2009•Zhongguo linchuang yixueRequires access

Effect of Paclitaxel-induced Apoptosis in Human Ovarian Cancer Cell Line SKOV-3 Pretreated with Dexamethasone

Hua Zhu

Open publisher page 0 citations

Abstract

Objective:To investigate the effect of paclitaxel-induced apoptosis in human ovarian cancer cell when pretreated with dexamethasone.Methods:MTT assay was used to examine the effect of paclitaxel-inhibited cell proliferation when pretreated with dexamethasone.The cell apoptosis on morphology was detected by TUNEL assay.The percentage of apoptosis of human ovarian cancer cell line SKOV-3 induced by paclitaxel in the presence or absence of dexamethasone was measured by PI-staining and then analyzed by FCM.Results:Dexamethasone can protect differently the inhibition of SKOV-3 cell proliferation induced by paclitaxel.TUNEL assay showed that dexamethasone inhibited the SKOV-3 cell apoptosis induced by paclitaxel.The apoptosis percentage of human ovarian cancer cell line SKOV-3 induced by paclitaxel and pretreated with dexamethasone measured by PI-staining was (5.55±0.53)%.The apoptosis percentage treated only with paclitaxe was (13.90±1.62)%.The apoptosis percentage decreased significantly when pretreated with dexamethasone ( P0.01).The percentage of cell arrested by PTX in the G2/M phase was no significant difference in paclitaxel in the presence or absence of dexamethasone group (P0.05).Conclusion:Pretreatment with dexamethasone can protect the inhibion of SKOV-3 cell proliferation induced by paclitaxel.Dexamethasone can inhibit apoptosis of human ovarian cancer cell line SKOV-3 induced by paclitaxel without affecting the ability of paclitaxel to induce mitotic division arrest in the G2/M phase.

About this research paper

What this paper is about

Objective:To investigate the effect of paclitaxel-induced apoptosis in human ovarian cancer cell when pretreated with dexamethasone.Methods:MTT assay was used to examine the effect of paclitaxel-inhibited cell proliferation when pretreated with dexamethasone.The cell apoptosis on morphology was detected by TUNEL assay.The percentage of apoptosis of human ovarian cancer cell line SKOV-3 induced by paclitaxel in the presence or absence of dexamethasone was measured by PI-staining and then analyzed by FCM.Results:Dexamethasone can protect differently the inhibition of SKOV-3 cell proliferation induced by paclitaxel.TUNEL assay showed that dexamethasone inhibited the SKOV-3 cell apoptosis induced by paclitaxel.The apoptosis percentage of human ovarian cancer cell line SKOV-3 induced by paclitaxel and pretreated with dexamethasone measured by PI-staining was (5.55±0.53)%.The apoptosis percentage treated only with paclitaxe was (13.90±1.62)%.The apoptosis percentage decreased significantly when pretreated with dexamethasone ( P0.01).The percentage of cell arrested by PTX in the G2/M phase was no significant difference in paclitaxel in the presence or absence of dexamethasone group (P0.05).Conclusion:Pretreatment with dexamethasone can protect the inhibion of SKOV-3 cell proliferation induced by paclitaxel.Dexamethasone can inhibit apoptosis of human ovarian cancer cell line SKOV-3 induced by paclitaxel without affecting the ability of paclitaxel to induce mitotic division arrest in the G2/M phase.

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 paclitaxel-induced apoptosis in human ovarian cancer cell when pretreated with dexamethasone.Methods:MTT assay was used to examine the effect of paclitaxel-inhibited cell proliferation when pretreated with dexamethasone.The cell apoptosis on morphology was detected by TUNEL assay.The percentage of apoptosis of human ovarian cancer cell line SKOV-3 induced by paclitaxel in the presence or absence of dexamethasone was measured by PI-staining and then analyzed by FCM.Results:Dexamethasone can protect differently the inhibition of SKOV-3 cell proliferation induced by paclitaxel.TUNEL assay showed that dexamethasone inhibited the SKOV-3 cell apoptosis induced by paclitaxel.The apoptosis percentage of human ovarian cancer cell line SKOV-3 induced by paclitaxel and pretreated with dexamethasone measured by PI-staining was (5.55±0.53)%.The apoptosis percentage treated only with paclitaxe was (13.90±1.62)%.The apoptosis percentage decreased significantly when pretreated with dexamethasone ( P0.01).The percentage of cell arrested by PTX in the G2/M phase was no significant difference in paclitaxel in the presence or absence of dexamethasone group (P0.05).Conclusion:Pretreatment with dexamethasone can protect the inhibion of SKOV-3 cell proliferation induced by paclitaxel.Dexamethasone can inhibit apoptosis of human ovarian cancer cell line SKOV-3 induced by paclitaxel without affecting the ability of paclitaxel to induce mitotic division arrest in the G2/M phase.

Key concepts: Paclitaxel, Apoptosis, Dexamethasone, Medicine, TUNEL assay, Cell growth, Ovarian cancer, MTT assay

Related papers

Back to paper searchBrowse research topicsOriginal source
Effect of Paclitaxel-induced Apoptosis in Human Ovarian Cancer Cell Line SKOV-3 Pretreated with Dexamethasone — Research Paper | ScholarLens