突变体
癌症研究
计算生物学
突变
点突变
生物
药物发现
头颈部鳞状细胞癌
抑制器
头颈部癌
癌症
遗传学
基因
生物信息学
作者
Danielle L. Swaney,Dana J. Ramms,Zhiyong Wang,Jisoo Park,Yusuke Goto,Margaret Soucheray,Neil E. Bhola,Kyumin Kim,Fan Zheng,Yan Zeng,Michael McGregor,Kari A. Herrington,Rachel A. O’Keefe,Nan Jin,Nathan K. VanLandingham,Helene Foussard,John Von Dollen,Mehdi Bouhaddou,David Jimenez‐Morales,Kirsten Obernier
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2021-09-30
卷期号:374 (6563)
被引量:56
标识
DOI:10.1126/science.abf2911
摘要
We outline a framework for elucidating tumor genetic complexity through multidimensional protein-protein interaction maps and apply it to enhancing our understanding of head and neck squamous cell carcinoma. This network uncovers 771 interactions from cancer and noncancerous cell states, including WT and mutant protein isoforms. Prioritization of cancer-enriched interactions reveals a previously unidentified association of the fibroblast growth factor receptor tyrosine kinase 3 with Daple, a guanine-nucleotide exchange factor, resulting in activation of Gαi- and p21-activated protein kinase 1/2 to promote cancer cell migration. Additionally, we observe mutation-enriched interactions between the human epidermal growth factor receptor 3 (HER3) receptor tyrosine kinase and PIK3CA (the alpha catalytic subunit of phosphatidylinositol 3-kinase) that can inform the response to HER3 inhibition in vivo. We anticipate that the application of this framework will be valuable for translating genetic alterations into a molecular and clinical understanding of the underlying biology of many disease areas.
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