ORIGINAL RESEARCH article
Genetic Variations of CD40 and LTβR Genes Are Associated With Increased Susceptibility and Clinical Outcome of Non-Small-Cell Carcinoma Patients
- 1Division of Oncology, Department of Medicine, University of Patras, Patras, Greece
- 2Molecular Oncology Laboratory, Division of Oncology, Department of Medicine, University of Patras, Patras, Greece
- 3Centre for Bio-Inspired Technology, Institute of Biomedical Engineering, Imperial College London, London, United Kingdom
- 4Department of Cardiothoracic Surgery, University of Patras, Patras, Greece
- 5Department of Pathology, University of Patras, Patras, Greece
Background: Immune system-related receptors CD40 (tumor necrosis factor receptor superfamily member 5), BAFFR (tumor necrosis factor receptor superfamily member 13C), and LTβR (tumor necrosis factor receptor superfamily member 3) play a pivotal role in non-small-cell lung cancer (NSCLC). To further evaluate their role in NSCLC, CD40 rs1883832 (T>C), BAFFR rs7290134 (A>G), and LTβR rs10849448 (A>G) single-nucleotide polymorphisms (SNPs) were investigated regarding their impact in risk and clinical outcome of NSCLC patients.
Methods: The three selected SNPs were evaluated in 229 NSCLC patients and 299 healthy controls, while CD40, BAFFR, and LTβR protein expression was assessed by immunohistochemistry in 96 tumor specimens from NSCLC patients.
Results: In total, CD40 rs1883832 was associated with NSCLC risk, with the T allele, after adjusting for cofactors, being related to increased risk (p = 0.007; OR 1.701). Moreover, the CT genotype was associated with increased risk (p = 0.024; OR 1.606) and poorer 5-year overall survival (OS) after adjusting for cofactors (p = 0.001, HR 1.829), while CC was associated with higher CD40 expression in tumorous cells (p = 0.040) and in stromal cells (p = 0.036). In addition, AA homozygotes for the LTβR rs10849448 had increased risk for NSCLC in multivariate analysis (p = 0.008; OR, 2.106) and higher LTβR membranous expression (p = 0.035). Although BAFFR rs7290134 was associated with BAFFR membranous expression (p = 0.039), BAFFR rs7290134 was not associated with neither the disease risk nor the prognosis of NSCLC patients.
Conclusions: In conclusion, CD40 rs1883832 and LTβR rs10849448 seem to be associated with increased risk for NSCLC, while CD40 rs1883832 is also associated with OS of patients with NSCLC.
The last decade, NF-κB (nuclear factor kappa-light-chain-enhancer of activated B cells) has attracted interest regarding its role in NSCLC (non-small-cell lung cancer) (1). It has been documented that the main effectors of the classical, NF-κB1 and RelA (transcription factor P65), as well as of the alternative pathway, NF-κB2 and RelB (transcription factor RelB), are overexpressed and have prognostic value in NSCLC (1–5). On the contrary, published data on the pathobiology and the clinical significance in NSCLC of the surface receptors CD40 (tumor necrosis factor receptor superfamily member 5), BAFFR (tumor necrosis factor receptor superfamily member 13C), and LTβR (tumor necrosis factor receptor superfamily member 3), which mainly leads to signal transduction through the NF-κB alternative pathway, are limited. Recently, our group has reported that these receptors are expressed in NSCLC revealing significant clinical associations (6). According to our studies as well as to other studies, CD40 expression in lung cancer patients has been associated with metastatic progression (7) as well as with prognosis (6, 8). Similarly, BAFFR expression in NSCLC has also been reported to be deregulated (6), while its expression in CAFs (cancer-associated fibroblasts) has interestingly been associated with overall survival (OS) and response to platinum-based chemotherapy in NSCLC (9).
More limited are also the published data on genetic variations of CD40, BAFFR, and LTβR and especially of the three single-nucleotide polymorphisms (SNPs) CD40 rs1883832 (T>C), BAFFR rs7290134 (A>G), and LTβR rs10849448 (A>G), which were evaluated in the current study, as well as their potent clinical value in NSCLC. In particular, CD40 SNP rs1883832 has been associated with many nonmalignant clinical entities, such as atherosclerosis (10), acute coronary syndrome (11, 12), ischemic stroke (13), chronic obstructive pulmonary disease (14), chronic HBV infection (15), and later onset of Graves’ disease (16). It has also been related to cervical carcinoma in a subset of a Malaysian population (17) and to sporadic breast cancer risk in Chinese Han women (18). Interestingly, in a small study in the Chinese population, it has also been correlated with the susceptibility to lung cancer (19). Regarding the BAFFR rs7290134, no association with the risk for CLL (chronic lymphocytic leukemia) was found (20, 21), while no study has been published regarding its role in epithelial tumors. In addition, the published data regarding the clinical value of LTβR rs10849448 (A>G) refer to its association with individuals’ risk of undergoing tonsillectomy (22) and juvenile idiopathic arthritis (23), while no data exist regarding its significance in cancer.
In the present study, we present our findings on the clinical significance of CD40 rs1883832 (T>C), BAFFR rs7290134 (A>G), and LTβR rs10849448 (A>G) SNPs in NSCLC patients in regard to the risk over NSCLC initiation and OS.
Materials and Methods
Study Design, Population, Tissue Specimens, and Data Collection
The current study was performed following Helsinki Declaration on ethical principles for medical research (2013) (24). In this study, we investigated the selected SNPs of CD40, BAFFR, and LTβR in relation to clinicopathological data, protein expression of the same molecules, and the clinical outcome of NSCLC patients. Initially, the selected SNPs were studied in a retrospectively collected group which was followed by a second prospectively collected patient cohort. Although our preliminary results from the retrospective group were validated in the prospective group, statistical analysis presented here was performed in the pool of the cases to achieve more robust statistical results.
Data (clinicopathological, disease outcome, and vital status) used in the analysis were obtained from pathology reports, from medical records, or through direct communication with the patients. Survival outcome was evaluated after the 60-month follow-up period. Clinicopathological characteristics of our cohort and relevant information are included in Table 1.
Histopathologically or cytologically confirmed NSCLC (squamous cell carcinoma or adenocarcinoma or large-cell carcinoma) patients were exclusively enrolled in the study. Totally, 229 previously untreated patients with confirmed NSCLC of all ages were enrolled, with 109 of them being retrospectively collected (Group R). Tissue specimens from the patients were collected from the archives of the Department of Pathology of the University Hospital of Patras, Greece: tumor-adjacent, nonmalignant, and macroscopically normal tissue specimens. Additionally, peripheral blood specimens from 120 newly diagnosed NSCLC patients, which were managed from 2008 to 2010, were prospectively collected (Group P). All cases were diagnosed and medically managed at the Division of Medical Oncology and the Department of Cardiothoracic Surgery at the University Hospital of Patras between 2004 and 2015. All patients of the study were treated based on the standard-of-care treatment options according to disease characteristics, the comorbidities, and the performance status following the current treatment guidelines. Uncertain histology, non-Greek Caucasian ethnic origin, and past medical history with cancer were the exclusion criteria for this study.
A healthy control group was also used, including 299 peripheral blood specimens from healthy control donors (Group H) who were collected in the context of annual medical checkup. Groups of controls and patients were age- and sex-matched (Table 2). In this study, only individuals with Greek Caucasian origin were recruited in order to ensure the similarity of the genetic background. Past medical history related to cancer or family history linked to any disease (including cancer) was set as exclusion criterion.
Selection of SNPs
The selection of the particular SNPs located within the CD40, BAFFR, and LTβR genes was performed by reviewing literature (PubMed, Google Scholar) using as keywords the words SNPs, CD40, BAFFR, LTβR, cancer, NSCLC, and lung cancer. Five percent was set as the cutoff point for minor allele frequencies, and the coefficient of determination r2 = 0.8 was captured. Genomic location, minor allele frequencies (MAF), and other specific characteristics of SNPs are presented in Table 3.
The commercial kit “QIAamp Blood Mini Kit” (Qiagen Ltd., Crawley, UK) was used for the extraction of genomic DNA from whole blood samples from 124 cancer patients and 279 healthy donors according to the manufacturer’s instructions. Furthermore, DNA was also isolated from 148 tumor adjacent, nonmalignant FFPE, tissue specimens using the “QIAamp DNA FFPE Tissue Kit” (Qiagen Ltd., Crawley, UK). DNA was stored at -20°C until required.
Genotyping was performed using real-time PCR followed by high-resolution melt curve (HRM) analysis on a StepOnePlus™ real-time PCR system (Thermo Fisher Scientific, Waltham, MA USA). Reactions were performed using SNP-specific primers (CD40 rs1883832: forward 5′-GCCTGGTCTCACCTCGC-3′ and reverse 5′-GCCCCAGAGGACGCAC-3′; BAFFR rs7290134: forward 5′-GCTGAATGCTGTGGTCTGTAGTG-3′ and reverse 5′-CATGCACATGCCCTCTTTCTG-3′; LtBR rs10849448 forward 5′-CGGCCAGCTCGCTCCAC-3′ and reverse 5′-GCCTCCAGGGCTCCCA-3′) and MeltDoctor™ HRM Master Mix (Thermo Fisher Scientific, Waltham, MA USA). HRM genotyping data were analyzed using the High-Resolution Melt Software v3.0 (Applied Biosystems, Thermo Fisher Scientific, Waltham, MA USA).
Further validation of the genotyping method as well as genotyping in some subgroups of participants due to the observed deviation from the Hardy–Weinberg equilibrium (HWE) was achieved through sequencing of several samples, representative of all three genotypes. The sequences of the primers and PCR conditions that were used for sequencing can be provided upon request. Sequencing was performed at Cemia SA (University of Thessaly, Greece). All obtained sequences were in agreement with the genotyping results of our method.
CD40, BAFFR, and LTβR protein expression was studied by immunohistochemistry in a cohort of patients, the vast majority of whom had undergone curative resection of a lung tumor in the University Hospital of Patras between 2005 and 2010 (Table 4). Selection of patients was serially and retrospectively done while patient data analysis was performed blindly based on the archive and database of the Pathology Department of the University Hospital of Patras. Invasive, formalin-fixed paraffin-embedded (FFPE) NSCLC tissue specimens as well as adjacent non-neoplastic lung parenchyma were retrieved.
Table 4 Clinicopathological characteristics and survival data of NSCLC patients studied by immunohistochemistry.
Mouse monoclonal antibodies against CD40 and BAFFR and a rabbit polyclonal antibody against LTβR were used for antigen detection. Specific conditions regarding clonality, clone, dilution, antigen retrieval, and incubation time have been described in depth in previous publications (6); thus, here they are presented briefly (Table 5). Detection and visualization were performed using the EnVision Detection Kit (DAKO) and diaminobenzidine (DAB) chromogen following the manufacturer’s instructions. In addition, dehydrated Harris’ hematoxylin was used to counterstain the sections.
Table 5 Primary antibodies and their clonality, clone, dilution, antigen retrieval, and incubation time information.
Evaluation of Immunohistochemistry
An evaluation of immunohistochemical staining has been described in detail in a previous publication (6). Briefly, an experienced pathologist (VT) assessed and scored each slide in a blind fashion. Tumor as well as stromal cells (myofibroblasts), tumor-infiltrating lymphocytes (TILs), and tumor-associated macrophages (TAMs) were scored. An initial selection of representative areas was performed at low (×100) magnification. A minimum number of 1,000 cells per tissue section was counted at a ×400 magnification. Cytoplasmic staining was evaluated for both epithelial and stromal cells, while membranous staining was performed only for epithelial cells. Microphotographs were taken by using a Nikon DXM1200C digital camera mounted on a Nikon Eclipse 80i microscope and ACT-1C software (Nikon Instruments Inc., Melville, NY, USA).
Statistical analysis was performed by using Statistical Package for Social Sciences version 17 (SPSS, Chicago, IL, USA). Categorical nominal variables were evaluated using the chi-square test or Fisher’s exact test. The T test was used for continuous variables with normal distribution. Analysis by using the Kruskal–Wallis or Mann–Whitney test was performed for ordinal or continuous data. Spearman’s correlations were used to assess associations between variables. The Kaplan–Meier method and the log-rank test were used for plotting of survival rates and their comparison, respectively. p<0.05 was considered statistically significant for all comparisons.
Frequencies of Genotypes and Alleles Across Subpopulations
In the current study, genotyping of the three studied polymorphisms was achieved in the vast majority of patients and controls, who were enrolled in the study. In particular, genotyping for CD40 rs1883832 (T>C) was successfully performed in 228 patients and all healthy controls (Table 6). The frequencies of the three CD40 rs1883832 genotypes (TT, CT, CC) were 23.6%, 26.8%, and 49.6%, in the NSCLC cases and 24.4%, 39.5%, and 36.1% in healthy controls, respectively. In addition, BAFFR rs7290134 (A>G) was successfully detected in all patients and 298 healthy controls. The frequencies of the three BAFFR rs7290134 (A>G) genotypes (AA, AG, GG) were 64.2%, 31.9%, and 3.9% in lung cancer patients and 62.4%, 3.9%, and 5.7% in healthy controls, respectively (Table 7). Furthermore, 223 NSCLC patients and all healthy controls were genotyped for LTβR rs10849448 (A>G). The frequencies for the three genotypes AA, AG, and GG of LTβR rs10849448 (A>G) were 10.8%, 27.4%, and 61.8% in the NSCLC subcohort and 18.4%, 25.8%, and 55.8% in healthy controls, respectively (Table 8).
Table 6 Relationships between clinicopathological variables of NSCLC patients and CD40 rs1883832 genotypes.
Table 7 Relationships between clinicopathological variables of NSCLC patients and BAFFR rs7290134 genotypes.
Table 8 Relationships between clinicopathological variables of NSCLC patients and LtBR rs10849448 genotypes.
CD40 rs1883832 (T>C) and LTβR rs10849448 (A>G) SNPs Were Associated With Increased NSCLC Risk
As shown in Table 9, a statistically significant difference was observed in the allele frequency of CD40 rs1883832 (T) between lung cancer patients and controls (p=0.021) as well as between the frequencies of the studied genotypes (p=0.003). Statistically significant was also the difference between genotypes in NSCLC patients and healthy controls following the dominant model for the T allele (p = 0.002). In univariate analysis, T allele carriers (TT+CT) for CD40 rs1883832 had a higher risk for lung cancer (p = 0.002; OR 1.738, 95% CI 1.224–2.468). The same relation remained statistically significant under a multivariate model, in which age, smoking history, and genotype for CD40 rs1883832 SNP were entered as covariates (p = 0.007; OR 1.701, 95% CI 1.154–2.506). In addition, using an overdominant gene model (CT vs. CC+ TT), the CT genotype was also associated with increased risk for NSCLC not only in univariate analysis (p = 0.002; OR 1.785, 95% CI 1.228–2.594) but also after adjusting for cofactors (p = 0.024; OR 1.606, 95% CI 1.065–2.422).
In addition, LTβR rs10849448 (A>G) SNP was also associated with the development of NSCLC. Particularly, homozygosity for the alternative allele A was related to higher risk for NSCLC in univariate (p=0.016; OR, 1.869; 95% 1.117–3.127) and multivariate analyses using age as cofactor (p=0.008; OR, 2.106; 95% 1.210–3.667). On the contrary, no association was observed between BAFFR rs7290134 SNP and the risk for NSCLC following any model.
CD40 rs1883832 (T>C) Was Associated With Overall Survival
Among all NSCLC cases, the CD40 rs1883832 CT heterozygotes had poorer OS compared to TT and CC homozygotes after 2, 3, and 5 years of observation on univariate analysis (p=0.015, p=0.005, and p=0.017, respectively, Figure 1). Prognostic significance for 2-, 3-, and 5-year OS persisted in multivariate analyses adjusted for age, sex, stage, and histological subtypes (p=0.023, p<0.001, and p=0.001, respectively). The same correlation was also observed after stratifying with histological subtype (p=0.075 and p=0.001, respectively). Interestingly, further analysis by stage stratification revealed that the observed correlation was limited in stages I and II (p=0.001), while it disappeared in patients of stages III and IV (p=0.151).
Figure 1 Kaplan–Meier curves depicting overall survival (OS) of NSCLC patients in relation to (A) CD40 rs1883832 genotypes in the whole sub-cohort of NSCLC patients, (B) CD40 rs1883832 genotypes in SQ patients, (C) CD40 rs1883832 genotypes in ADC patients, (D) CD40 rs1883832 genotypes in stage I and II patients, (E) CD40 rs1883832 genotypes in NSCLC patients with N = 0, (F) CD40 rs1883832 genotypes in NSCLC patients with N = 1. SQ, squamous cell carcinoma; ADC, adenocarcinoma.
On the contrary, although BAFFR rs7290134 (A>G) SNP seemed to be associated with the OS, finally it did not reach the level of statistical significance (p=0.087). In particular, G allele carriers had better 5-year survival compared to AA homozygotes; however, this difference was not statistically significant.
CD40 rs1883832 (T>C), LTβR rs10849448 (A>G), and BAFFR rs7290134 (A>G) Were Associated With Protein Expression
CD40 rs1883832 was associated with CD40 expression. In particular, CD40 rs1883832 was associated with total (cytoplasmic and membranous) CD40 expression with CC homozygotes having higher tumorous CD40 (Mann–Whitney U test, p=0.040). In addition, CC homozygotes had higher CD40 expression in stromal cells compared to T allele carriers (Mann–Whitney U test, p=0.036). In addition, LTβR rs10849448 SNP was associated with LTβR membranous expression, with AA homozygotes having higher protein levels (p=0.035). Furthermore, the third SNP, BAFFR rs7290134 (A>G), was associated with BAFFR membranous expression with A minor allele carriers having lower protein levels (p=0.039).
CD40 rs1883832 (T>C) SNP Was Associated With Development of Metastases
CD40 rs1883832 was associated with development of metastases after the initial assessment. Patients with no development of metastatic disease were mainly CC homozygotes (p=0.022). The same association was also observed in multivariate analysis using age, sex, lymph node infiltration, and histological subtype as cofactors (p=0.019).
During the last years, accumulating evidence supports the role of NF-κB in the pathobiology and management of NSCLC (25). In this context, CD40, BAFFR, and LTβR cell surface receptors, which mainly activate NF-κβ pathways, also seem to be important for NSCLC. In this study, we assessed the clinical value of three SNPs CD40 (rs1883832), BAFFR (rs7290134), and LTβR (rs10849448) in NSCLC, with the results further supporting previous findings from our and other groups on the role of these molecules in NSCLC. One of the major findings of the study was the association of CD40 rs1883832 with NSCLC risk. In line with our observation, Krishnappa et al. reported that the rs1883832 T allele is associated with increased susceptibility to cervical cancer in the Malaysian population (17). Similarly, Shuang et al. have also shown that the rs1883832 T allele is related to sporadic breast cancer risk in Han Chinese women (18). Interestingly, the same allele of rs1883832 (T) has also been documented in a small study (n = 105 cases) and has been correlated with the susceptibility to lung cancer in the Chinese population including not only NSCLC but also SCLC patients (19). Furthermore, TT genotype has also been associated with an increased risk for follicular lymphoma (26).
Another intriguing finding of the present study was the association of CD40 rs1883832 with OS. Although the role of this SNP has been studied in many nonmalignant diseases, as mentioned in the introduction, there has not been yet any reported finding on its prognostic significance in solid tumors or hematological malignancies. However, some indirect results are supportive of our observation. Our group has shown that CD40 overexpression in NSCLC patients is associated with improved 5-year OS (6), a finding, which is confirmed by using publicly available data and the KM plotter (Figure 2A) (27). In addition, in the current study, we show that CD40 rs1883832 is associated with total CD40 expression in tumorous cells as well as in stromal cells, suggesting a possible mechanism through which CD40 rs1883832 may influence survival outcome of NSCLC patients. From a biological point of view, this association could be justified by the genomic position of rs1883832, since it is located on the promoter region and in particular at the -1 base from the start codon of the CD40 and within the Kozak sequence (28). Also supportive is the observation by Skibola et al. according to which follicular lymphoma patients and healthy controls with TT genotypes had decreased plasma circulating soluble CD40 as well as CD40 cell surface expression in dendritic cells from healthy individuals compared to CC homozygotes (26).
Figure 2 (A) Kaplan–Meier curves depicting 5-year OS of NSCLC patients in relation to CD40 mRNA levels as provided by KM plotter, (B) Kaplan–Meier curves depicting 5-year OS of NSCLC patients in relation to LTβR mRNA levels as provided by the KM plotter.
Our study also showed that LTβR rs10849448 (A>G) SNP is associated with NSCLC risk, with homozygosity for the alternative A allele being related to lower risk for NSCLC, a finding that correlates for the first time this variant with cancer risk. Additionally, our group has reported that LTβR expression in NSCLC has prognostic significance (6). The prognostic significance of LTβR expression has also been confirmed using the KM plotter and the 203005_at dataset, with higher expression being correlated with poorer outcome (Figure 2B). In line with these findings, we also observed that LTβR rs10849448 (A>G) SNP was associated with LTβR membranous expression with AA homozygotes having higher protein levels, providing concurrently a potent explanation for the increased risk for NSCLC.
Despite the promising results of our study, we must acknowledge some weak points. A major limitation of our study is that the retrospectively collected samples as well as the size of the cohort did not permit a separate analysis for the discovery and validation subgroups; thus, despite our initial intention to follow a two-phase design, the final analysis was based on the study of the whole cohort. A larger cohort could permit the separate analysis and lead to more robust results. Moreover, molecular profiling of driver mutations and PD-L1 status was not available since the patients were enrolled before immunotherapy era.
In conclusion, this study shows that two (CD40 rs1883832 and LTβR rs10849448) of the three studied genetic variants are associated with an increased risk for NSCLC, while CD40 rs1883832 was also significantly associated with OS of patients with NSCLC. However, our findings need to be further validated in another population and more data are needed regarding the functionality of the studied polymorphisms.
Data Availability Statement
The datasets from sequencing presented in this study can be found in online repository as well as are also available upon request from the corresponding author. The name of the repository and accession number can be found below: European Nucleotide Archive (ENA) (accession number: PRJEB47384).
This study was conducted according to the guidelines of the Declaration of Helsinki and was performed upon approval by the Scientific Committee and the Committee on Research and Ethics of the University Hospital of Patras (Greece, 22/18.2.2015). Written informed consent was obtained from all participants unless the Committee had granted a waiver.
Conceptualization, F-ID, AA, AK, and HK. Methodology, AA, AK, F-ID, and VT. Formal analysis, F-ID and AA. Investigation, F-ID, AA, AK, NP, DD, TM, AngK, and HK. Resources, F-ID and HK. Writing—original draft preparation, F-ID, AA, and AK. Writing—review and editing, F-ID, MK, and HK. All authors contributed to the article and approved the submitted version.
This research was cofunded by the Hellenic Society of Medical Oncology (HeSMO) through a research funding program as well as from EOGE, an Oncology Research Fund non-profit organization, in Greece.
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.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
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Keywords: SNP, NSCLC, rs1883832, rs10849448, rs7290134, prognosis, risk
Citation: Dimitrakopoulos F-ID, Antonacopoulou AG, Kottorou AE, Kalofonou M, Panagopoulos N, Dougenis D, Makatsoris T, Tzelepi V, Koutras A and Kalofonos HP (2021) Genetic Variations of CD40 and LTβR Genes Are Associated With Increased Susceptibility and Clinical Outcome of Non-Small-Cell Carcinoma Patients. Front. Oncol. 11:721577. doi: 10.3389/fonc.2021.721577
Received: 07 June 2021; Accepted: 10 August 2021;
Published: 17 September 2021.
Edited by:Umberto Malapelle, University of Naples Federico II, Italy
Reviewed by:Jelena Stojsic, University of Belgrade, Serbia
Pasquale Pisapia, University of Naples Federico II, Italy
Copyright © 2021 Dimitrakopoulos, Antonacopoulou, Kottorou, Kalofonou, Panagopoulos, Dougenis, Makatsoris, Tzelepi, Koutras and Kalofonos. 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.
†These authors have contributed equally to this work and share first authorship