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mTOR 通路遗传变异与欧洲癌症前瞻性调查(EPIC)中的前列腺癌风险。

Genetic variability of the mTOR pathway and prostate cancer risk in the European Prospective Investigation on Cancer (EPIC).

机构信息

German Cancer Research Center (DKFZ), Heidelberg, Germany.

出版信息

PLoS One. 2011 Feb 23;6(2):e16914. doi: 10.1371/journal.pone.0016914.

Abstract

The mTOR (mammalian target of rapamycin) signal transduction pathway integrates various signals, regulating ribosome biogenesis and protein synthesis as a function of available energy and amino acids, and assuring an appropriate coupling of cellular proliferation with increases in cell size. In addition, recent evidence has pointed to an interplay between the mTOR and p53 pathways. We investigated the genetic variability of 67 key genes in the mTOR pathway and in genes of the p53 pathway which interact with mTOR. We tested the association of 1,084 tagging SNPs with prostate cancer risk in a study of 815 prostate cancer cases and 1,266 controls nested within the European Prospective Investigation into Cancer and Nutrition (EPIC). We chose the SNPs (n = 11) with the strongest association with risk (p<0.01) and sought to replicate their association in an additional series of 838 prostate cancer cases and 943 controls from EPIC. In the joint analysis of first and second phase two SNPs of the PRKCI gene showed an association with risk of prostate cancer (OR(allele) = 0.85, 95% CI 0.78-0.94, p = 1.3 x 10⁻³ for rs546950 and OR(allele) = 0.84, 95% CI 0.76-0.93, p = 5.6 x 10⁻⁴ for rs4955720). We confirmed this in a meta-analysis using as replication set the data from the second phase of our study jointly with the first phase of the Cancer Genetic Markers of Susceptibility (CGEMS) project. In conclusion, we found an association with prostate cancer risk for two SNPs belonging to PRKCI, a gene which is frequently overexpressed in various neoplasms, including prostate cancer.

摘要

mTOR(哺乳动物雷帕霉素靶蛋白)信号转导通路整合了各种信号,根据可用能量和氨基酸调节核糖体生物发生和蛋白质合成,并确保细胞增殖与细胞大小增加适当偶联。此外,最近的证据表明 mTOR 和 p53 通路之间存在相互作用。我们研究了 mTOR 通路和与 mTOR 相互作用的 p53 通路中 67 个关键基因的遗传变异。我们在欧洲癌症与营养前瞻性调查(EPIC)中对 815 例前列腺癌病例和 1266 例对照进行了一项研究,测试了 1084 个标记 SNP 与前列腺癌风险的关联。我们选择了与风险相关性最强的 11 个 SNP(p<0.01),并试图在 EPIC 中另外 838 例前列腺癌病例和 943 例对照的系列中复制其关联。在第一阶段和第二阶段的联合分析中,PRKCI 基因的两个 SNP 显示与前列腺癌风险相关(OR(等位基因)=0.85,95%CI 0.78-0.94,p=1.3×10⁻³ 对于 rs546950 和 OR(等位基因)=0.84,95%CI 0.76-0.93,p=5.6×10⁻⁴ 对于 rs4955720)。我们在使用我们研究的第二阶段数据与癌症遗传易感性标记物(CGEMS)项目的第一阶段联合作为复制集的荟萃分析中证实了这一点。总之,我们发现两个属于 PRKCI 的 SNP 与前列腺癌风险相关,PRKCI 是一种在包括前列腺癌在内的各种肿瘤中经常过度表达的基因。

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