Study of As2O3 regulating proliferation and apoptosis of Tca8113 cells by inhibiting the expression of Id-1

Our study aims to investigate the effect of arsenic trioxide (As 2 O 3 ) on proliferation and apoptosis of Tca8113 tongue squamous carcinoma cells. 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 q...

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Veröffentlicht in:Artificial cells, nanomedicine, and biotechnology nanomedicine, and biotechnology, 2019-12, Vol.47 (1), p.1932-1937
Hauptverfasser: Zhu, Yanfeng, Chen, Weihui, Guan, Weiqun, Fang, Yihong, Hao, Chunfeng
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container_title Artificial cells, nanomedicine, and biotechnology
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creator Zhu, Yanfeng
Chen, Weihui
Guan, Weiqun
Fang, Yihong
Hao, Chunfeng
description Our study aims to investigate the effect of arsenic trioxide (As 2 O 3 ) on proliferation and apoptosis of Tca8113 tongue squamous carcinoma cells. 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. 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. As 2 O 3 could regulate the proliferation and apoptosis of Tca8113 cells by inhibiting the expression of Id-1.
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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. 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. 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subjects Apoptosis
Arsenic
Arsenic trioxide
BAX protein
Bcl-2 protein
Caspase-3
Cell growth
Cell proliferation
Flow cytometry
Gene expression
Id-1
Id1 protein
mRNA
proliferation
Protein expression
Proteins
siRNA
tongue squamous cell carcinoma
Transfection
title Study of As2O3 regulating proliferation and apoptosis of Tca8113 cells by inhibiting the expression of Id-1
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