Bixel Kristin, Saini Uksha, Kumar Bid Hemant, Fowler John, Riley Maria, Wanner Ross, Deepa Priya Dorayappan Kalpana, Rajendran Sneha, Konishi Ikuo, Matsumura Noriomi, Cohn David E, Selvendiran Karuppaiyah
Division of Gynecologic Oncology, Comprehensive Cancer Center, The Ohio State University Wexner Medical Center, Columbus, OH.
Cancer Therapeutics, Life Sciences Institute University of Michigan campus, Ann Arbor, MI.
Int J Cancer. 2017 Nov 1;141(9):1856-1866. doi: 10.1002/ijc.30847. Epub 2017 Jul 24.
Advanced ovarian clear cell carcinoma (OCCC) carries a very poor prognosis in large part secondary to the extremely high rate of resistance to standard platinum and taxane chemotherapy. Signal transducer and activator of transcription 3(STAT3) expression and activation has been shown to regulate tumor progression in various human cancers, though has not been well studied in OCCC. Preliminary work in our lab has demonstrated constitutive activation of STAT3 (pSTAT3Tyr705 or pSTAT3727) in OCCC cell lines as well as human OCCC tumor tissue samples. Significantly, pSTAT3 is expressed in the absence of other forms of activated STAT (pSTAT1, 2, 6). Therefore, this work was planned to investigate the role of STAT3 and examine the efficacy of a novel anti-cancer compound -HO-3867, which is an inhibitor of STAT3, using known OCCC cell lines. Results demonstrate that treatment with HO-3867 decreased expression of pSTAT3 Tyr705 as well pSTAT3 Ser727, while total STAT3 remained constant. STAT3 overexpression increased the migration capability in OVTOKO cells in vitro and led to an increased tumor size when injected in vivo. The inhibitory effect of HO-3867 on cell proliferation and cell survival was accompanied by increased apoptosis, within 24 h post treatment. Treatment with HO-3867 resulted in a decrease in Bcl-2 and increase of cleavage of caspase 3, caspase 7, and PARP, confirming induction of apoptosis after treatment with HO-3867. In addition, HO-3867 significantly inhibited formation of human umbilical vein endothelial cells capillary-like structures and invasion at both 5 and 10 µM concentrations. STAT3 expression plays an important role in the spread of OCCC in vitro as well as in vivo. Thus, we can exploit the STAT3 pathway for targeted drug therapy. Inhibition of pSTAT3 using HO-3867in OCCC cell lines appears to be a promising therapy. This is of utmost importance given the poor response of OCCC to standard chemotherapy regimens.
晚期卵巢透明细胞癌(OCCC)的预后非常差,很大程度上是由于对标准铂类和紫杉烷化疗的耐药率极高。信号转导和转录激活因子3(STAT3)的表达和激活已被证明在多种人类癌症中调节肿瘤进展,尽管在OCCC中尚未得到充分研究。我们实验室的初步工作已经证明,在OCCC细胞系以及人类OCCC肿瘤组织样本中存在STAT3(pSTAT3Tyr705或pSTAT3727)的组成性激活。值得注意的是,pSTAT3在没有其他形式的活化STAT(pSTAT1、2、6)的情况下表达。因此,本研究旨在利用已知的OCCC细胞系,研究STAT3的作用,并检验一种新型抗癌化合物-HO-3867(一种STAT3抑制剂)的疗效。结果表明,HO-3867处理可降低pSTAT3 Tyr705以及pSTAT3 Ser727的表达,而总STAT3保持不变。STAT3过表达增加了OVTOKO细胞在体外的迁移能力,并在体内注射时导致肿瘤大小增加。HO-3867对细胞增殖和细胞存活的抑制作用伴随着处理后24小时内细胞凋亡的增加。HO-3867处理导致Bcl-2减少,caspase 3、caspase 7和PARP的裂解增加,证实HO-3867处理后诱导了细胞凋亡。此外,HO-3867在5和10μM浓度下均显著抑制人脐静脉内皮细胞毛细血管样结构的形成和侵袭。STAT3表达在OCCC的体外和体内扩散中起重要作用。因此,我们可以利用STAT3途径进行靶向药物治疗。在OCCC细胞系中使用HO-3867抑制pSTAT3似乎是一种有前景的治疗方法。鉴于OCCC对标准化疗方案反应不佳,这一点至关重要。