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Update on HER-2 as a target for cancer therapy: The ERBB2 promoter and its exploitation for cancer treatment

Overexpression of the ERBB2 proto-oncogene is associated with amplification of the gene in breast cancer but increased activity of the promoter also plays a significant role. Members of two transcription factor families (AP-2 and Ets) show increased binding to the promoter in over-expressing cells....

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Detalles Bibliográficos
Autor principal: Hurst, Helen C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138707/
https://www.ncbi.nlm.nih.gov/pubmed/11737892
http://dx.doi.org/10.1186/bcr329
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author Hurst, Helen C
author_facet Hurst, Helen C
author_sort Hurst, Helen C
collection PubMed
description Overexpression of the ERBB2 proto-oncogene is associated with amplification of the gene in breast cancer but increased activity of the promoter also plays a significant role. Members of two transcription factor families (AP-2 and Ets) show increased binding to the promoter in over-expressing cells. Consequently, strategies have been devised to target promoter activity, either through the DNA binding sites for these factors, or through another promoter sequence, a polypurine-polypyrimidine repeat structure. The promoter has also been exploited for its tumour-specific activity to direct the accumulation of cytotoxic compounds selectively within cancer cells. Our current understanding of the ERBB2 promoter is reviewed and the status of these therapeutic avenues is discussed.
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spelling pubmed-1387072003-02-27 Update on HER-2 as a target for cancer therapy: The ERBB2 promoter and its exploitation for cancer treatment Hurst, Helen C Breast Cancer Res Review Overexpression of the ERBB2 proto-oncogene is associated with amplification of the gene in breast cancer but increased activity of the promoter also plays a significant role. Members of two transcription factor families (AP-2 and Ets) show increased binding to the promoter in over-expressing cells. Consequently, strategies have been devised to target promoter activity, either through the DNA binding sites for these factors, or through another promoter sequence, a polypurine-polypyrimidine repeat structure. The promoter has also been exploited for its tumour-specific activity to direct the accumulation of cytotoxic compounds selectively within cancer cells. Our current understanding of the ERBB2 promoter is reviewed and the status of these therapeutic avenues is discussed. BioMed Central 2001 2001-10-01 /pmc/articles/PMC138707/ /pubmed/11737892 http://dx.doi.org/10.1186/bcr329 Text en Copyright © 2001 BioMed Central Ltd
spellingShingle Review
Hurst, Helen C
Update on HER-2 as a target for cancer therapy: The ERBB2 promoter and its exploitation for cancer treatment
title Update on HER-2 as a target for cancer therapy: The ERBB2 promoter and its exploitation for cancer treatment
title_full Update on HER-2 as a target for cancer therapy: The ERBB2 promoter and its exploitation for cancer treatment
title_fullStr Update on HER-2 as a target for cancer therapy: The ERBB2 promoter and its exploitation for cancer treatment
title_full_unstemmed Update on HER-2 as a target for cancer therapy: The ERBB2 promoter and its exploitation for cancer treatment
title_short Update on HER-2 as a target for cancer therapy: The ERBB2 promoter and its exploitation for cancer treatment
title_sort update on her-2 as a target for cancer therapy: the erbb2 promoter and its exploitation for cancer treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138707/
https://www.ncbi.nlm.nih.gov/pubmed/11737892
http://dx.doi.org/10.1186/bcr329
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