Suppr超能文献

基质金属蛋白酶-1启动子中的单核苷酸多态性增强肺癌易感性。

A single nucleotide polymorphism in the matrix metalloproteinase-1 promoter enhances lung cancer susceptibility.

作者信息

Zhu Y, Spitz M R, Lei L, Mills G B, Wu X

机构信息

Department of Epidemiology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.

出版信息

Cancer Res. 2001 Nov 1;61(21):7825-9.

Abstract

Extracellular matrix-degrading matrix metalloproteinase-1 (MMP-1) is one of the interstitial collagenases likely to be involved in tumor invasion and metastasis. MMP-1 may also contribute to tumor initiation and development by altering the cellular microenvironment that facilitates tumor formation. Recent studies have found that overexpression of MMP-1 is associated with the initial stages of cancer development in addition to promoting cellular invasion; however, preexisting oncogenic mutations or chemical carcinogens are required to initiate tumorigenesis as well. There is a single nucleotide polymorphism located in the promoter region of MMP-1 that partially regulates gene expression. The 2G/2G genotype enhances transcriptional activity and may be associated with an increased lung cancer risk. Using a case-control study, we tested the hypotheses that (a) individuals with the 2G/2G genotype may be at an increased risk for lung cancer; and (b) the risk should be greatly elevated in smoking individuals. PCR-RFLP was used to determine the MMP-1 genotypes in 456 lung-cancer cases and 451 frequency-matched controls of Caucasian ethnicity. Overall, there was a significant association between the 2G/2G genotype and lung cancer risk [odds ratio (OR), 1.76; 95% confidence interval (CI), 1.29-2.39]. In current smokers, the lung cancer risk associated with the 2G/2G genotype was significantly elevated (OR, 3.16; 95% CI, 1.87-5.35). However, this association was less evident in former smokers (OR, 1.23; 95% CI, 0.81-1.87) and absent in never smokers (OR, 1.09; 95% CI, 0.31-3.91). Similarly, this risk was more evident in heavy smokers (OR, 2.55; 95% CI, 1.61-4.03) than in light smokers (OR, 1.40; 95% CI, 0.84-2.32). Interestingly, men were observed to have a 2.15-fold increased lung cancer risk (OR, 2.15; 95% CI, 1.42-3.26) compared with women (OR, 1.34; 95% CI, 0.84-2.15). Furthermore, subjects with 2G/2G genotype developed lung cancer earlier (60.94 +/- 0.64 years old) than patients with 1G/1G and 1G/2G genotypes (62.91 +/- 0.59 years old; P = 0.024). Our data demonstrate that the 2G/2G genotype enhances lung cancer susceptibility especially in current smokers. To our knowledge, these results report the first molecular epidemiological evidence of the MMP-1 promoter polymorphism associated with the development of lung cancer in the presence of continuing carcinogenic exposure.

摘要

细胞外基质降解酶基质金属蛋白酶-1(MMP-1)是一种间质胶原酶,可能参与肿瘤侵袭和转移。MMP-1还可能通过改变促进肿瘤形成的细胞微环境,对肿瘤的起始和发展产生影响。最近的研究发现,MMP-1的过表达除了促进细胞侵袭外,还与癌症发展的初始阶段相关;然而,肿瘤发生还需要预先存在的致癌突变或化学致癌物。MMP-1启动子区域存在一个单核苷酸多态性,可部分调节基因表达。2G/2G基因型增强转录活性,可能与肺癌风险增加有关。通过病例对照研究,我们检验了以下假设:(a)2G/2G基因型个体患肺癌的风险可能增加;(b)吸烟个体的风险应大幅升高。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,对456例肺癌病例和451例频率匹配的高加索族对照个体的MMP-1基因型进行了检测。总体而言,2G/2G基因型与肺癌风险之间存在显著关联[比值比(OR)为1.76;95%置信区间(CI)为1.29 - 2.39]。在当前吸烟者中,与2G/2G基因型相关的肺癌风险显著升高(OR为3.16;95%CI为1.87 - 5.35)。然而,这种关联在前吸烟者中不太明显(OR为1.23;95%CI为0.81 - 1.87),在从不吸烟者中则不存在(OR为1.09;95%CI为0.31 - 3.91)。同样,重度吸烟者的这种风险(OR为2.55;95%CI为1.61 - 4.03)比轻度吸烟者(OR为1.40;95%CI为0.84 - 2.32)更明显。有趣的是,与女性(OR为1.34;95%CI为0.84 - 2.15)相比,男性患肺癌的风险增加了2.15倍(OR为2.15;95%CI为1.42 - 3.26)。此外,2G/2G基因型的受试者患肺癌的时间比1G/1G和1G/2G基因型的患者更早(60.94±0.64岁)(1G/1G和1G/2G基因型患者为62.91±0.59岁;P = 0.024)。我们的数据表明,2G/2G基因型增加了肺癌易感性,尤其是在当前吸烟者中。据我们所知,这些结果首次报道了在持续致癌暴露情况下,MMP-启动子多态性与肺癌发生相关的分子流行病学证据。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验