2. Academic Validation
  3. SHP2 inhibition mitigates adaptive resistance to MEK inhibitors in KRAS-mutant gastric cancer through the suppression of KSR1 activity

SHP2 inhibition mitigates adaptive resistance to MEK inhibitors in KRAS-mutant gastric cancer through the suppression of KSR1 activity

  • Cancer Lett. 2022 Dec 7;555:216029. doi: 10.1016/j.canlet.2022.216029.
Wenfang Zheng 1,  Zhiyi Yang 2,  Ping Song 3,  Yingchao Sun 4,  Pan Liu 3,  Lei Yue 4,  Kaiqi Lv 5,  Xinjie Wang 4,  Yuqin Shen 4,  Jianmin Si 4,  Xue Zhang 6,  Yuehai Ke 6,  Hongqiang Cheng 7,  Weiling Hu 8
Affiliations

Affiliations

  • 1 Department of Gastroenterology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China; Institute of Gastroenterology, Zhejiang University, Hangzhou, China; Department of Gastroenterology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
  • 2 Department of Pathology and Pathophysiology and Department of Cardiology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
  • 3 Department of Pathology and Pathophysiology, Zhejiang University School of Medicine, Hangzhou, China.
  • 4 Department of Gastroenterology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China; Institute of Gastroenterology, Zhejiang University, Hangzhou, China.
  • 5 Department of Gastroenterology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
  • 6 Department of Pathology and Pathophysiology and Department of Respiratory Medicine, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
  • 7 Department of Pathology and Pathophysiology and Department of Cardiology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China. Electronic address: hqcheng11@zju.edu.cn.
  • 8 Department of Gastroenterology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China; Institute of Gastroenterology, Zhejiang University, Hangzhou, China; Cancer Center, Zhejiang University, Hangzhou, China. Electronic address: huweiling@zju.edu.cn.
PMID: 36493900 DOI: 10.1016/j.canlet.2022.216029
Abstract

Despite the promising antitumor activity of Raf/MEK inhibitors for RAS-driven cancers, not all patients respond to these therapies. Adaptive resistance has been reported as a major culprit in non-responders, which can be reversed by SHP2 inhibitors (SHP2is) in multiple Cancer cells; however, the underlying mechanisms remain unknown. In this study, we found that KRAS-mutant gastric Cancer cells respond to MEK inhibitors (MEKis) with adaptive resistance. Markedly, SHP2 activation accompanied by ERK signaling restoration in MEKi-treated cells, and a MEKi and SHP2i combination had a synergistic effect on downstream signaling blockade. In vivo, SHP099 combined with AZD6244 (selumetinib) was highly efficacious for the treatment of xenografts. Mechanistically, SHP2 was found to interact with the scaffold protein KSR1 through its protein tyrosine Phosphatase domain. KSR1 knockdown sensitized cells to AZD6244, whereas a KSR1 activating mutation (S269A) diminished the synergistic anti-proliferative effect of SHP2i and MEKi. Interestingly, activated SHP2, during adaptive resistance to MEKis, impaired the interaction with KSR1, activating KSR1 to promote MAPK signaling. In conclusion, SHP2 promotes adaptive resistance to MEKis by activating KSR1; selumetinib combined with SHP099 might be an available therapeutic strategy for KRAS-mutant gastric cancers.

Keywords

KRAS-Mutant gastric cancer; KSR1; MAPK signaling; MEK inhibitor; SHP2.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-100510
    99.45%, RAF抑制剂
    Raf
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