Tobacco, alcohol, and p53 overexpression in early colorectal neoplasia
Tobacco, alcohol, and p53 overexpression in early colorectal neoplasia
复制标题
早期结直肠肿瘤中的烟草、酒精和 p53 过度表达
作者:
M. Terry;A. Neugut;M. Mansukhani;J. Waye;N. Harpaz;H. Hibshoosh
BackgroundThe 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).MethodsWe 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).Resultsp53 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).ConclusionOur 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.
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影响因子:
5
作者:
Terry,MB;Neugut,AI
通讯作者:
Neugut,AI
影响因子:
56.9
作者:
HOLLSTEIN, M;SIDRANSKY, D;HARRIS, CC
通讯作者:
HARRIS, CC
DOI:
10.1093/jnci/92.22.1831
发表时间:
2000-11-15
期刊:
JOURNAL OF THE NATIONAL CANCER INSTITUTE
影响因子:
--
作者:
Slattery, ML;Curtin, K;Samowitz, WS
通讯作者:
Samowitz, WS
DOI:
--
发表时间:
1993
期刊:
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
影响因子:
--
作者:
Neugut,AI;Jacobson,JS;DeVivo,I
通讯作者:
DeVivo,I
影响因子:
8.8
作者:
Freedman, AN;Michalek, AM;Marshall, JR;Mettlin, CJ;Petrelli, NJ;Zhang, ZF;Black, JD;Satchidanand, S;Asirwatham, JE
通讯作者:
Asirwatham, JE