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Variant Messenger RNAs between Normal Human Breast Tissue and Primary Breast Carcinomas1
Division of Experimental Therapy [M. A. J. v. D., L. J. v. V.], and Departments of Radiotherapy [A. A. M. H.] and Pathology [L. J. v. V.], Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, the Netherlands
We evaluated the differences in prevalence and functional activity of
human estrogen receptor
(hER) variant mRNA between 21 normal breast
tissues and 41 primary breast carcinomas using a functional assay in
yeast for the hER. First, we found that the presence of wild-type hER,
relative to the total amount of hER, differs markedly
(P < 0.0001) between normal breast
tissue (median, 85% wild-type hER) and breast tumors (median, 74%
wild-type hER). Second, the hER variants with altered function that are
present in normal breast tissue are mainly one-exon deleted splicing
variants (median, 100%), whereas in breast tumors only half of all
variants lack just one single exon (median, 50%;
P < 0.0001). Our results suggest that
hER-dependent estrogen responsiveness of breast tissue may change
during tumor outgrowth, indicating that specific hER variants may play
a role in breast cancer development or progression.
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