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PAK4 confers the malignance of cervical cancers and contributes to the cisplatin-resistance in cervical cancer cells via PI3K/AKT pathway

机译:PAK4赋予宫颈癌恶性作用,并通过PI3K / AKT途径促进宫颈癌细胞的顺铂耐药性

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Background Multiple protein or microRNA markers have been recognized to contribute to the progression and recurrence of cervical cancers. Particular those, which are associated with the chemo- or radio-resistance of cervical cancers, have been proposed to be promising and to facilitate the definition for cervical cancer treatment options. Methods This study was designed to explore the potential prognosis value of p21-activated kinase (PAK)-4 in cervical cancer, via the Kaplan–Meier analysis, log-rank test and Cox regression analysis, and then to investigate the regulatory role of PAK4 in the cisplatin resistance in cervical cancer cells, via the strategies of both PAK4 overexpression and PAK4 knockout. Results It was demonstrated that PAK4 was upregulated in cervical cancer tissues, in an association with the cancer’s malignance variables such as FIGO stage, lymph node or distant metastasis and the poor histological grade. The high PAK4 expression was also independently associated with poor prognosis to cervical cancer patients. Moreover, PAK4 confers cisplatin resistance in cervical cancer Hela or Caski cells. In addition, the PI3K/Akt pathway has been implicated in the PAK4-confered cisplatin resistance. And the PI3K/Akt inhibitor, LY294002, markedly deteriorated the cisplatin-mediated viability reduction of Hela or Caski cells, indicating the involvement of PI3K/Akt pathway in the cisplatin resistance in cervical cancer cells. Conclusion This study has confirmed the significant prognostic role of PAK4 level in cervical cancer patients and has recognized the regulatory role in cervical cancer progression. Moreover, our study has indicated that PAK4 also confers the chemoresistance of cervical cancer cells in a PI3K/Akt-dependent way. Thus, our study indicates PAK4 as a promising marker for cervical cancer treatment.
机译:背景技术已经认识到多种蛋白质或microRNA标记物有助于宫颈癌的进展和复发。已经提出特别是与子宫颈癌的化学或放射抗性有关的那些是有前途的,并有助于定义子宫颈癌的治疗选择。方法本研究旨在通过Kaplan-Meier分析,对数秩检验和Cox回归分析探讨p21活化激酶(PAK)-4在宫颈癌中的潜在预后价值,然后研究PAK4的调节作用。通过PAK4过表达和PAK4敲除的策略来抑制宫颈癌细胞的顺铂耐药性。结果表明,PAK4在宫颈癌组织中上调,与癌症的恶性变量(例如FIGO分期,淋巴结或远处转移以及不良的组织学分级)相关。 PAK4的高表达还与宫颈癌患者的不良预后相关。此外,PAK4在宫颈癌Hela或Caski细胞中赋予顺铂耐药性。此外,PI3K / Akt途径与PAK4赋予的顺铂耐药性有关。 PI3K / Akt抑制剂LY294002显着恶化了顺铂介导的Hela或Caski细胞活力的降低,表明PI3K / Akt通路参与了子宫颈癌细胞的顺铂耐药性。结论这项研究已证实PAK4水平在宫颈癌患者中具有重要的预后作用,并已认识到其在宫颈癌进展中的调节作用。此外,我们的研究表明,PAK4还以PI3K / Akt依赖性方式赋予宫颈癌细胞化学耐药性。因此,我们的研究表明PAK4是治疗宫颈癌的有前途的标志物。

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