Cutaneous wound healing through paradoxical MAPK activation by BRAF inhibitors

BRAF inhibitors often show skin-hyperproliferative side effects in melanoma patients. Here, the authors demonstrate that BRAF inhibitors can be used to enhance skin wound healing through the MAPK- ERK pathway activation that positively regulates the proliferation of keratinocytes.

Bibliographic Details
Main Authors: Helena Escuin-Ordinas, Shuoran Li, Michael W. Xie, Lu Sun, Willy Hugo, Rong Rong Huang, Jing Jiao, Felipe Meira de-Faria, Susan Realegeno, Paige Krystofinski, Ariel Azhdam, Sara Marie D. Komenan, Mohammad Atefi, Begoña Comin-Anduix, Matteo Pellegrini, Alistair J. Cochran, Robert L. Modlin, Harvey R. Herschman, Roger S. Lo, William H. McBride, Tatiana Segura, Antoni Ribas
Format: Article
Language:English
Published: Nature Publishing Group 2016-08-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/ncomms12348
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spelling doaj-4df7cfd06ae5433d88273671aa9365b62021-05-11T10:49:27ZengNature Publishing GroupNature Communications2041-17232016-08-017111010.1038/ncomms12348Cutaneous wound healing through paradoxical MAPK activation by BRAF inhibitorsHelena Escuin-Ordinas0Shuoran Li1Michael W. Xie2Lu Sun3Willy Hugo4Rong Rong Huang5Jing Jiao6Felipe Meira de-Faria7Susan Realegeno8Paige Krystofinski9Ariel Azhdam10Sara Marie D. Komenan11Mohammad Atefi12Begoña Comin-Anduix13Matteo Pellegrini14Alistair J. Cochran15Robert L. Modlin16Harvey R. Herschman17Roger S. Lo18William H. McBride19Tatiana Segura20Antoni Ribas21Division of Hematology/Oncology, Department of Medicine, University of California, Los Angeles (UCLA)Department of Chemical and Biomolecular Engineering, University of California, Los Angeles (UCLA)Division of Experimental Radiation Oncology, Department of Radiation Oncology, University of California, Los Angeles (UCLA)Division of Dermatology, Department of Medicine, University of California, Los Angeles (UCLA)Division of Dermatology, Department of Medicine, University of California, Los Angeles (UCLA)Department of Pathology and Laboratory Medicine, University of California, Los Angeles (UCLA)Department of Molecular and Medical Pharmacology, University of California, Los Angeles (UCLA)Department of Molecular and Medical Pharmacology, University of California, Los Angeles (UCLA)Department of Microbiology, Immunology & Molecular Genetics, University of California, Los Angeles (UCLA)Division of Hematology/Oncology, Department of Medicine, University of California, Los Angeles (UCLA)Division of Hematology/Oncology, Department of Medicine, University of California, Los Angeles (UCLA)Division of Surgical Oncology, Department of SurgeryDivision of Hematology/Oncology, Department of Medicine, University of California, Los Angeles (UCLA)Division of Surgical Oncology, Department of SurgeryDepartment of Molecular, Cell, and Developmental Biology, University of California, Los Angeles (UCLA)Department of Pathology and Laboratory Medicine, University of California, Los Angeles (UCLA)Division of Dermatology, Department of Medicine, University of California, Los Angeles (UCLA)Department of Molecular and Medical Pharmacology, University of California, Los Angeles (UCLA)Division of Dermatology, Department of Medicine, University of California, Los Angeles (UCLA)Division of Experimental Radiation Oncology, Department of Radiation Oncology, University of California, Los Angeles (UCLA)Department of Chemical and Biomolecular Engineering, University of California, Los Angeles (UCLA)Division of Hematology/Oncology, Department of Medicine, University of California, Los Angeles (UCLA)BRAF inhibitors often show skin-hyperproliferative side effects in melanoma patients. Here, the authors demonstrate that BRAF inhibitors can be used to enhance skin wound healing through the MAPK- ERK pathway activation that positively regulates the proliferation of keratinocytes.https://doi.org/10.1038/ncomms12348
collection DOAJ
language English
format Article
sources DOAJ
author Helena Escuin-Ordinas
Shuoran Li
Michael W. Xie
Lu Sun
Willy Hugo
Rong Rong Huang
Jing Jiao
Felipe Meira de-Faria
Susan Realegeno
Paige Krystofinski
Ariel Azhdam
Sara Marie D. Komenan
Mohammad Atefi
Begoña Comin-Anduix
Matteo Pellegrini
Alistair J. Cochran
Robert L. Modlin
Harvey R. Herschman
Roger S. Lo
William H. McBride
Tatiana Segura
Antoni Ribas
spellingShingle Helena Escuin-Ordinas
Shuoran Li
Michael W. Xie
Lu Sun
Willy Hugo
Rong Rong Huang
Jing Jiao
Felipe Meira de-Faria
Susan Realegeno
Paige Krystofinski
Ariel Azhdam
Sara Marie D. Komenan
Mohammad Atefi
Begoña Comin-Anduix
Matteo Pellegrini
Alistair J. Cochran
Robert L. Modlin
Harvey R. Herschman
Roger S. Lo
William H. McBride
Tatiana Segura
Antoni Ribas
Cutaneous wound healing through paradoxical MAPK activation by BRAF inhibitors
Nature Communications
author_facet Helena Escuin-Ordinas
Shuoran Li
Michael W. Xie
Lu Sun
Willy Hugo
Rong Rong Huang
Jing Jiao
Felipe Meira de-Faria
Susan Realegeno
Paige Krystofinski
Ariel Azhdam
Sara Marie D. Komenan
Mohammad Atefi
Begoña Comin-Anduix
Matteo Pellegrini
Alistair J. Cochran
Robert L. Modlin
Harvey R. Herschman
Roger S. Lo
William H. McBride
Tatiana Segura
Antoni Ribas
author_sort Helena Escuin-Ordinas
title Cutaneous wound healing through paradoxical MAPK activation by BRAF inhibitors
title_short Cutaneous wound healing through paradoxical MAPK activation by BRAF inhibitors
title_full Cutaneous wound healing through paradoxical MAPK activation by BRAF inhibitors
title_fullStr Cutaneous wound healing through paradoxical MAPK activation by BRAF inhibitors
title_full_unstemmed Cutaneous wound healing through paradoxical MAPK activation by BRAF inhibitors
title_sort cutaneous wound healing through paradoxical mapk activation by braf inhibitors
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2016-08-01
description BRAF inhibitors often show skin-hyperproliferative side effects in melanoma patients. Here, the authors demonstrate that BRAF inhibitors can be used to enhance skin wound healing through the MAPK- ERK pathway activation that positively regulates the proliferation of keratinocytes.
url https://doi.org/10.1038/ncomms12348
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