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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2020-04-01
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Series: | Experimental and Molecular Medicine |
Online Access: | https://doi.org/10.1038/s12276-020-0412-2 |
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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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AT hyeongsunmoon newinsightsintothefunctionsofcox2inskinandesophagealmalignancies AT andrewcwhite newinsightsintothefunctionsofcox2inskinandesophagealmalignancies AT alexanderdborowsky newinsightsintothefunctionsofcox2inskinandesophagealmalignancies |
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