在头部和部状细胞癌中罕见的驱动突变汇聚在NOTCH信号上
Sampath K Loganathan1, Krista Schleicher1,2, Ahmad Malik1,2
1Centre for Molecular and Systems Biology, Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada.
研究人员发现了15个抑制瘤的基因,包括ADAM10和AJUBA,这些基因可以抑制头平细胞癌 (HNSCC). 这些基因促进NOTCH受体信号传递,它们的失活是HNSCC的标志.
科学领域:
- 癌症学
- 遗传学
- 分子生物学
背景情况:
- 大多数人类癌症都表现出一些高频突变和许多低频"长尾"突变,其功能作用尚不清楚.
- 低频基因变异在癌症发展中的意义在很大程度上仍未被探索.
研究的目的:
- 研究"长尾"突变在头部和部状细胞癌 (HNSCC) 的功能后果.
- 鉴定突变导致HNSCC瘤发展的基因.
主要方法:
- 在小鼠体内使用CRISPR查来评估HNSCC中484个"长尾"基因突变的影响.
- 分析了基因突变,单基因损失,以及它们与人类HNSCC样本中的NOTCH受体信号和突变的关联.
主要成果:
- 鉴定出抑制小鼠HNSCC发育的15个瘤抑制基因.
- 通过增强NOTCH受体信号传递,发现ADAM10和AJUBA作为瘤抑制剂.
- 发现ADAM10和AJUBA突变或单基因损失发生在28%的HNSCC病例中,并且与NOTCH受体突变相互排斥.
结论:
- 在67%的人类HNSCC病例中,NOTCH信号通路的失活是关键事件.
- 在HNSCC中,ADAM10和AJUBA是关键的瘤抑制剂,这凸显了NOTCH途径在这种癌症类型中的重要性.
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