STAT3 as a target of molecular targeting therapy for oral cancer: Cell-based screening using inhibitor screening kits

Tatsuhito Nagumo , Daisuke Ito , Hikari Tsukamoto , Arisa Yasuda , Satoru Shintani
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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.

STAT3作为口腔癌分子靶向治疗的靶点:基于细胞的抑制剂筛选试剂盒筛选
分子靶向治疗因其对癌细胞的高特异性而受到关注;许多研究人员一直在努力寻找新的靶分子。在这项研究中,我们试图通过抑制剂面板试剂盒的细胞筛选来确定新的靶点。研究人员在口腔鳞状细胞癌(OSCC)细胞系中评估了来自抗癌药物筛选委员会抑制剂试剂盒的抑制剂的生长抑制作用,该试剂盒含有173种化学抑制剂。部分抑制剂强烈抑制OSCC细胞的增殖。在这些抑制剂中,我们选择了STAT3的特异性抑制剂JSI-124进行进一步研究。JSI-124显著抑制OSCC细胞株的生长,进而诱导DNA断裂、聚(adp -核糖)聚合酶裂解和caspase 3激活,并呈剂量依赖性。用JSI-124处理导致STAT3磷酸化水平降低,STAT3信号级联的下游分子survivin表达下调。我们的数据表明,JSI-124抑制STAT3信号传导可能是一种有希望的OSCC分子治疗策略。
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