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Molecular epidemiology of prostate cancer: hormone-related genetic loci.

机译:前列腺癌的分子流行病学:激素相关的遗传基因座。

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Prostate cancer is the most common non-skin cancer and the second leading cause of cancer deaths among men in most Western countries. Despite its high morbidity and mortality, the etiology of prostate cancer remains obscure. Although compelling laboratory data suggest a role for androgens in prostate carcinogenesis, most epidemiologic data, including serological and genetic studies, are inconclusive. In this chapter, we review the status of serologic studies and discuss the importance of intra-prostatic hormone levels in possibly clarifying the often-contradictory data on serologic studies. To provide insights and directions for epidemiologic research on hormones and prostate cancer, this review centers on the molecular epidemiology of hormone-related genetic loci. These loci have been investigated in a number of studies to date and will undoubtedly expand even further as rich new genetic information sources and high-throughput genotyping and analysis methods become available. Due to the enormous number of these loci, we recommend careful analysis and cautious interpretation of studies of genetic markers, including microsatellites and single nucleotide polymorphisms (SNPs), as false positive and negative results are likely due to limited statistical power, multiple hypothesis testing, population stratification, or non-representative population sampling. This review also highlights the need for replication in various populations, as well as reasons for performing functional analyses of SNPs, a critical and often under-appreciated component of molecular epidemiologic investigations. The time is ripe for concerted, large-scale multidisciplinary investigations that incorporate molecular genetics, biochemistry, histopathology, and endocrinology into traditional epidemiologic studies. Such collaboration will lead to a deeper understanding of the etiologic pathways of prostate cancer, ultimately yielding better preventive, diagnostic, and therapeutic strategies.
机译:在大多数西方国家中,前列腺癌是最常见的非皮肤癌,并且是导致癌症死亡的第二大主要原因。尽管其高发病率和高死亡率,但是前列腺癌的病因仍然不清楚。尽管令人信服的实验室数据表明雄激素在前列腺癌的发生中起作用,但大多数流行病学数据,包括血清学和遗传学研究,尚无定论。在本章中,我们回顾了血清学研究的现状,并讨论了前列腺内激素水平在阐明血清学研究中经常矛盾的数据方面的重要性。为了提供有关激素和前列腺癌的流行病学研究的见识和方向,本综述着重于激素相关遗传基因座的分子流行病学。迄今为止,已经在许多研究中对这些基因座进行了研究,并且毫无疑问,随着可获得丰富的新遗传信息资源以及高通量基因分型和分析方法,这些基因座将进一步扩大。由于这些基因座数量众多,我们建议对遗传标记物(包括微卫星和单核苷酸多态性(SNP))进行仔细的分析和谨慎的解释,因为错误的阳性和阴性结果可能是由于有限的统计能力,多重假设检验,人口分层或非代表性人口抽样。这篇综述还强调了在各种人群中进行复制的必要性,以及进行SNP功能分析的原因,SNP是分子流行病学研究的一个关键且经常被低估的组成部分。进行大规模,多学科协作研究的时机已经成熟,该研究将分子遗传学,生物化学,组织病理学和内分泌学纳入了传统的流行病学研究。这种合作将使人们对前列腺癌的病因学途径有更深入的了解,最终产生更好的预防,诊断和治疗策略。

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