Department of Otorhinolaryngology.
Precision Medicine Center, Tianjin Medical University General Hospital, Tianjin, China.
Anticancer Drugs. 2019 Sep;30(8):846-853. doi: 10.1097/CAD.0000000000000783.
Abnormal activation of signal transducer and activator of transcription 3 (STAT3) is complicated in the tumor progression of multiple cancers including human head and neck squamous cell carcinoma (HNSCC) and, therefore, serves as a potent therapeutic target. In this study, we identify that C188-9, a small-molecule STAT3 inhibitor, exhibits an antitumor effect on HNSCC in vitro. C188-9 significantly inhibits cell growth, arrests cell cycle at G0/G1 phase, and induces apoptosis in HNSCC. Besides, the capacities of migration and invasion of HNSCC cells are impaired with the exposure to C188-9. In addition, C188-9 treatment enhanced the chemosensitivity of HNSCC cellsin vitro. Moreover, C188-9 inactivates STAT3 by reducing its phosphorylation at Tyr705. Taken together, these results indicate that C188-9 could be a promising therapeutic strategy for patients suffered from HNSCC by suppressing the STAT3 pathway.
信号转导子和转录激活子 3(STAT3)的异常激活参与了多种癌症的肿瘤进展,包括人类头颈部鳞状细胞癌(HNSCC),因此是一个潜在的治疗靶点。在这项研究中,我们发现小分子 STAT3 抑制剂 C188-9 在体外对 HNSCC 具有抗肿瘤作用。C188-9 可显著抑制细胞生长,将细胞周期阻滞在 G0/G1 期,并诱导 HNSCC 细胞凋亡。此外,C188-9 还可抑制 HNSCC 细胞的迁移和侵袭能力。此外,C188-9 处理可增强 HNSCC 细胞的体外化疗敏感性。此外,C188-9 通过降低 Tyr705 处的磷酸化来使 STAT3 失活。综上所述,这些结果表明,通过抑制 STAT3 通路,C188-9 可能成为治疗 HNSCC 患者的一种有前途的治疗策略。