蛋白激酶B
MAPK/ERK通路
mTORC2型
癌症研究
PI3K/AKT/mTOR通路
激酶
细胞生物学
磷酸化
化学
细胞生长
信号转导衔接蛋白
信号转导
mTORC1型
蛋白激酶A
支架蛋白
三阴性乳腺癌
生物
细胞
原癌基因蛋白质c-akt
靶向治疗
FOXO3公司
癌症
IQGAP1型
细胞迁移
乳腺癌
p38丝裂原活化蛋白激酶
丝裂原活化蛋白激酶
作者
Zhenbo Tu,Leah Moses,Yi Hu,Sworaj Sapkota,Liza M. Quintana,Leismi Guerrero,George W. Bell,Antoine E. Karnoub
出处
期刊:Science Signaling
[American Association for the Advancement of Science]
日期:2026-02-10
卷期号:19 (924): eadr4063-eadr4063
标识
DOI:10.1126/scisignal.adr4063
摘要
Triple-negative breast cancers (TNBCs) lack targeted therapeutics that can inhibit their growth and progression. The long intergenic noncoding RNA LINC01133 promotes TNBC pathogenesis by increasing the abundance of proline-rich protein 5 (PRR5), an mTORC2 component that activates the kinase AKT in a PI3K-independent, mTORC2-dependent manner. Here, however, we found that TNBC cell proliferation was incompletely sensitive to AKT inhibitors alone because PRR5 also stimulated the mitogen-activated protein kinase (MAPK) cascade in an mTORC2-dependent manner. PRR5 associated with and prevented the ubiquitin-dependent proteasomal degradation of IQGAP1, an adaptor protein that promotes activation of the MAP kinase ERK. ERK signaling was essential for LINC01133-mediated TNBC proliferation in two- and three-dimensional cultures, and ERK inhibitors synergized with AKT blockade to suppress LINC01133-induced TNBC cell growth. Furthermore, PRR5 abundance was particularly enriched and correlated with that of phosphorylated ERK in samples from patients with TNBC. Our results highlight cross-talk between mTORC2 and ERK signaling downstream of LINC01133 and PRR5 that may be therapeutically targeted to treat TNBC.
科研通智能强力驱动
Strongly Powered by AbleSci AI