2008•Di-Si Junyi Daxue xuebaoRequires access

Inhibition on growth of ovarian carcinoma cells by recombinant adenovirus carrying pten gene

Lin Guan

Open publisher page 0 citations

Abstract

AIM:To observe the expression of pten in human highly metastatic ovarian carcinoma cell line HO-8910PM after in vitro infection and investigate the effects of pten gene on the proli-feration and metastatic ability of human ovarian carcinoma HO-8910PM cells.METHODS:Ad-pten was constructed through Ad-Easy adenovirus vector system and the expression of pten gene in HO-8910PM cells was determined by Western Blot.The transfection efficiency of Ad-pten was determined by fluorescence microscope.The inhibitive effect of Ad-pten on proliferation of HO-8910PM cells was determined by MTT assay.The morpho-logic changes of HO-8910PM cells transfected with Ad-pten were observed by light microscopy(HE staining).The metastatic ability was analyzed by cell scratching model in vitro.Hoechest33258 staining was used to study the cell apoptosis.RESULTS:The expression of PTEN protein in HO-8910PM cells was confirmed by Western Blot.The efficiency of adenovirus mediated Ad-pten gene transfer was above 90% when the multiplicities of infection(MOI)was 100.Exogenous pten gene significantly suppressed the growth and metastatic ability of HO-8910PM cells and induced the apoptosis of the cells.CONCLUSION:The constructed Ad-pten transfection system is highly efficient in transferring wild-type pten gene into human endometrial carcinoma cells.Ad-pten can strongly inhibit the proliferation and metastasis of the cells,and also induce the apoptosis of the cells.

About this research paper

What this paper is about

AIM:To observe the expression of pten in human highly metastatic ovarian carcinoma cell line HO-8910PM after in vitro infection and investigate the effects of pten gene on the proli-feration and metastatic ability of human ovarian carcinoma HO-8910PM cells.METHODS:Ad-pten was constructed through Ad-Easy adenovirus vector system and the expression of pten gene in HO-8910PM cells was determined by Western Blot.The transfection efficiency of Ad-pten was determined by fluorescence microscope.The inhibitive effect of Ad-pten on proliferation of HO-8910PM cells was determined by MTT assay.The morpho-logic changes of HO-8910PM cells transfected with Ad-pten were observed by light microscopy(HE staining).The metastatic ability was analyzed by cell scratching model in vitro.Hoechest33258 staining was used to study the cell apoptosis.RESULTS:The expression of PTEN protein in HO-8910PM cells was confirmed by Western Blot.The efficiency of adenovirus mediated Ad-pten gene transfer was above 90% when the multiplicities of infection(MOI)was 100.Exogenous pten gene significantly suppressed the growth and metastatic ability of HO-8910PM cells and induced the apoptosis of the cells.CONCLUSION:The constructed Ad-pten transfection system is highly efficient in transferring wild-type pten gene into human endometrial carcinoma cells.Ad-pten can strongly inhibit the proliferation and metastasis of the cells,and also induce the apoptosis of the 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

AIM:To observe the expression of pten in human highly metastatic ovarian carcinoma cell line HO-8910PM after in vitro infection and investigate the effects of pten gene on the proli-feration and metastatic ability of human ovarian carcinoma HO-8910PM cells.METHODS:Ad-pten was constructed through Ad-Easy adenovirus vector system and the expression of pten gene in HO-8910PM cells was determined by Western Blot.The transfection efficiency of Ad-pten was determined by fluorescence microscope.The inhibitive effect of Ad-pten on proliferation of HO-8910PM cells was determined by MTT assay.The morpho-logic changes of HO-8910PM cells transfected with Ad-pten were observed by light microscopy(HE staining).The metastatic ability was analyzed by cell scratching model in vitro.Hoechest33258 staining was used to study the cell apoptosis.RESULTS:The expression of PTEN protein in HO-8910PM cells was confirmed by Western Blot.The efficiency of adenovirus mediated Ad-pten gene transfer was above 90% when the multiplicities of infection(MOI)was 100.Exogenous pten gene significantly suppressed the growth and metastatic ability of HO-8910PM cells and induced the apoptosis of the cells.CONCLUSION:The constructed Ad-pten transfection system is highly efficient in transferring wild-type pten gene into human endometrial carcinoma cells.Ad-pten can strongly inhibit the proliferation and metastasis of the cells,and also induce the apoptosis of the cells.

Key concepts: PTEN, Transfection, Cancer research, Cell culture, Biology, Cell growth, Apoptosis, Western blot

Related papers

Back to paper searchBrowse research topicsOriginal source
Inhibition on growth of ovarian carcinoma cells by recombinant adenovirus carrying pten gene — Research Paper | ScholarLens