前列腺癌的分子遗传学。

Annales chirurgiae et gynaecologiae Pub Date : 1999-01-01
T Visakorpi
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引用次数: 0

摘要

尽管前列腺癌具有重要的临床意义,但其发生和发展的分子机制尚不清楚。分子遗传学的目的是揭示参与疾病过程的遗传改变和基因。连锁分析已经暗示了四个染色体位点可能含有前列腺癌易感基因。此外,染色体改变在前列腺肿瘤已经研究使用几种技术,如比较基因组杂交。这些分析表明,6q、8p、10q、13q和16q染色体的缺失以及7q、8q和Xq染色体的增加在前列腺癌中尤为常见。也有强有力的证据表明,雄激素受体基因(AR)、e-cadherin和PTEN等基因参与了前列腺癌的发生和发展。然而,上述大多数染色体改变的靶基因以及易患前列腺癌的基因尚未被克隆。识别这些基因应该是目前前列腺癌基础研究的最高目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular genetics of prostate cancer.

Despite the substantial clinical importance of prostate cancer, the molecular mechanisms underlying the development and progression of the disease are poorly understood. The aim of molecular genetics is to reveal the genetic alterations and genes that are involved in disease processes. Linkage analysis have already implicated four chromosomal loci that may harbour prostate cancer susceptibility genes. In addition, chromosomal alterations in prostate tumors have been studied using several techniques, such as comparative genomic hybridization. These analyses have indicated that losses of chromosomes 6q, 8p, 10q, 13q, and 16q, as well as gains of 7, 8q, and Xq are particularly common in prostate cancer. There is also a strong evidence, that genes, such as androgen receptor gene (AR), e-cadherin, and PTEN, are involved in the development and progression of prostate cancer. However, the target genes for most of the above mentioned chromosomal alterations as well as the genes predisposing to prostate cancer have not been cloned yet. The identification of those genes should be the utmost goal of basic research of prostate cancer, today.

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