{"title":"STAT3 as a target of molecular targeting therapy for oral cancer: Cell-based screening using inhibitor screening kits","authors":"Tatsuhito Nagumo , Daisuke Ito , Hikari Tsukamoto , Arisa Yasuda , Satoru Shintani","doi":"10.1016/j.ajoms.2011.06.007","DOIUrl":null,"url":null,"abstract":"<div><p>Molecular targeting therapy has recently received attention owing to its high specificity for cancer cells; numerous researchers have been working to identify novel target molecules. In this study, we attempted to identify new targets through cell-based screening with inhibitor panel kits. The growth-inhibitory effects of inhibitors from the Screening Committee of Anticancer Drugs inhibitor kits, which contain 173 chemical inhibitors, were evaluated in oral squamous-cell carcinoma (OSCC) cell lines. Some of the inhibitors strongly suppressed the proliferation of OSCC cells. Of these inhibitors, we chose JSI-124, a specific inhibitor of STAT3, to investigate further. JSI-124 significantly inhibited the growth of OSCC cell lines and then induced DNA fragmentation, poly (ADP-ribose) polymerase cleavage, and caspase 3 activation in a dose-dependent manner. Treatment with JSI-124 resulted in a decrease of phosphorylated STAT3 and a downregulated expression of survivin, a downstream molecule of the STAT3 signaling cascade. Our data suggest that inhibition of STAT3 signaling by JSI-124 might be promising as a molecular therapy strategy against OSCC.</p></div>","PeriodicalId":100128,"journal":{"name":"Asian Journal of Oral and Maxillofacial Surgery","volume":"23 4","pages":"Pages 167-171"},"PeriodicalIF":0.0000,"publicationDate":"2011-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.ajoms.2011.06.007","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Oral and Maxillofacial Surgery","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0915699211000963","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4
Abstract
Molecular targeting therapy has recently received attention owing to its high specificity for cancer cells; numerous researchers have been working to identify novel target molecules. In this study, we attempted to identify new targets through cell-based screening with inhibitor panel kits. The growth-inhibitory effects of inhibitors from the Screening Committee of Anticancer Drugs inhibitor kits, which contain 173 chemical inhibitors, were evaluated in oral squamous-cell carcinoma (OSCC) cell lines. Some of the inhibitors strongly suppressed the proliferation of OSCC cells. Of these inhibitors, we chose JSI-124, a specific inhibitor of STAT3, to investigate further. JSI-124 significantly inhibited the growth of OSCC cell lines and then induced DNA fragmentation, poly (ADP-ribose) polymerase cleavage, and caspase 3 activation in a dose-dependent manner. Treatment with JSI-124 resulted in a decrease of phosphorylated STAT3 and a downregulated expression of survivin, a downstream molecule of the STAT3 signaling cascade. Our data suggest that inhibition of STAT3 signaling by JSI-124 might be promising as a molecular therapy strategy against OSCC.