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DBC1 Functions as a Tumor Suppressor by Regulating p53 Stability

DBC1 (deleted in breast cancer 1), also known as CCAR2 or KIAA1967 is an important negative regulator of SIRT1 and cellular stress response. Although the Dbc1 gene localizes at a region that is homozygously deleted in breast cancer, its role in tumorigenesis remains unclear. It has been suggested to...

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Autores principales: Qin, Bo, Minter-Dykhouse, Katherine, Yu, Jia, Zhang, Jun, Liu, Tongzheng, Zhang, Haoxing, Lee, Seung Baek, Kim, Jung Jin, Wang, Liewei, Lou, Zhenkun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351187/
https://www.ncbi.nlm.nih.gov/pubmed/25732823
http://dx.doi.org/10.1016/j.celrep.2015.01.066
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author Qin, Bo
Minter-Dykhouse, Katherine
Yu, Jia
Zhang, Jun
Liu, Tongzheng
Zhang, Haoxing
Lee, Seung Baek
Kim, Jung Jin
Wang, Liewei
Lou, Zhenkun
author_facet Qin, Bo
Minter-Dykhouse, Katherine
Yu, Jia
Zhang, Jun
Liu, Tongzheng
Zhang, Haoxing
Lee, Seung Baek
Kim, Jung Jin
Wang, Liewei
Lou, Zhenkun
author_sort Qin, Bo
collection PubMed
description DBC1 (deleted in breast cancer 1), also known as CCAR2 or KIAA1967 is an important negative regulator of SIRT1 and cellular stress response. Although the Dbc1 gene localizes at a region that is homozygously deleted in breast cancer, its role in tumorigenesis remains unclear. It has been suggested to be either a tumor suppressor or an oncogene. Therefore, the function of DBC1 in cancer needs to be further explored. Here we report that Dbc1 knockout mice are tumor prone, supporting that DBC1 functions as a tumor suppressor in vivo. Our data suggest that the increased tumor incidence in Dbc1 knockout mice is independent of Sirt1. Instead, we found that DBC1 loss results in less p53 protein in vitro and in vivo. DBC1 directly binds p53 and stabilizes it through competition with MDM2. These studies reveal that DBC1 plays an important role in tumor suppression through p53 regulation.
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spelling pubmed-43511872016-03-03 DBC1 Functions as a Tumor Suppressor by Regulating p53 Stability Qin, Bo Minter-Dykhouse, Katherine Yu, Jia Zhang, Jun Liu, Tongzheng Zhang, Haoxing Lee, Seung Baek Kim, Jung Jin Wang, Liewei Lou, Zhenkun Cell Rep Article DBC1 (deleted in breast cancer 1), also known as CCAR2 or KIAA1967 is an important negative regulator of SIRT1 and cellular stress response. Although the Dbc1 gene localizes at a region that is homozygously deleted in breast cancer, its role in tumorigenesis remains unclear. It has been suggested to be either a tumor suppressor or an oncogene. Therefore, the function of DBC1 in cancer needs to be further explored. Here we report that Dbc1 knockout mice are tumor prone, supporting that DBC1 functions as a tumor suppressor in vivo. Our data suggest that the increased tumor incidence in Dbc1 knockout mice is independent of Sirt1. Instead, we found that DBC1 loss results in less p53 protein in vitro and in vivo. DBC1 directly binds p53 and stabilizes it through competition with MDM2. These studies reveal that DBC1 plays an important role in tumor suppression through p53 regulation. 2015-02-26 2015-03-03 /pmc/articles/PMC4351187/ /pubmed/25732823 http://dx.doi.org/10.1016/j.celrep.2015.01.066 Text en © 2015 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc/4.0/ This manuscript version is made available under the CC BY-NC-ND 4.0 license.
spellingShingle Article
Qin, Bo
Minter-Dykhouse, Katherine
Yu, Jia
Zhang, Jun
Liu, Tongzheng
Zhang, Haoxing
Lee, Seung Baek
Kim, Jung Jin
Wang, Liewei
Lou, Zhenkun
DBC1 Functions as a Tumor Suppressor by Regulating p53 Stability
title DBC1 Functions as a Tumor Suppressor by Regulating p53 Stability
title_full DBC1 Functions as a Tumor Suppressor by Regulating p53 Stability
title_fullStr DBC1 Functions as a Tumor Suppressor by Regulating p53 Stability
title_full_unstemmed DBC1 Functions as a Tumor Suppressor by Regulating p53 Stability
title_short DBC1 Functions as a Tumor Suppressor by Regulating p53 Stability
title_sort dbc1 functions as a tumor suppressor by regulating p53 stability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4351187/
https://www.ncbi.nlm.nih.gov/pubmed/25732823
http://dx.doi.org/10.1016/j.celrep.2015.01.066
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