首页> 外文期刊>Cancer letters >The CCR5 antagonist maraviroc causes remission of pancreatic cancer liver metastasis in nude rats based on cell cycle inhibition and apoptosis induction
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The CCR5 antagonist maraviroc causes remission of pancreatic cancer liver metastasis in nude rats based on cell cycle inhibition and apoptosis induction

机译:基于细胞周期抑制和细胞凋亡诱导,CCR5拮抗剂马拉维病导致裸鼠胰腺癌肝转移的缓解

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摘要

Pancreatic ductal adenocarcinoma (PDAC) is a highly lethal disease, and novel therapeutic strategies are urgently needed. Recently, expression of the C-C chemokine receptor 5 (CCR5) and its ligands has been found to play an important role in cancer progression and metastasis. In this study, we blocked the CCR5 receptor by the FDA approved antagonist maraviroc (MVC) in Suit2-007 and MIA-PaCa-2 human PDAC cells. The treatment significantly inhibited their proliferation and induced apoptosis of exposed cells as evidenced by caspases activation and increased Bax levels. Moreover, MVC inhibited the cell cycle by down regulating the proteins of the complexes of cyclin dependent kinase (CDK) 4/6 - Cyclin D and CDK2 - Cyclin E, as well as by increasing the protein levels of CDK inhibitors p18, p21 and p27. In line with this, MVC caused significant retardation of Suit2-007 cells growing in a PDAC liver metastasis xenograft model (p < 0.05). These results suggest that maraviroc could be a promising treatment strategy for PDAC patients with liver metastases.
机译:胰腺导管腺癌(PDAC)是一种高度致命的疾病,迫切需要新的治疗策略。最近,已发现C-C趋化因子受体5(CCR5)及其配体的表达在癌症进展和转移中起重要作用。在这项研究中,我们通过SIT2-007和MIA-PACA-2人PDAC细胞的FDA批准的拮抗剂Maraviroc(MVC)阻断了CCR5受体。该治疗显着抑制了其扩散和诱导暴露细胞的细胞凋亡,其通过Caspases活化和增加的Bax水平证明。此外,MVC通过向下调节细胞周期蛋白依赖性激酶(CDK)4/6 - Cyclin D和CDK2 - Cyclin E的络合物的蛋白质来抑制细胞周期,以及通过增加CDK抑制剂P18,P21和P27的蛋白质水平。符合此,MVC引起PDAC肝转移异种移植模型中生长的SIT2-007细胞的显着延迟(P <0.05)。这些结果表明,Maraviroc可能是肝转移患者的PDAC患者的有希望的治疗策略。

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