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Anticancer Research 2020-Aug

MK615 Suppresses Hypoxia Tolerance by Up-regulation of E-cadherin in Colorectal Cancer Cells With Mutant KRAS

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Kensuke Nishi
Toshiyuki Tsunoda
Yoshinori Uchida
Takayuki Sueta
Motohiro Sawatsubashi
Takafumi Yamano
Yasuko Hashiguchi
Anthony Swain
Senji Shirasawa
Toshifumi Sakata

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Astratto

Background/aim: The Japanese apricot "Prunus mume" is a traditional Japanese medicine. MK615, a compound extract from Prunus mume has been reported to have anti-tumor effects. Herein, we used 3D floating (3DF) culture to evaluate the anticancer effects of MK615 against human colorectal cancer (CRC) cells that contain mutant (mt) KRAS.

Materials and methods: HKe3 cells exogenously expressing mtKRAS (HKe3-mtKRAS) were treated with MK615 in 3DF cultures. The protein levels of hypoxia-inducible factor 1 (HIF-1) and E-cadherin were quantified by western blotting.

Results: MtKRAS enhanced hypoxia tolerance via up-regulation of HIF-1. The expression of HIF-1 protein was suppressed by constitutive overexpression of E-cadherin in CRC HCT116 spheroids. MK615 increased the expression of E-cadherin and decreased the expression of HIF-1 in HKe3-mtKRAS. These results suggest that MK615 suppresses hypoxia tolerance by up-regulation of E-cadherin in CRC cells with mtKRAS.

Conclusion: MK615 exhibits properties useful for the potential treatment of CRC patients with mtKRAS.

Keywords: E-cadherin; HIF; KRAS; MK615; Prunus mume; colon cancer.

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