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二甲双胍在肾透明细胞癌细胞系 Caki 中诱导不同的反应。

Metformin Induces Different Responses in Clear Cell Renal Cell Carcinoma Caki Cell Lines.

机构信息

Pharmaceutical Sciences Department, College of Pharmacy, Qatar University, P.O. Box 2713, Doha, Qatar.

Interim Translational Research Institute, Academic Health System, Hamad Medical Corporation, P.O. Box 3050, Doha, Qatar.

出版信息

Biomolecules. 2019 Mar 22;9(3):113. doi: 10.3390/biom9030113.

Abstract

Clear cell renal cell carcinoma (ccRCC) is the most common and lethal form of urological cancer diagnosed globally. Mutations of the von Hippel-Lindau tumor-suppressor gene and the resultant overexpression of hypoxia-inducible factor (HIF)-1α protein are considered hallmarks of ccRCC. Persistently activated HIF-1α is associated with increased cell proliferation, angiogenesis, and epithelial⁻mesenchymal transition (EMT), consequently leading to ccRCC progression and metastasis to other organs. However, the status alone cannot predict the differential sensitivity of ccRCC to cancer treatments, which suggests that other molecular differences may contribute to the differential response of ccRCC cells to drug therapies. In this study, we investigated the response to metformin (an antidiabetic drug) of two human ccRCC cell lines Caki-1 and Caki-2, which express wild-type . Our findings demonstrate a differential response between the two ccRCC cell lines studied, with Caki-2 cells being more sensitive to metformin compared to Caki-1 cells, which could be linked to the differential expression of HIF-1 despite both cell lines carrying a wild-type . Our study unveils the therapeutic potential of metformin to inhibit the progression of ccRCC in vitro. Additional preclinical and clinical studies are required to ascertain the therapeutic efficacy of metformin against ccRCC.

摘要

透明细胞肾细胞癌(ccRCC)是全球诊断出的最常见和最致命的泌尿系统癌症。von Hippel-Lindau 肿瘤抑制基因的突变和由此导致的缺氧诱导因子(HIF)-1α蛋白的过表达被认为是 ccRCC 的标志。持续激活的 HIF-1α与细胞增殖、血管生成和上皮⁻间充质转化(EMT)的增加有关,从而导致 ccRCC 的进展和转移到其他器官。然而,仅 的状态不能预测 ccRCC 对癌症治疗的差异敏感性,这表明其他分子差异可能导致 ccRCC 细胞对药物治疗的反应不同。在这项研究中,我们研究了二甲双胍(一种抗糖尿病药物)对两种表达野生型 的人 ccRCC 细胞系 Caki-1 和 Caki-2 的反应。我们的研究结果表明,在研究的两种 ccRCC 细胞系之间存在差异反应,与 Caki-1 细胞相比,Caki-2 细胞对二甲双胍更敏感,这可能与尽管两种细胞系都携带野生型 但 HIF-1 的差异表达有关。我们的研究揭示了二甲双胍在体外抑制 ccRCC 进展的治疗潜力。需要进行额外的临床前和临床研究来确定二甲双胍对 ccRCC 的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cfc/6468376/2bc7de19a518/biomolecules-09-00113-g001.jpg

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