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...

Full description

Bibliographic Details
Main Authors: Amish J. Patel, Chung-Ping Liao, Zhiguo Chen, Chiachi Liu, Yong Wang, Lu Q. Le
Format: Article
Language:English
Published: Elsevier 2014-01-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124713007316
id doaj-39b99f00a8a44294b0cd0b667f9858f9
record_format Article
spelling 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
work_keys_str_mv AT amishjpatel betbromodomaininhibitiontriggersapoptosisofnf1associatedmalignantperipheralnervesheathtumorsthroughbiminduction
AT chungpingliao betbromodomaininhibitiontriggersapoptosisofnf1associatedmalignantperipheralnervesheathtumorsthroughbiminduction
AT zhiguochen betbromodomaininhibitiontriggersapoptosisofnf1associatedmalignantperipheralnervesheathtumorsthroughbiminduction
AT chiachiliu betbromodomaininhibitiontriggersapoptosisofnf1associatedmalignantperipheralnervesheathtumorsthroughbiminduction
AT yongwang betbromodomaininhibitiontriggersapoptosisofnf1associatedmalignantperipheralnervesheathtumorsthroughbiminduction
AT luqle betbromodomaininhibitiontriggersapoptosisofnf1associatedmalignantperipheralnervesheathtumorsthroughbiminduction
_version_ 1725152428363350016