Andersen T I
Avdeling for medisinsk genetikk Ullevål sykehus, Blindern, Oslo.
Tidsskr Nor Laegeforen. 1998 May 30;118(14):2196-8.
Studies of molecular genetic changes in prostate carcinomas are slowly improving our understanding of the biological process which leads to a normal prostate epithelial cell becoming an adenocarcinoma cell with invasive and metastatic properties. Carriers of germ-line mutations in still unidentified prostate cancer susceptibility genes, one of which has been localised to chromosome arm lq, seem to be particularly prone to develop the disease. The susceptibility genes have to be identified and the effects of carrier detection evaluated before genetic testing for prostate cancer predisposition can be performed in a clinical setting. The identification of specific molecular genetic changes in prostate carcinomas may become clinically useful diagnostic and prognostic tools. An improved understanding of the molecular genetic mechanisms underlying the development of prostate cancer may eventually yield novel therapeutic strategies, attacking specific genetic changes in the prostate carcinomas.
对前列腺癌分子遗传学变化的研究正在逐步增进我们对这一生物学过程的理解,该过程使得正常前列腺上皮细胞转变为具有侵袭性和转移性的腺癌细胞。在仍未明确的前列腺癌易感基因中携带种系突变的个体,其中一个基因已定位到染色体臂1q,似乎特别容易患上这种疾病。在临床环境中进行前列腺癌易感性基因检测之前,必须先鉴定出这些易感基因,并评估携带者检测的效果。鉴定前列腺癌中特定的分子遗传学变化可能会成为临床上有用的诊断和预后工具。对前列腺癌发生发展背后分子遗传机制的深入理解最终可能会产生新的治疗策略,针对前列腺癌中的特定基因变化进行攻击。