0%, and 46.4% versus 50.6%, respectively). When evaluating the combined effect of CD151, MMP9, and MVD on the prognosis of HCC, we classified patients into three subgroups according

to their CD151, MMP9, and MVD-CD34 density: group I had high expression of all three markers, group II had high expression of one or two www.selleckchem.com/products/Romidepsin-FK228.html of the three markers, and group III had low expression of all three markers. We found that the 3-, 5-, and 7-year OS in group I was 50.9%, 39.1%, and 30.0%, respectively, significantly lower than the OS for groups II and III (Fig. 6A). The 3-, 5-, and 7-year cumulative recurrence rates in group I were 58.2%, 63.6%, and 64.5%, respectively, which were significantly higher than those for groups II and III (Fig. 6B). Individual clinicopathological features that showed significance by univariate analysis were adopted as covariates in a multivariate Cox proportional hazards model, and then combined variables were further analyzed. Multivariate Cox proportional hazards analysis also showed that overexpression of CD151, MMP9, and MVD together was independent of other prognostic markers (large size, microvascular invasion, and multiple tumors) for both OS (P < 0.001) and cumulative recurrence (Table 1; P < 0.001). Traditionally, tetraspanin

CD151 may activate Rac and Cdc42 by facilitating the integrins beta-catenin inhibitor and growth factor receptor signals or redistribute integrins by endocytosis and/or trafficking, with the end result being the promotion of motility and metastasis of tumor cells.4, 35, 36 In the present

study, we consistently observed that overexpression of CD151 facilitated tumor-associated neoangiogenesis in HCC and apparently did so by engaging MMP9 as an agent via the PI3K/Akt/GSK-3β/Snail signal, and thus it promoted the progression of HCC. An earlier study reported that homophilic interactions of tetraspanin CD151 up-regulated the expression of MMP9 in human melanoma (MelJuSo) cells through the FAK/p38/MAPK/JNK/c-Jun pathway.17 In contrast to the results with MelJuSo cells,17 we found that overexpression of medchemexpress CD151 in HCC cells up-regulated the expression of MMP9 by facilitating the PI3K/Akt/GSK-3β/Snail signal in HCC cells. One of the reasons for this inconsistency may reside in the special structural and functional characteristics of the tetraspanins.4 These proteins can assemble themselves into complexes consisting of a core structure surrounded by other specific proteins. This complex formation provides a great deal of variability, which in turn allows for specificity and functional differences to occur in different cell types.4, 37 Tetraspanin complexes can also present different functional profiles at different cell development stages, even though they may share several common components.4, 35 To our knowledge, the present study is the first to clearly demonstrate that overexpression of CD151 promotes MMP9 expression via the PI3K/Akt/GSK-3β/Snail cascade.