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Clinical and molecular insights into adenoid cystic carcinoma: Neural crest‐like stemness as a target

OBJECTIVES: This review surveys trialed therapies and molecular defects in adenoid cystic carcinoma (ACC), with an emphasis on neural crest‐like stemness characteristics of newly discovered cancer stem cells (CSCs) and therapies that may target these CSCs. DATA SOURCES: Articles available on Pubmed...

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Autores principales: Yarbrough, Wendell G., Panaccione, Alexander, Chang, Michael T., Ivanov, Sergey V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5510248/
https://www.ncbi.nlm.nih.gov/pubmed/28894804
http://dx.doi.org/10.1002/lio2.22
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author Yarbrough, Wendell G.
Panaccione, Alexander
Chang, Michael T.
Ivanov, Sergey V.
author_facet Yarbrough, Wendell G.
Panaccione, Alexander
Chang, Michael T.
Ivanov, Sergey V.
author_sort Yarbrough, Wendell G.
collection PubMed
description OBJECTIVES: This review surveys trialed therapies and molecular defects in adenoid cystic carcinoma (ACC), with an emphasis on neural crest‐like stemness characteristics of newly discovered cancer stem cells (CSCs) and therapies that may target these CSCs. DATA SOURCES: Articles available on Pubmed or OVID MEDLINE databases and unpublished data. REVIEW METHODS: Systematic review of articles pertaining to ACC and neural crest‐like stem cells. RESULTS: Adenoid cystic carcinoma of the salivary gland is a slowly growing but relentless cancer that is prone to nerve invasion and metastases. A lack of understanding of molecular etiology and absence of targetable drivers has limited therapy for patients with ACC to surgery and radiation. Currently, no curative treatments are available for patients with metastatic disease, which highlights the need for effective new therapies. Research in this area has been inhibited by the lack of validated cell lines and a paucity of clinically useful markers. The ACC research environment has recently improved, thanks to the introduction of novel tools, technologies, approaches, and models. Improved understanding of ACC suggests that neural crest‐like stemness is a major target in this rare tumor. New cell culture techniques and patient‐derived xenografts provide tools for preclinical testing. CONCLUSION: Preclinical research has not identified effective targets in ACC, as confirmed by the large number of failed clinical trials. New molecular data suggest that drivers of neural crest‐like stemness may be required for maintenance of ACC; as such, CSCs are a target for therapy of ACC.
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spelling pubmed-55102482017-09-11 Clinical and molecular insights into adenoid cystic carcinoma: Neural crest‐like stemness as a target Yarbrough, Wendell G. Panaccione, Alexander Chang, Michael T. Ivanov, Sergey V. Laryngoscope Investig Otolaryngol Head and Neck, and Tumor Biology OBJECTIVES: This review surveys trialed therapies and molecular defects in adenoid cystic carcinoma (ACC), with an emphasis on neural crest‐like stemness characteristics of newly discovered cancer stem cells (CSCs) and therapies that may target these CSCs. DATA SOURCES: Articles available on Pubmed or OVID MEDLINE databases and unpublished data. REVIEW METHODS: Systematic review of articles pertaining to ACC and neural crest‐like stem cells. RESULTS: Adenoid cystic carcinoma of the salivary gland is a slowly growing but relentless cancer that is prone to nerve invasion and metastases. A lack of understanding of molecular etiology and absence of targetable drivers has limited therapy for patients with ACC to surgery and radiation. Currently, no curative treatments are available for patients with metastatic disease, which highlights the need for effective new therapies. Research in this area has been inhibited by the lack of validated cell lines and a paucity of clinically useful markers. The ACC research environment has recently improved, thanks to the introduction of novel tools, technologies, approaches, and models. Improved understanding of ACC suggests that neural crest‐like stemness is a major target in this rare tumor. New cell culture techniques and patient‐derived xenografts provide tools for preclinical testing. CONCLUSION: Preclinical research has not identified effective targets in ACC, as confirmed by the large number of failed clinical trials. New molecular data suggest that drivers of neural crest‐like stemness may be required for maintenance of ACC; as such, CSCs are a target for therapy of ACC. John Wiley and Sons Inc. 2016-08-04 /pmc/articles/PMC5510248/ /pubmed/28894804 http://dx.doi.org/10.1002/lio2.22 Text en © 2016 The Authors Laryngoscope Investigative Otolaryngology published by Wiley Periodicals, Inc. on behalf of The Triological Society This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Head and Neck, and Tumor Biology
Yarbrough, Wendell G.
Panaccione, Alexander
Chang, Michael T.
Ivanov, Sergey V.
Clinical and molecular insights into adenoid cystic carcinoma: Neural crest‐like stemness as a target
title Clinical and molecular insights into adenoid cystic carcinoma: Neural crest‐like stemness as a target
title_full Clinical and molecular insights into adenoid cystic carcinoma: Neural crest‐like stemness as a target
title_fullStr Clinical and molecular insights into adenoid cystic carcinoma: Neural crest‐like stemness as a target
title_full_unstemmed Clinical and molecular insights into adenoid cystic carcinoma: Neural crest‐like stemness as a target
title_short Clinical and molecular insights into adenoid cystic carcinoma: Neural crest‐like stemness as a target
title_sort clinical and molecular insights into adenoid cystic carcinoma: neural crest‐like stemness as a target
topic Head and Neck, and Tumor Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5510248/
https://www.ncbi.nlm.nih.gov/pubmed/28894804
http://dx.doi.org/10.1002/lio2.22
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