Gao Y, Killian K, Zhang H, Yu K, Li QZ, Weinstein S, Virtamo J, Tucker M, Taylor P, Albanes D, Meltzer P, Caporaso N. Leukocyte DNA methylation and colorectal cancer among male smokers. World J Gastrointest Oncol 2012; 4(8): 193-201 [PMID: 22912915 DOI: 10.4251/wjgo.v4.i8.193]
Corresponding Author of This Article
Ying Gao, MD, PhD, Professor, Genetic Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 6120 Executive Boulevard, Bldg. EPS/Room 7110, NIH/NCI, Bethesda, MD 20892, United States. gaoying@mail.nih.gov
Article-Type of This Article
Original Article
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This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Ying Gao, Kai Yu, Stephanie Weinstein, Margaret Tucker, Philip Taylor, Demetrius Albanes, Neil Caporaso, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20852, United States
Keith Killian, Paul Meltzer, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20852, United States
Hong Zhang, Institute of Biostatistics, School of Life Science, Fudan University, Shanghai 200433, China
Qi-Zhai Li, Department of Statistics, Chinese Academy of Sciences, Beijing 100190, China
Jarmo Virtamo, National Public Health Institute, Helsinki FI-00271, Finland
ORCID number: $[AuthorORCIDs]
Author contributions: Gao Y and Caporaso N designed the study; Gao Y, Zhang H, Yu K and Li QZ analyzed the data; Gao Y and Caporaso N wrote the report; Killian K and Meltzer P conducted laboratory assays; all authors read, gave comments, and approved the final version of the manuscript; Gao Y had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
Supported by Grants from the Intramural Research Program of the Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health
Correspondence to: Ying Gao, MD, PhD, Professor, Genetic Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 6120 Executive Boulevard, Bldg. EPS/Room 7110, NIH/NCI, Bethesda, MD 20892, United States. gaoying@mail.nih.gov
Telephone: +1-301-4969249 Fax: +1-301-4024489
Received: January 13, 2012 Revised: July 13, 2012 Accepted: July 20, 2012 Published online: August 15, 2012
Abstract
AIM: To explore the association between methylation in leukocyte DNA and colorectal cancer (CRC) risk in male smokers using the α-tocopherol, β-carotene cancer prevention study.
METHODS: About 221 incident CRC cases, and 219 controls, frequency-matched on age and smoking intensity were included. DNA methylation of 1505 CpG sites selected from 807 genes were evaluated using Illumina GoldenGate Methylation Cancer Panel I in pre-diagnostic blood leukocytes of study subjects. Tertiles of methylation level classified according to the distribution in controls for each CpG site were used to analyze the association between methylation level and CRC risk with logistic regression. The time between blood draw to cancer diagnosis (classifying cases according to latency) was incorporated in further analyses using proportional odds regression.
RESULTS: We found that methylation changes of 31 CpG sites were associated with CRC risk at P < 0.01 level. Though none of these 31 sites remained statistically significant after Bonferroni correction, the most statistically significant CpG site associated with CRC risk achieved a P value of 1.0 × 10-4. The CpG site is located in DSP gene, and the risk estimate was 1.52 (95% CI: 0.91-2.53) and 2.62 (95% CI: 1.65-4.17) for the second and third tertile comparing with the lowest tertile respectively. Taking the latency information into account strengthened some associations, suggesting that the methylation levels of corresponding sites might change over time with tumor progression.
CONCLUSION: The results suggest that the methylation level of some genes were associated with cancer susceptibility and some were related to tumor development over time. Further studies are warranted to confirm and refine our results.
Citation: Gao Y, Killian K, Zhang H, Yu K, Li QZ, Weinstein S, Virtamo J, Tucker M, Taylor P, Albanes D, Meltzer P, Caporaso N. Leukocyte DNA methylation and colorectal cancer among male smokers. World J Gastrointest Oncol 2012; 4(8): 193-201
Although its incidence and mortality have declined in the past decades, colorectal cancer (CRC) remains the third most common cancer worldwide[1]. Epigenetic changes, which affect gene expression and subsequent phenotypes by mechanisms other than DNA sequence change, have been shown to play important roles in etiology of various cancers[2]. Studying the roles of epigenetic and genetic factors, as well as their interaction with environmental exposures, should lead to better understanding on the pathogenesis of CRC, and ultimately contribute to the prevention and treatment.
DNA methylation, the covalent addition of a methyl group, is an epigenetic event that alters gene expression. It has a degree of dependence on host status, including age[3,4] and genetic background[5-7], as well as environmental exposures, including dietary availability of methyl groups[8], smoking[9], and other factors. Variation in DNA methylation helps explain genetic diversity, which might mediate gene-environment interaction; mechanistically it might represent a key mechanism whereby changing environment modulates gene action. Alterations of the normal DNA methylation pattern, which is unique for each gene, have been considered an important step in many human diseases and been associated with all cancers examined to date, including CRC[2]. Promoter hypermethylation of many genes, associated with silencing (tumor suppressor genes) or activation (oncogenes) of downstream genes, has been linked to CRC carcinogenesis[10-14]. The key pathways in CRC carcinogenesis, including loss of cell cycle regulation control (p16INK4α), silencing of DNA mismatch repair genes (MLH1, MGMT), loss of function of apoptosis genes (DAPK), and abolishment of carcinogen metabolism (GSTP1), involve changes in promoter methylation[15]. Accumulating evidence suggests that epigenetic, including DNA methylation, abnormalities are a driving force of carcinogenesis[16]. Notably, a recent study induced cancer in Apc Min/+ mice through over expressing the de novo DNA methyltransferases Dnmt3a1 and Dnmt3b1 and thereby established a direct causal connection between DNA hypermethylation and the development of colon tumors[17]. However, evidence for the role that these mechanisms play in human populations remains incomplete. Case control studies are unable to differentiate methylation changes associated with tumor susceptibility from those changes that derive solely from tumor progression. For this reason, prospective studies are needed to examine whether certain DNA methylation changes precede cancer development.
Notable DNA methylation pattern changes have been observed in CRC tissue[18-22], which could classify CRC molecular subtypes. For example, the CpG island methylator phenotype (panels of four to eight CpG islands)[23-26] has distinct pathogenic features that could have prognostic implications and suggest avenues for prevention or therapy. However to date, prospective data on DNA methylation and risk of incident CRC have not been reported, and data from non-target tissue, including leukocytes, are sparse. Study in mice have shown that changes of methylation in leukocyte DNA were parallel those observed in other somatic tissues[27]. Emerging data suggest that leukocyte DNA methylation might be linked to susceptibility of bladder cancer[28], lung cancer[29], cervical intraepithelial neoplasia[30]. The study of DNA methylation status in peripheral leukocytes in relation to CRC risk has mainly been conducted among hereditary nonpolyposis CRC patients to compare methylation status between tissues[31-35]. Limited epidemiological studies have only examined small sets of genes[36,37] in case-control settings. To date, no report has examined the association between DNA methylation and CRC risk in a prospective study setting.
We conducted a nested case-control study within the α-tocopherol, β-carotene (ATBC) cancer prevention study to explore the relationship between CRC risk and gene-specific DNA methylation from pre-diagnostic leukocytes.
MATERIALS AND METHODS
ATBC study
The ATBC cancer prevention study was a double-blinded, placebo-controlled, 2 × 2 factorial design trial, which assessed the effect of ATBC, or both, on the incidence of cancer in male smokers[38-40]. The prospective cohort comprised of 29 133 Finish men, aged 50-69 years at study entry (1985-1988), who smoked at least 5 cigarettes per day. Participants were randomly assigned to groups receiving ATBC, both supplements, or placebo for 5-8 years until April 30, 1993 or death. Incident cases were identified through the Finnish Cancer Registry. Medical records for each cancer case were reviewed centrally by study physicians or oncologists for diagnosis confirmation. Questionnaire based general risk factor, education, family history, medical history, detailed smoking, and dietary information, as well as anthropometry, were collected at baseline. Whole blood biospecimens were collected from subjects close to the end of the intervention (before 1993).
This trial was approved by the institutional review boards of the National Institute for Health and Welfare of Finland and the National Cancer Institute of USA. All participants provided written informed consent.
Study subjects
We conducted a nested case-control study within the ATBC study. All participants were male smokers. All the incident cases with colon and rectal adenocarcinomas (International Classification of Diseases 9, codes 153 and 154) identified through the latest follow-up (April 2006) that had a pre-diagnostic blood sample were included in this study. Controls were cancer-free subjects identified through April 2006, who provided a blood sample, were frequency matched to the cases by age at study entry (± 5 years), date of blood draw (± 90 d), and smoking intensity (± 10 cigarettes/d). Leukocyte DNA was extracted from pre-diagnostic buffy coat sample of all study subjects.
DNA methylation assay
For the current study, 1 μg DNA from each study subject was treated with the bisulfate conversion kit from Zymo Research (D5008) (http://www.zymoresearch.com ) to convert unemthylated cytosines to uracil and leave methylated ones intact. Bisulfite converted DNA was then genotyped using a commercially available chip, the Illumina GoldenGate Methylation Cancer Panel 1 (Appendix 3) (http://www.illumina.com/pages.ilmnID=193), to differentiate the methylated and unmethylated cytosine. The chip covers 1505 CpG sites, which are located in the promoter regions of 807 genes reflecting a broad spectrum of carcinogenic processes including tumor suppressor genes, oncogenes, genes involved in DNA repair, cell cycle control, differentiation, apoptosis, X-linked, and imprinted genes. All of the 454 samples (224 cases and 230 controls) were tested in five 96 well-plate chips/ batches. Matched case and control samples were placed within the same batch in random order. Duplicates from each of 2 QC subjects in each of 5 batches were randomly and blindly dispersed among study samples in order to assess variability of the assay.
Statistical analysis
Raw data for methylated (M) alleles and unmethylated (U) alleles of each CpG site were exported from GenomeStudio Data Analysis Software (Illumina). Ten samples were excluded because 5% or more of the markers exceeded the threshold for non-specific cross-hybridization (P value of detection > 0.1). Then quantile normalization[41] was conducted on both M and U, and β values for each CpG site were generated for statistical analysis. The β value was expressed as percentage of methylated cytosines as follows: β = min (M, 0)/[min (U, 0) + min (M, 0) + 100], and was used as the proxy of methylation level at each CpG site. Principal component analysis was conducted based on overall β values of each individual to detect outlier individuals: the first two (principal) components, which explained most of the variance between individuals, were selected. Four samples which were outside the range of ± 5 SD of each principal component were excluded. A total of 440 subjects were eligible for the final analysis.
Methylation levels for each CpG site were classified into tertiles according to the distribution among controls. Logistic regression was used to estimate the association between the risk for CRC and each CpG site. Adjustment for date of blood draw and smoking intensity did not modify the results substantially so we only included age as covariate among the matching factors. Batch differences of QC samples were non-negligible and adjustment for batch variable modified the results significantly. Therefore, we reported the results from logistic regression adjusted for age and batch factor.
Taking advantage of the prospective design of the current study, we explored the effect of latency, which was defined as the difference in days between the date of blood draw to reported date of cancer diagnosis (for CRC cases). The range of latency (ranging 0-13.4 years) allowed us to classify cases into three categories: short (0-4.8 years), medium (4.9-8.9 years), and long latency groups (9.0-13.4 years). Proportional odds regression was used to estimate the association between DNA methylation and CRC risk by coding cases according to latency. In addition, another set of logistic regression analyses (partial logistic regression) were conducted with cases restricted to those having short and medium latencies. If we assume methylation of some CpG sites changes over time in relation to tumor progression, this model should enhance the detection of these markers by excluding subjects with long latency.
To evaluate the potential false positive findings due to multiple testing, we adjusted the P values using a Bonferroni correction for the total number of all the CpG sites tested in the current analysis (1505 sites). All the analyses were conducted with SAS9.1 or R software and all the tests are two sided.
RESULTS
A total of 221 CRC cases and 219 frequency matched controls with successful DNA methylation measurements were included in the current analysis. Cases and controls were similar with regard to age, supplement treatment, family history of CRC, smoking starting age, and smoking duration (years) (Table 1). Cases had relatively higher body mass index than controls. The median age of cancer diagnosis of cases was 69.5 years old, which is over 10 years after study entry (median = 58 years old). The histograms (Figure 1) show the data distribution of β values for all CpG sites in controls, suggesting most CpG sites in controls were unmethylated.
Table 1 Characteristics of cases and controls n (%).
Figure 1 Histogram for data distribution.
A: Means of β for all CpG sites in controls; B: SD of β for all CpG sites in controls.
In analysis comparing all cases to all controls using logistic regression model, the CpG sites with differential methylation are candidate sites potentially related to susceptibility. Of the 1505 CpG sites analyzed, 25 sites were associated with CRC risk at P < 0.01 level and are shown in Table 2. None of these 25 sites exceeded a Bonferroni threshold for significance (threshold is 3.3 × 10-5 for 1500 tests). However, the most statistically significant CpG site associated with risk was DSP_P440_R (P = 6.0 × 10-4) with the second tertile displaying a 1.01-fold risk (95% CI: 0.96-1.26) and the third tertile displaying a 1.26-fold risk (95% CI: 1.12-1.43) comparing with the lowest tertile of methylation.
Table 2 Methylation of CpG sites associated with colorectal cancer development (P value < 0.01 before multiple testing correction)1.
To capture markers whose status changed over time (potentially reflecting tumor progression), we incorporated the time variable, latency, in analysis using proportional odds regression by coding the cases as three categories according to latency. Of the 1505 CpG sites analyzed, 31 sites were associated with CRC risk at P < 0.01 level (Table 3). Though none of these 31 sites remained statistically significant after Bonferroni correction, the most statistically significant CpG site associated with CRC risk achieved a P value of 1.0 × 10-4. The CpG site is located in DSP gene, and the risk estimate was 1.52 (95% CI: 0.91-2.53) and 2.62 (95% CI: 1.65-4.17) for the second and third tertile comparing with the lowest tertile respectively.
Table 3 Methylation of CpG sites related to colorectal cancer development with different latencies (P value < 0.01 before multiple testing correction)1.
To further explore the time-related DNA methylation change, we conducted partial logistic regression analysis by excluding the one third of the cases with the longest latency, and only comparing cases with short and medium latency to controls. In this analysis, 26 sites were associated with CRC risk at P < 0.01 level (Table 4). None of them remain statistically significant after Bonferroni correction. GLA_E98_R was the top hit with over 30% elevated risk (P = 1.3 × 10-4) for subjects with highest methylation level compared to those at the lower level.
Table 4 Methylation of CpG sites associated with colorectal cancer with short to mediate latency (P value < 0.01 before multiple testing correction)1.
As stated in methods, changes in methylation of CpG sites over time, can suggest a relationship to tumor progression; models incorporating time/latency information (the proportional odds model and the partial logistic regression model) are designed to detect such a pattern. The regular logistic regression model comparing all cases to all controls should select all risk-associated markers. These include both susceptibility-related markers (which differ between cases and controls and do not change over time), as well as progression-related, (which change over time with tumor progression). To differentiate the CpG sites whose methylation levels are susceptibility related from those that are potentially tumor progression- related, we compared the top CpG sites selected from the three models (full logistic regression, proportional odds, and partial logistic regression). We found that methylation levels of some CpG sites, like those in the DSP gene, were consistently associated with CRC risk across three models, suggesting these associations were unaltered by time prior to diagnosis, or tumor progression; the available evidence therefore suggests that they are related to cancer predisposition. On the other hand, the methylation levels of some other sites, such as B3GALT5 and GLA genes, were associated with CRC risk at lower p values in analysis from models incorporating latency information than from standard model (the all logistic regression model); the time/latency pattern observed suggests that the markers are tumor progression- related.
DISCUSSION
In our study, more than 1500 CpG sites from 807 genes were evaluated among 440 study subjects, which is the first prospective study for CRC risk focusing on gene-specific DNA methylation to date. By comparing all the cases with all the controls, we found that the methylation levels of some CpG sites were associated with CRC risk. The methylation of these genes might be related to CRC susceptibility. By incorporating latency information in the analysis, we found some associations between DNA methylation and CRC risk were latency-related, suggesting the methylation in these genes altered with tumor progression. However, these results are cross-sectional, and further studies with repeated blood draws from the same subjects are needed to refine the temporal pattern prior to cancer diagnosis among same individuals.
Following the report from Feinberg and colleagues that colon cancer cells had different DNA methylation patterns in some genes compared to their normal counterparts[42], many studies have been conducted using colon cancer as a cancer model for methylation regulation in the past three decades. Methylation in several genes had been reported to be involved in the pathogenesis of colorectal precursor lesions and adenomas, as well as adenocarcinomas[43]. However, epidemiological studies to date have only tested limited sets of CpG sites in small numbers of subjects[36,44,45]. The reported associations require confirmation and methylation levels of other genes remained to be described. Although further replication is needed, our study is among the most comprehensive and large studies.
Epigenetic regulation of gene expression is specific for each cell type, within different tissues, according to stages of development or differentiation[11,46]. Most studies of DNA methylation in CRC have been conducted by comparing tumor tissue DNA with adjacent normal tissue DNA from cancer patients[47]. Circulating DNA from serum also has been studied[48-50], although this might reflect methylation status in DNA released from tumor tissue, and could be influenced by tumor volume, vascularity, stage, grade, metastasis, et al. Methylation patterns from other DNA sources have only had fragmentary study[36,51]. Selected epigenetic markers could be heritable from one generation to the next[52], or affected by aging or environmental exposures throughout life[53]. It is reasonable to hypothesize that DNA methylation status in some genes is associated with cancer susceptibility. Therefore, methylation patterns of germline tissue, including that derived from blood leukocyte DNA might be related to cancer risk. Changes of methylation in leukocyte DNA have been shown to parallel other somatic tissues in mice[27], and have been linked to susceptibility of certain cancers[28]. Certainly, we could not rule out the possibility that different tissues have different response to environmental exposure and that methylation status in leukocytes may not fully reflect the changes in the target tissue[27]. In the current study, we found methylation levels of some genes, like DSP, were consistently associated with CRC risk across all three models, suggesting a relationship to cancer risk that is invariant over time, that is unaffected by tumor progression. We recognize that the procedure that favor tumor initiation and progression may have both similar (as we observed) and independent elements and specifically targeted populations will be required to explore the later hypothesis in future studies. Though further confirmation is required, our results provide some evidence that DNA methylation of some genes could be related to cancer susceptibility.
Aberrantly increased DNA methylation in the promoter region of hMLH1 gene in germline DNA has been reported among nonpolyposis CRC patients[32-35]. Hypermethylation in the MSH2 gene of germline DNA was also observed among early onset CRC patients[31]. Interestingly, the inverse relationship between leukocyte DNA genomic methylation and colorectal adenoma progression was found stronger for nonadvanced rather than advanced adenoma in a case-control study, which suggests that leukocyte DNA genomic methylation may be more important as an etiologic factor in early adenomas[54]. All these data suggest that the methylation levels of some genes either increase or decrease over time with tumor progression. Though further studies are required to replicate and confirm, our results suggest that methylation levels of some genes, i.e., GLA, B3GALT5, et al, could be markers of tumor progression, and methylation levels of some genes, i.e., DSP et al, were more likely markers of susceptibility. Also, some genes whose methylation levels were positively associated with CRC risk, i.e., DSP, MLH3, et al, suggest they might be tumor suppressing-like genes, and those showed negative association, i.e., PLAL1, et al, might be oncogenic-like genes.
Our study has several advantages. First, it is nested within the ATBC cohort, which offers a substantial, representative, well characterized, and relatively homogeneous population of male smokers. Second, data on cancer diagnoses and key covariates were systematically collected. Third, this is the first prospective population-based study to explore the role of gene-specific DNA methylation in colorectal carcinogenesis with a large number of CpG sites. DNA obtained from blood samples at baseline allows us to assess methylation status prior to cancer diagnosis, and explore the latency effect on the associations. Although to our knowledge the sample size is among the largest reported to date, variations of DNA methylation in leukocytes are less prominent than those observed in colorectal tissue/tumor comparisons; thus we had limited power to detect markers with moderate and small effect sizes. Another limitation is that this study is restricted to male Finnish smokers. The advantage of homogeneity implies the limitation that the results are not entirely generalizable to other populations. Furthermore, we only have one blood draw from each subject, which limits our power to precisely explore the direct effect of latency on the association between DNA methylation and cancer risk.
In summary, the results from this prospective study suggest that the methylation level of some genes were associated with cancer susceptibility and some were related with tumor progression. Further studies are warranted to confirm and refine our results.
ACKNOWLEDGMENTS
The authors thank Tim Sheehy and Dominick Parisi for sample preparation, and Kirk Snyder, Information Management Services, Silver Spring, MD, for data management. Finally, we acknowledge the study participants for donating their time and making this study possible.
COMMENTS
Background
Recent data suggest a link between leukocyte DNA methylation and cancer risk. However, data on DNA methylation from a prospective study, which may provide evidence for causality, are sparse.
Research frontiers
Results may provide new insights into the etiology of colorectal cancer (CRC) and suggest new cancer prevention strategies.
Innovations and breakthroughs
Data on DNA methylation from a prospective study, which could provide causality evidence, are missing. This is among the first prospective studies to examine gene-specific methylation status in germ-line DNA prior to CRC diagnosis.
Applications
Results may provide new insights into the etiology of CRC and suggest new cancer prevention strategies. The approach we propose, methylation profiling of PBMC DNA from prospectively obtained samples and its relation to CRC risk, should be relevant to other cancers.
Terminology
Methylation: Methylation is the covalent addition of a methyl group to cytosine residue, which is an epigenetic event that affects cell function by altering gene expression. Prospective study: Prospective study follows over time a group of similar individuals who differ with respect to certain factors under study, to determine how these factors affect rates of a certain disease.
Peer review
The comparison was made between ca. 200 pairs, thus small case-control study with comprehensive methylation pattern. There were no sites where methylation differences survived Bonferroni threshold of significance. Time-dependent DNA methylation was suspected, but no cases gave DNA at different times. However, the design is ambitious and the results are potentially important.
Footnotes
Peer reviewer: Haruhiko Sugimura, MD, PhD, Department of Investigative Pathology I, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ward, Hamamatsu 431-3192, Japan
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