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Malignant inflammation in cutaneous T‐cell lymphoma—a hostile takeover

Cutaneous T-cell lymphomas (CTCL) are characterized by the presence of chronically inflamed skin lesions containing malignant T cells. Early disease presents as limited skin patches or plaques and exhibits an indolent behavior. For many patients, the disease never progresses beyond this stage, but i...

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Autores principales: Krejsgaard, Thorbjørn, Lindahl, Lise M., Mongan, Nigel P., Wasik, Mariusz A., Litvinov, Ivan V., Iversen, Lars, Langhoff, Erik, Woetmann, Anders, Odum, Niels
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368200/
https://www.ncbi.nlm.nih.gov/pubmed/27717961
http://dx.doi.org/10.1007/s00281-016-0594-9
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author Krejsgaard, Thorbjørn
Lindahl, Lise M.
Mongan, Nigel P.
Wasik, Mariusz A.
Litvinov, Ivan V.
Iversen, Lars
Langhoff, Erik
Woetmann, Anders
Odum, Niels
author_facet Krejsgaard, Thorbjørn
Lindahl, Lise M.
Mongan, Nigel P.
Wasik, Mariusz A.
Litvinov, Ivan V.
Iversen, Lars
Langhoff, Erik
Woetmann, Anders
Odum, Niels
author_sort Krejsgaard, Thorbjørn
collection PubMed
description Cutaneous T-cell lymphomas (CTCL) are characterized by the presence of chronically inflamed skin lesions containing malignant T cells. Early disease presents as limited skin patches or plaques and exhibits an indolent behavior. For many patients, the disease never progresses beyond this stage, but in approximately one third of patients, the disease becomes progressive, and the skin lesions start to expand and evolve. Eventually, overt tumors develop and the malignant T cells may disseminate to the blood, lymph nodes, bone marrow, and visceral organs, often with a fatal outcome. The transition from early indolent to progressive and advanced disease is accompanied by a significant shift in the nature of the tumor-associated inflammation. This shift does not appear to be an epiphenomenon but rather a critical step in disease progression. Emerging evidence supports that the malignant T cells take control of the inflammatory environment, suppressing cellular immunity and anti-tumor responses while promoting a chronic inflammatory milieu that fuels their own expansion. Here, we review the inflammatory changes associated with disease progression in CTCL and point to their wider relevance in other cancer contexts. We further define the term “malignant inflammation” as a pro-tumorigenic inflammatory environment orchestrated by the tumor cells and discuss some of the mechanisms driving the development of malignant inflammation in CTCL.
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spelling pubmed-53682002017-04-11 Malignant inflammation in cutaneous T‐cell lymphoma—a hostile takeover Krejsgaard, Thorbjørn Lindahl, Lise M. Mongan, Nigel P. Wasik, Mariusz A. Litvinov, Ivan V. Iversen, Lars Langhoff, Erik Woetmann, Anders Odum, Niels Semin Immunopathol Review Cutaneous T-cell lymphomas (CTCL) are characterized by the presence of chronically inflamed skin lesions containing malignant T cells. Early disease presents as limited skin patches or plaques and exhibits an indolent behavior. For many patients, the disease never progresses beyond this stage, but in approximately one third of patients, the disease becomes progressive, and the skin lesions start to expand and evolve. Eventually, overt tumors develop and the malignant T cells may disseminate to the blood, lymph nodes, bone marrow, and visceral organs, often with a fatal outcome. The transition from early indolent to progressive and advanced disease is accompanied by a significant shift in the nature of the tumor-associated inflammation. This shift does not appear to be an epiphenomenon but rather a critical step in disease progression. Emerging evidence supports that the malignant T cells take control of the inflammatory environment, suppressing cellular immunity and anti-tumor responses while promoting a chronic inflammatory milieu that fuels their own expansion. Here, we review the inflammatory changes associated with disease progression in CTCL and point to their wider relevance in other cancer contexts. We further define the term “malignant inflammation” as a pro-tumorigenic inflammatory environment orchestrated by the tumor cells and discuss some of the mechanisms driving the development of malignant inflammation in CTCL. Springer Berlin Heidelberg 2016-10-07 2017 /pmc/articles/PMC5368200/ /pubmed/27717961 http://dx.doi.org/10.1007/s00281-016-0594-9 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Krejsgaard, Thorbjørn
Lindahl, Lise M.
Mongan, Nigel P.
Wasik, Mariusz A.
Litvinov, Ivan V.
Iversen, Lars
Langhoff, Erik
Woetmann, Anders
Odum, Niels
Malignant inflammation in cutaneous T‐cell lymphoma—a hostile takeover
title Malignant inflammation in cutaneous T‐cell lymphoma—a hostile takeover
title_full Malignant inflammation in cutaneous T‐cell lymphoma—a hostile takeover
title_fullStr Malignant inflammation in cutaneous T‐cell lymphoma—a hostile takeover
title_full_unstemmed Malignant inflammation in cutaneous T‐cell lymphoma—a hostile takeover
title_short Malignant inflammation in cutaneous T‐cell lymphoma—a hostile takeover
title_sort malignant inflammation in cutaneous t‐cell lymphoma—a hostile takeover
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368200/
https://www.ncbi.nlm.nih.gov/pubmed/27717961
http://dx.doi.org/10.1007/s00281-016-0594-9
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