Role of JNK in a Trp53-dependent mouse model of breast cancer.

The cJun NH2-terminal kinase (JNK) signal transduction pathway has been implicated in mammary carcinogenesis. To test the role of JNK, we examined the effect of ablation of the Jnk1 and Jnk2 genes in a Trp53-dependent model of breast cancer using BALB/c mice. We detected no defects in mammary gland...

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Main Authors: Cristina Cellurale, Claire R Weston, Judith Reilly, David S Garlick, D Joseph Jerry, Hayla K Sluss, Roger J Davis
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-08-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2930003?pdf=render
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author Cristina Cellurale
Claire R Weston
Judith Reilly
David S Garlick
D Joseph Jerry
Hayla K Sluss
Roger J Davis
author_facet Cristina Cellurale
Claire R Weston
Judith Reilly
David S Garlick
D Joseph Jerry
Hayla K Sluss
Roger J Davis
author_sort Cristina Cellurale
collection DOAJ
description The cJun NH2-terminal kinase (JNK) signal transduction pathway has been implicated in mammary carcinogenesis. To test the role of JNK, we examined the effect of ablation of the Jnk1 and Jnk2 genes in a Trp53-dependent model of breast cancer using BALB/c mice. We detected no defects in mammary gland development in virgin mice or during lactation and involution in control studies of Jnk1(-/-) and Jnk2(-/-) mice. In a Trp53(-/+) genetic background, mammary carcinomas were detected in 43% of control mice, 70% of Jnk1(-/-) mice, and 53% of Jnk2(-/-) mice. These data indicate that JNK1 and JNK2 are not essential for mammary carcinoma development in the Trp53(-/+) BALB/c model of breast cancer. In contrast, this analysis suggests that JNK may partially contribute to tumor suppression. This conclusion is consistent with the finding that tumor-free survival of JNK-deficient Trp53(-/+) mice was significantly reduced compared with control Trp53(-/+) mice. We conclude that JNK1 and JNK2 can act as suppressors of mammary tumor development.
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spelling doaj.art-e3edcc8710984e838f206fbeb95f0e602022-12-21T18:51:34ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-08-0158e1246910.1371/journal.pone.0012469Role of JNK in a Trp53-dependent mouse model of breast cancer.Cristina CelluraleClaire R WestonJudith ReillyDavid S GarlickD Joseph JerryHayla K SlussRoger J DavisThe cJun NH2-terminal kinase (JNK) signal transduction pathway has been implicated in mammary carcinogenesis. To test the role of JNK, we examined the effect of ablation of the Jnk1 and Jnk2 genes in a Trp53-dependent model of breast cancer using BALB/c mice. We detected no defects in mammary gland development in virgin mice or during lactation and involution in control studies of Jnk1(-/-) and Jnk2(-/-) mice. In a Trp53(-/+) genetic background, mammary carcinomas were detected in 43% of control mice, 70% of Jnk1(-/-) mice, and 53% of Jnk2(-/-) mice. These data indicate that JNK1 and JNK2 are not essential for mammary carcinoma development in the Trp53(-/+) BALB/c model of breast cancer. In contrast, this analysis suggests that JNK may partially contribute to tumor suppression. This conclusion is consistent with the finding that tumor-free survival of JNK-deficient Trp53(-/+) mice was significantly reduced compared with control Trp53(-/+) mice. We conclude that JNK1 and JNK2 can act as suppressors of mammary tumor development.http://europepmc.org/articles/PMC2930003?pdf=render
spellingShingle Cristina Cellurale
Claire R Weston
Judith Reilly
David S Garlick
D Joseph Jerry
Hayla K Sluss
Roger J Davis
Role of JNK in a Trp53-dependent mouse model of breast cancer.
PLoS ONE
title Role of JNK in a Trp53-dependent mouse model of breast cancer.
title_full Role of JNK in a Trp53-dependent mouse model of breast cancer.
title_fullStr Role of JNK in a Trp53-dependent mouse model of breast cancer.
title_full_unstemmed Role of JNK in a Trp53-dependent mouse model of breast cancer.
title_short Role of JNK in a Trp53-dependent mouse model of breast cancer.
title_sort role of jnk in a trp53 dependent mouse model of breast cancer
url http://europepmc.org/articles/PMC2930003?pdf=render
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