Huang Wei, Dong Zizheng, Wang Fang, Peng Hui, Liu Jing-Yuan, Zhang Jian-Ting
Department of Pharmacology and Toxicology and ‡IU Simon Cancer Center, Indiana University School of Medicine , 980 W. Walnut Street, Indianapolis, Indiana 46202, United States.
ACS Chem Biol. 2014 May 16;9(5):1188-96. doi: 10.1021/cb500071v. Epub 2014 Mar 24.
Signal transducer and activator of transcription 3 (STAT3) plays important roles in multiple aspects of cancer aggressiveness including migration, invasion, survival, self-renewal, angiogenesis, and tumor cell immune evasion by regulating the expression of multiple downstream target genes. STAT3 is constitutively activated in many malignant tumors and its activation is associated with high histological grade and advanced cancer stages. Thus, inhibiting STAT3 promises an attracting strategy for treatment of advanced and metastatic cancers. Herein, we identified a STAT3 inhibitor, inS3-54, by targeting the DNA-binding domain of STAT3 using an improved virtual screening strategy. InS3-54 preferentially suppresses proliferation of cancer over non-cancer cells and inhibits migration and invasion of malignant cells. Biochemical analyses show that inS3-54 selectively inhibits STAT3 binding to DNA without affecting the activation and dimerization of STAT3. Furthermore, inS3-54 inhibits expression of STAT3 downstream target genes and STAT3 binding to chromatin in situ. Thus, inS3-54 represents a novel probe for development of specific inhibitors targeting the DNA-binding domain of STAT3 and a potential therapeutic for cancer treatments.
信号转导与转录激活因子3(STAT3)通过调节多个下游靶基因的表达,在癌症侵袭的多个方面发挥重要作用,包括迁移、侵袭、存活、自我更新、血管生成和肿瘤细胞免疫逃逸。STAT3在许多恶性肿瘤中持续激活,其激活与高组织学分级和晚期癌症阶段相关。因此,抑制STAT3有望成为治疗晚期和转移性癌症的一种有吸引力的策略。在此,我们通过使用改进的虚拟筛选策略靶向STAT3的DNA结合结构域,鉴定出一种STAT3抑制剂inS3-54。inS3-54优先抑制癌细胞而非非癌细胞的增殖,并抑制恶性细胞的迁移和侵袭。生化分析表明,inS3-54选择性抑制STAT3与DNA的结合,而不影响STAT3的激活和二聚化。此外,inS3-54抑制STAT3下游靶基因的表达以及STAT3与染色质的原位结合。因此,inS3-54代表了一种用于开发靶向STAT3 DNA结合结构域的特异性抑制剂的新型探针,以及一种潜在的癌症治疗药物。