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Type I Interferons: Key Players in Normal Skin and Select Cutaneous Malignancies

Interferons (IFNs) are a family of naturally existing glycoproteins known for their antiviral activity and their ability to influence the behavior of normal and transformed cell types. Type I Interferons include IFN-α and IFN-β. Currently, IFN-α has numerous approved antitumor applications, includin...

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Detalles Bibliográficos
Autores principales: Ismail, Aimen, Yusuf, Nabiha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913103/
https://www.ncbi.nlm.nih.gov/pubmed/24516470
http://dx.doi.org/10.1155/2014/847545
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author Ismail, Aimen
Yusuf, Nabiha
author_facet Ismail, Aimen
Yusuf, Nabiha
author_sort Ismail, Aimen
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description Interferons (IFNs) are a family of naturally existing glycoproteins known for their antiviral activity and their ability to influence the behavior of normal and transformed cell types. Type I Interferons include IFN-α and IFN-β. Currently, IFN-α has numerous approved antitumor applications, including malignant melanoma, in which IFN-α has been shown to increase relapse free survival. Moreover, IFN-α has been successfully used in the intralesional treatment of cutaneous squamous cell carcinoma (SCC) and basal cell carcinoma (BCC). In spite of these promising clinical results; however, there exists a paucity of knowledge on the precise anti-tumor action of IFN-α/β at the cellular and molecular levels in cutaneous malignancies such as SCC, BCC, and melanoma. This review summarizes current knowledge on the extent to which Type I IFN influences proliferation, apoptosis, angiogenesis, and immune function in normal skin, cutaneous SCC, BCC, and melanoma.
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spelling pubmed-39131032014-02-10 Type I Interferons: Key Players in Normal Skin and Select Cutaneous Malignancies Ismail, Aimen Yusuf, Nabiha Dermatol Res Pract Review Article Interferons (IFNs) are a family of naturally existing glycoproteins known for their antiviral activity and their ability to influence the behavior of normal and transformed cell types. Type I Interferons include IFN-α and IFN-β. Currently, IFN-α has numerous approved antitumor applications, including malignant melanoma, in which IFN-α has been shown to increase relapse free survival. Moreover, IFN-α has been successfully used in the intralesional treatment of cutaneous squamous cell carcinoma (SCC) and basal cell carcinoma (BCC). In spite of these promising clinical results; however, there exists a paucity of knowledge on the precise anti-tumor action of IFN-α/β at the cellular and molecular levels in cutaneous malignancies such as SCC, BCC, and melanoma. This review summarizes current knowledge on the extent to which Type I IFN influences proliferation, apoptosis, angiogenesis, and immune function in normal skin, cutaneous SCC, BCC, and melanoma. Hindawi Publishing Corporation 2014 2014-01-05 /pmc/articles/PMC3913103/ /pubmed/24516470 http://dx.doi.org/10.1155/2014/847545 Text en Copyright © 2014 A. Ismail and N. Yusuf. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Ismail, Aimen
Yusuf, Nabiha
Type I Interferons: Key Players in Normal Skin and Select Cutaneous Malignancies
title Type I Interferons: Key Players in Normal Skin and Select Cutaneous Malignancies
title_full Type I Interferons: Key Players in Normal Skin and Select Cutaneous Malignancies
title_fullStr Type I Interferons: Key Players in Normal Skin and Select Cutaneous Malignancies
title_full_unstemmed Type I Interferons: Key Players in Normal Skin and Select Cutaneous Malignancies
title_short Type I Interferons: Key Players in Normal Skin and Select Cutaneous Malignancies
title_sort type i interferons: key players in normal skin and select cutaneous malignancies
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913103/
https://www.ncbi.nlm.nih.gov/pubmed/24516470
http://dx.doi.org/10.1155/2014/847545
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