Sanshimao formula inhibits the hypoxia-induced pro-angiogenesis of hepatocellular carcinoma cells partly through regulating MKK6/p38 signaling pathway

Author:

Chen Zhe12,Wang Man3ORCID,Lv Xiang4,Xu Yannan3,Wang Xionghui3,Li Bai1,Ling Changquan3,Du Juan3

Affiliation:

1. Department of Rehabilitation Medicine, Changhai Hospital, Naval Medical University , Shanghai , China

2. Qingdao Special Servicemen Recuperation Center of PLA Navy , Qingdao , China

3. Department of Traditional Chinese Medicine, Changhai Hospital, Naval Medical University , Shanghai , China

4. Drug Clinical Trial Institutions, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine , Shanghai , China

Abstract

Abstract Objectives Sanshimao (SSM) is a traditional Chinese medicine formula for advanced hepatocellular carcinoma (HCC). This study was designed to investigate the effect of SSM on HCC-induced angiogenesis and to explore the potential mechanism. Methods The endothelial cells were cultured with HCC cells conditioned medium in the 1% oxygen atmosphere to imitate tumor hypoxia microenvironment. EA.hy926 cells migration and tubulogenesis were detected by tube formation and scratch-wound assay. The protein microarray was employed to explore SSM-targeted proteins in Huh7 cells. We also established an animal model to observe the effects of SSM on angiogenesis in vivo. Results The data indicated that SSM reduced HCC-induced migration and tube formation of EA.hy926 cells at low dose under hypoxic conditions. These effects might be partly owing to suppression of HIF-1α-induced vascular endothelial growth factorα expression in Huh7 cells. Moreover, this inhibition was in an MKK6/P38-dependent way. Besides, Huh7 subcutaneous tumor models in nude mice further demonstrated the inhibition of SSM on tumor weight might be exerted partly by reduction of angiogenesis via blocking MKK6/P38 signaling pathways. Conclusion SSM inhibits HCC-induced pro-angiogenesis under hypoxic conditions via suppression of MKK6/P38 signaling pathways, which is favorable for HCC tumor growth.

Funder

National Natural Science Foundation of China

Shanghai Municipal Health Commission

Publisher

Oxford University Press (OUP)

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