Review: Mechanisms and perspective treatment of radioresistance in non-small cell lung cancer

Radiotherapy is the major treatment of non-small cell lung cancer (NSCLC). The radioresistance and toxicity are the main obstacles that leading to therapeutic failure and poor prognosis. Oncogenic mutation, cancer stem cells (CSCs), tumor hypoxia, DNA damage repair, epithelial-mesenchymal transition (EMT), and tumor microenvironment (TME) may dominate the occurrence of radioresistance at different stages of radiotherapy. Chemotherapy drugs, targeted drugs, and immune checkpoint inhibitors are combined with radiotherapy to treat NSCLC to improve the efficacy. This article reviews the potential mechanism of radioresistance in NSCLC, and discusses the current drug research to overcome radioresistance and the advantages of Traditional Chinese medicine (TCM) in improving the efficacy and reducing the toxicity of radiotherapy.


Introduction
Radiotherapy is the mainstay of treatment for patients with non-small cell lung cancer (NSCLC), and usually combined with surgery, chemotherapy, immunotherapy, and targeted therapy (1)(2)(3)(4)(5)(6). The radiation commonly used in radiotherapy mainly includes photo radiation, such as X-ray and g-ray and particle rays such as neutrons, electrons, protons and heavy ions (2,(7)(8)(9)(10). However, no matter what radiation and dose segmentation methods are used, radioresistance will inevitably occur, leading to radiotherapy failure and local recurrence. Simply increasing the radiation dose does not improve survival benefits but leads to adverse reactions and poor prognosis (11).
Targeted drugs or small molecule drugs combined with radiotherapy are used in the treatment of NSCLC. However, there is no systematic review on the mechanism of radioresistance and radiosensitizers of NSCLC. Therefore, we will discuss the radioresistance mechanisms of NSCLC and the study of drugs that can enhance the efficacy and reduce the toxicity of radiotherapy, especially TCM. So as to provide a theoretical basis for clinical development of anti-tumor drugs in combination with radiotherapy.

Mechanisms of acquired radioresistance
Acquired radioresistance occurs mainly with radiation induction, the underlying mechanisms involve DNA damage repair and EMT in cancer cell itself, as well as changes in TME such as inflammation, immune response, tumor metabolic reprogramming etc. (15,16,19,(30)(31)(32). Acquired radioresistance may enhance invasion and metastasis of surviving cancer cells after primary radiotherapy and affect the prognosis and life quality of patients.
It can be seen from the above that tumor cells have multiple ways to repair radiation-induced DNA damage. Drugs targeting a single target may not have obvious effect on overcoming radioresistance, and are prone to drug resistance. Therefore, the combination of multiple targets for DNA repair will be the direction of tumor treatment in the future, but how to effectively combine the targets still needs more research.

Tumor microenvironment remodeling and radioresistance
Tumor microenvironment (TME) is closely related to tumor progression, and the remodeling of TME after radiotherapy can lead to radioresistance (18). Here, we focus on the effects of inflammation and immune response, tumor microbiota, tumor metabolic reprogramming, and cell senescence on TME to clarify the role of radiation-induced TME remodeling in the radioresistance of NSCLC (Figure 2).

Inflammation and immune response
Radiation generated ROS and RNS can activate NF-kB, Janusassociated kinase (JAK)2/signal transducer and activator of transcription (STAT)3 pathway to increase the release of growth TME remodeling may lead to radioresistance of NSCLC. The TME changed in NSCLC cells surviving after radiotherapy. Radiation induced inflammation and immune response can cause immunosuppression. The local lung microbiota can induce tumor growth by regulating the immune cells. Tumor metabolic reprogramming after radiation will lead to increase of acidity, hypoxia, and GSH production, unbalance of ferroptosis, and redox homeostasis maintaining, being conductive to tumor growth. Cell senescence after radiotherapy can also induce cell proliferation and tumor growth. The above factors together form TME remodeling that promotes tumor growth, metastasis and recurrence after radiotherapy. (This figure is adapted from an image created from BioRender.com).
factors and cytokines, such as VEGF, TGF-b, IL-1, IL-8, TNF-a and IL-6 etc. (15, 31, 55, 56), which are involved in inflammation and immune response (18,(57)(58)(59)(60). TGFb and TNFa in TME are very important in the formation and development of tumor (61). Our previous study found that irradiation of NSCLC cell lines A549 and H1299 can cause overexpression of TGFb and TNFa, resulting in HIF1a activation and cause genomic instability of BMSCs and may promote tumor progression (62). We also found that TGFb mainly causes short-term side effects, while TNFa mainly causes long-term side effects. This may provide a guideline for clinical use of combined drugs at different stages of radiotherapy for NSCLC. In addition, radiation-induced inflammation reduces tumor-suppressing immune cells such as CD4+T cells, CD8+T cells, and natural killer (NK) cells, while tumor-promoting immune cells such as regulatory T cells (Treg), myeloid-derived suppressor cells (MDSC), and M2 tumorassociated macrophages (TAMs) increase, eventually forming an immunosuppressive environment, and high level of TGFb (19,63). Moreover, M2 macrophages and B cells infiltrate into TME also participate in the radioresistance of NSCLC (64, 65). Thus targeting inflammation not only enhance the tumor killing effects of radiotherapy, but also protect the normal cells and tissues from radiation-induced bystander effects.

Tumor microbiota
It is well known that intestinal microbiome can regulate host physiological and pathological processes through metabolism, inflammation and immune response (66, 67). On the one hand, tumor microbiota can enhance anti-tumor immunity through STING signal activation, T and NK cell activation. On the other hand, it can upregulate ROS, induce anti-inflammatory environment, and inactivate T cell to promote immunosuppression and cancer progression (68). Moreover, tumor microbiota stimulates gdT cells to produce IL-17 that triggering inflammation and cancer progression (69), and increases Th17 cells that enhancing lung cancer proliferation and angiogenesis (70). It is found that the dysbiosis of local lung microbiota in patients with advanced lung cancer can lead to Th1, Th17, gdT cells and PD-1 positive T cells increase, neutrophils recruitment, dendritic cells (DCs) activation, CD4+T cells decrease, cytokines IL-1, IL-1b, IL-6, IL-17, IL-23 upregulation, as well as upregulation of ERK/MAPK and inflammation pathways, all these above alterations promoted tumor progression (71). Although there is no research report on the correlation between tumor microbiota and radioresistance, there is no doubt that tumor microbiota will participate in tumor response to radiotherapy through inflammation and immune response and affect the final efficacy. The microbiome may serve as an indicator for cancer diagnosis or prognostic assessment and could be used as potential targets to develop new cancer therapies.

Tumor metabolic reprogramming
Tumor metabolic reprogramming after radiotherapy, such as glucose metabolism, lipid metabolism, and redox metabolism, contributes to TME remodeling and acquired radioresistance (19). The increased expression of glucose transporter1 (GLUT1), pyruvate kinase M2 isoform (PKM2), and lactate dehydrogenase (LDHA) after irradiation promoted glycolysis (19,72,73), while the expression of glycogen synthetase 1 (GYS1) was also up-regulated, leading to glycogen accumulation (74). These changes enable cancer cells to survive, proliferate and resist radiation. In addition, pentose phosphate pathway (PPP) after radiation induced more NADPH production, which promoted the production of reduced glutathione (GSH) (19), may lead to radioresistance of NSCLC.
IR can induce the expression of ACSL4, which is a lipid metabolizing enzyme in cancer cells, to increase lipid peroxidation and ferroptosis (75). Intriguingly, IR can also induce the expression of ferroptosis inhibitors SLC7A11 and GPX4, causing radioresistance (75). Perhaps, radioresistant cells have formed a balance between promoting ferroptosis and inhibiting ferroptosis, enabling cells to survive. In radioresistant lung cancer cells, the expression of lipid Droplet (LD) and ferritin heavy chain (FTH1) increased and correlated with each other, which can be targeted and synergistically inhibit tumor radioresistance (76). In addition, the activation of sPLA2-PKCd-MAPKs-cPLA2a pathway promoted tumor progression and radioresistance in NSCLC (77).
In conclusion, NSCLC cells that survived after radiation have altered metabolism that favors cell proliferation and tumor progression. Therefore, targeting tumor metabolism will be an effective measure to improve the radiotherapy prognosis and survival rate of NSCLC patients.

Cell senescence
Studies have shown that induction of premature senescence can radiosensitize NSCLC cells (80). On the contrary, the cytokines secreted by senescent cells which not killed by radiation will affect the adjacent surviving cancer cells in TME, stimulate tumor cell proliferation, invasion and metastasis, escape apoptosis, induce angiogenesis, and promote tumor phenotype (20). In addition, lung cancer cells survived from radiotherapy experienced senescence and entered a dormant state, reprogrammed their biology months or years after irradiation, reactivated stemness, and produced tumors with enhanced growth and metastasis (81).
To sum up, the TME itself is inflammatory, radiation further promotes the release of inflammatory factors, aggravates inflammatory reaction, causes immunosuppression, and hinders anti-tumor immunity. In addition, tumor microbiota can activate inflammatory pathways to promote tumor progression. Moreover, the oxidative stress reaction induced by radiation promotes the occurrence of tumor metabolism reprogramming, causes the depletion of T cells, and makes tumor cells resistant to radiation. The senescent cells in TME can promote tumor proliferation, invasion and metastasis by secreting cytokines. The interaction of the above factors leads to TME remodeling and radioresistance. In addition to these above, tumor hypoxia also play a key role in TME. It is a challenge to overcome radioresistance by targeting TME, because any single targeting action may not achieve the desired therapeutic effect.

Mechanisms of inherent radioresistance
Inherent radioresistance is an important factor leading to radiotherapy failure, which is mainly related to the gene mutation status of tumor cells, hypoxia status, distribution of CSCs (28, 92, 93), etc.
EGFR is overexpressed in 40% to 80% of patients with NSCLC and is associated with poor prognosis (101,102). Radiation can stimulate wild-type EGFR to enter nucleus and bind with DNA-PK catalytic subunit (DNA-PKcs) to promote DNA repair, thus leading to radioresistance of NSCLC (103, 104). However, the NSCLC with Mechanisms of EMT contributes to radioresistance in NSCLC. The surviving cells included enriched CSCs subpopulations that highly expressed CSCs markers (CD24, CD44, CD133, and CD166). miR-30b was upregulated and targeted to FBXL14, activating the transcription factor Twist1, resulting in increased expression of Vimentin, N-cadherin and Fibronectin, and decreased E-cadherin expression. Integrin b1 is overexpressed after radiotherapy and targets YAP1 to activate ATM/Chk2 signaling, leading to EMT. Furthermore, RAC1 is upregulated in radioresistant NSCLCs, activates the RAC1/PAK1/ LIMK1/Cofilins pathway and the PAK1/Snail pathway, causes EMT and promotes tumor metastasis and invasion. LKB1/SIK1 signaling is downregulated after radiotherapy, prompting activation of the transcription factor ZEB1, leading to EMT and tumor metastasis and invasion. (This figure is adapted from an image created from BioRender.com). mutant EGFR is not necessarily more sensitive to radiation (94), since the mutant EGFR can trigger the downstream pathways, including extracellular signal-regulated kinase (RAS/ERK), p38MAPK, c-Jun Nterminal kinase (JNK), and ERK5, and also activate PI3K/AKT/ mTOR signaling pathway, leading to cell proliferation and antiapoptosis, migration, DNA repair, cell cycle arrest, etc., which in turn increases the radioresistance of NSCLC (22, 23, 103, 105-108).
KRAS can regulate cell growth, differentiation and apoptosis, its mutations mainly occur at codons 12 and 13, and have been found approximately in 20-30% of NSCLC tumor samples (109). KRASmutant NSCLC cells are more radioresistant than KRAS wild-type cells (96,110) or EGFR-mutant cells (21), because mutant KRAS can upregulate RAD51 expression through oncogene MYC, thereby enhancing DNA damage repair and cell survival (111). In addition, EGFR-dependent chromatin condensation, namely mitotic-like concentrated chromatin (MLCC), can protect KRAS-mutant NSCLC cells from ionizing radiation (IR)-induced DSBs and premature senescence (110), and enhance the expression of CSC marker protein CD133 via osteopontin/EGFR pathway, promoting tumor invasion and radioresistance (112). KEAP1/nuclear factor E2-related factor (NRF2) mutation happens approximately 30% of NSCLC (92), and 7% of patients have co-mutations of KEAP1/NRF2 and EGFR (113). Mutant KEAP1 lost its inhibitory effect on NRF2 in cytoplasm, the activated NRF2 translocated to the nucleus and activated the expression of antioxidant proteins by binding to antioxidant-responsive elements (AREs), resulting in the scavenging of ROS and anti-apoptosis of tumor cells, leading to unlimited proliferation, metastasis and radioresistance of NSCLC (114)(115)(116).
TP53 mutation occurs in more than half of human cancers, including NSCLC (92). p53 can not only induce cell cycle arrest, senescence, and apoptosis, but also regulate tumor metabolism, promote ferroptosis, and inhibit tumor development (117). Mutant p53 can neither induce the expression of pro-apoptotic protein Bax, nor inhibit the expression of anti-apoptotic proteins (Bcl-2, Bcl-xl) (118), which makes cancer cells survive in radiotherapy (119). Compared with single mutations in TP53, NSCLC with comutation in KRAS and TP53, or co-mutation in TP53 and KEAP1 are more resistance to IR-induced cell death (100, 114).
In addition to the oncogenic mutation, high levels of inhibitor of apoptosis proteins, such as cIAP1/2, XIAP, and survivin, participate in cell death and survival by binding and inhibiting caspases, leading to radioresistance of NSCLC (120)(121)(122)(123). In addition, microRNAs can also affect the radiosensitivity of NSCLC by regulating the cell proliferation and apoptosis. miR-99a and miR-770-5p can induce apoptosis and improve radiosensitivity (124,125). On the contrary, miR-410 and miR-208a promote radioresistance by inducing EMT and increasing cell proliferation respectively in NSCLC (126, 127). According to the potential mechanism of inherent radioresistance mentioned above, genome sequencing can be carried out before treatment to determine the mutation type and formulate effective treatment strategies, so as to improve the tumor-killing rate and reduce the tumor recurrence rate after primary radiotherapy of NSCLC.

Cancer stem cells and radioresistance
Cancer stem cells (CSCs) are subpopulations of tumor cells with the ability to self-renew and differentiate into heterogeneous tumor cells, promote tumor growth and metastasis through unlimited proliferation and migration, leading to tumor recurrence and treatment failure (128)(129)(130)(131). Antioxidant signaling pathways (NRF2, Wnt, etc.) in CSCs are activated, and more antioxidant proteins are expressed to clear ROS, so as to maintain a low level of ROS in cells, which contributes to the quiescence and self-renewal of CSCs (130, 132-134) ( Figure 5). In addition, CSCs have a strong ability to repair DNA damage (135). CD133 is one of the markers of CSCs. As early as 2006, Bao et al. reported that CD133-positive glioma cells showed higher expression of DNA damage checkpoint proteins (i.e. ATM, Rad17, Chk1 and Chk2) than CD133-negative cells (136). In 2014, Desai et al. clarified that CD133-positive NSCLC cells highly express DNA damage repair proteins RAD51 and Exo1, which can promote radioresistance, but had cell type specificity (137). Therefore, low levels of ROS and enhanced DNA damage repair make CSCs insensitive to radiotherapy, leading to tumor relapse (138). CD44 is another CSCs marker, which is related to tumor recurrence and metastasis, as well as prediction of the outcome after radiotherapy (139,140). The overexpression of CD44 promotes the proliferation of NSCLC, and up-regulates the expression of PD-L1 to promote tumorigenesis, immunosuppression and chemotherapy resistance (141,142). It is worth noting that due to the low sensitivity of CSCs to IR, the CSCs not killed by radiation will be enriched, which leads to acquired radioresistance. Therefore, the treatment efficiency of NSCLC can be improved by inducing CSCs to differentiate to reduce their proportion in tumor tissues, or by combining drugs targeting key proteins of CSCs antioxidant pathways or surface marker proteins with radiotherapy.

Tumor hypoxia and radioresistance
As one of the cancer hallmarks, hypoxia induces angiogenesis, tumor invasion, metastasis, and treatment resistance (27, 28). Hypoxic tumor cells are very insensitive to radiation (143). In this article, we mainly introduce the research on HIFs and radioresistance in NSCLC ( Figure 6). Hypoxia environment and radiation activate HIFs (144, 145), activated HIF-1a and its partner subunits HIF-1b enter nucleus and bind to hypoxia-responsive element (HRE) to trigger gene transcription regulating VEGF and glucose metabolism etc., leading to cell survival (146)(147)(148). HIF-2a mainly induces angiogenic factors, such as VEGF, VEGFR, EGFR etc., promoting angiogenesis and tumor growth (149-151). Research showed that the upregulation of HIF-1a enhanced the radioresistance of NSCLC (152). Conversely, the decrease of HIF-1a in acidic environment caused radioresistance in NSCLC cells and blocking simultaneously of both HIF-1a and HIF-2a radiosensitized NSCLC, suggesting the role of HIF-2a in radioresistance (153). In addition, miR-210 promoted the hypoxic phenotype of NSCLC cells and increased radioresistance by inducing and stabilizing HIF-1a (154). By contrast, another microRNA, miR-320a targeted HIF-1a to promote methylation of PTEN, thereby reducing the radioresistance of NSCLC in vitro and in vivo (155). In conclusion, targeting HIFs may enhance radiosensitivity of NSCLC in clinical, but the pH value should be considered when targeting HIF-1a.
4 Radiosensitizing non-small cell lung cancer As we discussed above, the mechanisms of radioresistance of NSCLC are complex and not isolated from each other. Whether surgery, chemotherapy, targeted therapy, or immunotherapy, the goal of their combination with radiotherapy is to kill tumor cells, but what cannot be avoided is limited effect, tumor recurrence and metastasis, as well as side effects.
At present, chemotherapy drugs, targeted drugs, immune checkpoint inhibitors, etc. can be used as radiosensizitizers in NSCLC, but these drugs are prone to drug resistance and toxic side effects (11,30,156,157). In addition, most of the current studies about radiosensitizers used in NSCLC is still limited to experimental research, and only a few drugs have been used in clinical. We summarized the drugs or agents for NSCLC radiosensitization in Table 1, including antibody drugs and small molecule inhibitors from non-natural sources. In addition to drug toxicity, radiotherapy itself can also cause lung toxicity in patients, manifesting as different grades of pneumonia, pulmonary fibrosis (32, 183). In addition, the mechanisms of radioresistance are complex, and the efficacy of these single targeted drugs is limited. Therefore, it is an urgent need to develop drugs targeting multiple targets, with synergistic effects and low toxicity in NSCLC radiotherapy.

Application and advantages of TCM in radiotherapy for NSCLC
As an auxiliary means of radiotherapy for NSCLC, TCM can increase the apoptosis of cancer cells, inhibit tumor metastasis, enhance the anti-tumor immunity of patients, regulate the TME homeostasis, thus improving the efficacy of radiotherapy and reducing the recurrence rate (184,185), which reflecting the basic principles of treating tumor by reinforcing healthy qi to eliminate pathogenic factors of TCM. Some single herbs are frequently used in the treatment of NSCLC (186). Commonly used TCM for reinforcing healthy qi to eliminate pathogenic factors include Ginseng, Codonopsis pilosula, Astragalus, Angelica, and Polygonatum, etc. Astraglus has immunoregulatory, antioxidant, anti-inflammatory, and anti-cancer activities and combined with chemotherapy to increase the efficacy and reduce the toxicity in patients with advanced NSCLC (187,188). Our previous research found that Astragalus polysaccharides can reduce the radiation induced AND-1 CH-3 compound In vitro and in vivo Inhibition of AND-1 will be a promising strategy for enhancing radiosensitivity in NSCLC. (42)

RUVBL1/2 Compound B
In vitro and in vivo RUVBL1/2 inhibition combined with radiotherapy may be effective treatment for NSCLC.
Targeting cell cycle

BET JQ1
In vitro and in vivo BET inhibition may be a potential treatment for radiosensitizing NSCLC.

CDK4/6 Abemaciclib
In vitro and in vivo Abemacilcib combined with radiotherapy radiosensitized NSCLC in preclinical models.
Targeting inflammation

IKKb IMD03544
In vitro and/or in vivo Blockade of IKK-NF-kB signaling will be benefit for radiotherapy in NSCLC.

TGF-b LY364947
In vitro and in vivo TGF-b inhibition combined with radiotherapy enhanced therapeutic efficacy in NSCLC.

STAT3 Niclosamide
In vitro and in vivo Inhibition of STAT3 signaling will be effective treatment for NSCLC to radiotherapy. (59)

JAK2 TG101209
In vitro and in vivo Targeting JAK2 may enhance radiotherapy response in KRASmutant NSCLC.
Targeting immune suppression PD-L1 anti-PD-L1 antibody In vitro and in vivo Anti-PD-L1 antibody combined with radiotherapy synergistically enhanced anti-tumor immunity in NSCLC.

Clinical
Heat-clearing and toxin-removing, eliminating stasis and resolve masses. Aidi injection improved PSF and immune function in lung cancer patients and alleviated the myelosuppression, radiation pneumonitis, radiation esophagitis. (197,198) Shengqi Fuzheng injection Compound prescription, composed of extracts from Codonopsis and Astragalus.
Clinical Supplement and tonify lung qi. Reduced the inflammatory response and improved immune function by regulating the expression of TNF-a and TGF-b. (199)

Compound kushen injection
Compound prescription, composed of extracts from Sophorae and Rhizoma Smilacis Glabrae.

Clinical
Clear heat and drain dampness, resolve masses and alleviate pain. Improved efficacy and reduced radiation pneumonitis, radiation esophagitis, and myelosuppression.
Kangai injection Compound prescription, composed of extracts from Astragalus, Ginseng, and Oxymatrine.

In vitro
Increased FOXO3a-mediated apoptosis and autophagic cell death in cisplatin-resistance A549 cells. Frontiers in Immunology frontiersin.org bystander effects (RIBE) of bone marrow mesenchymal stem cells (BMSCs) caused by X-rays and heavy ions, and reduce the toxicity of normal cells and tissues in lung cancer radiotherapy (189)(190)(191). In addition, our research also found that Guiqi Baizhu Decoction, which composed of Astragalus, Angelica, Atractylodes, Paeonia lactiflora, Tangerine peel, Rhubarb, and Licorice, can significantly reduce the radiation inflammatory reaction and immune damage, and prevent intestinal microbial imbalance and metabolic disorders caused by radiation (192). We further found that Guiqi Baizhu Decoction can regulate HIF-1a, AQP4 and Na+/K+-ATPase to reduce hypoxia and oxidative stress, thus treating radiation-induced intestinal edema (193). Moreover, in the study of gastric cancer, we used chemical informatics and cell experiments to verify that Guiqi Baizhu decoction plays a dual role of anti-tumor and immunoregulation by targeting HER2 and PD-L1 through its active components quercetin and isorhamnetin respectively, reflecting the mechanism of multipoint and synergistic effect of TCM in tumor treatment (194). In recent decades, the advantages of natural products in antitumor have become more and more obvious, such as paclitaxel (195) and vinorelbine (196) has been used in clinical for decades. Here we listed the application of TCM compound prescription, single herb, herbal extracts, and small molecules from TCM in the preclinical and clinical research of radiotherapy toxicity reduction and efficiency enhancement for NSCLC ( Table 2). The various factors that cause radioresistance are not independent, nor only appear in a certain period of time. Moreover, at different stages of radiotherapy, the mechanism that dominates radioresistance is variable and complex. However, TCM can adjust the radiation anti-tumor effect in different ways with the advantage of multi-component and multi-target, improve the efficacy of radiotherapy, reduce the toxicity of radiotherapy and improve the quality of life of patients.

Conclusions
In conclusion, the radioresistance mechanisms of NSCLC are complex. Therefore, prior to radiotherapy gene sequencing should be performed for NSCLC patients to determine the type of mutation, or abnormally expressed genes, proteins, and signaling pathways, thus to develop more effective treatment strategies. In the early stage of radiotherapy, it is suggested to combine EGFR, KRAS and other mutant targeted drugs, drugs to improve DNA damage, immune checkpoint drugs or drugs to target hypoxia. In the middle and late stage of radiotherapy, it is suggested that the combination of drugs targeting EMT or regulating TME can improve the curative effect. TCM can run through the whole radiotherapy process. However, the specific mechanism of TCM in the sensitization of NSCLC radiotherapy needs to be further explored. The combination of Astragalus polysaccharide Herbal extractions from Astragalus.

In vitro
Micheliolide enhanced radiosensitivity via inducing the ubiquitination degradation of HIF-1a in p53-null NSCLC.
Quercetin Small molecule, derived from a variety of TCM such as Bupleurum, Hypericum, Astragalus, etc.
Isorhamnetin Small molecule, derived from a variety of TCM such as Folium Ginkgo, Astragalus, etc.

In vitro
Upregulated IL-13, suppressed NF-kB signaling and increased cell apoptosis.
Cucurbitacin I Small molecule, mainly distributed in Cucurbitaceae.

In vitro and in vivo
Inhibition of STAT3 signaling in CD133-positive NSCLC may enhance radiotherapy effect.

In vitro
Induce lung cancer cell apoptosis via inhibiting survivin.

In vitro
Celastrol radiosensitized NSCLC by suppressing the ATP-binding activity of Hsp90.
Curcumin Small molecule, isolated from Curcuma longa L.

In vitro and in vivo
Promoted cell apoptosis via down-regulating AKT/mTOR pathway.
effective small molecules extracted from TCM and radiotherapy may provide a new application prospect for the future clinical treatment of NSCLC.

Author contributions
TZ is responsible for literature review and article writing. LZ and JH are responsible for revising articles. ZM, YYL, YZ, and ZL are responsible for collecting and sorting materials. SZ, YC, and GZ are responsible for sorting charts. YQL provides ideas and guidance for the article. All authors contributed to the article and approved the submitted version.

Conflict of interest
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.

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