EXPRESSION OF CYTOKERATIN MESSENGER-RNA VERSUS PROTEIN IN THE NORMAL MAMMARY-GLAND AND IN BREAST-CANCER

Citation
L. Su et al., EXPRESSION OF CYTOKERATIN MESSENGER-RNA VERSUS PROTEIN IN THE NORMAL MAMMARY-GLAND AND IN BREAST-CANCER, Human pathology, 27(8), 1996, pp. 800-806
Citations number
37
Categorie Soggetti
Pathology
Journal title
ISSN journal
00468177
Volume
27
Issue
8
Year of publication
1996
Pages
800 - 806
Database
ISI
SICI code
0046-8177(1996)27:8<800:EOCMVP>2.0.ZU;2-6
Abstract
It is not known how tightly regulation of cytokeratin (CK) protein exp ression is correlated with transcriptional activity in breast cancer. The level of control of CK expression in the normal mammary gland and in breast cancer has been assessed by combining in situ hybridization with riboprobes, and with immunohistochemistry using monospecific anti bodies. In normal mammary gland, luminal cells showed abundant hybridi zation with complementary RNA (cRNA) probes for CK7, CK8, CK18, and CK 19. Proteins of these CKs were correspondingly distributed except for that of CK19, which showed a heterogeneous staining. In primary carcin omas, both messenger RNAs (mRNAs) and proteins of CK8 and CK18 were ge nerally expressed to a degree similar to that of normal epithelia, but a lower level of mRNA and protein of CK18 was observed in metastatic carcinomas. Reduced expression of CK7 and CK14 was observed in all car cinomas, and the correlation between mRNA and protein for these two cy tokeratins was unbalanced, whereas the expression of CK19 mRNA and the proportion of its protein-positive cells were increased. The results suggest that these major CKs in normal mammary gland epithelia are reg ulated at the transcriptional level except for CK19, which is partiall y under the posttranscriptional control. The alterations observed in b reast cancer are not only refleted by the reduced or increased express ion of individual cytokeratins, but characterized by partial loss of t he normal regulation of cytokeratin expression. Copyright (C) 1996 by W.B. Saunders Company.