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TIP30: A Novel Tumor-Suppressor Gene

TIP30/CC3 was first identified and characterized as a “candidate” tumor-suppressor gene in 1997. Recently, the TIP30 tumor-suppressor status has been fully established since several studies have described that TIP30 protein expression is frequently downregulated in diverse types of human tumors, and...

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Detalles Bibliográficos
Autores principales: Yu, Xin, Li, Zheng, Wu, William K. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cognizant Communication Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842584/
https://www.ncbi.nlm.nih.gov/pubmed/26629947
http://dx.doi.org/10.3727/096504015X14424348426116
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author Yu, Xin
Li, Zheng
Wu, William K. K.
author_facet Yu, Xin
Li, Zheng
Wu, William K. K.
author_sort Yu, Xin
collection PubMed
description TIP30/CC3 was first identified and characterized as a “candidate” tumor-suppressor gene in 1997. Recently, the TIP30 tumor-suppressor status has been fully established since several studies have described that TIP30 protein expression is frequently downregulated in diverse types of human tumors, and the downregulation is often associated with tumor progression. TIP30 is involved in the control of cell apoptosis, growth, metastasis, angiogenesis, DNA repair, and tumor cell metabolism. Moreover, TIP30(−/−) mice spontaneously develop hepatocellular carcinoma and other tumors at a higher incidence than that of wild-type mice. In this review, we provide an overview of current knowledge concerning the role of TIP30 in tumor development and progression. To our knowledge, this is the first review about the role of novel tumor-suppressor gene TIP30 in tumor development and progression.
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spelling pubmed-78425842021-02-16 TIP30: A Novel Tumor-Suppressor Gene Yu, Xin Li, Zheng Wu, William K. K. Oncol Res Review TIP30/CC3 was first identified and characterized as a “candidate” tumor-suppressor gene in 1997. Recently, the TIP30 tumor-suppressor status has been fully established since several studies have described that TIP30 protein expression is frequently downregulated in diverse types of human tumors, and the downregulation is often associated with tumor progression. TIP30 is involved in the control of cell apoptosis, growth, metastasis, angiogenesis, DNA repair, and tumor cell metabolism. Moreover, TIP30(−/−) mice spontaneously develop hepatocellular carcinoma and other tumors at a higher incidence than that of wild-type mice. In this review, we provide an overview of current knowledge concerning the role of TIP30 in tumor development and progression. To our knowledge, this is the first review about the role of novel tumor-suppressor gene TIP30 in tumor development and progression. Cognizant Communication Corporation 2015-11-25 /pmc/articles/PMC7842584/ /pubmed/26629947 http://dx.doi.org/10.3727/096504015X14424348426116 Text en Copyright © 2015 Cognizant Comm. Corp. http://creativecommons.org/licenses/by-nc-nd/4.0/ This article is licensed under a Creative Commons Attribution-NonCommercial NoDerivatives 4.0 International License.
spellingShingle Review
Yu, Xin
Li, Zheng
Wu, William K. K.
TIP30: A Novel Tumor-Suppressor Gene
title TIP30: A Novel Tumor-Suppressor Gene
title_full TIP30: A Novel Tumor-Suppressor Gene
title_fullStr TIP30: A Novel Tumor-Suppressor Gene
title_full_unstemmed TIP30: A Novel Tumor-Suppressor Gene
title_short TIP30: A Novel Tumor-Suppressor Gene
title_sort tip30: a novel tumor-suppressor gene
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7842584/
https://www.ncbi.nlm.nih.gov/pubmed/26629947
http://dx.doi.org/10.3727/096504015X14424348426116
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