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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Dis Esophagus. Author manuscript; available in PMC 2011 January 1.
Published in final edited form as:
PMCID: PMC2866140

p53 Arg72Pro, MDM2 T309G and CCND1 G870A polymorphisms are not associated with susceptibility to esophageal adenocarcinoma


p53 Arg72Pro, MDM2 T309G, and CCND1 G870A are functional single nucleotide polymorphisms (SNPs) in key genes that regulate apoptosis and cell cycle. Variant genotypes of these SNPs have been associated with increased risk and earlier age of onset in some cancers. We investigated the association of these SNPs with susceptibility to esophageal adenocarcinoma in a large, North American case-control study. 312 cases and 454 cancer-free controls recruited in Boston, USA were genotyped for each of the three SNPs, and demographic and clinical data were collected. Genotype frequencies for each of the three SNPs did not deviate from Hardy-Weinberg equilibrium, and did not differ between cases and controls. Odds ratios (OR), adjusted for clinical risk factors, for the homozygous variant genotypes were 0.99 (95% CI 0.57 – 1.72) for p53 Pro/Pro, 0.81 (95% CI 0.52 – 1.28) for MDM2 G/G, and 0.97 (95% CI 0.64 – 1.49) for CCND1 A/A. The analysis was adequately powered (80%) to detect ORs of 1.37. 1.35 and 1.34 for each SNP respectively. In contrast to the results of smaller published studies, no association between p53 Arg72Pro, MDM2 T309G, and CCND1 G870A SNPs and susceptibility to esophageal adenocarcinoma, age of onset, or stage of disease at diagnosis was detected.

Keywords: Esophageal adenocarcinoma, molecular epidemiology, single nucleotide polymorphism (SNP), risk factors, p53


Esophageal adenocarcinoma (EA) is the predominant form of esophageal cancer in Western populations, and its incidence is rising dramatically.1 Despite its high morbidity and mortality, there have been few studies examining the molecular epidemiology of this disease and, of those published, most are small and their results inconsistent.2 A better understanding of the genetic risk factors that underlie EA could lead to improved strategies for screening and prevention.

p53, its negative regulator MDM2, and cyclin D1 (CCND1) are important regulators of cell cycle and apoptosis; and each contains functional single nucleotide polymorphisms (SNPs) (p53 Arg72Pro, MDM2 T309G, and CCND1 G870A) that have been implicated in the susceptibility and outcome of various human malignancies.35 The variants alleles of both p53 Arg72Pro and MDM2 T309G putatively impair apoptosis, which could contribute to esophageal carcinogenesis: p53 Pro72 codes for a protein with reduced apoptotic potential, while MDM2 309G is a promoter SNP that results in the upregulation of MDM2 and the consequent downregulation of the p53 pathway. CCND1 G870A alters a transcriptional splice site, with the resulting transcript leading to constitutive nuclear cyclin D1 localization and an increased in vitro transforming capacity through mechanisms not fully elucidated.4 Two studies, with conflicting findings, have evaluated the association between CCND1 G870A and EA risk.6,7 p53 Arg72Pro and MDM2 T309G have not been studied in this disease despite the importance of the p53 pathway in esophageal cancer, and associations with risk in other aerodigestive cancers.812

We sought to evaluate the association of these SNPs with EA risk in a large North American case-control study. Subgroups of females and smokers, in whom the variant alleles might exert a stronger biologic effect,13 were analyzed. We also explored whether a relationship exists between these SNPs and age of onset and stage of disease at diagnosis, both of which have been demonstrated previously.13,14


Case and control population

Since 1999, patients with histologically-confirmed esophageal adenocarcinoma were recruited from Massachusetts General Hospital (Boston, MA).15 Patients were also enrolled from the Dana Farber Cancer Institute (Boston, MA) beginning in 2003. The current study includes the cohort enrolled up to September, 2005. Healthy unrelated age-, sex-, and gender-matched visitor controls with no history of cancer or GERD were recruited from the same institutions. A more detailed description of the recruitment of this cohort has been recently published.16 For both cases and controls, the rate of recruitment exceeded 85% of individuals who were approached for participation. Informed consent was provided by all participants, and the study protocol was approved by the institutional review boards of the participating hospitals and universities.


Demographic information, detailed medical and family histories, adult body mass index (BMI, defined using healthy weight between ages 20 and 30), smoking, and alcohol consumption habits were collected by trained interviewers. Smoking habits were defined as never, former, current smokers according to standard definitions. Alcohol use was dichotomized into never-drinker (lifetime average ≤1 standard drink/year) and drinkers.


DNA was extracted from peripheral blood using the Puregene DNA Isolation Kit (Gentra Systems, Minneapolis, USA). Genotyping for p53 Arg72Pro (rs1042522), MDM2 T309G (rs2279744) and CCND1 G870A (rs603965) were performed as previously described using Taqman assays.17 Probe and primer sequences are available upon request.

Statistical analysis

Sex and age distribution matching were confirmed between cases and controls. Demographic and clinical variables were compared across cases and controls, and across genotypes in the case cohort using Fisher`s exact tests (categorical variables) and non-parametric Wilcoxon rank sum tests (continuous variables) where appropriate. Unconditional logistic regression models were used to analyze associations between genotypes and risk of EA, as previously described.15 Recessive, additive and dominant models were considered. Analyses were adjusted for smoking status and adult BMI. Subgroup analyses were performed by gender and smoking status. Stage of disease and age at diagnosis were compared across genotypes using Fisher exact and Wilcoxon rank tests. P values of 0.05 were considered significant. All statistical testing was performed using SAS 9.1 (SAS Institute, Cary, NC, USA).


312 cases and 454 controls were included in the analysis. Demographic and clinical variables, as well as genotype frequencies are shown in Table 1. Smoking, BMI and alcohol use, all putative risk factors for esophageal cancer, were more common in cases than controls. Genotyping for each of the three SNPs was complete in 98–99.7% of individuals. Genotype frequencies, as well as crude and adjusted ORs for EA risk for all SNPs are shown in Table 2. There were no differences in genotype distribution between cases and control for any of the three SNPs. The observed frequencies were similar to previous reports, and both cases and controls did not deviate from Hardy Weinberg equilibrium (p>0.05).

Table 1
Demographic characteristics of cases and controls
Table 2
Genotype frequencies for p53 Arg72Pro, MDM2 T309G and CCND1 G870A polymorphisms and crude and adjusted ORs for their risk of esophageal adenocarcinoma.

Subgroup analyses were performed to examine the association of SNPs and EA risk by gender and smoking status. Analyses adjusted for alcohol consumption were also carried out in the subgroup of patients with available alcohol use data. No significant associations were shown in any subgroup explored (p>0.10 for each comparison).

Neither stage of disease at diagnosis, nor age at diagnosis was associated with any of the three SNPs (p>0.10 for each comparison).


In a large esophageal adenocarcinoma genetic case-control study, we found no association between p53 Arg72Pro, MDM2 T309G or CCND1 G870A and EA susceptibility. Our study was adequately powered (80%) to detect ORs of 1.37, 1.35, and 1.34 for the p53, MDM2 and CCND1 SNPs respectively, and included several times more patients than any previous study that has evaluated these associations. We considered subgroups of patients in whom the SNPs might be more likely to modulate disease risk, and no positive associations were found. In addition, we found no association between any of the three SNPs and age or stage of disease at diagnosis.

The lack of association between p53 Arg72Pro, MDM2 T309G and risk or age of onset in EA is important and adds to the growing literature about p53 pathway SNPs and cancer susceptibility. The conflicting reports among tumor types suggests that any impact on cancer susceptibility is likely disease-site specific, and may be limited to subgroups of patients within tumor types. In our study we had limited ability to examine the interaction between SNP genotypes and other patient factors and EA susceptibility; and as our population was almost entirely Caucasian, our null results may not apply to other ethnic groups. Furthermore, because these SNPs affect a common pathway, a combined analysis of the MDM2 and p53 SNPs is clearly warranted; however, because of the low prevalence of each variant allele, we had limited power to analyze SNP combinations.

Our null result for CCND1 G870A and EA risk contrasts with one small case-control study (cases, n=56; OR 5.99, 95% CI 1.89–18.96, for A/A vs. G/G), but consistent with another (n=56) that did not find a significant association.6,7 In addition, we did not confirm the results of a case series (n=124) that found a positive association between CCND1 A/- genotypes and both age of onset and frequency of distant metastases at diagnosis.14,18 While the affected population in that series had similar ethnic and sex distributions as our own, a greater proportion of our patients had stage IV disease. These results highlight the importance of validating SNP-susceptibility associations.

In conclusion, our findings do not support an association between p53 Arg72Pro, MDM2 T309G, and CCND1 G870A SNPs and esophageal adenocarcinoma susceptibility in a North American Caucasian-predominant population. As demonstrated in the current and other recently published studies,15,16,1921 the large and well-characterized cohort examined here provides a powerful resource for characterizing the molecular epidemiology of esophageal adenocarcinoma.



This work was supported by NIH R01 CA074386, Posluns Family Foundation, Alan Brown Chair in Molecular Genomics, FAMRI, CIHR and Doris Duke Charitable Foundation.



The authors have no conflicts to declare.


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