首页> 外文期刊>Cancer biology & therapy >Downregulation of a mitochondria associated protein SLP-2 inhibits tumor cell motility, proliferation and enhances cell sensitivity to chemotherapeutic reagents.
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Downregulation of a mitochondria associated protein SLP-2 inhibits tumor cell motility, proliferation and enhances cell sensitivity to chemotherapeutic reagents.

机译:线粒体相关蛋白SLP-2的下调抑制了肿瘤细胞的运动性,增殖并增强了细胞对化学治疗剂的敏感性。

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Results from tissue microarray in this study and our previous reports revealed that stomatin-like protein 2 (SLP-2) is notably associated with tumorigenesis and metastasis. Many members of stomatin family are involved in tumor as mitochondrial component, and recent study has revealed that SLP-2 may also function in mitochondria. To further investigate the function of SLP-2, we used siRNA target SLP-2. Data showed that knock-down of SLP-2 potently inhibited cell motility, proliferation and slightly altered cell cycle without any significant change of apoptosis. Moreover, by combined application with different chemotherapeutic reagents, we observed the enhancement of cell chemosensitivity by SLP-2 depletion. We also confirmed that, SLP-2 localizes in mitochondria, affects mitochondrial membrane potential (MMP) and ATP production. We conclude that, SLP-2 is a mitochondrial protein and therefore, functions in energy process by MMP maintenance, and subsequently affecting cell motility, proliferation and chemosensitivity.
机译:这项研究和我们以前的报道中的组织芯片结果表明,类生长激素样蛋白2(SLP-2)与肿瘤发生和转移密切相关。胃抑素家族的许多成员都以线粒体成分的形式参与了肿瘤的治疗,最近的研究表明SLP-2也可能在线粒体中起作用。为了进一步研究SLP-2的功能,我们使用了siRNA靶标SLP-2。数据显示,敲低SLP-2可以有效抑制细胞运动,增殖和细胞周期的轻微改变,而凋亡却没有任何明显变化。此外,通过与不同的化学治疗剂联合应用,我们观察到通过SLP-2耗竭提高了细胞化学敏感性。我们还证实,SLP-2位于线粒体中,影响线粒体膜电位(MMP)和ATP的产生。我们得出的结论是,SLP-2是一种线粒体蛋白,因此通过MMP维持而在能量过程中起作用,并随后影响细胞运动性,增殖和化学敏感性。

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