticancer activity. PLoS ONE. (2012) 7:e30890. doi: 10.1371/journal.pone.0030890

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Nagalingam A, Kuppusamy P, Singh SV, Sharma D, Saxena NK. Mechanistic elucidation of the antitumor properties of Withaferin A in breast cancer. Cancer Res. (2014) 74:2617–29. doi: 10.1158/0008-5472.CAN-13-2081

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Stan SD, Hahm ER, Warin R, Singh SV. Withaferin A causes FOXO3a- and Bim-dependent apoptosis and inhibits growth of human breast cancer cells in vivo. Cancer Res. (2008) 68:7661–9. doi: 10.1158/0008-5472.CAN-08-1510

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Thaiparambil JT, Bender L, Ganesh T, Kline E, Patel P, Liu Y, et al. Withaferin A inhibits breast cancer invasion and metastasis at sub-cytotoxic doses by inducing vimentin disassembly and serine 56 phosphorylation. Int J Cancer. (2011) 129:2744–55. doi: 10.1002/ijc.25938

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Vyas AR, Singh SV. Molecular targets and mechanisms of cancer prevention and treatment by Withaferin A, a naturally occurring steroidal lactone. AAPS J. (2014) 16:1–10. doi: 10.1208/s12248-013-9531-1

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Wadegaonkar VP, Wadegaonkar PA. Withanone as an inhibitor of survivin: a potential drug candidate for cancer therapy. J Biotechnol. (2013) 168:229–33. doi: 10.1016/j.jbiotec.2013.08.028

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Wadhwa R, Singh R, Gao R, Shah N, Widodo N, Nakamoto T, et al. Water extract of Ashwagandha leaves has anticancer activity: identification of an active component and its mechanism of action. PLoS ONE. (2013) 8:e77189. doi: 10.1371/journal.pone.0077189

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Kataria H, Shah N, Kaul SC, Wadhwa R, Kaur G. Water extract of Ashwagandha leaves limits proliferation and migration and induces differentiation in glioma cells. Evid Based Complement Alternat Med. (2011) 2011:267614. doi: 10.1093/ecam/nep188

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Yu Y, Katiyar SP, Sundar D, Kaul Z, Miyako E, Zhang Z, et al. Withaferin-A kills cancer cells with and without telomerase: chemical, computational and experimental evidences. Cell Death Dis. (2017) 8:e2755. doi: 10.1038/cddis.2017.33

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Gao R, Shah N, Lee J-S, Katiyar SP, Li L, Oh E, et al. Withanone-rich combination of Ashwagandha withanolides restricts metastasis and angiogenesis through hnRNP-K. Mol Cancer Ther. (2014) 13:2930–40. doi: 10.1158/1535-7163.MCT-14-0324

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Chaudhary A, Kalra RS, Huang C, Prakash J, Kaul SC, Wadhwa R. 2,3-Dihydro-3β-methoxy Withaferin-A protects normal cells against stress: molecular evidence of its potent cytoprotective activity. J Nat Prod. (2017) 80:2756–60. doi: 10.1021/acs.jnatprod.7b00573

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Grimaldi N, Andrade F, Segovia N, Ferrer-Tasies L, Sala S, Veciana J, et al. Lipid-based nanovesicles for nanomedicine. Chem Soc Rev. (2016) 45:6520–45. doi: 10.1039/c6cs00409a

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Parveen S, Sahoo SK. Nanomedicine: clinical applications of polyethylene glycol conjugated proteins and drugs. Clin Pharmacokinet. (2006) 45:965–88. doi: 10.2165/00003088-200645100-00002

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Suk JS, Xu Q, Kim N, Hanes J, Ensign LM. PEGylation as a strategy for improving nanoparticle-based drug and gene delivery. Adv Drug Deliv Rev. (2016) 99:28–51. doi: 10.1016/j.addr.2015.09.012

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Chen S, Yang K, Tuguntaev RG, Mozhi A, Zhang J, Wang PC, et al. Targeting tumor microenvironment with PEG-based amphiphilic nanoparticles to overcome chemoresistance. Nanomedicine. (2016) 12:269–86. doi: 10.1016/j.nano.2015.10.020

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Paolino D, Accolla ML, Cilurzo F, Cristiano MC, Cosco D, Castelli F, et al. Interaction between PEG lipid and DSPE/DSPC phospholipids: an insight of PEGylation degree and kinetics of de-PEGylation. Colloids Surf B Biointerfaces. (2017) 155:266–75. doi: 10.1016/j.colsurfb.2017.04.018

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Khutoryanskiy VV. Beyond PEGylation: alternative surface-modification of nanoparticles with mucus-inert biomaterials. Adv Drug Deliv Rev. (2018) 124:140–9. doi: 10.1016/j.addr.2017.07.015

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Cosco D, Paolino D, De Angelis F, Cilurzo F, Celia C, Di Marzio L, et al. Aqueous-core PEG-coated PLA nanocapsules for an efficient entrapment of water-soluble anticancer drugs and a smart therapeutic response. Eur J Pharm Biopharm. (2015) 89:30–9. doi: 10.1016/j.ejpb.2014.11.012

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Cosco D, Mare R, Paolino D, Salvatici MC, Cilurzo F, Fresta M. Sclareol-loaded hyaluronan-coated PLGA nanoparticles: physico-chemical properties and in vitro anticancer features. Int J Biol Macromol. (2019) 132:550–7. doi: 10.1016/j.ijbiomac.2019.03.241

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Yu Y, Nishikawa M, Liu M, Tei T, Kaul SC, Wadhwa R, et al. Self-assembled nanodiamond supraparticles for anticancer chemotherapy. Nanoscale. (2018) 10:8969–78. doi: 10.1039/c8nr00641e

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Yu Y, Yang X, Liu M, Nishikawa M, Tei T, Miyako E. Amphipathic nanodiamond supraparticles for anticancer drug loading and delivery. ACS Appl Mater Interfaces. (2019) 11:18978–87. doi: 10.1021/acsami.9b04792

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Matsumura Y, Maeda H. A new concept for macromolecular therapeutics in cancer chemotherapy: mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs. Cancer Res. (1986) 46:6387–92.

PubMed Abstract | Google Scholar

28. Maeda H, Tsukigawa K, Fang J. A retrospective 30 years after discovery of the enhanced permeability and retention effect of solid tumors: next-generation chemotherapeutics and photodynamic therapy–problems, solutions, and prospects. Microcirculation. (2016) 23:173–82. doi: 10.1111/micc.12228

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Di Francesco M, Celia C, Primavera R, D'Avanzo N, Locatelli M, Fresta M, et al. Physicochemical characterization of pH-responsive and fusogenic self-assembled non-phospholipid vesicles for a potential multiple targeting therapy. Int J Pharm. (2017) 528:18–32. doi: 10.1016/j.ijpharm.2017.05.055

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Cheung A, Bax HJ, Josephs DH, Ilieva KM, Pellizzari G, Opzoomer J, et al. Targeting folate receptor alpha for cancer treatment. Oncotarget. (2016) 7:52553–74. doi: 10.18632/oncotarget.9651

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Kurosaki A, Hasegawa K, Kato T, Abe K, Hanaoka T, Miyara A, et al. Serum folate receptor alpha as a biomarker for ovarian cancer: Implications for diagnosis, prognosis and predicting its local tumor expression. Int J Cancer. (2016) 138:1994–2002. doi: 10.1002/ijc.29937

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Chen YL, Chang MC, Huang CY, Chiang YC, Lin HW, Chen CA, et al. Serous ovarian carcinoma patients with high alpha-folate receptor had reducing survival and cytotoxic chemo-response. Mol Oncol. (2012) 6:360–9. doi: 10.1016/j.molonc.2011.11.010

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Kalli KR, Oberg AL, Keeney GL, Christianson TJH, Low PS, Knutson KL, et al. Folate receptor alpha as a tumor target in epithelial ovarian cancer. Gynecol Oncol. (2008) 108:619–26. doi: 10.1016/j.ygyno.2007.11.020

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Yao C, Evans CO, Stevens VL, Owens TR, Oyesiku NM. Folate receptor alpha regulates cell proliferation in mouse gonadotroph alphaT3-1 cells. Exp Cell Res. (2009) 315:3125–32. doi: 10.1016/j.yexcr.2009.05.006

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Doucette MM, Stevens VL. Folate receptor function is regulated in response to different cellular growth rates in cultured mammalian cells. J Nutr. (2001) 131:2819–25. doi: 10.1093/jn/131.11.2819

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Hou Z, Gattoc L, O'Connor C, Yang S, Wallace-Povirk A, George C, et al. Dual targeting of epithelial ovarian cancer via folate receptor alpha and the proton-coupled folate transporter with 6-substituted pyrrolo[2,3-d]pyrimidine antifolates. Mol Cancer Ther. (2017) 16:819–30. doi: 10.1158/1535-7163.MCT-16-0444

CrossRef Full Text | Google Scholar

37. Ledermann JA, Canevari S, Thigpen T. Targeting the folate receptor: diagnostic and therapeutic approaches to personalize cancer treatments. Ann Oncol. (2015) 26:2034–43. doi: 10.1093/annonc/mdv250

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Zwicke GL, Mansoori GA, Jeffery CJ. Utilizing the folate receptor for active targeting of cancer nanotherapeutics. Nano Rev. (2012) 3:1–11. doi: 10.3402/nano.v3i0.18496

PubMed Abstract | CrossRef Full Text | Google Scholar

39. van Dam GM, Themelis G, Crane LM, Harlaar NJ, Pleijhuis RG, Kelder W, et al. Intraoperative tumor-specific fluorescence imaging in ovarian cancer by folate receptor-alpha targeting: first in-human results. Nat Med. (2011) 17:1315–9. doi: 10.1038/nm.2472

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Pasut G, Canal F, Dalla Via L, Arpicco S, Veronese FM, Schiavon O. Antitumoral activity of PEG-gemcitabine prodrugs targeted by folic acid. J Control Release. (2008) 127:239–48. doi: 10.1016/j.jconrel.2008.02.002

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Paolino D, Licciardi M, Celia C, Giammona G, Fresta M, Cavallaro G. Folate-targeted supramolecular vesicular aggregates as a new frontier for effective anticancer treatment in in vivo model. Eur J Pharm Biopharm. (2012) 82:94–102. doi: 10.1016/j.ejpb.2012.06.001.

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Licciardi M, Paolino D, Celia C, Giammona G, Cavallaro G, Fresta M. Folate-targeted supramolecular vesicular aggregates based on polyaspartyl-hydrazide copolymers for the selective delivery of antitumoral drugs. Biomaterials. (2010) 31:7340–54. doi: 10.1016/j.biomaterials.2010.05.060.

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Zhang M, Zhou X, Iijima S, Yudasaka M. Small-sized carbon nanohorns enabling cellular uptake control. Small. (2012) 8:2524–31. doi: 10.1002/smll.201102595

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Han X, Liu J, Liu M, Xie C, Zhan C, Gu B, et al. 9-nitro-camptothecin-loaded folate-conjugated polymer micelles as tumor targeted drug delivery system: preparation and evaluation in vitro. Int J Pharm. (2009) 372:125–31. doi: 10.1016/j.ijpharm.2008.12.035

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Hayama A, Yamamoto T, Yokoyama M, Kawano K, Hattori Y, Maitani Y. Polymeric micelles modified by folate-PEG-lipid for targeted drug delivery to cancer cells in vitro. J Nanosci Nanotechnol. (2008)8:3085–90. doi: 10.1166/jnn.2008.093

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Guo Y, Chen W, Wang W, Shen J, Guo R, Gong F, et al. Simultaneous diagnosis and gene therapy of immuno-rejection in rat allogeneic heart transplantation model using a T-cell-targeted theranostic nanosystem. ACS Nano. (2012) 6:10646–57. doi: 10.1021/nn3037573

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Courtemanche C, Elson-Schwab I, Mashiyama ST, Kerry N, Ames BN. Folate deficiency inhibits the proliferation of primary human CD8+ T lymphocytes in vitro. J Immunol. (2004) 173:3186–92. doi: 10.4049/jimmunol.173.5.3186

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Zhang XM, Huang GW, Tian ZH, Ren DL, Wilson JX. Folate stimulates ERK1/2 phosphorylation and cell proliferation in fetal neural stem cells. Nutr Neurosci. (2009) 12:226–32. doi: 10.1179/147683009X423418

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Lim S, Kaldis P. Cdks, cyclins, and CKIs: roles beyond cell cycle regulation. Development. (2013) 140:3079–93. doi: 10.1242/dev.091744

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Danial NN, Korsmeyer SJ. Cell death: critical control points. Cell. (2004) 116:205–19. doi: 10.1016/S0092-8674(04)00046-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: Withania somnifera, folic acid, i-Extract, nanomedicine, chemotherapy

Citation: Yu Y, Wang J, Kaul SC, Wadhwa R and Miyako E (2019) Folic Acid Receptor-Mediated Targeting Enhances the Cytotoxicity, Efficacy, and Selectivity of Withania somnifera Leaf Extract: In vitro and in vivo Evidence. Front. Oncol. 9:602. doi: 10.3389/fonc.2019.00602

Received: 14 March 2019; Accepted: 18 June 2019;
Published: 04 July 2019.

Edited by:

Brian Gabrielli, University of Queensland, Australia

Reviewed by:

Felisa Cilurzo, Università degli Studi G. d'Annunzio Chieti e Pescara, Italy
Frederick E. Williams, University of Toledo, United States

Copyright © 2019 Yu, Wang, Kaul, Wadhwa and Miyako. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Renu Wadhwa, renu-wadhwa@aist.go.jp; Eijiro Miyako, e-miyako@aist.go.jp

These authors have contributed equally to this work