Dded to the upper chamber, while 750 ml DMEM containing 10 FBS was placed in the lower chamber. After 48 h of incubation, Matrigel and cells remaining in the upper chamber were removed by cotton swabs. Cells on the lower surface of the membrane were fixed in 4 paraformaldehyde and stained with Giemsa. Cells in 5 microscopic fields (magnification, 6200) were counted and photographed. All LED-209 web experiments were performed in triplicate.Immunoblotting and Immunofluorescence AssayTotal cell extract protein (30 mg) was separated by SDSpolyacrylamide gel electrophoresis, transferred onto GSK -3203591 polyvinylidene difluoride membranes, and incubated with the corresponding antibodies. The membranes were developed with the enhanced chemiluminescence method (Pierce, Rockford, IL, USA). Mouse anti-human CD151(11G5a, 1:200; Serotec, UK) and anti-integrin a3 monoclonal antibodies (P1B5, 1:300; Chemicon International, Temecula, CA) were used to detect the expression of CD151 and integrin a3, respectively. GAPDH (1:5,000; Chemicon, USA) was used as an internal control. All experiments were performed in triplicate. HGC-27 cells were used to detect the location of CD151 and integrin a3 as described previously [13]. Mouse anti-human CD151 monoclonal antibody (11G5a, 1:200; Serotec, UK) and mouse anti-human integrin a3 antibody (P1B5, 1:300; Chemicon International, Temecula, CA) were used. The slices were analyzed by fluorescence 
microscopy (Leica Microsystems Imaging Solutions).In Vivo Metastasis AssaysFor in vivo metastasis assays, MGC-803-Mock, MGC-803vshRNACD151 and MGC-803-vshRNA CD151-cDNA-CD151 cells were transplanted into nude mice (5-week-old BALB/c-nu/ nu, 5 per group, 16106 cells for each mouse) through the lateral tail vein [14]. After 7 weeks, mice were sacrificed. Their lungs were removed and subjected to hematoxylin and eosin (H E) staining. All research involving animals was performed in compliance with protocols approved by the Shaoxing Second People’s Hospital Animal Care Commission.Co-immunoprecipitation (Co-ip) AssaysCells were lysed with RIPA lysis buffer supplemented with 40 mM NaF, 100 mM Na3VO4, and Complete Protease Inhibitor (Roche). After removing the insoluble material by centrifugation at 12,0006g, the precleared lysates were incubated with primary mAb pre-absorbed protein A- and G-Sepharose beads (Pierce Biotechnology) overnight at 4uC. The precipitates were washed three times with lysis buffer, boiled in 26SDS sample buffer for 5 minutes, and proteins were resolved by SDS-PAGE on 10 gradient gels. Subsequent immunoblots were probed with the appropriate antibody and detected by ECL.Transfection of Lentiviral Vectors with Small Hairpin RNA Against CD151 and Integrin aThe pGMLV/Neo-shRNA-CD151 vector was constructed according to the manufacturer’s instructions (pGMLV, a small hairpin RNA (shRNA)i Vector, Shanghai Genomeditch Co. Ltd). Three shRNA-CD151 lentiviral vectors (pGMLV-GFPshRNA -CD151) were generated to silence the expression of CD151 in HGC-27 cells (shRNA-CD151-HGC-27). The shRNA targeting sequences for CD151 were as follows: #1, 59-CATGTGGCACCGTTTGCCT-39; #2, 59TACCTGCTGTTTACCTACA-39; #3, 59-CATACAGGTGCTCAA TAAA-39. The shRNA targeting sequence for integrin a3 was 
as follows: 59- CCTCTATATTGGGTACACGAT-39 (Shanghai Genomeditech, Shanghai, China). Stably transfected clones were characterized by RT-PCR and analyzed by immunoblotting for the expression levels of the CD151 and integrin a3 proteins.Construction of Tissue Microarrays and.Dded to the upper chamber, while 750 ml DMEM containing 10 FBS was placed in the lower chamber. After 48 h of incubation, Matrigel and cells remaining in the upper chamber were removed by cotton swabs. Cells on the lower surface of the membrane were fixed in 4 paraformaldehyde and stained with Giemsa. Cells in 5 microscopic fields (magnification, 6200) were counted and photographed. All experiments were performed in triplicate.Immunoblotting and Immunofluorescence AssayTotal cell extract protein (30 mg) was separated by SDSpolyacrylamide gel electrophoresis, transferred onto polyvinylidene difluoride membranes, and incubated with the corresponding antibodies. The membranes were developed with the enhanced chemiluminescence method (Pierce, Rockford, IL, USA). Mouse anti-human CD151(11G5a, 1:200; Serotec, UK) and anti-integrin a3 monoclonal antibodies (P1B5, 1:300; Chemicon International, Temecula, CA) were used to detect the expression of CD151 and integrin a3, respectively. GAPDH (1:5,000; Chemicon, USA) was used as an internal control. All experiments were performed in triplicate. HGC-27 cells were used to detect the location of CD151 and integrin a3 as described previously [13]. Mouse anti-human CD151 monoclonal antibody (11G5a, 1:200; Serotec, UK) and mouse anti-human integrin a3 antibody (P1B5, 1:300; Chemicon International, Temecula, CA) were used. The slices were analyzed by fluorescence microscopy (Leica Microsystems Imaging Solutions).In Vivo Metastasis AssaysFor in vivo metastasis assays, MGC-803-Mock, MGC-803vshRNACD151 and MGC-803-vshRNA CD151-cDNA-CD151 cells were transplanted into nude mice (5-week-old BALB/c-nu/ nu, 5 per group, 16106 cells for each mouse) through the lateral tail vein [14]. After 7 weeks, mice were sacrificed. Their lungs were removed and subjected to hematoxylin and eosin (H E) staining. All research involving animals was performed in compliance with protocols approved by the Shaoxing Second People’s Hospital Animal Care Commission.Co-immunoprecipitation (Co-ip) AssaysCells were lysed with RIPA lysis buffer supplemented with 40 mM NaF, 100 mM Na3VO4, and Complete Protease Inhibitor (Roche). After removing the insoluble material by centrifugation at 12,0006g, the precleared lysates were incubated with primary mAb pre-absorbed protein A- and G-Sepharose beads (Pierce Biotechnology) overnight at 4uC. The precipitates were washed three times with lysis buffer, boiled in 26SDS sample buffer for 5 minutes, and proteins were resolved by SDS-PAGE on 10 gradient gels. Subsequent immunoblots were probed with the appropriate antibody and detected by ECL.Transfection of Lentiviral Vectors with Small Hairpin RNA Against CD151 and Integrin aThe pGMLV/Neo-shRNA-CD151 vector was constructed according to the manufacturer’s instructions (pGMLV, a small hairpin RNA (shRNA)i Vector, Shanghai Genomeditch Co. Ltd). Three shRNA-CD151 lentiviral vectors (pGMLV-GFPshRNA -CD151) were generated to silence the expression of CD151 in HGC-27 cells (shRNA-CD151-HGC-27). The shRNA targeting sequences for CD151 were as follows: #1, 59-CATGTGGCACCGTTTGCCT-39; #2, 59TACCTGCTGTTTACCTACA-39; #3, 59-CATACAGGTGCTCAA TAAA-39. The shRNA targeting sequence for integrin a3 was as follows: 59- CCTCTATATTGGGTACACGAT-39 (Shanghai Genomeditech, Shanghai, China). Stably transfected clones were characterized by RT-PCR and analyzed by immunoblotting for the expression levels of the CD151 and integrin a3 proteins.Construction of Tissue Microarrays and.