人群中的交响乐:癌症前列腺的关键基因改变

Cancer Innovation Pub Date : 2023-02-09 DOI:10.1002/cai2.52
Neshat Masud
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引用次数: 0

摘要

雄激素受体(AR)信号传导经常被靶向用于治疗癌症(PCa)。尽管主要患者通过靶向AR信号轴获得了良好的治疗效果,但最终它通过改变前列腺细胞的基因组成而产生耐药性。然而,为了开发一种有效的治疗方案,识别前列腺癌的关键基因改变是至关重要的。引起不同雄激素不同分化状态的最常见的遗传改变是TMPRSS2与ETS家族基因的基因融合、肿瘤抑制因子PTEN和TP53基因的缺失或突变、AR的扩增或剪接、改变的DNA修复基因。在这篇综述中,我们描述了已被认为有助于改变前列腺环境的关键基因和遗传变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Symphony in the crowd: Key genetic alterations in prostate cancer

Androgen receptor (AR) signaling have been frequently targeted for treating prostate cancer (PCa). Even though primarily patients receive a good therapeutic outcome by targeting AR signaling axis, eventually it emerges resistance by altering the genetic makeup of prostate cells. However, to develop an effective therapeutic regime, it is essential to recognize key genetic alterations in PCa. The most common genetic alterations that give rise to distinct androgen different differentiation states are gene fusion of TMPRSS2 with ETS family genes, deletion, or mutation of tumor suppressor PTEN and TP53 gene, amplification or splicing of AR, altered DNA repair genes. In this review, we describe key genes and genetic changes that have been recognized to contribute to altered prostate environment.

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