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dc.contributor.authorWang, Zhuoyingen_US
dc.contributor.authorWang, Chongrenen_US
dc.contributor.authorZhou, Zifeien_US
dc.contributor.authorSun, Mengxiongen_US
dc.contributor.authorZhou, Chenghaoen_US
dc.contributor.authorChen, Jianen_US
dc.contributor.authorYin, Feien_US
dc.contributor.authorWang, Hongshengen_US
dc.contributor.authorLin, Binhuien_US
dc.contributor.authorZuo, Dongqingen_US
dc.contributor.authorLi, Suoyuanen_US
dc.contributor.authorFeng, Lijinen_US
dc.contributor.authorDuan, Zhenfengen_US
dc.contributor.authorCai, Zhengdongen_US
dc.contributor.authorHua, Yingqien_US
dc.date.accessioned2017-04-06T03:19:16Z
dc.date.issued2016en_US
dc.identifier.citationWang, Z., C. Wang, Z. Zhou, M. Sun, C. Zhou, J. Chen, F. Yin, et al. 2016. “CD151-mediated adhesion is crucial to osteosarcoma pulmonary metastasis.” Oncotarget 7 (37): 60623-60638. doi:10.18632/oncotarget.11380. http://dx.doi.org/10.18632/oncotarget.11380.en
dc.identifier.issnen
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:32072058
dc.description.abstractCD151, a tetraspanin family protein involved in cell-cell and cell-extracellular matrix interaction, is differentially expressed in osteosarcoma cell membranes. Thus, this study aimed to investigate the role of CD151 in osteosarcoma metastasis. We analyzed CD151 expression in patient tissue samples using immunohistochemistry. CD151 expression was also silenced with shRNA in osteosarcoma cells of high metastatic potential, and cell adhesion, migration and invasion were evaluated in vitro and pulmonary metastasis was investigated in vivo. Mediators of cell signaling pathways were also examined following suppression of CD151 expression. Overall survival for patients with low versus high CD151 expression level was 94 vs. 41 months (p=0.0451). CD151 expression in osteosarcoma cells with high metastatic potential was significantly higher than in those with low metastatic potential (p<0.001). shRNA-mediated silencing of CD151 did not influence cell viability or proliferation; however, cell adhesion, migration and invasion were all inhibited (all p<0.001). In mice inoculated with shRNA-transduced osteosarcoma cells, the number and size of lung metastatic lesions were reduced compared to the mice inoculated with control-shRNA transduced cells (p<0.001). In addition, CD151 knockdown significantly reduced Akt, p38, and p65 phosphorylation as well as focal adhesion kinase, integrin β1, p70s6, and p-mTOR levels. Taken together, CD151 induced osteosarcoma metastasis likely by regulating cell function through adhesion signaling. Further studies are necessary to fully explore the diagnostic and prognostic value of determining CD151 expression in osteosarcoma patients.en
dc.language.isoen_USen
dc.publisherImpact Journals LLCen
dc.relation.isversionofdoi:10.18632/oncotarget.11380en
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312406/pdf/en
dash.licenseLAAen_US
dc.subjectosteosarcomaen
dc.subjecttetraspaninen
dc.subjectCD151en
dc.subjectmetastasisen
dc.subjectadhesionen
dc.titleCD151-mediated adhesion is crucial to osteosarcoma pulmonary metastasisen
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden
dc.relation.journalOncotargeten
dc.date.available2017-04-06T03:19:16Z
dc.identifier.doi10.18632/oncotarget.11380*
dash.authorsorderedfalse


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