| Literature DB >> 30145835 |
Jian Gao1, Yingxue Rong1, Yuxing Huang1, Peng Shi1, Xitao Wang2, Xuan Meng3,4, Jiahong Dong5, Congying Wu1.
Abstract
A majority of hepatocellular carcinomas (HCCs) combine with liver cirrhosis. The cirrhotic liver has been implicated in interfering with the effects of HCC-targeted drugs, including sorafenib. Alterations in the tumor microenvironment of the cirrhotic liver include both biochemical and biomechanical factors. In this study, we induced sorafenib resistance in HCC cells. We observed changes in cell morphology, cytoskeletal architecture, and cellular stiffness in these sorafenib-resistant cells, resembling those adapted to stiffer substrates. To examine the contribution of mechanical factors in HCC cell growth and drug resistance, we used an in vitro cell culture system with adjustable stiffness mimicking the normal or cirrhotic liver tissues. We identified that mechanical adaptation conferred HCC cells with increased motility and sorafenib resistance. We further reported the mechanism underlying the involvement of the transcription coactivator YAP. Our results underline the important role of mechanical factors in the interaction between tumor cells and their microenvironment.Entities:
Keywords: YAP; drug resistance; hepatocellular carcinoma (HCC); sorafenib; tumor biomechanics; tumor cell migration
Year: 2018 PMID: 30145835 DOI: 10.1002/jcp.27078
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384