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Inflammation, Cancer and Immunity—Implication of TRPV1 Channel

Process of inflammation and complex interactions between immune and cancer cells within tumor microenvironment are known to drive and shape the outcome of the neoplastic disease. Recent studies increasingly show that ion channels can be used as potential targets to modulate immune response and to tr...

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Autores principales: Bujak, Joanna Katarzyna, Kosmala, Daria, Szopa, Iwona Monika, Majchrzak, Kinga, Bednarczyk, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805766/
https://www.ncbi.nlm.nih.gov/pubmed/31681615
http://dx.doi.org/10.3389/fonc.2019.01087
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author Bujak, Joanna Katarzyna
Kosmala, Daria
Szopa, Iwona Monika
Majchrzak, Kinga
Bednarczyk, Piotr
author_facet Bujak, Joanna Katarzyna
Kosmala, Daria
Szopa, Iwona Monika
Majchrzak, Kinga
Bednarczyk, Piotr
author_sort Bujak, Joanna Katarzyna
collection PubMed
description Process of inflammation and complex interactions between immune and cancer cells within tumor microenvironment are known to drive and shape the outcome of the neoplastic disease. Recent studies increasingly show that ion channels can be used as potential targets to modulate immune response and to treat inflammatory disorders and cancer. The action of both innate and adaptive immune cells is tightly regulated by ionic signals provided by a network of distinct ion channels. TRPV1 channel, known as a capsaicin receptor, was recently documented to be expressed on the cells of the immune system but also aberrantly expressed in the several tumor types. It is activated by heat, protons, proinflammatory cytokines, and associated with pain and inflammation. TRPV1 channel is not only involved in calcium signaling fundamental for many cellular processes but also takes part in cell-environment crosstalk influencing cell behavior. Furthermore, in several studies, activation of TRPV1 by capsaicin was associated with anti-cancer effects. Therefore, TRPV1 provides a potential link between the process of inflammation, cancer and immunity, and offers new treatment possibilities. Nevertheless, in many cases, results regarding TRPV1 are contradictory and need further refinement. In this review we present the summary of the data related to the role of TRPV1 channel in the process of inflammation, cancer and immunity, limitations of the studies, and directions for future research.
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spelling pubmed-68057662019-11-01 Inflammation, Cancer and Immunity—Implication of TRPV1 Channel Bujak, Joanna Katarzyna Kosmala, Daria Szopa, Iwona Monika Majchrzak, Kinga Bednarczyk, Piotr Front Oncol Oncology Process of inflammation and complex interactions between immune and cancer cells within tumor microenvironment are known to drive and shape the outcome of the neoplastic disease. Recent studies increasingly show that ion channels can be used as potential targets to modulate immune response and to treat inflammatory disorders and cancer. The action of both innate and adaptive immune cells is tightly regulated by ionic signals provided by a network of distinct ion channels. TRPV1 channel, known as a capsaicin receptor, was recently documented to be expressed on the cells of the immune system but also aberrantly expressed in the several tumor types. It is activated by heat, protons, proinflammatory cytokines, and associated with pain and inflammation. TRPV1 channel is not only involved in calcium signaling fundamental for many cellular processes but also takes part in cell-environment crosstalk influencing cell behavior. Furthermore, in several studies, activation of TRPV1 by capsaicin was associated with anti-cancer effects. Therefore, TRPV1 provides a potential link between the process of inflammation, cancer and immunity, and offers new treatment possibilities. Nevertheless, in many cases, results regarding TRPV1 are contradictory and need further refinement. In this review we present the summary of the data related to the role of TRPV1 channel in the process of inflammation, cancer and immunity, limitations of the studies, and directions for future research. Frontiers Media S.A. 2019-10-16 /pmc/articles/PMC6805766/ /pubmed/31681615 http://dx.doi.org/10.3389/fonc.2019.01087 Text en Copyright © 2019 Bujak, Kosmala, Szopa, Majchrzak and Bednarczyk. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Bujak, Joanna Katarzyna
Kosmala, Daria
Szopa, Iwona Monika
Majchrzak, Kinga
Bednarczyk, Piotr
Inflammation, Cancer and Immunity—Implication of TRPV1 Channel
title Inflammation, Cancer and Immunity—Implication of TRPV1 Channel
title_full Inflammation, Cancer and Immunity—Implication of TRPV1 Channel
title_fullStr Inflammation, Cancer and Immunity—Implication of TRPV1 Channel
title_full_unstemmed Inflammation, Cancer and Immunity—Implication of TRPV1 Channel
title_short Inflammation, Cancer and Immunity—Implication of TRPV1 Channel
title_sort inflammation, cancer and immunity—implication of trpv1 channel
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805766/
https://www.ncbi.nlm.nih.gov/pubmed/31681615
http://dx.doi.org/10.3389/fonc.2019.01087
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