Soliman A S, Bondy M L, Guan Y, El-Badawi S, Mokhtar N, Bayomi S, Raouf A A, Ismail S, McPherson R S, Abdel-Hakim T F, Beasley R P, Levin B, Wei Q
Department of Epidemiology, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Int J Oncol. 1998 Jun;12(6):1315-9. doi: 10.3892/ijo.12.6.1315.
An Egyptian hospital-based pilot case-control study was conducted to investigate the relationship between the expression level of mismatch repair (MMR) genes and the risk of colorectal cancer. The relative expression of five known MMR genes, i.e., hMSH2, hMLH1, hPMS1, hPMS2, and GTBP/hMSH6, was measured by a multiplex reverse transcriptase (RT)-polymerase chain reaction (PCR) in peripheral blood lymphocytes from 31 colorectal cancer patients and 47 age- and-sex matched controls. The expression of hMSH2, GTBP/hMSH6, hPMS1 and hPMS2 tended to be lower in patients than controls, but only the difference in hPMS2 expression was statistically significant (p<0. 01). Although 50% of the cases had chemotherapy or radiotherapy within the last six months before the blood was drawn, their gene expression was not statistically different from those who had not undergone such therapies. After adjustment for age and sex, the odds ratios (OR) calculated from a logistical regression model, using the median levels of gene expression of controls as cut-off values, indicated that increased risk was associated with reduced expressions of both hPMS1 (OR = 3.97, 95% confidence interval (CI) = 1.04 to 7.65) and hPMS2 (OR = 2.86, 95% CI = 1.05 to 7.76). Although the results of this study were inconclusive because of the small sample size and use of prevalent cases, it is biologically plausible that patients with colorectal cancers may have a lower expression of MMR genes than healthy controls because malfunction of these genes has been shown in hereditary nonpolyposis colon cancer. The involvement of low hPMS2 expression in colon cancer risk seems to be unique in the Egyptian population. Further studies with newly diagnosed patients before they begin therapy will provide more convincing data about the role of MMR gene expression in the etiology of colorectal cancers in Egypt.
一项基于埃及医院的病例对照试验研究旨在探究错配修复(MMR)基因的表达水平与结直肠癌风险之间的关系。通过多重逆转录酶(RT)-聚合酶链反应(PCR)测定了31例结直肠癌患者及47例年龄和性别匹配的对照者外周血淋巴细胞中5种已知MMR基因,即hMSH2、hMLH1、hPMS1、hPMS2和GTBP/hMSH6的相对表达。患者中hMSH2、GTBP/hMSH6、hPMS1和hPMS2的表达往往低于对照者,但只有hPMS2表达的差异具有统计学意义(p<0.01)。尽管50%的病例在采血前的最后6个月内接受了化疗或放疗,但其基因表达与未接受此类治疗的患者相比无统计学差异。在对年龄和性别进行校正后,使用对照者基因表达的中位数水平作为截断值,通过逻辑回归模型计算的优势比(OR)表明,hPMS1(OR = 3.97,95%置信区间(CI) = 1.04至7.65)和hPMS2(OR = 2.86,95%CI = 1.05至7.76)表达降低均与风险增加相关。尽管由于样本量小以及使用的是现患病例,本研究结果尚无定论,但结直肠癌患者的MMR基因表达可能低于健康对照者,这在生物学上是合理的,因为这些基因的功能异常已在遗传性非息肉病性结肠癌中得到证实。hPMS2低表达与结肠癌风险的关联在埃及人群中似乎是独特的。对新诊断患者在开始治疗前进行进一步研究,将为MMR基因表达在埃及结直肠癌病因学中的作用提供更有说服力的数据。