个人信息Personal Information
教授
博士生导师
硕士生导师
性别:男
毕业院校:日本京都大学
学位:博士
所在单位:化工海洋与生命学院
电子邮箱:jnzhang@dlut.edu.cn
CD147 stimulates hepatoma cells escaping from immune surveillance of T cells by interaction with Cyclophilin A
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论文类型:期刊论文
发表时间:2016-05-01
发表刊物:BIOMEDICINE & PHARMACOTHERAPY
收录刊物:SCIE、PubMed、Scopus
卷号:80
页面范围:289-297
ISSN号:0753-3322
关键字:Tumor immunesurveillance; Hepatocellular carcinoma; CD147; Cyclophilin A; Chemotaxis
摘要:T cells play an important role in tumor immune surveillance. CD147 is a member of immunoglobulin superfamily present on the surface of many tumor cells and mediates malignant cell behaviors. Cyclophilin A (CypA) is an intracellular protein promoting inflammation when released from cells. CypA is a natural ligand for CD147. In this study, CD147 specific short hairpin RNAs (shRNA) were transfected into murine hepatocellular carcinoma Hepa1-6 cells to assess the effects of CD147 on hepatoma cells escaping from immune surveillance of T cells. We found extracellular CypA stimulated cell proliferation through CD147 by activating ERK1/2 signaling pathway. Downregulation of CD147 expression on Hepa16 cells significantly suppressed tumor progression in vivo, and decreased cell viability when co-cultured with T cells in vitro. Importantly, knockdown of CD147 on Hepa1-6 cells resulted in significantly increased T cells chemotaxis induced by CypA both in vivo and in vitro. These findings provide novel mechanisms how tumor cells escaping from immune surveillance of T cells. We provide a potential therapy for hepatocellular carcinoma by targeting CD147 or CD147-CypA interactions. (C) 2016 Elsevier Masson SAS. All rights reserved.