MAPK/ERK通路
抗凋亡Ras信号级联
癌症研究
癌变
细胞生物学
支架蛋白
信号转导
癌基因
化学
生物
癌症
细胞周期
遗传学
作者
Qiwei Jiang,Deyu Zhang,Juan Liu,Chaoyang Liang,Ronghui Yang,Cheng Zhang,Jun Wu,Jing Lin,Tianxing Ye,Lihua Ding,Jianbin Li,Shan Gao,Binghui Li,Qinong Ye
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2023-06-09
卷期号:9 (23)
被引量:2
标识
DOI:10.1126/sciadv.ade1155
摘要
The EGFR-RAS-ERK pathway plays a key role in cancer development and progression. However, the integral assembly of EGFR-RAS-ERK signaling complexes from the upstream component EGFR to the downstream component ERK is largely unknown. Here, we show that hematopoietic PBX-interacting protein (HPIP) interacts with all classical components of the EGFR-RAS-ERK pathway and forms at least two complexes with overlapping components. Experiments of HPIP knockout or knockdown and chemical inhibition of HPIP expression showed that HPIP is required for EGFR-RAS-ERK signaling complex formation, EGFR-RAS-ERK signaling activation, and EGFR-RAS-ERK signaling–mediated promotion of aerobic glycolysis as well as cancer cell growth in vitro and in vivo. HPIP expression is correlated with EGFR-RAS-ERK signaling activation and predicts worse clinical outcomes in patients with lung cancer. These results provide insights into EGFR-RAS-ERK signaling complex formation and EGFR-RAS-ERK signaling regulation and suggest that HPIP may be a promising therapeutic target for cancer with dysregulated EGFR-RAS-ERK signaling.
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