SHR6390 combined with cabozantinib inhibits tumor progression in hepatocellular carcinoma mouse model

Author:

Liu Caiqi1,Shi Jiaqi2,Lin Binlin2,Zhou Meng2,Shan Dan2,Nie Jianhua2,Wang Yan3,Zhang Yanqiao2,Han Peng4,Zheng Tongsen2ORCID

Affiliation:

1. Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, People's Republic of China

2. Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, People\'s Republic of China

3. Department of Colorectal Surgery, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, People\'s Republic of China

4. Department of General Surgery, the First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People\'s Republic of China

Abstract

Background: A novel CDK4/6 inhibitor SHR6390 has shown significant anti-tumor effects. However, its role in hepatocellular carcinoma(HCC) remains unknown. Objective: To explore the inhibitory effect of combination treatment with SHR6390 and cabozantinib in HCC, and its antitumor mechanism, so as to provide more effective therapeutic strategy for HCC patients. Methods: We investigated SHR6390, monotherapy or combined with cabozantinib, by CCK8, wound healing, transwell, western blotting, immunohistochemistry and mouse model of subcutaneous tumor. Results: Our results show that SHR6390 exhibited potent anti-proliferative activity against HCC in a dose-dependent manner. SHR6390 combined with cabozantinib exhibited more potent inhibition of cell viability, migration and invasion. In terms of potential mechanisms, we found that cabozantinib could lead to phosphorylation of Rb, which was reduced in SHR6390 and combined groups. SHR6390 monotherapy inhibited the growth of subcutaneous HCC tumors, besides the combination treatment with SHR6390 and cabozantinib exerted synergistic anti-tumor activity in vivo. Conclusion: SHR6390 is effective against HCC, monotherapy or combined with cabozantinib.

Publisher

Bentham Science Publishers Ltd.

Subject

Genetics (clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

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