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Toward a Biology-Driven Treatment Strategy for Peripheral T-cell Lymphoma
T-cell and natural killer–cell lymphomas are a relatively rare and heterogeneous group of diseases that are difficult to treat and usually have poor outcomes. To date, therapeutic interventions are of limited efficacy and there is a pressing need to find better treatments. In recent years, advances...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428136/ https://www.ncbi.nlm.nih.gov/pubmed/28579857 http://dx.doi.org/10.1177/1179545x17705863 |
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author | Hildyard, CAT Shiekh, S Browning, JAB Collins, GP |
author_facet | Hildyard, CAT Shiekh, S Browning, JAB Collins, GP |
author_sort | Hildyard, CAT |
collection | PubMed |
description | T-cell and natural killer–cell lymphomas are a relatively rare and heterogeneous group of diseases that are difficult to treat and usually have poor outcomes. To date, therapeutic interventions are of limited efficacy and there is a pressing need to find better treatments. In recent years, advances in molecular biology have helped to elucidate the underlying genetic complexity of this group of diseases and to identify mutations and signaling pathways involved in lymphomagenesis. In this review, we highlight the unique biological characteristics of some of the different subtypes and discuss how these may be targeted to provide more individualized and effective treatment approaches. |
format | Online Article Text |
id | pubmed-5428136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-54281362017-06-02 Toward a Biology-Driven Treatment Strategy for Peripheral T-cell Lymphoma Hildyard, CAT Shiekh, S Browning, JAB Collins, GP Clin Med Insights Blood Disord Perspective T-cell and natural killer–cell lymphomas are a relatively rare and heterogeneous group of diseases that are difficult to treat and usually have poor outcomes. To date, therapeutic interventions are of limited efficacy and there is a pressing need to find better treatments. In recent years, advances in molecular biology have helped to elucidate the underlying genetic complexity of this group of diseases and to identify mutations and signaling pathways involved in lymphomagenesis. In this review, we highlight the unique biological characteristics of some of the different subtypes and discuss how these may be targeted to provide more individualized and effective treatment approaches. SAGE Publications 2017-04-24 /pmc/articles/PMC5428136/ /pubmed/28579857 http://dx.doi.org/10.1177/1179545x17705863 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (http://www.uk.sagepub.com/aboutus/openaccess.htm). |
spellingShingle | Perspective Hildyard, CAT Shiekh, S Browning, JAB Collins, GP Toward a Biology-Driven Treatment Strategy for Peripheral T-cell Lymphoma |
title | Toward a Biology-Driven Treatment Strategy for Peripheral T-cell Lymphoma |
title_full | Toward a Biology-Driven Treatment Strategy for Peripheral T-cell Lymphoma |
title_fullStr | Toward a Biology-Driven Treatment Strategy for Peripheral T-cell Lymphoma |
title_full_unstemmed | Toward a Biology-Driven Treatment Strategy for Peripheral T-cell Lymphoma |
title_short | Toward a Biology-Driven Treatment Strategy for Peripheral T-cell Lymphoma |
title_sort | toward a biology-driven treatment strategy for peripheral t-cell lymphoma |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428136/ https://www.ncbi.nlm.nih.gov/pubmed/28579857 http://dx.doi.org/10.1177/1179545x17705863 |
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