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Combined treatment with acetazolamide and cisplatin enhances chemosensitivity in laryngeal carcinoma Hep-2 cells

机译:乙酰唑胺和顺铂联合治疗可增强喉癌Hep-2细胞的化学敏感性

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摘要

The aim of the present study was to determine whether acetazolamide (Ace) treatment enhances the chemosensitivity of Hep-2 laryngeal cells to cisplatin (Cis). At the logarithmic growth phase, Hep-2 cells were treated with Ace, Cis or both, and cell viability was detected using an MTT assay. The degree of apoptosis was detected using flow cytometry. Expression levels of apoptosis-related proteins, including BCL2 apoptosis regulator (bcl-2), BCL2 associated X (bax) and caspase-3, and of proliferation-related proteins, including proliferating cell nuclear antigen (PCNA) and tumor protein p53 (P53), were detected using western blotting. mRNA expression levels of aquaporin-1 (AQP1) in each group were detected using reverse transcription-polymerase chain reaction. Compared with the drugs used alone, treatment with both Ace and Cis displayed synergistic effects on the growth inhibition and apoptosis induction in Hep-2 cells. The Ace/Cis combination decreased the expression of PCNA but increased the expression of p53. In addition, the combination treatment decreased the ratio of bcl-2/bax and increased the expression of caspase-3, as well as decreased the expression of AQP1. These results demonstrated that the combined use of Ace and Cis enhanced the chemosensitivity of laryngeal carcinoma cells.
机译:本研究的目的是确定乙酰唑胺(Ace)处理是否能增强Hep-2喉细胞对顺铂(Cis)的化学敏感性。在对数生长期,用Ace,Cis或两者同时处理Hep-2细胞,并使用MTT分析检测细胞活力。使用流式细胞仪检测细胞凋亡的程度。凋亡相关蛋白的表达水平,包括BCL2凋亡调节剂(bcl-2),BCL2相关X(bax)和caspase-3,以及增殖相关蛋白的表达水平,包括增殖细胞核抗原(PCNA)和肿瘤蛋白p53(P53 ),使用蛋白质印迹法检测。使用逆转录-聚合酶链反应检测每组中aquaporin-1(AQP1)的mRNA表达水平。与单独使用的药物相比,Ace和Cis均对Hep-2细胞的生长抑制和凋亡诱导具有协同作用。 Ace / Cis组合降低PCNA的表达,但增加p53的表达。此外,联合治疗降低了bcl-2 / bax的比例,增加了caspase-3的表达,并降低了AQP1的表达。这些结果表明,Ace和Cis的组合使用增强了喉癌细胞的化学敏感性。

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