Association between Vitamin D Receptor Single-Nucleotide Polymorphisms and Colorectal Cancer in the Thai Population: A Case-Control Study

Suksawatamnuay, Sirinporn; Sriphoosanaphan, Supachaya; Aumpansub, Prapimphan; Aniwan, Satimai; Thanapirom, Kessarin; Tanasanvimon, Suebpong; Thaimai, Panarat; Wiangngoen, Sumitra; Ponauthai, Yuwadee; Sumdin, Sakolkan; Angspatt, Pattama; Rerknimitr, Rungsun; Poovorawan, Yong; Komolmit, Piyawat

doi:https://doi.org/10.1155/2020/7562958

BioMed Research International

On this page

Abstract Introduction Materials and Methods Results Discussion Conclusions Data Availability Ethical Approval Consent Disclosure Conflicts of Interest Authors’ Contributions Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2020 | Article ID 7562958 | https://doi.org/10.1155/2020/7562958

Association between Vitamin D Receptor Single-Nucleotide Polymorphisms and Colorectal Cancer in the Thai Population: A Case-Control Study

Sirinporn Suksawatamnuay,^1,2,3Supachaya Sriphoosanaphan,^1,2Prapimphan Aumpansub,¹Satimai Aniwan,¹Kessarin Thanapirom,^1,2,3Suebpong Tanasanvimon,⁴Panarat Thaimai,¹Sumitra Wiangngoen,¹Yuwadee Ponauthai,¹Sakolkan Sumdin,¹Pattama Angspatt,⁴and Rungsun Rerknimitr¹ et al.

Academic Editor: Toshimi Chiba

Received19 Feb 2020

Revised12 May 2020

Accepted18 May 2020

Published15 Jun 2020

Abstract

Vitamin D and its cognate intracellular nuclear receptor, namely, vitamin D receptor (VDR), are involved in the regulation of a variety of body metabolic processes, immune function, and oncogenesis. A large number of studies demonstrated the association of low vitamin D levels and variations in five common single nucleotide polymorphisms (SNPs), FokI, BsmI, Tru9I, ApaI, and TaqI, with the risk of several cancers, including colorectal cancers. However, these associations vary among different populations. This case-control study was aimed at analysing whether common single-nucleotide polymorphisms (SNPs) and haplotypes of the vitamin D receptor (VDR) gene contribute to colorectal carcinogenesis in the Thai population. We enrolled 364 Thai participants from King Chulalongkorn Memorial Hospital between 2014 and 2015. Half of the participants underwent colonoscopy and showed a normal colon without polyps (control group) and another half were newly diagnosed patients with colorectal cancer (CRC) by colonoscopy during the index period, were under treatment, or were followed up at the outpatient clinic (case group). Differences in allele and genotype frequencies of five common VDR SNPs, between the case and control groups, were the primary outcome measures. Differences in haplotype frequencies of the five SNPs between the case and control groups were the secondary outcome measures. Among the 364 participants, baseline characteristics were not significantly different between the case and control groups, except for the higher proportion of males in the CRC group. The mean vitamin D level was also not significantly different between the case and control groups ( vs. ng/mL, ). None of the five VDR SNPs was associated with CRC development (). However, haplotype analysis of these polymorphisms demonstrated that the AGGT haplotype was associated with a decreased risk of CRC (odds ratio 0.24, 95% confidence interval 0.07-0.81, ). The AGGT haplotype was associated with a lower risk of CRC in the Thai population. This genetic linkage might support the role of vitamin D in colorectal carcinogenesis. However, this finding requires further study within a larger population and a multivariate analysis of other established risk factors.

1. Introduction

Colorectal cancer (CRC) is one of the most common malignancies worldwide. It is estimated that the incidence and burden of CRC will increase to 60% by 2030, especially in low-income and middle-income countries [1]. The prevention and early detection of CRC are therefore crucial to decrease morbidity and mortality. Besides the development of an effective strategy for prioritising a screening program based on patient risk, further study of CRC risk factors also has its benefits [2]. Vitamin D deficiency is one of the nutritional factors related to CRC risk. A previous epidemiologic study showed a higher prevalence of CRC in areas with low solar ultraviolet B exposure. Recent reviews, both in vitro and in vivo, also suggested an association between vitamin D deficiency and an increased risk of various malignancies, including breast cancer, prostate cancer, and CRC [3, 4]. Furthermore, maintaining a normal vitamin D level has been shown to reduce CRC risk [5–7].

Vitamin D is thought to affect cancer development via the cell-cycle processes, including cell proliferation, differentiation, and apoptosis, and through modification of immune activity [8, 9]. Vitamin D metabolism occurs primarily in the liver, kidney, and other tissues, including intestinal epithelial cells and immune cells. The active form of vitamin D exerts its effects through interaction with its cognate intracellular nuclear receptor, the vitamin D receptor (VDR), which subsequently activates a number of genes involved in immune cell proliferation, oncogenesis, and tumour suppression [9, 10].

The VDR gene is located on the long arm of chromosome 12 (12q13-14), spanning approximately 75 kb. It contains nine exons. Even though many SNPs associated with VDR function have been discovered, five common SNPs, namely, FokI, BsmI, Tru9I, ApaI, and TaqI, were mostly used in association studies, as they are usually coinherited as blocks of haplotypes [11]. Among the five SNPs, only FokI is a nonsynonymous SNP located at the 5 end of exon 2. The other four SNPs are the nonsynonymous variations. BsmI, Tru9I, and ApaI are inside intron 8, and only TaqI is in exon 9, which is unlikely to affect the translated forms of VDR polypeptides [12]. Only the variation in FokI genotypes (T>C allele) caused a change in the translation start site, which in turn resulted in a smaller protein with increased activity [13].

The downstream signals of the VDR involve different functions, including bone mineral metabolism, immune regulation, and cell growth and differentiation [14]. Studies of common polymorphisms in the VDR gene have demonstrated association of the polymorphisms with several chronic diseases such as systemic lupus erythematosus and osteoporosis and various malignancies, including CRC [15–18]. However, the previous data on the association between VDR polymorphisms and CRC risk were mostly from Western countries, and the collective results were inconsistent [15, 19]. These discrepancies might stem from the divergence of VDR allele frequencies among ethnic groups. As there is not enough data on the Thai population, this study was aimed at analysing whether common single-nucleotide polymorphisms (SNPs) and specific haplotypes of the VDR gene contribute to colorectal carcinogenesis in the Thai population.

2. Materials and Methods

2.1. Participants

This case-control study was conducted between 2014 and 2015 at King Chulalongkorn Memorial Hospital, a tertiary care centre in Bangkok, Thailand. The inclusion criteria for the CRC cases included the patients who were diagnosed at the time colonoscopy for CRC screening or those requiring investigation of the clinical cases for pathological confirmation. In addition, the CRC patients who were currently on follow-up treatment in the oncology clinic were also included in the study. The controlled cases were the patients who underwent colonoscopy examination for the routine CRC screening and showed normal colon without any type of colorectal polyps. In addition, the cases of patients who had current or previous diagnosis of inflammatory bowel diseases were excluded. The other exclusion criteria for both groups included having a history of other malignancies and declination to participate in the study. The study protocol was approved by the Institutional Review Board of the Faculty of Medicine of Chulalongkorn University (number 192/58). All participants provided written informed consent. We enrolled a total 364 Thai participants, of whom 182 underwent colonoscopy and showed a normal colon without any polyps (control group) and 182 had CRC (case group). The case group consisted of 90 patients who were newly diagnosed with CRC by colonoscopy during the index period and 92 patients who were undergoing treatment or were followed up at the outpatient clinic. All cases were diagnosed as positive malignancies based on pathological reports. Demographic variables, including age, sex, height, and weight, were recorded, and body mass index (BMI) was calculated. Each participant provided a blood sample collected in a 6 mL tube with ethylenediaminetetraacetic acid (EDTA) and stored at 4°C until analysis for vitamin D level and VDR genotype.

2.2. Vitamin D Assays

Vitamin D levels in the plasma samples were measured using the LIAISON® 25 OH Vitamin D TOTAL Assay (DiaSorin, Saluggia, Italy) and LIAISON® analyser, following the manufacturer’s instructions. The final measurements were indicated in nanograms per millilitre.

2.3. Genotype Analysis

Genomic DNA was extracted from peripheral blood leukocytes in 6 mL of whole blood sample using standard phenol-chloroform protocols. Samples were sent to the lab consecutively in the order they were collected and genotyped by scientists who were blinded to the disease status of the patients in the study. Five SNPs of the VDR gene—namely, FokI (rs228570 C>T), BsmI (rs1544410 A>G), Tru9I (rs757343 G>A), ApaI (rs7975232 G>T), and TaqI (rs731236 C>T)—were genotyped using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis. Human genomic DNA was extracted from 100 μL of peripheral blood mononuclear cells by first incubating with proteinase K in a lysis buffer and then performing standard phenol-chloroform extraction and ethanol precipitation. The resultant pellet was dissolved in 50 μL sterile water and stored at -20°C until analysis. Specific primer pairs for each locus of the VDR gene were used for amplification (Supplementary Table 1). Two microlitres of DNA was used to set up 25 μL PCR reactions using the PerfectTaq™ Plus Master Mix (5 Prime GmbH, Hamburg, Germany). A total volume of 10 μL was digested overnight with 2 units of restriction endonucleases (New England Biolabs, Hitchin, UK) using the buffers and temperatures recommended by the manufacturer. The resultant DNA fragments were resolved by 2% agarose gel electrophoresis, and the RFLP result was visualized under ultraviolet light after staining with ethidium bromide. To validate the RFLP genotyping results, we selected the DNA product of each RFLP pattern in the 5 SNPs for DNA sequencing. Sanger sequencing of the DNA products was conducted using Macrogen (Seoul, Korea). All sequences were aligned with their reference sequence of the VDR gene obtained from GenBank (accession number NC_000012.12).

2.4. Statistical Methods

Statistical analyses were performed using SPSS software (version 20, 2015; SPSS Inc., Chicago, IL, USA). Numerical data are presented as means and standard deviations and categorical data as numbers and percentages. To compare associations between cases and controls, numerical and categorical variables were calculated using independent sample -tests, chi-squared test, and Fisher’s exact test, as appropriate. The normality of continuous variables was assessed by visually inspecting histograms and conducting a Shapiro-Wilk test. The reported values were obtained from a two-sided statistical test, and a value of <0.05 was considered statistically significant, except for logistic regression analyses where values of 0.01 were considered significant based on a Bonferroni adjusted with 5 comparisons. The Hardy-Weinberg equilibrium (HWE) of genotype frequencies among participants, linkage disequilibrium (LD), haplotype construction, and genetic association were analysed using SHEsis software [20].

Sample size was calculated for an unmatched case-control study using a web-based calculator at http://www.openepi.com. We assumed the prevalence of BsmI homozygous recessives in the control group was 14%; the OR for the CRC group versus the control group was 2.7, based on a study by Rasool et al. [21]. Using Fleiss’s method, enrolling 184 patients in each group would provide 80% power to detect this minimum odds ratio at a 1% significance level (a Bonferroni adjusted alpha with 5 SNP comparisons).

3. Results

3.1. Clinical Characteristics

A total of 364 participants, including 182 with CRC (cases) and 182 without CRC (controls), were included in this study. The mean age of participants in the case and control groups was and years, respectively, which was not significantly different (). The case group had a significantly higher proportion of males than the control group (103 [57%] vs. 59 [32%], ). Baseline characteristics such as age, history of CRC in first-degree relatives, and BMI were not significantly different between both groups. The mean vitamin D levels were also not significantly different between the case and control groups ( vs. , ). Moreover, vitamin D deficiency/insufficiency was detected in 76.1% and 79.9% in the case and control groups, respectively, but there was no significant difference. The baseline characteristics of the participants are summarized in Table 1.

3.2. Allele Frequencies of VDR SNPs

The case and control groups showed similar proportions of allele frequencies for each VDR SNP, and thus, no significant difference in allelic frequencies was found between both groups. The major allele frequencies for each polymorphism are shown in Table 2. The representative PCR-RFLP and the respective sequences of all SNPs analysed are demonstrated in Figure 1.

(a)

(b)

(c)

(d)

(e)

(f)

Figure 1

Representative RFLP patterns of each VDR polymorphism of the 5 VDR-SNPs and example of DNA sequencing results of three PCR products of three cases with different Tru9I genotypes. (a) FokI (rs228570 C>T): product sizes were 266 bp for the C allele and 205 and 61 bp for the T allele, (b) BsmI (rs1544410 A>G): product sizes were 357 bp for the A allele and 254 and 103 bp for the G allele, (c) ApaI (rs7975232 G>T): product sizes were 340 bp for the T allele and 229 and 111 bp for the G allele, (d) TaqI (rs731236 C>T): product sizes were 340 bp for the T allele and 191 and 149 bp for the C allele, (e) Tru9I (rs757343 G>A): product sizes were 357 bp for the G allele and 26 and 93 bp for the A allele, and (f) DNA sequencing results of the PCR products with Tru9I (rs757343 G>A) genotypes GG, GA, and AA. The arrow indicates the polymorphism; M: a molecular marker of the 100 bp ladder.

3.3. Genotype Frequencies of VDR SNPs

For all VDR SNPs, the genotype frequencies were in line with the HWE. Most of the participants in both the case and control groups had the CT genotype, GG genotype, GG genotype, GT genotype, and TT genotype for FokI, BsmI, Tru9I, ApaI, and TaqI, respectively. However, no significant difference in genotype frequency was observed when the case group was compared with the control group (Table 2). The subanalysis comparing vitamin D levels according to genotypic variances in the SNPs showed no significant differences between CRC and control groups (Table 3).

3.4. Haplotype Frequencies of VDR SNPs

A strong LD () was observed among BsmI, Tru9I, ApaI, and TaqI (Figure 2). The distribution of the BsmI/Tru9I/ApaI/TaqI haplotype frequencies in the case and control groups is shown in Table 4. The GGGT haplotype was the most frequent haplotype in both the cases and controls (65.8% and 61.5%, respectively). Importantly, the AGGT haplotype was significantly associated with a decreased risk of CRC (odds ratio 0.24, 95% confidence interval 0.07-0.81, ), whereas other haplotypes did not show any significant difference in frequencies between the cases and controls. Eleven patients with a definite AGGT haplotype were identified, two in the case group and nine in the control group. The vitamin D level was normal in three cases (27.3%), and there was vitamin D insufficiency in five cases (45.4%) and vitamin D deficiency in three cases (27.3%). The detailed data is submitted in Supplementary Table 2.

(a)

(b)

4. Discussion

Most epidemiological and scientific studies have strongly suggested that vitamin D and the VDR gene may have a role in colorectal pathogenesis [22, 23] and that variations in VDR SNPs are also associated with CRC [19]. This case-control study demonstrated no significant differences in the serum vitamin D levels between CRC cases and controls in the Thai population, as well as no association of the five common VDR SNPs, with CRC risk. However, a specific haplotype, AGGT, significantly predicted a lower risk of CRC.

Many studies have attempted to prove the association of common SNPs, including FokI, BsmI, Tru9I, ApaI, and TaqI, with CRC in various populations. A meta-analysis in 2011 including 17 published studies suggested that BsmI is associated with a lower risk of CRC. However, only two studies were conducted in Asian countries, and these studies showed that BsmI and FokI were associated with CRC risk in China and Korea, respectively [24, 25]. A meta-analysis in 2017 by a Chinese study group, which analysed 39 studies worldwide, 9 of which were from Asian countries, showed a strong association between BsmI and CRC risk and a probable but not statistically proven association between FokI and CRC risk [15]. Our study in the Thai population did not reveal any association of the five common SNPs with CRC. The number of cases in each arm of our study was based on a study from Kashmir showing an increased risk (with 2.7 relative risk) of CRC with the BsmI genotype [21]. However, our study not only showed an absence of association between SNPs and CRC but also showed a difference between the BsmI genotypes of our population and that of the study from Kashmir [21]. Such difference due to ethnicity, even within the same geographic area, might help explain the null results in our study. Our results are consistent with those of a large genetic association study of >1700 sibships with and without CRC from North America, Honolulu, and Australia, which clearly showed no statistical association between CRC and 43 VDR SNPs, including BsmI and TaqI, but not Tru9I, ApaI, and FokI [26].

In this study, the analysis of the haplotype AGGT of BsmI, Tru9I, ApaI, and TaqI showed statistically significant results in relation to CRC. However, the association was quite minimal, with allele frequencies of only 0.9% and 3.6% in the case and control arms, compared to that of genetic association studies. The significant association from our haplotype analysis was only based on a number of cases initially calculated to prove an association between CRC and a single SNP, specifically BsmI. Thus, to prove the association between the AGGT haplotype and CRC in our population, the next study will require at least >1000 cases in each arm. Several case-control studies found some specific haplotypes that are associated with CRC. A case-control study in the USA with >3000 White, Hispanic, African-American, and Asian cases and controls examined the haplotypes of three SNPs spanning across the VDR gene, including BsmI (intron 8), poly(A) long (18-22 repeats), and FokI (exon 2), and reported an association of the bLF and BLF haplotypes with the risk of colon cancer [27]. Other studies showed a significant association of BsmI/ApaI/TaqI and BsmI/TaqI haplotypes with a decreased risk of CRC in Korean and European populations, respectively [25, 28]. However, our study demonstrated that in the Thai population, all SNPs did not deviate from the HWE, and that BsmI, Tru9I, and ApaI in intron 8 and TaqI in exon 9 were more likely to have low recombination rates and be inherited together, with BsmI and ApaI showing high and moderate LD scores only in the control group. The importance of the HWE and LD in genetic association studies has been reviewed and should be assessed for this type of studies [29, 30]. In our study, we found that the LD of the BsmI/Tru9I/ApaI/TaqI haplotype was within block B, spanning approximately 40 kilobases (kb) and containing exons 3-9, of the three LD block patterns reported in European studies, which showed that these patterns are likely to be inherited together even in different European ethnicities [30].

The association between CRC and these specific haplotypes from different populations, including ours, points to the same hypothesis that some specific variations in the genome, likely in the VDR gene or possibly in a nearby gene, affect the VDR functions. The haplotype AGGT in our study is a nonsynonymous variation, which is located on intron 8 and exon 9, nearer to the 3-UTR. It is unlikely to affect the translated VDR polypeptides [12]. There are several speculations of the effect of these 3-UTR variations that might affect the transcription ability of the VDR gene in osteoblast cell lines [31]. Two of the most important genetic tools to elucidate in vivo protein-gene interactions that have been recently developed are chromatin immunoprecipitation (ChIP) and ChIP with massively parallel sequencing (ChIP-seq) [32, 33]. These methods open new insights not only into the vitamin D response element (VDRE), which is located in the promoter region of hundreds of genes involved in different cellular functions, but also into the biology of VDR, especially the transcriptional activation of the VDR gene. Importantly, the VDR has its own autoregulation through several enhancer elements far upstream from the transcription start site and also inside the VDR gene, reported to be 20-30 kb downstream inside the introns [34, 35]. The haplotype associated with CRC in our and other studies might be linked to these enhancer elements; however, further study is required to prove this hypothesis. The VDR has low expression in intestinal epithelial cells. Enhanced VDR-mediated transcripts in stromal fibroblasts surrounding cancer cells could predict better survival outcomes [36]. Hence, this specific haplotype associated with a decreased CRC risk in the Thai population might represent or be associated with the enhancer variants inside the VDR intron.

Several epidemiological studies, mostly from Western countries, including meta-analyses, affirm the link between lower vitamin D levels and a higher risk of CRC [22, 37]. In other words, adequate vitamin D levels protect against CRC development [37]. In this study, even though the population was from the tropical regions with high sunlight exposure throughout the year, nearly 80% of the participants from the case and control groups had vitamin D levels below 30 ng/mL, and one-third of the participants from the case group had vitamin D levels below 20 ng/mL or had vitamin insufficiency/deficiency. Moreover, participants in both the case and control groups showed no difference in vitamin D levels. We were able to identify 11 patients with the AGGT haplotype, and the vitamin D levels were normal in three cases (27.3%), insufficient in five cases (45.4%), and deficient in three cases (27.3%). These findings could be attributed to the lack of association between the haplotype and vitamin D levels, as nearly three quarters of the patients had vitamin D levels below 30 ng/mL; however, a larger sample size is required to prove this assumption. In addition, these serum vitamin D levels do not always reflect its local tissue levels and the magnitude of VDR gene activation in different haplotype variants.

This study has some limitations. As mentioned earlier, the number of cases is quite small, calculated only to prove the association between CRC and a single SNP, and the analysis was based on data obtained from another Asian study [21]. The haplotype analysis also requires a second larger study to confirm the results. Furthermore, the vitamin D levels measured in this study were cross-sectional results and therefore cannot represent long-term levels to reflect patient lifestyles and several other factors. Lastly, we could not entirely prove that low vitamin D levels can influence the risk of CRC in the Thai population, as reported in other studies [37].

5. Conclusions

In conclusion, this study revealed that it remains difficult to confirm the association of low vitamin D levels and VDR gene variations with colorectal carcinogenesis in the Thai population. The five SNPs, namely, FokI, BsmI, Tru9I, ApaI, and TaqI, were not associated with CRC. Interestingly though, a specific haplotype, AGGT, of the BsmI, Tru9I, ApaI, and TaqI SNPs was associated with a decreased risk of CRC, but further study with a larger sample is required to confirm such association. Our study indicates that further research should not focus on the common VDR SNPs but should explore some recently discovered enhancer elements associated with CRC.

Data Availability

The genotype data of participants were submitted in Dryad (identifier number: 336 doi:10.5061/dryad.6hdr7sqx0).

Ethical Approval

The study protocol was approved by the Institutional Review Board of the Faculty of Medicine of Chulalongkorn University (number 192/58).

All participants provided written informed consent.

Disclosure

The funding sources had no role in the study design; in the collection, analysis, and interpretation of the data; in the writing of the manuscript; or in the process of submission for publication.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

Authors’ Contributions

S Suksawatamnuay contributed to the conception of the study, laboratory works, data collection and analysis, and writing of the manuscript. S Sriphoosanaphan was involved in the conception of the study, data analysis, and writing of the manuscript. PA contributed to the study design, data analysis, and drafting of some parts of the manuscript. SA, KT, and ST contributed to the study design and data acquisition. PT, SW, YP, S Sumdin, and PAng were involved in collecting the samples and carrying out the protocol. RR was involved in the conception of the study and revision of the manuscript. YP contributed to the study concept and provided advice on genetic aspects. PK contributed to the study design, data analysis, and writing of the manuscript and was the principal investigator of this study. All authors have read and approved the final manuscript. S Suksawatamnuay and S Sriphoosanaphan contributed equally to this study.

Acknowledgments

We would like to thank Professor Stephen Kerr, BPharm (Hons), MIPH, PhD, Director, Biostatistics Excellence Centre, Faculty of Medicine, Chulalongkorn University and Biostatistics at HIV-NAT for his valuable advice on statistical analysis. This work was supported by the Ratchadapisek Sompoch Research Grant under grant numbers GRU 6105530009-1, RA59/074, and RA60/101; the Research Chair Grant from the National Science and Technology Development Agency under grant number P-15-50004; and the Center of Excellence in Clinical Virology of Chulalongkorn University and King Chulalongkorn Memorial Hospital under grant number GCE 59-009-30-005.

Supplementary Materials

Supplementary 1. Supplementary Table 1: primer sequences and PCR-RFLP analysis.

Supplementary 2. Supplementary Table 2: vitamin D levels in eleven patients with a definite AGGT haplotype among CRC and control groups.

References

J. Ferlay, I. Soerjomataram, R. Dikshit et al., “Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012,” International Journal of Cancer, vol. 136, no. 5, pp. E359–E386, 2015.
View at: Publisher Site | Google Scholar
M. Arnold, M. S. Sierra, M. Laversanne, I. Soerjomataram, A. Jemal, and F. Bray, “Global patterns and trends in colorectal cancer incidence and mortality,” Gut, vol. 66, no. 4, pp. 683–691, 2017.
View at: Publisher Site | Google Scholar
K. K. Deeb, D. L. Trump, and C. S. Johnson, “Vitamin D signalling pathways in cancer: potential for anticancer therapeutics,” Nature Reviews Cancer, vol. 7, no. 9, pp. 684–700, 2007.
View at: Publisher Site | Google Scholar
M. L. McCullough, R. M. Bostick, and T. L. Mayo, “Vitamin D gene pathway polymorphisms and risk of colorectal, breast, and prostate cancer,” Annual Review of Nutrition, vol. 29, no. 1, pp. 111–132, 2009.
View at: Publisher Site | Google Scholar
M. L. McCullough, A. S. Robertson, C. Rodriguez et al., “Calcium, vitamin D, dairy products, and risk of colorectal cancer in the Cancer Prevention Study II Nutrition Cohort (United States),” Cancer Causes & Control, vol. 14, no. 1, pp. 1–12, 2003.
View at: Publisher Site | Google Scholar
V. Fedirko, E. Riboli, A. Tjonneland et al., “Prediagnostic 25-hydroxyvitamin D, VDR and CASR polymorphisms, and survival in patients with colorectal cancer in western European ppulations,” Cancer Epidemiology Biomarkers & Prevention, vol. 21, no. 4, pp. 582–593, 2012.
View at: Publisher Site | Google Scholar
G. Bjelakovic, L. L. Gluud, D. Nikolova et al., “Vitamin D supplementation for prevention of mortality in adults,” Cochrane Database of Systematic Reviews, no. 1, article CD007470, 2014.
View at: Publisher Site | Google Scholar
Y. Ma, P. Zhang, F. Wang, J. Yang, Z. Liu, and H. Qin, “Association between vitamin D and risk of colorectal cancer: a systematic review of prospective studies,” Journal of Clinical Oncology, vol. 29, no. 28, pp. 3775–3782, 2011.
View at: Publisher Site | Google Scholar
M. G. Thomas, S. Tebbutt, and R. C. Williamson, “Vitamin D and its metabolites inhibit cell proliferation in human rectal mucosa and a colon cancer cell line,” Gut, vol. 33, no. 12, pp. 1660–1663, 1992.
View at: Publisher Site | Google Scholar
D. Feldman, A. V. Krishnan, S. Swami, E. Giovannucci, and B. J. Feldman, “The role of vitamin D in reducing cancer risk and progression,” Nature Reviews Cancer, vol. 14, no. 5, pp. 342–357, 2014.
View at: Publisher Site | Google Scholar
A. G. Uitterlinden, Y. Fang, J. B. J. van Meurs, H. A. P. Pols, and J. P. T. M. van Leeuwen, “Genetics and biology of vitamin D receptor polymorphisms,” Gene, vol. 338, no. 2, pp. 143–156, 2004.
View at: Publisher Site | Google Scholar
J. M. Valdivielso and E. Fernandez, “Vitamin D receptor polymorphisms and diseases,” Clinica Chimica Acta, vol. 371, no. 1-2, pp. 1–12, 2006.
View at: Publisher Site | Google Scholar
M. O. Elnenaei, R. Chandra, T. Mangion, and C. Moniz, “Genomic and metabolomic patterns segregate with responses to calcium and vitamin D supplementation,” British Journal of Nutrition, vol. 105, no. 1, pp. 71–79, 2011.
View at: Publisher Site | Google Scholar
L. Adorini, K. Daniel, and G. Penna, “Vitamin D receptor agonists, cancer and the immune system: an intricate relationship,” Current Topics in Medicinal Chemistry, vol. 6, no. 12, pp. 1297–1301, 2006.
View at: Publisher Site | Google Scholar
Z. Pan, M. Chen, X. Hu et al., “Associations between VDR gene polymorphisms and colorectal cancer susceptibility: an updated meta-analysis based on 39 case-control studies,” Oncotarget, vol. 9, no. 16, pp. 13068–13076, 2018.
View at: Publisher Site | Google Scholar
V. Rai, J. Abdo, S. Agrawal, and D. K. Agrawal, “Vitamin D receptor polymorphism and cancer: an update,” Anticancer Research, vol. 37, no. 8, pp. 3991–4003, 2017.
View at: Publisher Site | Google Scholar
S. C. Bae and Y. H. Lee, “Vitamin D receptor FokI, TaqI, and ApaI polymorphisms and susceptibility to systemic lupus erythematosus: an updated meta-analysis,” Clinical Rheumatology, vol. 37, no. 6, pp. 1529–1537, 2018.
View at: Publisher Site | Google Scholar
L. Zhang, X. Yin, J. Wang et al., “Associations between VDR gene polymorphisms and osteoporosis risk and bone mineral density in postmenopausal women: a systematic review and meta-analysis,” Scientific Reports, vol. 8, no. 1, p. 981, 2018.
View at: Publisher Site | Google Scholar
M. Touvier, D. S. M. Chan, R. Lau et al., “Meta-analyses of vitamin D intake, 25-hydroxyvitamin D status, vitamin D receptor polymorphisms, and colorectal cancer risk,” Cancer Epidemiology Biomarkers & Prevention, vol. 20, no. 5, pp. 1003–1016, 2011.
View at: Publisher Site | Google Scholar
Y. Y. Shi and L. He, “SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci,” Cell Research, vol. 15, no. 2, pp. 97-98, 2005.
View at: Publisher Site | Google Scholar
S. Rasool, S. A. Kadla, V. Rasool et al., “Role of the VDR Bsm I and Apa I polymorphisms in the risk of colorectal cancer in Kashmir,” Oncology Research and Treatment, vol. 37, no. 6, pp. 345–349, 2014.
View at: Publisher Site | Google Scholar
M. Jenab, H. B. Bueno-de-Mesquita, P. Ferrari et al., “Association between pre-diagnostic circulating vitamin D concentration and risk of colorectal cancer in European populations: a nested case-control study,” BMJ, vol. 340, article b5500, 2010.
View at: Publisher Site | Google Scholar
R. Dou, K. Ng, E. L. Giovannucci, J. A. E. Manson, Z. R. Qian, and S. Ogino, “Vitamin D and colorectal cancer: molecular, epidemiological and clinical evidence,” British Journal of Nutrition, vol. 115, no. 9, pp. 1643–1660, 2016.
View at: Publisher Site | Google Scholar
C. Li, Y. Li, L. B. Gao et al., “Vitamin D receptor gene polymorphisms and the risk of colorectal cancer in a Chinese population,” Digestive Diseases and Sciences, vol. 54, no. 3, pp. 634–639, 2009.
View at: Publisher Site | Google Scholar
K. Park, M. Woo, J. H. Nam, and J. C. Kim, “Start codon polymorphisms in the vitamin D receptor and colorectal cancer risk,” Cancer Letters, vol. 237, no. 2, pp. 199–206, 2006.
View at: Publisher Site | Google Scholar
J. N. Poynter, E. T. Jacobs, J. C. Figueiredo et al., “Genetic variation in the vitamin D receptor (VDR) and the vitamin D-binding protein (GC) and risk for colorectal cancer: results from the Colon Cancer Family Registry,” Cancer Epidemiology, Biomarkers & Prevention, vol. 19, no. 2, pp. 525–536, 2010.
View at: Publisher Site | Google Scholar
C. Sweeney, K. Curtin, M. A. Murtaugh, B. J. Caan, J. D. Potter, and M. L. Slattery, “Haplotype analysis of common vitamin D receptor variants and colon and rectal cancers,” Cancer Epidemiology Biomarkers & Prevention, vol. 15, no. 4, pp. 744–749, 2006.
View at: Publisher Site | Google Scholar
J. Flügge, S. Krusekopf, M. Goldammer et al., “Vitamin D receptor haplotypes protect against development of colorectal cancer,” European Journal of Clinical Pharmacology, vol. 63, no. 11, pp. 997–1005, 2007.
View at: Publisher Site | Google Scholar
C. Minelli, J. R. Thompson, K. R. Abrams, A. Thakkinstian, and J. Attia, “How should we use information about HWE in the meta-analyses of genetic association studies?” International Journal of Epidemiology, vol. 37, no. 1, pp. 136–146, 2008.
View at: Publisher Site | Google Scholar
S. Nejentsev, L. Godfrey, H. Snook et al., “Comparative high-resolution analysis of linkage disequilibrium and tag single nucleotide polymorphisms between populations in the vitamin D receptor gene,” Human Molecular Genetics, vol. 13, no. 15, pp. 1633–1639, 2004.
View at: Publisher Site | Google Scholar
Y. Fang, J. B. J. van Meurs, A. d'Alesio et al., “Promoter and 3-Untranslated-Region Haplotypes in the Vitamin D Receptor Gene Predispose to Osteoporotic Fracture: The Rotterdam Study,” American Journal of Human Genetics, vol. 77, no. 5, pp. 807–823, 2005.
View at: Publisher Site | Google Scholar
Y. Shang, X. Hu, J. DiRenzo, M. A. Lazar, and M. Brown, “Cofactor dynamics and sufficiency in estrogen receptor-regulated transcription,” Cell, vol. 103, no. 6, pp. 843–852, 2000.
View at: Publisher Site | Google Scholar
W. J. Welboren, M. A. van Driel, E. M. Janssen-Megens et al., “ChIP-Seq of ERalpha and RNA polymerase II defines genes differentially responding to ligands,” The EMBO Journal, vol. 28, no. 10, pp. 1418–1428, 2009.
View at: Publisher Site | Google Scholar
L. A. Zella, S. Kim, N. K. Shevde, and J. W. Pike, “Enhancers located within two introns of the vitamin D receptor gene mediate transcriptional autoregulation by 1, 25-dihydroxyvitamin D3,” Molecular Endocrinology, vol. 20, no. 6, pp. 1231–1247, 2006.
View at: Publisher Site | Google Scholar
L. A. Zella, M. B. Meyer, R. D. Nerenz, S. M. Lee, M. L. Martowicz, and J. W. Pike, “Multifunctional enhancers regulate mouse and human vitamin D receptor gene transcription,” Molecular Endocrinology, vol. 24, no. 1, pp. 128–147, 2010.
View at: Publisher Site | Google Scholar
G. Ferrer-Mayorga, G. Gomez-Lopez, A. Barbachano et al., “Vitamin D receptor expression and associated gene signature in tumour stromal fibroblasts predict clinical outcome in colorectal cancer,” Gut, vol. 66, no. 8, pp. 1449–1462, 2017.
View at: Publisher Site | Google Scholar
M. L. McCullough, E. S. Zoltick, S. J. Weinstein et al., “Circulating vitamin D and colorectal cancer risk: an international pooling project of 17 cohorts,” JNCI: Journal of the National Cancer Institute, vol. 111, no. 2, pp. 158–169, 2019.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2020 Sirinporn Suksawatamnuay et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

742

Downloads

1063

Citations