2006Chinese Journal of Clinical GastroenterologyRequires access

A Study on the Apoptosis of BGC-823 Gastric Cancer Cells Induced by Sulindac

Qizhi Wang

Open publisher page 0 citations

Abstract

Objective To investigate the effect of sulindac on apoptsis of the human gastric cancer cells line-BGC-832 and its antineoplastic mechanisma. Methods Sulindac were incubated with human gastric cancer cell line-BGCC-823 in various concentrations for different time. The positive rates of apoptosis were determined by flow cytometry and TUNEL assay,expressions of apoptosis related genes protein,including bcl-2 and survivin were analysed by immunohistochemical staining,expressions of COX-2 protein was used to detect immunohistochemical staining. Results The apex of apoptosis was determined by flow cytometry. The rate of apoptosis in gastric cancer cell line-BGC-823 was significantly higher than that in comparison group by flow cytometry and TUNEL assay(P0.05). Some morphologic features of apoptotic and the a pportosis body were examined by transmission electron microscopy. The expressions of bcl-2, survivin and COX-2 were decreased in Sulindac treated cells as compared with the untreated control cells. All the effects were in a time-and dose-dependent manner(P0.05). Conclusion Sulindac can induce apoptosis in gastric cancer cell line-BGC-823 by inhibit apoptosis related genes protein, including bcl-2 and survivin expression, downergulation of COX-2 expression.

About this research paper

What this paper is about

Objective To investigate the effect of sulindac on apoptsis of the human gastric cancer cells line-BGC-832 and its antineoplastic mechanisma. Methods Sulindac were incubated with human gastric cancer cell line-BGCC-823 in various concentrations for different time. The positive rates of apoptosis were determined by flow cytometry and TUNEL assay,expressions of apoptosis related genes protein,including bcl-2 and survivin were analysed by immunohistochemical staining,expressions of COX-2 protein was used to detect immunohistochemical staining. Results The apex of apoptosis was determined by flow cytometry. The rate of apoptosis in gastric cancer cell line-BGC-823 was significantly higher than that in comparison group by flow cytometry and TUNEL assay(P0.05). Some morphologic features of apoptotic and the a pportosis body were examined by transmission electron microscopy. The expressions of bcl-2, survivin and COX-2 were decreased in Sulindac treated cells as compared with the untreated control cells. All the effects were in a time-and dose-dependent manner(P0.05). Conclusion Sulindac can induce apoptosis in gastric cancer cell line-BGC-823 by inhibit apoptosis related genes protein, including bcl-2 and survivin expression, downergulation of COX-2 expression.

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

Objective To investigate the effect of sulindac on apoptsis of the human gastric cancer cells line-BGC-832 and its antineoplastic mechanisma. Methods Sulindac were incubated with human gastric cancer cell line-BGCC-823 in various concentrations for different time. The positive rates of apoptosis were determined by flow cytometry and TUNEL assay,expressions of apoptosis related genes protein,including bcl-2 and survivin were analysed by immunohistochemical staining,expressions of COX-2 protein was used to detect immunohistochemical staining. Results The apex of apoptosis was determined by flow cytometry. The rate of apoptosis in gastric cancer cell line-BGC-823 was significantly higher than that in comparison group by flow cytometry and TUNEL assay(P0.05). Some morphologic features of apoptotic and the a pportosis body were examined by transmission electron microscopy. The expressions of bcl-2, survivin and COX-2 were decreased in Sulindac treated cells as compared with the untreated control cells. All the effects were in a time-and dose-dependent manner(P0.05). Conclusion Sulindac can induce apoptosis in gastric cancer cell line-BGC-823 by inhibit apoptosis related genes protein, including bcl-2 and survivin expression, downergulation of COX-2 expression.

Key concepts: Survivin, Apoptosis, Flow cytometry, Sulindac, TUNEL assay, Immunohistochemistry, Medicine, Cancer

Related papers

Back to paper searchBrowse research topicsOriginal source
A Study on the Apoptosis of BGC-823 Gastric Cancer Cells Induced by Sulindac — Research Paper | ScholarLens