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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Study of As2O3 regulating proliferation and apoptosis of Tca8113 cells by inhibiting the expression of Id-1
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Study of As2O3 regulating proliferation and apoptosis of Tca8113 cells by inhibiting the expression of Id-1

机译:As2O3通过抑制Id-1表达调控Tca8113细胞增殖和凋亡的研究

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Objective: Our study aims to investigate the effect of arsenic trioxide (As 2 O 3 ) on proliferation and apoptosis of Tca8113 tongue squamous carcinoma cells. Methods: Cell proliferation and the expression of Id-1 mRNA in Tca8113 cells after treatment with different concentrations of As 2 O 3 were detected by MTT and qRT-PCR, respectively. The expression of Id-1, cell proliferation and apoptosis in Id-1 silencing Tca8113 cells were detected by qRT-PCR, Western blot, MTT and flow cytometry, respectively. The pcDNA 3.1-Id-1 overexpression vector was transfected into Tca8113 cells combination with 3?μmol/L As 2 O 3 . The detection of cell proliferation, apoptosis and Caspase-3, Bax and Bcl-2 protein expression in transfected Tca8113 cells were performed by MTT, flow cytometry and Western blot assay, respectively. Results: As 2 O 3 of different concentration could inhibit the proliferation of Tca8113 cells and IC 50 value was 3.004?±?0.2379?μmol/L. The expression of Id-1 mRNA was down-regulated in Tca8113 cells treated with 3?μmol/L As 2 O 3 for 48?h. The results of qRT-PCR, Western blot, MTT and flow cytometry indicated that the expression level of Id-1 and cell proliferation ability were decreased while the apoptosis rate was increased in Tca8113 cells after transfection of Id-1 siRNA. Overexpression of Id-1 could attenuate the inhibition or promotion of As 2 O 3 on proliferation, apoptosis and Caspase-3, Bax and Bcl-2 protein expression in Tca8113 cells. Conclusion: As 2 O 3 could regulate the proliferation and apoptosis of Tca8113 cells by inhibiting the expression of Id-1.
机译:目的:本研究旨在探讨三氧化二砷(As 2 O 3)对Tca8113舌鳞癌细胞增殖和凋亡的影响。方法:分别用MTT法和qRT-PCR法检测不同浓度As 2 O 3处理后Tca8113细胞的增殖和Id-1 mRNA的表达。分别通过qRT-PCR,Western blot,MTT和流式细胞术检测Id-1沉默的Tca8113细胞中Id-1的表达,细胞增殖和凋亡。将pcDNA 3.1-Id-1过表达载体与3?μmol/ L As 2 O 3转染到Tca8113细胞中。 MTT法,流式细胞术和Western blot法分别检测转染的Tca8113细胞的细胞增殖,凋亡和Caspase-3,Bax和Bcl-2蛋白的表达。结果:不同浓度的2 O 3可抑制Tca8113细胞的增殖,IC 50值为3.004?±?0.2379?μmol/ L。在3?μmol/ L As 2 O 3处理48?h的Tca8113细胞中,Id-1 mRNA的表达下调。 qRT-PCR,Western blot,MTT和流式细胞仪检测结果表明,转染Id-1 siRNA后,Tca8113细胞中Id-1的表达水平和细胞增殖能力降低,凋亡率增加。 Id-1的过量表达可减弱As 2 O 3对Tca8113细胞增殖,凋亡以及Caspase-3,Bax和Bcl-2蛋白表达的抑制或促进。结论:As 2 O 3可以通过抑制Id-1的表达来调节Tca8113细胞的增殖和凋亡。

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