2010Xiandai shengwu yixue jinzhanRequires access

Trichostatin A induces cell cycle arrest and apoptosis in bladder cancer T24 cells

Danfeng Xu

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Abstract

Objective: To study the effect of trichostatin A (TSA) on inducing cell cycle arrest and apoptosis in bladder cancer T24 cells.Methods: T24 cells were exposed to varying concentrations of TSA (0.1μM,0.3μM and 1μM)for 24h.MTT assay was performed to evaluate cell viability.Apoptosis was analyzed with Annexin V-PI staining by flow cytometry.Active form of caspase-3 positive cells were measured by flow cytometry.Cell cycle distribution was analyzed by PI staining.Results: The results showed that TSA decreased cell viability in a dose dependent manner.TSA induced increased apoptotic cells evaluated by annexin V positive cells,which was accompanied with increased level of active caspase-3.TSA also induced G2/M arrest dose-dependently.Conclusions: These results suggest that TSA induces apoptosis by caspase-3 activation and promote G2/M cell cycle arrest.

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What this paper is about

Objective: To study the effect of trichostatin A (TSA) on inducing cell cycle arrest and apoptosis in bladder cancer T24 cells.Methods: T24 cells were exposed to varying concentrations of TSA (0.1μM,0.3μM and 1μM)for 24h.MTT assay was performed to evaluate cell viability.Apoptosis was analyzed with Annexin V-PI staining by flow cytometry.Active form of caspase-3 positive cells were measured by flow cytometry.Cell cycle distribution was analyzed by PI staining.Results: The results showed that TSA decreased cell viability in a dose dependent manner.TSA induced increased apoptotic cells evaluated by annexin V positive cells,which was accompanied with increased level of active caspase-3.TSA also induced G2/M arrest dose-dependently.Conclusions: These results suggest that TSA induces apoptosis by caspase-3 activation and promote G2/M cell cycle arrest.

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Available abstract

Objective: To study the effect of trichostatin A (TSA) on inducing cell cycle arrest and apoptosis in bladder cancer T24 cells.Methods: T24 cells were exposed to varying concentrations of TSA (0.1μM,0.3μM and 1μM)for 24h.MTT assay was performed to evaluate cell viability.Apoptosis was analyzed with Annexin V-PI staining by flow cytometry.Active form of caspase-3 positive cells were measured by flow cytometry.Cell cycle distribution was analyzed by PI staining.Results: The results showed that TSA decreased cell viability in a dose dependent manner.TSA induced increased apoptotic cells evaluated by annexin V positive cells,which was accompanied with increased level of active caspase-3.TSA also induced G2/M arrest dose-dependently.Conclusions: These results suggest that TSA induces apoptosis by caspase-3 activation and promote G2/M cell cycle arrest.

Key concepts: Apoptosis, Trichostatin A, Viability assay, Cell cycle, Flow cytometry, Annexin, Cell cycle checkpoint, Molecular biology

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