EIF3B通过TBK1和PI3K/AKT信号通路促进KRAS基因突变驱动的结肠腺癌进展

Chongren Ren1, Yaxin Qin1, Dujuan Cao2

  • 1Department of General Surgery, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, Taiyuan, China.

概括

准EIF3B对具有KRAS突变的结肠直肠癌 (CRC) 有前途. 抑制EIF3B可以减少瘤生长,并破坏KRAS突变结直肠腺癌的关键信号通路.

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