2006Zhongguo aizheng zazhiRequires access

The inhibition and induction of apoptosis in HeLa cell by As_4S_4

Tian Li

Open publisher page 0 citations

Abstract

Background and purpose:Tetra-arsenic tetra-sulfide (As_4S_4) is a major component in realgar. In recent years, a series of studies had been undertaken both in vitro and in vivo, and demonstrated that As_4S_4 is effective for the treatment of cancer such as Acute Promyelocytic Leukemia (APL), but the efficacy of the agent is not well studied for the treatment of cervical cancer. The study was to investigate the impact of As_4S_4 on HeLa cells in terms of cell growth inhibition and apoptosis.Methods:HeLa cells were incubated with As_4S_4 for the varieties of period (12,24,36,48,60 h) at different concentrations(7.5,15,30,60 mmol/L). Cell growth was measured by MTT. Apoptosis was detected by double staining flowcytometry (FCM) and DNA Ladder.Results:After treated with different concentrations of As_4S_4(7.5,15,30,60mmol/L), the cell growth was significantly suppressed in dose-and time-dependent manner, proliferative inhibition was statistically significant for the cells with and without the treatment of agent (P0.01). FCM analysis showed that As_4S_4 could markedly induce apoptosis, apoptotic rate for the cells exposure to different concentrations of As_4S_4(7.5,15,30,60 mmol/L) were (8.1±1.1)%,(29.6±2.5)%,(46±3)%,(62±4)%, respectively, there were significant differences compared to control group(2.8±1.8)%,(P0.01);DNA fragmentation gel analysis showed typical DNA ladder of apoptosis.Conclusions:As_4S_4 could inhibit the proliferation and induce apoptosis in human HeLa cells.

About this research paper

What this paper is about

Background and purpose:Tetra-arsenic tetra-sulfide (As_4S_4) is a major component in realgar. In recent years, a series of studies had been undertaken both in vitro and in vivo, and demonstrated that As_4S_4 is effective for the treatment of cancer such as Acute Promyelocytic Leukemia (APL), but the efficacy of the agent is not well studied for the treatment of cervical cancer. The study was to investigate the impact of As_4S_4 on HeLa cells in terms of cell growth inhibition and apoptosis.Methods:HeLa cells were incubated with As_4S_4 for the varieties of period (12,24,36,48,60 h) at different concentrations(7.5,15,30,60 mmol/L). Cell growth was measured by MTT. Apoptosis was detected by double staining flowcytometry (FCM) and DNA Ladder.Results:After treated with different concentrations of As_4S_4(7.5,15,30,60mmol/L), the cell growth was significantly suppressed in dose-and time-dependent manner, proliferative inhibition was statistically significant for the cells with and without the treatment of agent (P0.01). FCM analysis showed that As_4S_4 could markedly induce apoptosis, apoptotic rate for the cells exposure to different concentrations of As_4S_4(7.5,15,30,60 mmol/L) were (8.1±1.1)%,(29.6±2.5)%,(46±3)%,(62±4)%, respectively, there were significant differences compared to control group(2.8±1.8)%,(P0.01);DNA fragmentation gel analysis showed typical DNA ladder of apoptosis.Conclusions:As_4S_4 could inhibit the proliferation and induce apoptosis in human HeLa cells.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Background and purpose:Tetra-arsenic tetra-sulfide (As_4S_4) is a major component in realgar. In recent years, a series of studies had been undertaken both in vitro and in vivo, and demonstrated that As_4S_4 is effective for the treatment of cancer such as Acute Promyelocytic Leukemia (APL), but the efficacy of the agent is not well studied for the treatment of cervical cancer. The study was to investigate the impact of As_4S_4 on HeLa cells in terms of cell growth inhibition and apoptosis.Methods:HeLa cells were incubated with As_4S_4 for the varieties of period (12,24,36,48,60 h) at different concentrations(7.5,15,30,60 mmol/L). Cell growth was measured by MTT. Apoptosis was detected by double staining flowcytometry (FCM) and DNA Ladder.Results:After treated with different concentrations of As_4S_4(7.5,15,30,60mmol/L), the cell growth was significantly suppressed in dose-and time-dependent manner, proliferative inhibition was statistically significant for the cells with and without the treatment of agent (P0.01). FCM analysis showed that As_4S_4 could markedly induce apoptosis, apoptotic rate for the cells exposure to different concentrations of As_4S_4(7.5,15,30,60 mmol/L) were (8.1±1.1)%,(29.6±2.5)%,(46±3)%,(62±4)%, respectively, there were significant differences compared to control group(2.8±1.8)%,(P0.01);DNA fragmentation gel analysis showed typical DNA ladder of apoptosis.Conclusions:As_4S_4 could inhibit the proliferation and induce apoptosis in human HeLa cells.

Key concepts: Apoptosis, HeLa, DNA fragmentation, Fragmentation (computing), Molecular biology, Acute promyelocytic leukemia, MTT assay, Cell growth

Related papers

Back to paper searchBrowse research topicsOriginal source
The inhibition and induction of apoptosis in HeLa cell by As_4S_4 — Research Paper | ScholarLens