Tobacco, alcohol, and p53 overexpression in early colorectal neoplasia
© Terry et al; licensee BioMed Central Ltd. 2003
Received: 07 August 2003
Accepted: 06 November 2003
Published: 06 November 2003
The p53 tumor suppressor gene is commonly mutated in colorectal cancer. While the effect of p53 mutations on colorectal cancer prognosis has been heavily studied, less is known about how epidemiologic risk factors relate to p53 status, particularly in early colorectal neoplasia prior to clinically invasive colorectal cancer (including adenomas, carcinoma in situ (CIS), and intramucosal carcinoma).
We examined p53 status, as measured by protein overexpression, in 157 cases with early colorectal neoplasia selected from three New York City colonoscopy clinics. After collecting paraffin-embedded tissue blocks, immunohistochemistry was performed using an anti-p53 monoclonal mouse IgG2a [BP53-12-1] antibody. We analyzed whether p53 status was different for risk factors for colorectal neoplasia relative to a polyp-free control group (n = 508).
p53 overexpression was found in 10.3%, 21.7%, and 34.9%, of adenomatous polyps, CIS, and intramucosal cases, respectively. Over 90% of the tumors with p53 overexpression were located in the distal colon and rectum. Heavy cigarette smoking (30+ years) was associated with cases not overexpressing p53 (OR = 1.8, 95% CI = 1.1–2.9) but not with those cases overexpressing p53 (OR = 1.0, 95% CI = 0.4–2.6). Heavy beer consumption (8+ bottles per week) was associated with cases overexpressing p53 (OR = 4.0, 95% CI = 1.3–12.0) but not with cases without p53 overexpression (OR = 1.6, 95% CI = 0.7–3.7).
Our findings that p53 overexpression in early colorectal neoplasia may be positively associated with alcohol intake and inversely associated with cigarette smoking are consistent with those of several studies of p53 expression and invasive cancer, and suggest that there may be relationships of smoking and alcohol with p53 early in the adenoma to carcinoma sequence.
Keywordscolorectal adenoma colorectal cancer p53 risk factors
The molecular model of genetic changes along the colorectal adenoma-carcinoma sequence, first described by Vogelstein and colleagues, has become the framework for understanding the timing and role multiple mutations and genetic alterations play in carcinogenesis . It is thought that multiple mutations are needed for invasive cancer [1–4]. Although the number of mutations and not their order has been found to be paramount, there are general trends in terms of timing in the sequence. Of more common genes important to colorectal carcinogenesis (e.g., APC, K-ras, and p53), most data suggest that p53 is generally mutated later in the adenoma-carcinoma sequence [1, 3–9]. The prevalence of p53 protein overexpression, which is highly correlated with p53 gene mutations [10–12], increases along the adenoma-carcinoma sequence with as little as 7.1 percent overexpression in adenomas with mild dysplasia to over sixty percent in those with severe dysplasia and invasive cancer [13–15].
Although the majority of colorectal cancers are thought to originate from adenomas, most adenomas do not progress to cancer. In fact, even though the prevalence of adenomas in most high-risk populations is extremely high (as high as 20 percent in people under 50 and over 50 percent among people in their 70s , colorectal cancer is still a rare event. Estimates of the cumulative risk of invasive cancer after adenoma detected on screening exam range from 1 to 10 percent depending on the length of follow-up [16, 17]. Apart from pathologic characteristics such as larger size and villous histology, little is known about risk factors for intermediate steps along the adenoma-carcinoma sequence such as carcinoma in situ (CIS) and intramucosal carcinoma .
We undertook this investigation to examine if risk factors for early colorectal neoplasia differed by p53 status. Specifically, we were interested in whether colorectal cancer risk factors including alcohol use and cigarette smoking are associated with p53 status in early colorectal neoplasia and if these associations were similar to associations with invasive colorectal cancer. If so, such findings would suggest that processes contributing to the relationships between risk factors and p53 protein overexpression begin early in the adenoma-carcinoma sequence and may point to factors to target for intervention and future prevention. We conducted two analyses, one combining all cases of early colorectal neoplasia (subjects with adenomatous polyps, carcinoma in situ (CIS), and intramucosal carcinoma (IM)) and a second examining only cases with advanced adenomas (subjects with CIS and IM). Together these case groups represent steps along the adenoma carcinoma sequence prior to clinically relevant invasive colorectal cancer.
The cases and controls for this study come from a case-control study of newly diagnosed adenomas and polyp-free controls conducted in three New York City colonoscopy clinics between April 1986 to March 1988 [19, 20]. Both the parent study and this study were approved by Columbia's Institutional Review Board. There were 3,008 individuals who underwent colonoscopy during this time frame at the three colonoscopy clinics, of whom 2,443 (81.2%) were eligible to participate in this study. To be eligible, the subjects in this study were required to have had a complete colonoscopy; to be English- or Spanish-speaking; and to be between the ages of 35 and 84 years (18.8% of the subjects were not eligible because of incomplete colonoscopy, language restrictions and or age restrictions). Of the 2,443 eligible subjects, 2,001 subjects (81.9%) were successfully interviewed, both by telephone (71%) and by mailed questionnaire (29%) with follow-up telephone calls to complete incomplete items. The questionnaire contained information on demographics, past medical history, dietary habits, alcohol intake, smoking history, body size, physical activity, and other lifestyle factors.
The 2,001 interviewed subjects were subdivided into several categories, based on the diagnosis at the index colonoscopy and after a uniform pathologic review. Of these 2,001 subjects, there were 508 subjects free of any polyp (including adenomatous and hyperplastic) with a normal index colonoscopy and no prior history of colorectal neoplasia, 269 subjects with newly diagnosed adenoma, with no prior history of colorectal neoplasia, 57 carcinoma in situ (CIS) cases with or without a known history of adenomas, and 58 intramucosal carcinoma cases with or without a known history of adenomas (n = 58). The remaining subjects (n = 1,109) had pathologic diagnoses that were not of interest to this current investigation including hyperplastic polyps. For this study of early colorectal neoplasia, we collected paraffin-embedded tumor tissue blocks for the cases with intramucosal carcinoma, carcinoma in situ (CIS) and a random sample of cases with adenomatous polyps. Blocks with enough tissue for immunohistochemistry were retrieved for 46 (80%) of the CIS cases, 43 (75%) of the IM cases and a random sample of 25% of the adenomatous polyp cases (n = 68) frequency-matched by age (within 5 years) and sex to the other case groups. Risk factor data were not statistically significantly different between those with tumor blocks available and those without (data not shown). The cases were compared with polyp-free controls (n = 508).
Immunohistochemistry was performed on using five :m formalin-fixed, paraffin-embedded tissue sections, placing them on silane-coated slides and baking at 60° for 30 minutes. Afterwards, the slides are de paraffinized, hydrated, place in 10 mM citrate buffer (pH 6) and microwaved for a total of ten minutes (antigen retrieval). Appropriate blocking serum (Horse serum) and an anti-p53 monoclonal Mouse IgG2a [BP53-12-1] antibody (1:300 dilution, BioGenex, San Ramon, CA) was used. Detection method used Vectastain, Elite ABC kit (Vector Laboratory, Burlington, CA). Chromogen diamino-benzidine was used and sections were counter-stained with methyl green (Ethyl Green; Sigma Chemical Co; St. Louis MO). Nuclear staining of tumor tissue, from a single slide, was evaluated by a semiquantitative scoring system for intensity and percent positive nuclei. A positive control with known strongly positive p53 staining was used for comparison in each batch. Adjacent non-neoplastic colonic epithelium was used as a negative control for each batch. Two study pathologists (HH and MM) blinded to case status reviewed the stained slides and scored each case based on staining intensity and percent of cells on slide showing evidence of overexpression. Disagreements in ratings were resolved by consensus of the two pathologists. The following categories were used for scoring: intensity (None, Mild, Moderate, and Strong) and percent positive (none or rare, < 10% nuclear staining, 10–25%, 25–50%, and >50%). Cutoff levels reflect levels of staining not observed in normal colonic mucosa controls. Cases were classified as positive if the intensity score was strong and at least 10% or more of cells showing evidence of overexpression. For ease of presentation, we refer to these cases with protein overexpression as p53+ cases throughout the manuscript; those cases with no, mild or moderate staining intensity with any percent positive or those with strong staining but less than 10% positive nuclear staining are referred to as p53- cases. We also performed sensitivity analyses on the final models using a more stringent (intensity score strong and at least 25% or more of cells showing evidence of overexpression) as well as a less stringent definition (intensity score of moderate or strong with at least 10% or more of cells showing evidence of overexpression) of positivity.
First, univariate analyses comparing epidemiologic risk factors and p53 status were performed using analysis of variance for continuous variables and chi-square tests for categorical variables. All continuous variables were then categorized based on quantiles in the control group to test for linearity with respect to outcome status. Second, we used unordered polytomous logistic regression models to adjust for potential confounding variables . We performed two separate analyses: the first, combined all three groups (adenomas, CIS, and IM) into a single case group of early colorectal neoplasia; the second, examined only examined advanced adenomas (CIS and IM). Our sample size limited the use of multivariate models to analyze each type of case separately by p53 status, though univariate analyses suggested that the association between risk factors and p53 status were similar in magnitude across the separate types of cases (adenomas, CIS, and IM) (data not shown). There were a total of three outcome categories: p53 + cases, p53 - cases, and polyp-free controls and comparisons where made using odds ratios (OR) and 95% confidence intervals (CI) for p53+ cases versus polyp-free controls, p53- cases versus controls, and p53+ versus p53-cases.
All continuous variables that did not have a linear relationship with outcome status were categorized in categories based on homogeneity in risk . To account for the non-linear relationship with age, age adjustments were made by adding age and age squared (age2) to the regression model. Model building was based on log likelihood tests . Heterogeneity by p53 status was examined by examining the ratio of the odds ratio (which is equivalent to exponentiating the difference in the beta coefficients) and the 95% CI (based on the variance for the difference in the beta coefficients).
The prevalence of p53 protein overexpression increased steadily across the adenoma-carcinoma sequence from 10.3%, 21.7%, and 34.9% for adenomatous polyps, CIS, and intramucosal carcinoma (IM), respectively. Although, p53 protein overexpression differed by type of case group (p < .01), univariate associations between risk factors (including family history, alcohol use, tobacco use, body size, physical activity, dietary fiber and fat) and p53 status did not differ in magnitude or direction for the three types of cases, albeit numbers were small. Because of these similar univariate association and because of statistical power constraints we conducted two main multivariate analyses, one combining the three types of cases (adenomas, CIS, and IM) and a second only examining the more advanced adenomas (CIS and IM).
Descriptive Statistics by p53 status.
No p53 protein overexpression (n = 125)
p53 protein overexpression (n = 32)
Age (μ μ ;± σ)
Family History of Colorectal Cancer
Age at Starting (μ ± σ)
Total years (μ ± σ)
Cigs per day (μ ± σ)
Pipe or Cigar smoking
# of alcoholic drinks per week (μ ± σ)
Other risk factors
Body Mass Index (kg/m2) (μ ± σ)
Leisure Physical Activity Hours/week (μ ± σ)
Daily Fiber Intake Grams/day (μ ± σ)
Daily Fat Intake Grams/day (μ ± σ)
Age adjusted odds ratios by p53 status relative to polyp-free controls.
No p53 protein overexpression
p53 protein overexpression
Total number of years smoking*
< 15 years
15 – 29 years
Pipes or cigars
Beer 1–7 bottles/week
Beer 8+ bottles/week
Wine (any wine during week)
Liquor (any liquor during week)
Total alcohol (wine+beer+liquor)
Body Size and Physical Activity
Body mass index (kg/m2)
22.5 – <25.5
Leisure physical activity
Fiber: < 12.5 grams/day
12.5 – <17 grams/day
Fat: < 60 grams/day
60 – <85.5 grams/day
Multivariate adjusted* odds ratios by p53 status relative to polyp-free controls.
No p53 protein overexpression (-)
p53 protein overexpression (+)
(A) Associations using all cases (adenomas, CIS, IM)
Duration of Cigarette Smoking
< 15 years
15 – 29 years
Pipes or cigars
Body mass index (kg/m2)
22.5 – <25.5
(B) Associations using all only cases with advanced adenomas (CIS and IM)
Duration of Cigarette Smoking
< 15 years
15 – 29 years
Pipes or cigars
Body mass index (kg/m2)
22.5 – <25.5
We also examined these associations for only the cases of CIS and IM. These findings are also reported in Table 3 (panel B) and suggest little differences between the analyses for all three groups combined. Although these results suggest that cigarette smoking may be associated mainly with the tumors that do not overexpress p53 protein and beer consumption mainly with the tumors that overexpress p53 protein, statistical tests of heterogeneity were not significant (see the case/case comparisons reported in Table 3). Specifically, the comparison of heavy beer consumption for subjects with polyps that overexpress p53 protein relative to those without overexpression was over two-fold but not statistically significant (OR = 2.5, 95% CI = 0.7–8.1). Comparison of long duration of cigarette smoking for subjects with polyps that overexpress p53 protein relative to those without overexpression was 0.6 (95%CI = 0.2–1.5).
Sensitivity analyses altering the definition of p53 positivity.
Original a priori definition a
More stringent definition b
Less stringent definition c
Long duration of Cigarette Smoking (30+ years)
No p53 protein overexpression
p53 protein overexpression
Heavy Beer Consumption (8 + bottles per week)
No p53 protein overexpression
p53 protein overexpression
The p53 tumor suppressor gene is a commonly mutated gene in colorectal cancer . While the effect of p53 mutations on colorectal cancer prognosis has been heavily studied, less is known about how epidemiologic risk factors such as alcohol and tobacco consumption relate to p53 status. In many populations, colorectal adenomas are common [16, 24] but most adenomas will not advance to cancer. Understanding risk factors for early colorectal neoplasia is therefore is crucial to colon cancer prevention .
p53 status and polyp site
In this study, adenomatous polyps overexpressing p53 protein (with and without CIS and IM) were more likely to be found in the rectum and distal colon than in the proximal colon (p< 0.01). This findings agrees with a study by Diez and colleagues of invasive colorectal cancer which also found p53 overexpression more frequently in distal than proximal tumors (58.5% versus 41.7%, p = 0.03).
p53 status and cigarette smoking
We also found that long duration of cigarette smoking was related to adenomatous polyps (with and without CIS and IM) that did not overexpress p53 protein (OR = 1.8, 95% CI = 1.1–2.9) but not those polyps that did overexpress p53 protein. This association persisted when only examining CIS and IM cases compared to control and was robust to different definitions of p53 positivity. This finding also closely matches that of Freedman and colleagues in their case-control study of invasive colorectal cancer: OR = 1.84 (95% CI, 1.00–3.37) with heavy cigarette smoking (40+ pack years) for p53 negative colorectal cancer and no association with p53 positive colorectal cancer as determined by protein overexpression . Our findings also lend support to recent findings by Slattery and colleagues on the association between cigarette smoking and microsatellite instability (MSI) positive invasive colon cancers (OR = 1.6, 95%CI = 1.0–2.5 for men, OR = 2.2, 95%CI = 1.4–3.5 for women) but not MSI negative cancers. MSI and p53 are inversely associated suggesting two molecularly distinct forms of colorectal cancer, MSI-positive and MSI-negative, or, as referred to by Laurent-Puig, LOH (loss of heterozygosity)-positive, characterized by K-ras and p53 mutations, and MSI-positive colorectal cancers [28, 29].
The association between cigarette smoking and p53-negative tumors is interesting in light of the relationship between smoking, p53 mutation, and other tumor sites . People with p53 mutations who smoke may be more likely to get another cancer, as p53 mutations are associated with a number of tobacco-related tumors including lung, head and neck, and bladder cancers . Most of the p53 mutations in colonic tissue, however, are endogenous [4, 31] (i.e., spontaneous transitions at the CpG sites); endogenous mutations are not thought to be associated with exogenous environmental factors like cigarette smoking .
p53 status and alcohol intake
We found alcohol intake, specifically heavy beer consumption, to be more associated with polyps that overexpress p53 than those that do not (OR = 4.0, 95% CI = 1.3–12.0 for p53 protein overexpression relative to polyp-free controls versus OR = 1.6, 95%CI = 0.7–3.7). A similar association was found when restricting the analyses to just the advanced adenomas (CIS and IM). Sensitivity analyses, however, revealed that this finding was limited to our a priori definition of p53 positivity as well as a more strigent definition of positivity but not to a less strigent definition of positivity. Our finding with heavy alcohol consumption agrees with those of Fredrickson and colleagues who reported an increased association of p53-positive (as determined by protein overexpression) invasive colorectal cancer with alcohol use (OR = 3.4, 95%CI = 1.1–10).
The association between p53 protein overexpression and alcohol intake in the colon is interesting in light of the fact, as previously mentioned, that most p53 mutations in the colon are transitions rather than transversions. In contrast, other tumors such as those of the aerodigestive tract, which are highly associated with smoking and alcohol intake  have a higher prevalence of transversions . This suggests the possibility of a different mechanism for alcohol in the colon than aerodigestive tract tumors.
Strengths and Limitations
Our main findings that 1) polyps overexpressing p53 protein are more likely to be located in the distal colon and rectum, 2) long-term cigarette smoking is more likely to be related to early colorectal tumors that do not overexpress p53 protein, and 3) alcohol consumption, specifically beer consumption, is more likely to be associated with early colorectal tumors that overexpress p53 protein, all agree with the literature on invasive colorectal cancer. This suggests that underlying mechanisms that may explain associations between epidemiologic risk factors and p53 status are likely involved in early colorectal neoplasia as well.
Our study benefited from uniform pathologic review and classification of all lesions, reducing the degree of measurement error in the classification of lesions . p53 status was also assessed in a blinded fashion. We were able to obtain paraffin-embedded tissue blocks for 75% of the IM cases and 80% of the CIS cases. Risk factor data did not differ between those with tumor blocks available and those without (data not shown). Uniform classification, blinded assessment, and lack of selection bias in tumor block availability are strengths of this study.
Despite the agreement with the invasive cancer literature and the other study strengths, there are some limitations that warrant discussion. Tests of statistical heterogeneity were not significant. Thus, even though findings between p53 status and the risk factors were significant relative to polyp-free controls, tests comparing the odds ratios between subjects with p53 protein overexpression and those without were not statistically significant. Measurement error of p53 protein overexpression likely hampered the ability to detect heterogeneity . Third, we were limited by a small sample size to fully model differences stratified by p53 status and case group (adenomatous polyp, CIS, and IM). However, univariate assessment between risk factors and p53 status stratified by case group suggested similar associations irrespective of case group. Restriction of our final model to just cases with CIS and IM also did not alter any of our conclusions. As well, reliability analyses suggest that CIS and IM cases should be combined into a case group of "advanced adenomas" given the difficulty in reliably classifying these lesions .
In sum, we found similar associations between p53 status and polyp site, cigarette use, and alcohol consumption reported in several studies of invasive colorectal cancer.
Specifically, p53 protein overexpression, which has been associated with a worse overall survival after cancer diagnosis, is more likely to be found in polyps in the distal colon and rectum, more likely to be associated with alcohol intake, and less likely to be associated with cigarette smoking. We did not find any association between p53 status and other risk factors for colorectal neoplasia such as body size and physical activity. Additional studies of early colorectal neoplasia that investigate associations between epidemiologic risk factors and markers of genetic changes are needed to understand progression to invasive cancer from a relatively common precursor lesion. However, this study lends itself to the view that some colorectal risk factors may share the same association with respect to specific genotypic changes in precursor lesions and invasive cancer.
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