We then explored the molecular mechanism underlying modulation of CD151 in MMP9 expression in HCCLM3 cells through the zone-by-zone blockade of the PI3K/Akt/glycogen synthase kinase 3β (GSK-3β)/Snail

signal. We further explored the role of CD151 in tumor-associated neoangiogenesis and metastasis in vitro and in vivo. Finally, we evaluated the combined expression of CD151, MMP9, and MVD as a prognostic marker in HCC patients. AFP, alpha-fetoprotein; AKT, protein kinase B; bFGF, basic fibroblast growth DMXAA molecular weight factor; CDC42, cell division control protein 42 homologue; CI, confidence interval; ELISA, enzyme-linked immunosorbent assay; ERK, extracellular signal-regulated kinase; FAK, focal adhesion kinase; GAPDH, glyceraldehyde 3-phosphate dehydrogenase; selleck chemicals GSK, glycogen synthase kinase; H&E, hematoxylin and eosin; HBsAg, hepatitis B surface antigen; HCC, hepatocellular carcinoma; HR, hazard ratio; HUVEC, human umbilical vein endothelial cell; LY294002, 2-morpholin-4-yl-8-phenylchromen-4-one; MAPK, mitogen-activated protein kinase; MMP, matrix metalloproteinase; mRNA, messenger RNA; MVD, microvessel density; NA, not adopted; NS, not significant;

OS, overall survival; PI3K, phosphatidylinositol-3-kinase; qRT-PCR, quantitative real-time polymerase chain reaction; RT-PCR, reverse transcription polymerase chain reaction; shRNA, short hairpin RNA; siRNA, small interfering RNA; TNM, tumor node metastasis; U0126, 1,4-diamino-2,3-dicyano-1,4-bis(2-aminophenylthio)butadiene; VEGF, vascular endothelial growth factor. A highly metastatic human HCC

cell line (HCCLM3), low-metastatic human HCC cell lines (MHCC97-L, PLC/PRF/5, Hep3B, and HepG2; American Type Culture Collection),6, 18, 19 and human umbilical vein endothelial cells (HUVECs; American Type Culture Collection) were used in this study. Male, athymic BALB/c nude mice (8 weeks old; Shanghai Mephenoxalone Institute of Material Medicine, Chinese Academy of Science, Shanghai, China) were raised under specific pathogen-free conditions. Animal care and experimental protocols were in accordance with the guidelines established by the Shanghai Medical Experimental Animal Care Commission. Specimens taken from areas next to the margins of tumors were collected from 327 consecutive patients with HCC who underwent curative resection between 1997 and 2000 at the Liver Cancer Institute of Fudan University (Shanghai, China). The histopathological diagnosis was based on the World Health Organization criteria.20 The histological grade of tumor differentiation was determined according to the classification proposed by Edmondson and Steiner.21 Liver function was assessed by the Child-Pugh scoring system. Clinical tumor typing was performed according to the sixth edition of the tumor node metastasis (TNM) classification system of the Union Internationale Contre le Cancer. Ethical approval was obtained from the research ethics committee of Zhongshan Hospital, and written, informed consent was obtained from each patient.