王雨辰, 陈越, 季鸣, 薛妮娜, 陈晓光. STAT3靶点抑制剂Bt354抗前列腺癌作用及其分子机制研究J. 药学学报, 2019,54(10): 1851-1857. doi: 10.16438/j.0513-4870.2019-0668
引用本文: 王雨辰, 陈越, 季鸣, 薛妮娜, 陈晓光. STAT3靶点抑制剂Bt354抗前列腺癌作用及其分子机制研究J. 药学学报, 2019,54(10): 1851-1857. doi: 10.16438/j.0513-4870.2019-0668
WANG Yu-chen, CHEN Yue, JI Ming, XUE Ni-na, CHEN Xiao-guang. The antitumor activity of STAT3 target inhibitor Bt354 and molecular mechanism of anti-prostate cancer J. Acta Pharmaceutica Sinica, 2019,54(10): 1851-1857. doi: 10.16438/j.0513-4870.2019-0668
Citation: WANG Yu-chen, CHEN Yue, JI Ming, XUE Ni-na, CHEN Xiao-guang. The antitumor activity of STAT3 target inhibitor Bt354 and molecular mechanism of anti-prostate cancer J. Acta Pharmaceutica Sinica, 2019,54(10): 1851-1857. doi: 10.16438/j.0513-4870.2019-0668

STAT3靶点抑制剂Bt354抗前列腺癌作用及其分子机制研究

The antitumor activity of STAT3 target inhibitor Bt354 and molecular mechanism of anti-prostate cancer

  • 摘要: 在某些肿瘤组织中,信号传导与活化转录因子3(STAT3)信号通路处于异常激活状态。在这种情况下,抑制STAT3信号通路被认为是一种潜在的肿瘤治疗方法。在体外,STAT3靶点抑制剂Bt354可以抑制癌细胞的增殖;在体内,Bt354还抑制了DU145异种移植小鼠的肿瘤生长,而不影响体重。在Bt354给药组中,10、20和40 mg·kg-1组的瘤重抑制率分别为58.8%、62.7%和73.5%。另外,Bt354给药组均可见DU145移植瘤组织中Ki 67阳性细胞的数量显著降低。这些研究结果表明,Bt354可能是一种对STAT3激活的前列腺癌细胞有效的抗癌剂。此外,Bt354抑制了STAT3的核转位,从而诱导了DU145细胞的生长抑制和凋亡。动物实验中对动物的处理均遵循中国医学科学院药物研究所动物实验中心标准操作规程。

     

    Abstract: Signal transducer and activator of transcription 3 (STAT3) was found in an abnormal constitutively active status in certain cancer tissues, and under these circumstances the interruption of STAT3 signaling pathway was proposed with the potential anti-cancer efficacy. In this study, our previous reported STAT3 inhibitor Bt354 can inhibit tumor growth in DU145 xenograft mice without affecting body weight. In groups treated with Bt354, the inhibition rate of tumor weight was 58.8%, 62.7% and 73.5% in 10, 20, 40 mg·kg-1 group, respectively. Particularly, the number of Ki 67 positive cells in the tumor sections was significantly decreased in Bt354 groups. Furthermore, Bt354 inhibited the nuclear translocation of STAT3 and consequently induced cell growth inhibition, apoptosis in DU145 cells. These findings suggest that Bt354 may be a potent anticancer agent for STAT3 activated prostate cancer cells. Procedures for animal study were performed with approval of the Animal Care and Use Committee of the Chinese Academy of Medical Sciences and Peking Union Medical College.

     

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