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首页> 外文期刊>Neoplasma: Journal of Experimental and Clinical Oncology >MiR-200c sensitizes clear-cell renal cell carcinoma cells to sorafenib and imatinib by targeting heme oxygenase-1
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MiR-200c sensitizes clear-cell renal cell carcinoma cells to sorafenib and imatinib by targeting heme oxygenase-1

机译:MiR-200c通过靶向血红素加氧酶-1使透明细胞肾细胞癌细胞对索拉非尼和伊马替尼敏感

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摘要

Clear-cell renal cell carcinoma is a highly treatment-resistant tumor type. Heme oxygenase-1 plays an anti-apoptotic role in cancer chemotherapeutic inducing tumor-progression. The miR-200 family was involved in the process of mesenchymal-epithelial transition (MET) during renal development. In the present study, we demonstrated the regulatory relationship between miR-200c and HO-1. We provided evidences to elucidate that miR-200c could sensitize ccRCC cells to sorafenib or imatinib to inhibit cell proliferation, at least partly by targeting HO-1. Moreover, the correlation between miR-200c and HO-1 expression level and drug resistance in ccRCC was also determined. Combined application with chemotherapeutic drugs, miR-200c, a HO-1 inhibitor, may enhance the efficiency of therapy by promoting both apoptosis and autophagy.
机译:透明细胞肾细胞癌是高度耐药的肿瘤类型。血红素加氧酶-1在癌症化学治疗诱导肿瘤进展中起抗凋亡作用。 miR-200家族参与了肾脏发育过程中的间充质-上皮转化(MET)过程。在本研究中,我们证明了miR-200c和HO-1之间的调节关系。我们提供的证据阐明,miR-200c可以使ccRCC细胞对索拉非尼或伊马替尼敏感,至少部分地通过靶向HO-1来抑制细胞增殖。此外,还确定了ccRCC中miR-200c和HO-1表达水平与耐药性之间的相关性。与HO-1抑制剂miR-200c联合使用可通过促进细胞凋亡和自噬来提高治疗效率。

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