癌症研究
生物
调节器
子宫内膜间质肉瘤
转录组
抑制器
肉瘤
基因
免疫疗法
突变
间质细胞
恶性肿瘤
抑癌基因
子宫肉瘤
DNA错配修复
遗传学
靶向治疗
计算生物学
生殖系
基因敲除
种系突变
基因表达谱
融合基因
子宫内膜癌
生物信息学
作者
Tobias MP Hartwich,Seungji Choi,Ayoung Hwang,Stefania Bellone,Luca Palmieri,Hae Seo,Taekeun Kim,Juhyeon Hong,Camilla Krakstad,Jone Trovik,Ingunn M. Stefansson,Hans Kristian Haugland,Michelle Greenman,Victoria Ettorre,Sarah Ottum,Cem Demirkiran,Yang Yang-Hartwich,Natalia Buza,Pei Hui,Salvatore Lopez
标识
DOI:10.1073/pnas.2531105123
摘要
) and co-occurring deletions in metabolic regulator genes (TSC2, STK11). Finally, in an activating NRAS-mutant (p.Q61R) HG-ESS xenograft, the combination of MEK and FAK inhibition dramatically suppressed tumor growth and prolonged survival, highlighting a promising targeted treatment strategy. Overall, our comprehensive analysis defines the molecular basis of ESS and provides a strong preclinical rationale for precision therapies in this aggressive cancer.
科研通智能强力驱动
Strongly Powered by AbleSci AI