New insights into the functions of Cox-2 in skin and esophageal malignancies

Cancer: Inflammatory enzyme linked to skin and esophageal tumors Drugs that block a pro-inflammatory enzyme implicated in cancer initiation and progression could help suppress the development of skin and esophageal cancers that arise from abnormal squamous cells (skin cells and cells lining the resp...

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Main Authors: Hyeongsun Moon, Andrew C. White, Alexander D. Borowsky
Format: Article
Language:English
Published: Nature Publishing Group 2020-04-01
Series:Experimental and Molecular Medicine
Online Access:https://doi.org/10.1038/s12276-020-0412-2
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spelling doaj-1e006bd90b4f418c8b2ad19d12b2d8992021-04-04T11:41:41ZengNature Publishing GroupExperimental and Molecular Medicine1226-36132092-64132020-04-0152453854710.1038/s12276-020-0412-2New insights into the functions of Cox-2 in skin and esophageal malignanciesHyeongsun Moon0Andrew C. White1Alexander D. Borowsky2Center for Immunology and Infectious Diseases, University of CaliforniaDepartment of Biological Sciences, Cornell UniversityCenter for Immunology and Infectious Diseases, University of CaliforniaCancer: Inflammatory enzyme linked to skin and esophageal tumors Drugs that block a pro-inflammatory enzyme implicated in cancer initiation and progression could help suppress the development of skin and esophageal cancers that arise from abnormal squamous cells (skin cells and cells lining the respiratory and digestive tracts). In a review article, Hyeongsun Moon from the University of California, Davis, USA, and colleagues discuss experimental evidence from genetically engineered mouse models demonstrating that expression of an enzyme called cyclooxygenase-2 (Cox-2) is critical to the transformation of stem and progenitor cells in the skin and esophagus into cancer cells. Cox-2 is already the target of many drugs approved for treating inflammatory conditions such as arthritis. The preclinical data suggest that the same medications, or agents directed at mediators of Cox-2 signaling, may help tamp down the inflammation that can spur tumor-prone cells into turning malignant.https://doi.org/10.1038/s12276-020-0412-2
collection DOAJ
language English
format Article
sources DOAJ
author Hyeongsun Moon
Andrew C. White
Alexander D. Borowsky
spellingShingle Hyeongsun Moon
Andrew C. White
Alexander D. Borowsky
New insights into the functions of Cox-2 in skin and esophageal malignancies
Experimental and Molecular Medicine
author_facet Hyeongsun Moon
Andrew C. White
Alexander D. Borowsky
author_sort Hyeongsun Moon
title New insights into the functions of Cox-2 in skin and esophageal malignancies
title_short New insights into the functions of Cox-2 in skin and esophageal malignancies
title_full New insights into the functions of Cox-2 in skin and esophageal malignancies
title_fullStr New insights into the functions of Cox-2 in skin and esophageal malignancies
title_full_unstemmed New insights into the functions of Cox-2 in skin and esophageal malignancies
title_sort new insights into the functions of cox-2 in skin and esophageal malignancies
publisher Nature Publishing Group
series Experimental and Molecular Medicine
issn 1226-3613
2092-6413
publishDate 2020-04-01
description Cancer: Inflammatory enzyme linked to skin and esophageal tumors Drugs that block a pro-inflammatory enzyme implicated in cancer initiation and progression could help suppress the development of skin and esophageal cancers that arise from abnormal squamous cells (skin cells and cells lining the respiratory and digestive tracts). In a review article, Hyeongsun Moon from the University of California, Davis, USA, and colleagues discuss experimental evidence from genetically engineered mouse models demonstrating that expression of an enzyme called cyclooxygenase-2 (Cox-2) is critical to the transformation of stem and progenitor cells in the skin and esophagus into cancer cells. Cox-2 is already the target of many drugs approved for treating inflammatory conditions such as arthritis. The preclinical data suggest that the same medications, or agents directed at mediators of Cox-2 signaling, may help tamp down the inflammation that can spur tumor-prone cells into turning malignant.
url https://doi.org/10.1038/s12276-020-0412-2
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