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对头颈部鳞状细胞癌中组成性和诱导性JAK\STAT激活的治疗性抑制

Therapeutic suppression of constitutive and inducible JAK\STAT activation in head and neck squamous cell carcinoma.

作者信息

Kupferman Michael E, Jayakumar Arumugam, Zhou Ge, Xie Tong, Dakak-Yazici Yasemin, Zhao Mei, Ju Jun, Mandal Mahitosh, Jasser Samar, Madden Timothy, Myers Jeffrey N, Priebe Waldemar

机构信息

Department of Head and Neck Surgery, The University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA.

出版信息

J Exp Ther Oncol. 2009;8(2):117-27.

Abstract

The oncogenic role of STAT3 has been elucidated in a number of human malignancies including leukemia, lymphoma, malignant glioma and cancers of the breast, lung, and head and neck (HNSCC). Here we show that WP1066 has profound anti-neoplastic effects in HNSCC, mediated in part by suppression of JAK2-STAT3 signaling. WP1066 inhibited constitutive and inducible STAT3 phosphorylation in both dose- and time-dependant manners. Further, the nuclear translocation of STAT3 was completely inhibited, resulting in decreased DNA binding activity. In vivo testing of WP1066 in a nude mouse orthotopic model of HNSCC demonstrated significant anti-tumor effects, with histological evidence of decreased cellular proliferation and angiogenesis. Collectively, these data suggest that WP1066 suppresses squamous cell carcinoma cell growth, in part through its effects on JAK-STAT pathways, and establishes this small molecule as potentially efficacious agent in the treatment of HNSCC.

摘要

信号转导和转录激活因子3(STAT3)的致癌作用已在多种人类恶性肿瘤中得到阐明,包括白血病、淋巴瘤、恶性胶质瘤以及乳腺癌、肺癌和头颈部癌(HNSCC)。在此我们表明,WP1066在HNSCC中具有显著的抗肿瘤作用,部分是通过抑制JAK2-STAT3信号传导介导的。WP1066以剂量和时间依赖性方式抑制组成型和诱导型STAT3磷酸化。此外,STAT3的核转位被完全抑制,导致DNA结合活性降低。在HNSCC裸鼠原位模型中对WP1066进行的体内测试显示出显著的抗肿瘤作用,组织学证据表明细胞增殖和血管生成减少。总体而言,这些数据表明WP1066部分通过其对JAK-STAT途径的作用抑制鳞状细胞癌细胞生长,并确定这种小分子为治疗HNSCC的潜在有效药物。

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