RAD21 促进前列腺癌的瘤发生和致命进展
Xiaofeng A Su1,2,3,4,5, Konrad H Stopsack6,7, Daniel R Schmidt1,8
1David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139.
概括
积体,或异常的染色体数量,驱动致命的前列腺癌. 染色体8q上的凝聚素基因RAD21与致命的疾病进展密切相关,并通过减少DNA损伤来帮助侵略性瘤存活.
科学领域:
- 在瘤学瘤学.
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
背景情况:
- 不平衡的染色体数量 (aneuploidy) 与致命的前列腺癌进展有关.
- 人们还不太了解状积分症促进癌症攻击性的具体机制.
研究的目的:
- 在8q染色体上识别与致命前列腺癌进展相关的基因.
- 调查凝聚素基因RAD21在前列腺癌攻击性中的作用及其与形积分症的潜在联系.
主要方法:
- 对403名前列腺癌患者的基因表达的分析.
- 基因表达与长期转移风险和前列腺癌死亡的相关性.
- 评估RAD21在缓解前列腺癌器官和患者数据中的瘤性压力和DNA损伤方面的作用.
主要成果:
- 染色体8q上的一种凝聚素子单元基因RAD21显示,与致死性前列腺癌进展的最强相关性 (OR 3.7).
- 增加RAD21表达与TMPRSS2-ERG融合的瘤中减少有毒瘤性压力和DNA损伤有关.
- 似乎RAD21能够激进瘤的增殖和生存,这表明一个机制,由此形形有利于瘤.
结论:
- RAD21是致死性前列腺癌进展的关键驱动因素,可能会调解血管积分不全的好处.
- 准RAD21可能为侵袭性前列腺癌提供治疗策略.
- 这项研究提供了关于染色体不稳定如何导致癌症致死性的见解.
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