Department of Hepatobiliary Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi Province, China.
PLoS One. 2013 Aug 12;8(8):e67268. doi: 10.1371/journal.pone.0067268. eCollection 2013.
It has been reported that Annexin A2 (ANXA2) is up-regulated in hepatocellular carcinoma (HCC), but the roles of ANXA2 in the migration and invasion of HCC cells have not been determined. In this study, we found that ANXA2-specific siRNA (si-ANXA2) significantly inhibited the migration and invasion of HCC cells co-cultured with fibroblasts in vitro. In addition, the production of MMP-2 by fibroblasts cultured in supernatant collected from si-ANXA2-transfected HCC cells was notably down-regulated. ANXA2 was also found to be co-localized and co-immunoprecipitated with CD147. Further investigation revealed that the expression of ANXA2 in HCC cells affected the shedding of CD147-harboring membrane microvesicles, acting as a vehicle for CD147 in tumor-stromal interactions and thereby regulating the production of MMP-2 by fibroblasts. Together, these results suggest that ANXA2 enhances the migration and invasion potential of HCC cells in vitro by regulating the trafficking of CD147-harboring membrane microvesicles.
已有报道称,膜联蛋白 A2(ANXA2)在肝细胞癌(HCC)中上调,但 ANXA2 在 HCC 细胞迁移和侵袭中的作用尚未确定。在这项研究中,我们发现 Annexin A2 特异性 siRNA(si-ANXA2)可显著抑制与成纤维细胞共培养的 HCC 细胞的迁移和侵袭。此外,从转染 si-ANXA2 的 HCC 细胞上清液中培养的成纤维细胞产生的 MMP-2 明显下调。还发现 ANXA2 与 CD147 共定位和共免疫沉淀。进一步的研究表明,HCC 细胞中 ANXA2 的表达影响了携带 CD147 的膜微囊泡的脱落,作为肿瘤-基质相互作用中 CD147 的载体,从而调节成纤维细胞产生 MMP-2。综上所述,这些结果表明,ANXA2 通过调节携带 CD147 的膜微囊泡的运输,增强 HCC 细胞在体外的迁移和侵袭能力。