Laminin-332 gamma 2 Monomeric Chain Promotes Adhesion and Migration of Hepatocellular Carcinoma Cells

Simple Summary Extracellular matrix (ECM) molecules are believed to being critically involved in the progression of hepatocellular carcinoma (HCC). Laminin332 (Ln332) is an ECM protein complex that has been found to be implicated in the acquisition of aggressive phenotype of HCC cancer cells. Here, we focus on the pro-invasive function of the gamma 2 chain of Ln332 in monomeric form, highlighting its ability to stimulate the motility of HCC cell, independent of and to the same extent as the entire Ln332. Our data provide proof of principle that blocking interactions between the gamma 2 chain and related receptors on the HCC cell surface may be strategic to counteract HCC aggravation. Extracellular matrix (ECM) has a well-recognized impact on the progression of solid tumors, including hepatocellular carcinoma (HCC). Laminin 332 (Ln332) is a ECM molecule of epithelial basal lamina, composed of three polypeptide chains (alpha 3, beta 3, and gamma 2), that is usually poorly expressed in the normal liver but is detected at high levels in HCC. This macromolecule was shown to promote the proliferation, epithelial-to-mesenchymal transition (EMT), and drug resistance of HCC cells. The monomeric gamma 2 chain is up-regulated and localized preferentially at the invasive edge of metastatic intrahepatic HCC nodules, suggesting its potential involvement in the acquisition of invasive properties of HCC cells. HCC cells were tested in in vitro adhesion, scattering, and transwell migration assays in response to fibronectin and the Ln332 and Ln332 gamma 2 chains, and the activation status of major signaling pathways involved was evaluated. Here, we show that the Ln332 gamma 2 chain promotes HCC the cell adhesion, migration, and scattering of HCC cells that express the Ln332 receptor alpha 3 beta 1 integrin, proving to be a causal factor of the EMT program achievement. Moreover, we found that efficient HCC cell adhesion and migration on gamma 2 require the activation of the small cytosolic GTPase Rac1 and ERKs signaling. These data suggest that the gamma 2 chain, independently from the full-length Ln332, can contribute to the pro-invasive potential of aggressive HCC cell subpopulations.