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Role of Cell Division Autoantigen 1 (CDA1) in Cell Proliferation, Fibrosis
Cell Division Autoantigen 1 (CDA1) was discovered following screening a human expression library with serum from a patient with Discoid Lupus Erythematosus. CDA1, encoded by TSPYL2 on the X chromosome, shares anti-proliferative, pro‑fibrotic properties with TGF-β. It inhibits cell growth through p53...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966230/ https://www.ncbi.nlm.nih.gov/pubmed/24710090 http://dx.doi.org/10.3390/genes1030335 |
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author | Toh, Ban-Hock Tu, Yugang Cao, Zemin Cooper, Mark E. Chai, Zhonglin |
author_facet | Toh, Ban-Hock Tu, Yugang Cao, Zemin Cooper, Mark E. Chai, Zhonglin |
author_sort | Toh, Ban-Hock |
collection | PubMed |
description | Cell Division Autoantigen 1 (CDA1) was discovered following screening a human expression library with serum from a patient with Discoid Lupus Erythematosus. CDA1, encoded by TSPYL2 on the X chromosome, shares anti-proliferative, pro‑fibrotic properties with TGF-β. It inhibits cell growth through p53, pERK1/2, p21‑mediated pathways, is implicated in tumorigenesis, the DNA damage response. Its pro-fibrotic property is mediated through cross-talk with TGF-β that results in upregulation of extracellular matrix proteins. The latter properties have identified a key role for CDA1 in diabetes associated atherosclerosis. These dual properties place CDA1 as an attractive molecular target for treating tumors, vascular fibrosis including atherosclerosis, other vascular disorders associated with enhanced TGF-β action, tissue scarring. |
format | Online Article Text |
id | pubmed-3966230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-39662302014-03-26 Role of Cell Division Autoantigen 1 (CDA1) in Cell Proliferation, Fibrosis Toh, Ban-Hock Tu, Yugang Cao, Zemin Cooper, Mark E. Chai, Zhonglin Genes (Basel) Review Cell Division Autoantigen 1 (CDA1) was discovered following screening a human expression library with serum from a patient with Discoid Lupus Erythematosus. CDA1, encoded by TSPYL2 on the X chromosome, shares anti-proliferative, pro‑fibrotic properties with TGF-β. It inhibits cell growth through p53, pERK1/2, p21‑mediated pathways, is implicated in tumorigenesis, the DNA damage response. Its pro-fibrotic property is mediated through cross-talk with TGF-β that results in upregulation of extracellular matrix proteins. The latter properties have identified a key role for CDA1 in diabetes associated atherosclerosis. These dual properties place CDA1 as an attractive molecular target for treating tumors, vascular fibrosis including atherosclerosis, other vascular disorders associated with enhanced TGF-β action, tissue scarring. MDPI 2010-09-30 /pmc/articles/PMC3966230/ /pubmed/24710090 http://dx.doi.org/10.3390/genes1030335 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Toh, Ban-Hock Tu, Yugang Cao, Zemin Cooper, Mark E. Chai, Zhonglin Role of Cell Division Autoantigen 1 (CDA1) in Cell Proliferation, Fibrosis |
title | Role of Cell Division Autoantigen 1 (CDA1) in Cell Proliferation, Fibrosis |
title_full | Role of Cell Division Autoantigen 1 (CDA1) in Cell Proliferation, Fibrosis |
title_fullStr | Role of Cell Division Autoantigen 1 (CDA1) in Cell Proliferation, Fibrosis |
title_full_unstemmed | Role of Cell Division Autoantigen 1 (CDA1) in Cell Proliferation, Fibrosis |
title_short | Role of Cell Division Autoantigen 1 (CDA1) in Cell Proliferation, Fibrosis |
title_sort | role of cell division autoantigen 1 (cda1) in cell proliferation, fibrosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966230/ https://www.ncbi.nlm.nih.gov/pubmed/24710090 http://dx.doi.org/10.3390/genes1030335 |
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