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Complement System in Cutaneous Squamous Cell Carcinoma
Epidermal keratinocyte-derived cutaneous squamous cell carcinoma (cSCC) is the most common metastatic skin cancer with high mortality rates in the advanced stage. Chronic inflammation is a recognized risk factor for cSCC progression and the complement system, as a part of innate immunity, belongs to...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678994/ https://www.ncbi.nlm.nih.gov/pubmed/31331124 http://dx.doi.org/10.3390/ijms20143550 |
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author | Riihilä, Pilvi Nissinen, Liisa Knuutila, Jaakko Rahmati Nezhad, Pegah Viiklepp, Kristina Kähäri, Veli-Matti |
author_facet | Riihilä, Pilvi Nissinen, Liisa Knuutila, Jaakko Rahmati Nezhad, Pegah Viiklepp, Kristina Kähäri, Veli-Matti |
author_sort | Riihilä, Pilvi |
collection | PubMed |
description | Epidermal keratinocyte-derived cutaneous squamous cell carcinoma (cSCC) is the most common metastatic skin cancer with high mortality rates in the advanced stage. Chronic inflammation is a recognized risk factor for cSCC progression and the complement system, as a part of innate immunity, belongs to the microenvironment of tumors. The complement system is a double-edged sword in cancer, since complement activation is involved in anti-tumor cytotoxicity and immune responses, but it also promotes cancer progression directly and indirectly. Recently, the role of several complement components and inhibitors in the regulation of progression of cSCC has been shown. In this review, we will discuss the role of complement system components and inhibitors as biomarkers and potential new targets for therapeutic intervention in cSCC. |
format | Online Article Text |
id | pubmed-6678994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66789942019-08-19 Complement System in Cutaneous Squamous Cell Carcinoma Riihilä, Pilvi Nissinen, Liisa Knuutila, Jaakko Rahmati Nezhad, Pegah Viiklepp, Kristina Kähäri, Veli-Matti Int J Mol Sci Review Epidermal keratinocyte-derived cutaneous squamous cell carcinoma (cSCC) is the most common metastatic skin cancer with high mortality rates in the advanced stage. Chronic inflammation is a recognized risk factor for cSCC progression and the complement system, as a part of innate immunity, belongs to the microenvironment of tumors. The complement system is a double-edged sword in cancer, since complement activation is involved in anti-tumor cytotoxicity and immune responses, but it also promotes cancer progression directly and indirectly. Recently, the role of several complement components and inhibitors in the regulation of progression of cSCC has been shown. In this review, we will discuss the role of complement system components and inhibitors as biomarkers and potential new targets for therapeutic intervention in cSCC. MDPI 2019-07-19 /pmc/articles/PMC6678994/ /pubmed/31331124 http://dx.doi.org/10.3390/ijms20143550 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Riihilä, Pilvi Nissinen, Liisa Knuutila, Jaakko Rahmati Nezhad, Pegah Viiklepp, Kristina Kähäri, Veli-Matti Complement System in Cutaneous Squamous Cell Carcinoma |
title | Complement System in Cutaneous Squamous Cell Carcinoma |
title_full | Complement System in Cutaneous Squamous Cell Carcinoma |
title_fullStr | Complement System in Cutaneous Squamous Cell Carcinoma |
title_full_unstemmed | Complement System in Cutaneous Squamous Cell Carcinoma |
title_short | Complement System in Cutaneous Squamous Cell Carcinoma |
title_sort | complement system in cutaneous squamous cell carcinoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6678994/ https://www.ncbi.nlm.nih.gov/pubmed/31331124 http://dx.doi.org/10.3390/ijms20143550 |
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