追踪癌症演变揭示了转移的受限制路径:TRACERx脏
Samra Turajlic1, Hang Xu2, Kevin Litchfield2
1Translational Cancer Therapeutics Laboratory, the Francis Crick Institute, London NW1 1AT, UK; Renal and Skin Units, the Royal Marsden Hospital NHS Foundation Trust, London SW3 6JJ, UK.
Cell
|April 17, 2018
概括
转移性清细胞癌 (ccRCC) 的进展不同. 染色体复杂性,特别是9p损失,导致ccRCC转移和死亡率,影响传播模式.
科学领域:
- 癌症学
- 遗传学
- 病理学
背景情况:
- 清细胞癌 (ccRCC) 有多种转移性行为.
- 缺乏对ccRCC转移表型的系统研究.
研究的目的:
- 在清细胞癌中分析转移性表型.
- 确定ccRCC转移和死亡的遗传驱动因素.
主要方法:
- 来自100名患者的575个初级和335个转移性ccRCC活检的分析.
- 瘤样本的检查,包括尸体活检.
- 染色体复杂性与转移能力和生存的相关性.
主要成果:
- 转移能力与染色体复杂性有关.
- 染色体9p的丢失是导致ccRCC转移和死亡的一个关键事件 (p=0. 0014).
- 观察到不同的转移模式:从单克隆瘤迅速扩散而非异质瘤逐渐扩散.
结论:
- 在ccRCC转移中,染色体复杂性和9p损失等特定的遗传变化至关重要.
- 瘤异质性影响转移的进展速度和模式.
- 胰腺转移表现出早期克隆分离和长期潜伏期.
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