Journal of Enzyme Inhibition and Medicinal Chemistry (Jan 2021)

Discovery of N-aryl sulphonamide-quinazoline derivatives as anti-gastric cancer agents in vitro and in vivo via activating the Hippo signalling pathway

  • Jin-Bo Niu,
  • Chun-Hua Quan,
  • Yuan Liu,
  • Guang-Xi Yu,
  • Jia-Jia Yang,
  • Yin-Ru Li,
  • Yan-Bing Zhang,
  • Ying-Qiu Qi,
  • Jian Song,
  • Cheng-Yun Jin,
  • Sai-Yang Zhang

DOI
https://doi.org/10.1080/14756366.2021.1958211
Journal volume & issue
Vol. 36, no. 1
pp. 1715 – 1731

Abstract

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Hippo signalling pathway plays a crucial role in tumorigenesis and cancer progression. In this work, we identified an N-aryl sulphonamide-quinazoline derivative, compound 9i as an anti-gastric cancer agent, which exhibited potent antiproliferative ability with IC50 values of 0.36 μM (MGC-803 cells), 0.70 μM (HCT-116 cells), 1.04 μM (PC-3 cells), and 0.81 μM (MCF-7 cells), respectively and inhibited YAP activity by the activation of p-LATS. Compound 9i was effective in suppressing MGC-803 xenograft tumour growth in nude mice without obvious toxicity and significantly down-regulated the expression of YAP in vivo. Compound 9i arrested cells in the G2/M phase, induced intrinsic apoptosis, and inhibited cell colony formation in MGC-803 and SGC-7901 cells. Therefore, compound 9i is to be reported as an anti-gastric cancer agent via activating the Hippo signalling pathway and might help foster a new strategy for the cancer treatment by activating the Hippo signalling pathway regulatory function to inhibit the activity of YAP.

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