Piezo1 impairs hepatocellular tumor growth via deregulation of the MAPK-mediated YAP signaling pathway. (May 2021)

• Record Type: Journal Article
• Authors: Liu, Silin; Xu, Xiaohuang; Fang, Zhigang; Ning, Yile; Deng, Bo; Pan, Xianmei; He, Yu; Yang, Zhongqi; Huang, Keer; Li, Jing
• Is Part Of: Cell calcium. Volume 95(2021)
• Publication Date: 2021-05
• Subjects: Piezo1 -- Haploinsufficient mice -- Calcium -- YAP signal -- Hepatocellular carcinoma; Calcium -- Metabolism -- Periodicals; Vertebrates -- Physiology -- Periodicals; Calcium -- Physiological effect -- Periodicals; Cell physiology -- Periodicals; Calcium in the body -- Periodicals; 572.516
• DOI: 10.1016/j.ceca.2021.102367
• Languages: English
• ISSNs: 0143-4160

Abstract

Graphical abstract: Highlights: Knocking down of Piezo1 impaired proliferation, migration, and increased apoptosis in HepG2 cells. Piezo1/MAPK/YAP signaling cascade was essential for cell function. HCC tumor growth was inhibited in Piezo1 haploinsufficient mice. Abstract: Accumulating evidence has revealed the mechanosensitive ion channel protein Piezo1 is contributing to tumorigenesis. However, its role in hepatocellular carcinoma (HCC) remains unexplored. In this study, we demonstrated that Piezo1 was expressed in the HepG2 cell line and depletion of Piezo1 impaired proliferation and migration, as well as increased apoptosis in these cells. Using a Piezo1-specific activator, Yoda1, we identified that calcium entry induced by Yoda1 resulted in phosphorylation of JNK, p38, and ERK, thereby activating the mitogen-activated protein kinase (MAPK) pathway, in a dose- and time-dependent manner. More strikingly, Piezo1 activation integrated with YAP signaling to control the nuclear translocation of YAP and regulation of its target genes. JNK, p38, and ERK (MAPK signaling) regulated Yoda1-induced YAP activation. Consistent with the association of calpain with Piezo1, we also found that calpain activity was decreased by siRNA-mediated knockdown of Piezo1. In addition, the growth of HCC tumors was inhibited in Piezo1 haploinsufficient mice. Together, our findings establish that the Piezo1/MAPK/YAP signaling cascade is essential for HepG2 cell function. These results highlight the importance of Piezo1 in HCC and the potential utility of Piezo1 as a biomarker and therapeutic target.