Plasma membrane calcium-ATPase 2 and 4 in human breast cancer cell lines


Autoria(s): Lee, WJ; Roberts-Thomson, SJ; Monteith, GR
Contribuinte(s)

W. Baumeister

Data(s)

01/01/2005

Resumo

There is evidence to suggest that plasma membrane Ca2+-ATPase (PMCA) isoforms are important mediators of mammary gland physiology. PMCA2 in particular is upregulated extensively during lactation. Expression of other isoforms such as PMCA4 may influence mammary gland epithelial cell proliferation and aberrant regulation of PMCA isoform expression may lead or contribute to mammary gland pathophysiology in the form of breast cancers. To explore whether PMCA2 and PMCA4 expression may be deregulated in breast cancer, we compared mRNA expression of these PMCA isoforms in tumorigenic and non-tumorigenic human breast epithelial cell lines using real time RT-PCR. PMCA2 mRNA has a higher level of expression in some breast cancer cell lines and is overexpressed more than 100-fold in ZR-75-1 cells, compared to non-tumorigenic 184135 cells. Although differences in PMCA4 mRNA levels were observed between breast cell lines, they were not of the magnitude observed for PMCA2. We conclude that PMCA2 mRNA can be highly overexpressed in some breast cancer cells. The significance of PMCA2 overexpression on tumorigenicity and its possible correlation with other properties such as invasiveness requires further study. (c) 2005 Elsevier Inc. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:75312

Idioma(s)

eng

Publicador

Academic Press

Palavras-Chave #Biochemistry & Molecular Biology #Biophysics #Calcium #Pmca #Mammary Gland #Lactation #Breast Cancer #Mrna #Transcription #Time Rt-pcr #Mammary-gland #Calcineurin Controls #Calcium-atpase #Pump Isoforms #Ca2+ Atpase #Expression #Ca2+-atpase #Neurons #Stat5a #C1 #320599 Pharmacology not elsewhere classified #730108 Cancer and related disorders
Tipo

Journal Article