胰腺癌的危险因素与p53和K-ras密码子12突变的表达之间的关系

Jon P Fryzek, David H Garabrant, Maryjean Schenk, Margaret Kinnard, Joel K Greenson, Fazlul H Sarkar
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引用次数: 24

摘要

背景:胰腺癌是癌症死亡的主要原因。研究表明,一些风险因素,包括吸烟、体重指数、有胰腺癌亲属和糖尿病可能与胰腺癌风险有关。研究目的:我们在密歇根州东南部进行了病例对照研究,研究上述危险因素与K-ras癌基因和p53抑癌基因突变的关系。方法:245例新诊断胰腺癌患者和420例普通人群对照纳入研究。在本分析中,所有病例对象仅限于有组织阻滞可用于研究的胰腺癌患者(n = 51)。进行了面对面访谈,以确定人口统计和生活方式因素的信息。采用调整后的logistic回归分析,比较K-ras和p53突变的胰腺癌患者及其亚型与普通人群对照的各种受试者特征。结果:吸烟(校正优势比[aOR] = 2.0;95%可信区间[95% ci] = 0.9-4.3)和访谈前5年或更长时间诊断为糖尿病(aOR = 3.4;95%CI = 1.3-8.8)与K-ras密码子12突变阳性的胰腺癌患者相关,而与K-ras密码子12突变阴性的胰腺癌患者无关。另一方面,没有一个被检查的危险因素与p53突变的患者有意义的关系。结论:本研究提示一些公认的胰腺癌危险因素也可能与K-ras密码子12突变有关。然而,进一步的大规模研究是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The association between selected risk factors for pancreatic cancer and the expression of p53 and K-ras codon 12 mutations.

Background: Pancreatic cancer is a major contributor to cancer mortality. Studies suggest that a few risk factors, including cigarette smoking, body mass index, having a relative with pancreatic cancer, and diabetes may be related to pancreatic cancer risk.

Aim of the study: We conducted a case-control study in southeastern Michigan to examine the relation between the above mentioned risk factors and mutations of the K-ras oncogene and p53 tumor suppressor gene.

Methods: Two hundred forty-five patients with newly diagnosed pancreatic cancer and 420 general population controls were enrolled in the study. For this analysis, all case subjects were restricted to the pancreatic cancer patients that had tissue blocks available for study (n = 51). In-person interviews were conducted to ascertain information on demographic and lifestyle factors. Adjusted logistic regression analyses were conducted to compare various subject characteristics of pancreatic cancer patients with K-ras and p53 mutations and their subtypes to the characteristics of the general population controls.

Results: Smoking (adjusted odds ratio [aOR] = 2.0; 95% confidence interval [95%CI] = 0.9-4.3) and diabetes diagnosed 5 or more years before interview (aOR = 3.4; 95%CI = 1.3-8.8) were associated with pancreatic cancer patients positive for K-ras codon 12 mutations, but not with pancreatic cancer patients negative for K-ras codon 12 mutations. On the other hand, none of the examined risk factors were meaningfully related to patients with p53 mutations.

Conclusions: This study suggests that some recognized risk factors for pancreatic cancer may also be associated with K-ras codon 12 mutations. However, further large-scale studies are warranted.

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