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Enhanced expression of Hab18g/CD147 and activation of integrin pathway in HCC cells under 3‐D co‐culture conditions
Author(s) -
Wu YaMei,
Tang Juan,
Zhao Pu,
Chen ZhiNan,
Jiang JianLi
Publication year - 2009
Publication title -
cell biology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.932
H-Index - 77
eISSN - 1095-8355
pISSN - 1065-6995
DOI - 10.1016/j.cellbi.2008.11.006
Subject(s) - integrin , extracellular matrix , metastasis , matrix metalloproteinase , cell culture , cancer research , hepatocellular carcinoma , paxillin , biology , extracellular , cell adhesion , microbiology and biotechnology , cell , cancer , genetics
CD147 is reported to be correlated with the malignancy of some cancers, and its overexpression affects the progression of tumor. In the present study, we investigated the function of HAb18G/CD147, a member of CD147 family, on hepatocellular carcinoma (HCC) adhesion, invasion and metastasis in 3‐dimensional (3‐D) cell co‐culture model. The results showed that the extracellular microenvironment could determine the cellular phenotypes and then affected the cellular functions. The expressions of HAb18G/CD147 in HCC cells and fibroblasts were both obviously elevated in 3‐D co‐culture model. The overexpression of HAb18G/CD147 increased MMPs' (MMP‐2 and MMP‐9) production ( P < 0.01), and was obviously accompanied with enhanced expressions of paxillin, FAK and p‐FAK in 3‐D cell co‐culture model. All the results suggest that HAb18G/CD147 plays an important role in HCC adhesion, invasion and metastasis mainly via modulating synthesis of MMPs and activating integrin signal pathways in fibroblasts and tumor cells themselves under the 3‐D co‐culture conditions.