Cargando…
ICBP90 belongs to a new family of proteins with an expression that is deregulated in cancer cells
ICBP90 (Inverted CCAAT box Binding Protein of 90 kDa) is a recently identified nuclear protein that binds to one of the inverted CCAAT boxes of the topoisomerase IIα (TopoIIα) gene promoter. Here, we show that ICBP90 shares structural homology with several other proteins, including Np95, the human a...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2003
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394215/ https://www.ncbi.nlm.nih.gov/pubmed/12838312 http://dx.doi.org/10.1038/sj.bjc.6601068 |
_version_ | 1782155365751717888 |
---|---|
author | Mousli, M Hopfner, R Abbady, A-Q Monté, D Jeanblanc, M Oudet, P Louis, B Bronner, C |
author_facet | Mousli, M Hopfner, R Abbady, A-Q Monté, D Jeanblanc, M Oudet, P Louis, B Bronner, C |
author_sort | Mousli, M |
collection | PubMed |
description | ICBP90 (Inverted CCAAT box Binding Protein of 90 kDa) is a recently identified nuclear protein that binds to one of the inverted CCAAT boxes of the topoisomerase IIα (TopoIIα) gene promoter. Here, we show that ICBP90 shares structural homology with several other proteins, including Np95, the human and mouse NIRF, suggesting the emergence of a new family of nuclear proteins. Towards elucidating the functions of this family, we analysed the expression of ICBP90 in various cancer or noncancer cell lines and in normal or breast carcinoma tissues. We found that cancer cell lines express higher levels of ICBP90 and TopoIIα than noncancer cell lines. By using cell-cycle phase-blocking drugs, we show that in primary cultured human lung fibroblasts, ICBP90 expression peaks at late G1 and during G2/M phases. In contrast, cancer cell lines such as HeLa, Jurkat and A549 show constant ICBP90 expression throughout the entire cell cycle. The effect of overexpression of E2F-1 is more efficient on ICBP90 and TopoIIα expression in noncancer cells (IMR90, WI38) than in cancer cells (U2OS, SaOs). Together, these results show that ICBP90 expression is altered in cancer cell lines and is upregulated by E2F-1 overexpression with an efficiency depending on the cancer status of the cell line. |
format | Text |
id | pubmed-2394215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23942152009-09-10 ICBP90 belongs to a new family of proteins with an expression that is deregulated in cancer cells Mousli, M Hopfner, R Abbady, A-Q Monté, D Jeanblanc, M Oudet, P Louis, B Bronner, C Br J Cancer Molecular and Cellular Pathology ICBP90 (Inverted CCAAT box Binding Protein of 90 kDa) is a recently identified nuclear protein that binds to one of the inverted CCAAT boxes of the topoisomerase IIα (TopoIIα) gene promoter. Here, we show that ICBP90 shares structural homology with several other proteins, including Np95, the human and mouse NIRF, suggesting the emergence of a new family of nuclear proteins. Towards elucidating the functions of this family, we analysed the expression of ICBP90 in various cancer or noncancer cell lines and in normal or breast carcinoma tissues. We found that cancer cell lines express higher levels of ICBP90 and TopoIIα than noncancer cell lines. By using cell-cycle phase-blocking drugs, we show that in primary cultured human lung fibroblasts, ICBP90 expression peaks at late G1 and during G2/M phases. In contrast, cancer cell lines such as HeLa, Jurkat and A549 show constant ICBP90 expression throughout the entire cell cycle. The effect of overexpression of E2F-1 is more efficient on ICBP90 and TopoIIα expression in noncancer cells (IMR90, WI38) than in cancer cells (U2OS, SaOs). Together, these results show that ICBP90 expression is altered in cancer cell lines and is upregulated by E2F-1 overexpression with an efficiency depending on the cancer status of the cell line. Nature Publishing Group 2003-07-07 2003-07-01 /pmc/articles/PMC2394215/ /pubmed/12838312 http://dx.doi.org/10.1038/sj.bjc.6601068 Text en Copyright © 2003 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular and Cellular Pathology Mousli, M Hopfner, R Abbady, A-Q Monté, D Jeanblanc, M Oudet, P Louis, B Bronner, C ICBP90 belongs to a new family of proteins with an expression that is deregulated in cancer cells |
title | ICBP90 belongs to a new family of proteins with an expression that is deregulated in cancer cells |
title_full | ICBP90 belongs to a new family of proteins with an expression that is deregulated in cancer cells |
title_fullStr | ICBP90 belongs to a new family of proteins with an expression that is deregulated in cancer cells |
title_full_unstemmed | ICBP90 belongs to a new family of proteins with an expression that is deregulated in cancer cells |
title_short | ICBP90 belongs to a new family of proteins with an expression that is deregulated in cancer cells |
title_sort | icbp90 belongs to a new family of proteins with an expression that is deregulated in cancer cells |
topic | Molecular and Cellular Pathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394215/ https://www.ncbi.nlm.nih.gov/pubmed/12838312 http://dx.doi.org/10.1038/sj.bjc.6601068 |
work_keys_str_mv | AT mouslim icbp90belongstoanewfamilyofproteinswithanexpressionthatisderegulatedincancercells AT hopfnerr icbp90belongstoanewfamilyofproteinswithanexpressionthatisderegulatedincancercells AT abbadyaq icbp90belongstoanewfamilyofproteinswithanexpressionthatisderegulatedincancercells AT monted icbp90belongstoanewfamilyofproteinswithanexpressionthatisderegulatedincancercells AT jeanblancm icbp90belongstoanewfamilyofproteinswithanexpressionthatisderegulatedincancercells AT oudetp icbp90belongstoanewfamilyofproteinswithanexpressionthatisderegulatedincancercells AT louisb icbp90belongstoanewfamilyofproteinswithanexpressionthatisderegulatedincancercells AT bronnerc icbp90belongstoanewfamilyofproteinswithanexpressionthatisderegulatedincancercells |