Aberrant Activation of the RANK Signaling Receptor Induces Murine Salivary Gland Tumors.

Unlike cancers of related exocrine tissues such as the mammary and prostate gland, diagnosis and treatment of aggressive salivary gland malignancies have not markedly advanced in decades. Effective clinical management of malignant salivary gland cancers is undercut by our limited knowledge concernin...

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Main Authors: Maria M Szwarc, Ramakrishna Kommagani, Allison P Jacob, William C Dougall, Michael M Ittmann, John P Lydon
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4464738?pdf=render
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spelling doaj-4c53013ca1144500a2566ea2c57189972020-11-25T01:49:45ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01106e012846710.1371/journal.pone.0128467Aberrant Activation of the RANK Signaling Receptor Induces Murine Salivary Gland Tumors.Maria M SzwarcRamakrishna KommaganiAllison P JacobWilliam C DougallMichael M IttmannJohn P LydonUnlike cancers of related exocrine tissues such as the mammary and prostate gland, diagnosis and treatment of aggressive salivary gland malignancies have not markedly advanced in decades. Effective clinical management of malignant salivary gland cancers is undercut by our limited knowledge concerning the key molecular signals that underpin the etiopathogenesis of this rare and heterogeneous head and neck cancer. Without knowledge of the critical signals that drive salivary gland tumorigenesis, tumor vulnerabilities cannot be exploited that allow for targeted molecular therapies. This knowledge insufficiency is further exacerbated by a paucity of preclinical mouse models (as compared to other cancer fields) with which to both study salivary gland pathobiology and test novel intervention strategies. Using a mouse transgenic approach, we demonstrate that deregulation of the Receptor Activator of NFkB Ligand (RANKL)/RANK signaling axis results in rapid tumor development in all three major salivary glands. In line with its established role in other exocrine gland cancers (i.e., breast cancer), the RANKL/RANK signaling axis elicits an aggressive salivary gland tumor phenotype both at the histologic and molecular level. Despite the ability of this cytokine signaling axis to drive advanced stage disease within a short latency period, early blockade of RANKL/RANK signaling markedly attenuates the development of malignant salivary gland neoplasms. Together, our findings have uncovered a tumorigenic role for RANKL/RANK in the salivary gland and suggest that targeting this pathway may represent a novel therapeutic intervention approach in the prevention and/or treatment of this understudied head and neck cancer.http://europepmc.org/articles/PMC4464738?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Maria M Szwarc
Ramakrishna Kommagani
Allison P Jacob
William C Dougall
Michael M Ittmann
John P Lydon
spellingShingle Maria M Szwarc
Ramakrishna Kommagani
Allison P Jacob
William C Dougall
Michael M Ittmann
John P Lydon
Aberrant Activation of the RANK Signaling Receptor Induces Murine Salivary Gland Tumors.
PLoS ONE
author_facet Maria M Szwarc
Ramakrishna Kommagani
Allison P Jacob
William C Dougall
Michael M Ittmann
John P Lydon
author_sort Maria M Szwarc
title Aberrant Activation of the RANK Signaling Receptor Induces Murine Salivary Gland Tumors.
title_short Aberrant Activation of the RANK Signaling Receptor Induces Murine Salivary Gland Tumors.
title_full Aberrant Activation of the RANK Signaling Receptor Induces Murine Salivary Gland Tumors.
title_fullStr Aberrant Activation of the RANK Signaling Receptor Induces Murine Salivary Gland Tumors.
title_full_unstemmed Aberrant Activation of the RANK Signaling Receptor Induces Murine Salivary Gland Tumors.
title_sort aberrant activation of the rank signaling receptor induces murine salivary gland tumors.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Unlike cancers of related exocrine tissues such as the mammary and prostate gland, diagnosis and treatment of aggressive salivary gland malignancies have not markedly advanced in decades. Effective clinical management of malignant salivary gland cancers is undercut by our limited knowledge concerning the key molecular signals that underpin the etiopathogenesis of this rare and heterogeneous head and neck cancer. Without knowledge of the critical signals that drive salivary gland tumorigenesis, tumor vulnerabilities cannot be exploited that allow for targeted molecular therapies. This knowledge insufficiency is further exacerbated by a paucity of preclinical mouse models (as compared to other cancer fields) with which to both study salivary gland pathobiology and test novel intervention strategies. Using a mouse transgenic approach, we demonstrate that deregulation of the Receptor Activator of NFkB Ligand (RANKL)/RANK signaling axis results in rapid tumor development in all three major salivary glands. In line with its established role in other exocrine gland cancers (i.e., breast cancer), the RANKL/RANK signaling axis elicits an aggressive salivary gland tumor phenotype both at the histologic and molecular level. Despite the ability of this cytokine signaling axis to drive advanced stage disease within a short latency period, early blockade of RANKL/RANK signaling markedly attenuates the development of malignant salivary gland neoplasms. Together, our findings have uncovered a tumorigenic role for RANKL/RANK in the salivary gland and suggest that targeting this pathway may represent a novel therapeutic intervention approach in the prevention and/or treatment of this understudied head and neck cancer.
url http://europepmc.org/articles/PMC4464738?pdf=render
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