2009•Journal of Jilin Medical CollegeRequires access

Experimental study of inhabitation of lower concentration of paclitaxel to the proliferation of SPCA-1 cel

Wenbin Li

Open publisher page 0 citations

Abstract

Objective To study the effect of lower concentration paclitaxel on the proliferation,cell cycle,apoptosis and mitosis of non-small cell SPCA-1.Methods SPCA-1 cells were treated by different concentration of paclitaxel for 16 hours,paclitaxel containing medium was replaced by drug free medium.After additional 56 hours,cells were counted and the growth inhibition rates were calculated.SPCA-1 cells were treated by 0,1.5,3 and 6 nmol/L paclitaxel with or without 10 μmol/L SP600125 for 16 hours,the cell cycle and apoptosis were determined by flow cytometry.Results Lower concentration of paclitaxel could inhibit the proliferation SPCA-1 cells significantly.The IC50,IC70 and IC90 were 1.75、3.25 and 4.50 nmol/L respectively.The apoptosis rate induced by 0,1.5,3 and 6 nmol/L were(0.5±0.36)%,(17.0±0.55)%,(27.0±0.63)%,(21.0±3.02)% and(22.7±1.68)%,(19.4±1.43)%,(26.2±0.97)%,(42.6±3.36%)were blocked at G2/M phase by the same concentration of paclitaxel.The apoptosis induced by paclitaxel was reduced significantly by 10 μmol/L SP600125,a JNK inhibitor.Conclusion Lower concentration of paclitaxel inhibited SPCA-1 cell growth by apoptosis induction and mitosis blocking,and JNK inhibitor could reduce paclitaxel-induced apoptosis.

About this research paper

What this paper is about

Objective To study the effect of lower concentration paclitaxel on the proliferation,cell cycle,apoptosis and mitosis of non-small cell SPCA-1.Methods SPCA-1 cells were treated by different concentration of paclitaxel for 16 hours,paclitaxel containing medium was replaced by drug free medium.After additional 56 hours,cells were counted and the growth inhibition rates were calculated.SPCA-1 cells were treated by 0,1.5,3 and 6 nmol/L paclitaxel with or without 10 μmol/L SP600125 for 16 hours,the cell cycle and apoptosis were determined by flow cytometry.Results Lower concentration of paclitaxel could inhibit the proliferation SPCA-1 cells significantly.The IC50,IC70 and IC90 were 1.75、3.25 and 4.50 nmol/L respectively.The apoptosis rate induced by 0,1.5,3 and 6 nmol/L were(0.5±0.36)%,(17.0±0.55)%,(27.0±0.63)%,(21.0±3.02)% and(22.7±1.68)%,(19.4±1.43)%,(26.2±0.97)%,(42.6±3.36%)were blocked at G2/M phase by the same concentration of paclitaxel.The apoptosis induced by paclitaxel was reduced significantly by 10 μmol/L SP600125,a JNK inhibitor.Conclusion Lower concentration of paclitaxel inhibited SPCA-1 cell growth by apoptosis induction and mitosis blocking,and JNK inhibitor could reduce paclitaxel-induced apoptosis.

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 study the effect of lower concentration paclitaxel on the proliferation,cell cycle,apoptosis and mitosis of non-small cell SPCA-1.Methods SPCA-1 cells were treated by different concentration of paclitaxel for 16 hours,paclitaxel containing medium was replaced by drug free medium.After additional 56 hours,cells were counted and the growth inhibition rates were calculated.SPCA-1 cells were treated by 0,1.5,3 and 6 nmol/L paclitaxel with or without 10 μmol/L SP600125 for 16 hours,the cell cycle and apoptosis were determined by flow cytometry.Results Lower concentration of paclitaxel could inhibit the proliferation SPCA-1 cells significantly.The IC50,IC70 and IC90 were 1.75、3.25 and 4.50 nmol/L respectively.The apoptosis rate induced by 0,1.5,3 and 6 nmol/L were(0.5±0.36)%,(17.0±0.55)%,(27.0±0.63)%,(21.0±3.02)% and(22.7±1.68)%,(19.4±1.43)%,(26.2±0.97)%,(42.6±3.36%)were blocked at G2/M phase by the same concentration of paclitaxel.The apoptosis induced by paclitaxel was reduced significantly by 10 μmol/L SP600125,a JNK inhibitor.Conclusion Lower concentration of paclitaxel inhibited SPCA-1 cell growth by apoptosis induction and mitosis blocking,and JNK inhibitor could reduce paclitaxel-induced apoptosis.

Key concepts: Paclitaxel, Apoptosis, Cell cycle, Flow cytometry, Cell growth, Chemistry, IC50, Mitosis

Related papers

Back to paper searchBrowse research topicsOriginal source
Experimental study of inhabitation of lower concentration of paclitaxel to the proliferation of SPCA-1 cel — Research Paper | ScholarLens