BET Bromodomain Inhibition Triggers Apoptosis of NF1-Associated Malignant Peripheral Nerve Sheath Tumors through Bim Induction
Malignant peripheral nerve sheath tumors (MPNSTs) are highly aggressive sarcomas that develop sporadically or in neurofibromatosis type 1 (NF1) patients. There is no effective treatment for MPNSTs and they are typically fatal. To gain insights into MPNST pathogenesis, we utilized an MPNST mouse mode...
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doaj-39b99f00a8a44294b0cd0b667f9858f92020-11-25T01:15:34ZengElsevierCell Reports2211-12472014-01-0161819210.1016/j.celrep.2013.12.001BET Bromodomain Inhibition Triggers Apoptosis of NF1-Associated Malignant Peripheral Nerve Sheath Tumors through Bim InductionAmish J. Patel0Chung-Ping Liao1Zhiguo Chen2Chiachi Liu3Yong Wang4Lu Q. Le5Department of Dermatology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX, 75390-9133, USADepartment of Dermatology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX, 75390-9133, USADepartment of Dermatology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX, 75390-9133, USADepartment of Dermatology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX, 75390-9133, USADepartment of Dermatology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX, 75390-9133, USADepartment of Dermatology, University of Texas Southwestern Medical Center at Dallas, Dallas, TX, 75390-9133, USAMalignant peripheral nerve sheath tumors (MPNSTs) are highly aggressive sarcomas that develop sporadically or in neurofibromatosis type 1 (NF1) patients. There is no effective treatment for MPNSTs and they are typically fatal. To gain insights into MPNST pathogenesis, we utilized an MPNST mouse model that allowed us to study the evolution of these tumors at the transcriptome level. Strikingly, in MPNSTs we found upregulation of a chromatin regulator, Brd4, and show that BRD4 inhibition profoundly suppresses both growth and tumorigenesis. Our findings reveal roles for BET bromodomains in MPNST development and report a mechanism by which bromodomain inhibition induces apoptosis through induction of proapoptotic Bim, which may represent a paradigm shift in therapy for MPNST patients. Moreover, these findings indicate epigenetic mechanisms underlying the balance of anti- and proapoptotic molecules and that bromodomain inhibition can shift this balance in favor of cancer cell apoptosis.http://www.sciencedirect.com/science/article/pii/S2211124713007316 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Amish J. Patel Chung-Ping Liao Zhiguo Chen Chiachi Liu Yong Wang Lu Q. Le |
spellingShingle |
Amish J. Patel Chung-Ping Liao Zhiguo Chen Chiachi Liu Yong Wang Lu Q. Le BET Bromodomain Inhibition Triggers Apoptosis of NF1-Associated Malignant Peripheral Nerve Sheath Tumors through Bim Induction Cell Reports |
author_facet |
Amish J. Patel Chung-Ping Liao Zhiguo Chen Chiachi Liu Yong Wang Lu Q. Le |
author_sort |
Amish J. Patel |
title |
BET Bromodomain Inhibition Triggers Apoptosis of NF1-Associated Malignant Peripheral Nerve Sheath Tumors through Bim Induction |
title_short |
BET Bromodomain Inhibition Triggers Apoptosis of NF1-Associated Malignant Peripheral Nerve Sheath Tumors through Bim Induction |
title_full |
BET Bromodomain Inhibition Triggers Apoptosis of NF1-Associated Malignant Peripheral Nerve Sheath Tumors through Bim Induction |
title_fullStr |
BET Bromodomain Inhibition Triggers Apoptosis of NF1-Associated Malignant Peripheral Nerve Sheath Tumors through Bim Induction |
title_full_unstemmed |
BET Bromodomain Inhibition Triggers Apoptosis of NF1-Associated Malignant Peripheral Nerve Sheath Tumors through Bim Induction |
title_sort |
bet bromodomain inhibition triggers apoptosis of nf1-associated malignant peripheral nerve sheath tumors through bim induction |
publisher |
Elsevier |
series |
Cell Reports |
issn |
2211-1247 |
publishDate |
2014-01-01 |
description |
Malignant peripheral nerve sheath tumors (MPNSTs) are highly aggressive sarcomas that develop sporadically or in neurofibromatosis type 1 (NF1) patients. There is no effective treatment for MPNSTs and they are typically fatal. To gain insights into MPNST pathogenesis, we utilized an MPNST mouse model that allowed us to study the evolution of these tumors at the transcriptome level. Strikingly, in MPNSTs we found upregulation of a chromatin regulator, Brd4, and show that BRD4 inhibition profoundly suppresses both growth and tumorigenesis. Our findings reveal roles for BET bromodomains in MPNST development and report a mechanism by which bromodomain inhibition induces apoptosis through induction of proapoptotic Bim, which may represent a paradigm shift in therapy for MPNST patients. Moreover, these findings indicate epigenetic mechanisms underlying the balance of anti- and proapoptotic molecules and that bromodomain inhibition can shift this balance in favor of cancer cell apoptosis. |
url |
http://www.sciencedirect.com/science/article/pii/S2211124713007316 |
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