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CCAAT/enhancer binding proteins in normal mammary development and breast cancer

CCAAT/enhancer binding proteins (C/EBPs) are a family of leucine zipper, transcription factors that bind to DNA as homodimers and heterodimers. They regulate cellular proliferation, differentiation and apoptosis in the mammary gland. Multiple protein isoforms, including truncated, dominant negatives...

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Detalles Bibliográficos
Autor principal: Zahnow, Cynthia A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138725/
https://www.ncbi.nlm.nih.gov/pubmed/12052253
http://dx.doi.org/10.1186/bcr428
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author Zahnow, Cynthia A
author_facet Zahnow, Cynthia A
author_sort Zahnow, Cynthia A
collection PubMed
description CCAAT/enhancer binding proteins (C/EBPs) are a family of leucine zipper, transcription factors that bind to DNA as homodimers and heterodimers. They regulate cellular proliferation, differentiation and apoptosis in the mammary gland. Multiple protein isoforms, including truncated, dominant negatives, are generated by translation of the C/EBPβ transcript or via proteolytic cleavage of the full-length C/EBPβ protein. Gene deletion of individual C/EBP family members has demonstrated an essential role for C/EBPβ in normal mammary development, while transgenic and overexpression studies provide evidence that the dominant-negative C/EBPβ-liver-enriched inhibitory protein isoform induces proliferation in mammary epithelial cells. Mounting evidence suggests that alterations in the ratio of the C/EBPβ-liver-enriched inhibitory protein isoform and the C/EBPβ-liver-enriched activating protein isoform may play a role in the development of breast cancer. This review will consequently focus on C/EBP actions in normal mammary development and on the emerging data that supports a role in breast cancer.
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spelling pubmed-1387252003-02-27 CCAAT/enhancer binding proteins in normal mammary development and breast cancer Zahnow, Cynthia A Breast Cancer Res Review CCAAT/enhancer binding proteins (C/EBPs) are a family of leucine zipper, transcription factors that bind to DNA as homodimers and heterodimers. They regulate cellular proliferation, differentiation and apoptosis in the mammary gland. Multiple protein isoforms, including truncated, dominant negatives, are generated by translation of the C/EBPβ transcript or via proteolytic cleavage of the full-length C/EBPβ protein. Gene deletion of individual C/EBP family members has demonstrated an essential role for C/EBPβ in normal mammary development, while transgenic and overexpression studies provide evidence that the dominant-negative C/EBPβ-liver-enriched inhibitory protein isoform induces proliferation in mammary epithelial cells. Mounting evidence suggests that alterations in the ratio of the C/EBPβ-liver-enriched inhibitory protein isoform and the C/EBPβ-liver-enriched activating protein isoform may play a role in the development of breast cancer. This review will consequently focus on C/EBP actions in normal mammary development and on the emerging data that supports a role in breast cancer. BioMed Central 2002 2002-04-19 /pmc/articles/PMC138725/ /pubmed/12052253 http://dx.doi.org/10.1186/bcr428 Text en Copyright © 2002 BioMed Central Ltd
spellingShingle Review
Zahnow, Cynthia A
CCAAT/enhancer binding proteins in normal mammary development and breast cancer
title CCAAT/enhancer binding proteins in normal mammary development and breast cancer
title_full CCAAT/enhancer binding proteins in normal mammary development and breast cancer
title_fullStr CCAAT/enhancer binding proteins in normal mammary development and breast cancer
title_full_unstemmed CCAAT/enhancer binding proteins in normal mammary development and breast cancer
title_short CCAAT/enhancer binding proteins in normal mammary development and breast cancer
title_sort ccaat/enhancer binding proteins in normal mammary development and breast cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138725/
https://www.ncbi.nlm.nih.gov/pubmed/12052253
http://dx.doi.org/10.1186/bcr428
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