Carcinogenesis, Vol 18, 251-257, Copyright © 1997 by Oxford University Press
KS Kang, I Morita, A Cruz, YJ Jeon, JE Trosko and CC Chang
Although approximately two-thirds of breast cancers are estrogen receptor
(ER)-positive, only a small proportion of epithelial cells in the mammary
gland express the ER. The origin of the ER-positive breast cancers is
unknown. Recently, we have developed a culture method to grow two
morphologically and antigenically distinguishable types of normal human
breast epithelial cells (HBEC) derived from reduction mammoplasty. In this
report, we studied the expression of ER in these two types of cells and
their transformed cell lines. The results indicate that Type I HBEC with
luminal and stem cell characteristics expressed a variant ER (approximately
48 kd) by Western blot analysis. This variant ER contains a deletion in the
DNA binding domain (exon 2) as revealed by RT-PCR analysis. The lack of the
DNA-binding domain of the variant ER was also confirmed by the ER-estrogen
responsive element binding assay, as well as by the immunofluorescence
staining of the ER using anti-ER antibodies which recognize either the
C-terminal or N- terminal region. In contrast, Type II HBEC with basal
epithelial phenotype are ER-negative. Simian virus 40 (SV40) transformed
Type I and Type II HBEC lines also expressed the variant ER. Tumors formed
in athymic nude mice by in vitro transformed tumorigenic Type I cell lines,
however, expressed a high level of wild type ER which was undetectable in
these cells grown in vitro before and after tumor formation. Thus, there
appears to be a differential ER mRNA splicing between the in vitro and in
vivo mileu.
ARTICLES
Expression of estrogen receptors in a normal human breast epithelial cell type with luminal and stem cell characteristics and its neoplastically transformed cell lines
Department of Pediatrics/Human Development, College of Human Medicine, Michigan State University, East Lansing 48824-1317, USA.
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