DocumentCode :
2513994
Title :
MRTF- A Decreases the Anti-Tumor Effect of Tamoxifen on MCF-7 Human Breast Cancer Cells
Author :
Liu, Zhi-Peng ; Luo, Xue-Gang ; Guo, Shu ; Wang, Jian-Xin ; Zhang, Xin ; Wang, Nan ; Jiang, Yong ; Zhang, Tong-Cun
Author_Institution :
Key Lab. of Ind. Microbiol., Tianjin Univ. of Sci. & Technol., Tianjin, China
fYear :
2009
fDate :
11-13 June 2009
Firstpage :
1
Lastpage :
4
Abstract :
Myocardin-related transcription factors A (MRTF-A) is a myocardin-related transcription factor that has been found strongly activated CarG box - containing genes through its direct binding to serum response factor (SRF). In the present study, the MRTF-A expression vector was constructed. The MTT assay showed that transfection of MRTF-A could significantly decrease the anti-tumor effect of tamoxifen on MCF-7 human breast cancer cells. The bioinformatics analysis found that the CarG element existed in the promoter region of COMT gene of many familiar vertebrates, including of human, rhesus macaque, chimpanzee, etc. The results of RT-PCR assay further showed that MRTF-A could enhance the transcription level of COMT. These results are the first to indicate that COMT might be a target gene which could be regulated by MRTF-A/SRF, and such transactivation event might be involved in the process of tamoxifen resistance.
Keywords :
biochemistry; cancer; cellular biophysics; drugs; proteins; proteomics; tumours; COMT gene promoter region; CarG box containing genes; MCF-7 human breast cancer cells; MRTF-A expression vector; MRTF-A transfection; MTT assay; RT-PCR assay; SRF MRTF-A binding; bioinformatics analysis; myocardin related transcription factor A; serum response factor; tamoxifen antitumor effect; tamoxifen resistance; Biotechnology; Breast cancer; Cells (biology); Chemical technology; Educational institutions; Humans; Laboratories; Medical treatment; Muscles; RNA;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
Conference_Location :
Beijing
Print_ISBN :
978-1-4244-2901-1
Electronic_ISBN :
978-1-4244-2902-8
Type :
conf
DOI :
10.1109/ICBBE.2009.5163090
Filename :
5163090
Link To Document :
بازگشت