Interleukin-17 Receptor D in Physiology, Inflammation and Cancer

Interleukin-17 receptor D (IL-17RD) is an evolutionarily conserved member of the IL-17 receptor family. Originally identified as a negative regulator of fibroblast growth factor (FGF) signaling under the name of Sef (Similar expression to FGF genes), IL-17RD was subsequently reported to regulate oth...

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Main Authors: Charlotte Girondel, Sylvain Meloche
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-03-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2021.656004/full
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spelling doaj-1225e4c97aa14cd3afe87618836f16bb2021-03-23T06:42:04ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2021-03-011110.3389/fonc.2021.656004656004Interleukin-17 Receptor D in Physiology, Inflammation and CancerCharlotte Girondel0Charlotte Girondel1Sylvain Meloche2Sylvain Meloche3Sylvain Meloche4Institute for Research in Immunology and Cancer, Montreal, QC, CanadaDepartment of Pharmacology and Physiology, Faculty of Medicine, Université de Montréal, Montreal, QC, CanadaInstitute for Research in Immunology and Cancer, Montreal, QC, CanadaDepartment of Pharmacology and Physiology, Faculty of Medicine, Université de Montréal, Montreal, QC, CanadaMolecular Biology Program, Université de Montréal, Montreal, QC, CanadaInterleukin-17 receptor D (IL-17RD) is an evolutionarily conserved member of the IL-17 receptor family. Originally identified as a negative regulator of fibroblast growth factor (FGF) signaling under the name of Sef (Similar expression to FGF genes), IL-17RD was subsequently reported to regulate other receptor tyrosine kinase signaling pathways. In addition, recent studies have shown that IL-17RD also modulates IL-17 and Toll-like receptor (TLR) signaling. Combined genetic and cell biology studies have implicated IL-17RD in the control of cell proliferation and differentiation, cell survival, lineage specification, and inflammation. Accumulating evidence also suggest a role for IL-17RD in tumorigenesis. Expression of IL-17RD is down-regulated in various human cancers and recent work has shown that loss of IL-17RD promotes tumor formation in mice. However, the exact mechanisms underlying the tumor suppressor function of IL-17RD remain unclear and some studies have proposed that IL-17RD may exert pro-tumorigenic effects in certain contexts. Here, we provide an overview of the signaling functions of IL-17RD and review the evidence for its involvement in cancer.https://www.frontiersin.org/articles/10.3389/fonc.2021.656004/fullIL-17RDcancertumor suppressorMAPK signalinginflammation
collection DOAJ
language English
format Article
sources DOAJ
author Charlotte Girondel
Charlotte Girondel
Sylvain Meloche
Sylvain Meloche
Sylvain Meloche
spellingShingle Charlotte Girondel
Charlotte Girondel
Sylvain Meloche
Sylvain Meloche
Sylvain Meloche
Interleukin-17 Receptor D in Physiology, Inflammation and Cancer
Frontiers in Oncology
IL-17RD
cancer
tumor suppressor
MAPK signaling
inflammation
author_facet Charlotte Girondel
Charlotte Girondel
Sylvain Meloche
Sylvain Meloche
Sylvain Meloche
author_sort Charlotte Girondel
title Interleukin-17 Receptor D in Physiology, Inflammation and Cancer
title_short Interleukin-17 Receptor D in Physiology, Inflammation and Cancer
title_full Interleukin-17 Receptor D in Physiology, Inflammation and Cancer
title_fullStr Interleukin-17 Receptor D in Physiology, Inflammation and Cancer
title_full_unstemmed Interleukin-17 Receptor D in Physiology, Inflammation and Cancer
title_sort interleukin-17 receptor d in physiology, inflammation and cancer
publisher Frontiers Media S.A.
series Frontiers in Oncology
issn 2234-943X
publishDate 2021-03-01
description Interleukin-17 receptor D (IL-17RD) is an evolutionarily conserved member of the IL-17 receptor family. Originally identified as a negative regulator of fibroblast growth factor (FGF) signaling under the name of Sef (Similar expression to FGF genes), IL-17RD was subsequently reported to regulate other receptor tyrosine kinase signaling pathways. In addition, recent studies have shown that IL-17RD also modulates IL-17 and Toll-like receptor (TLR) signaling. Combined genetic and cell biology studies have implicated IL-17RD in the control of cell proliferation and differentiation, cell survival, lineage specification, and inflammation. Accumulating evidence also suggest a role for IL-17RD in tumorigenesis. Expression of IL-17RD is down-regulated in various human cancers and recent work has shown that loss of IL-17RD promotes tumor formation in mice. However, the exact mechanisms underlying the tumor suppressor function of IL-17RD remain unclear and some studies have proposed that IL-17RD may exert pro-tumorigenic effects in certain contexts. Here, we provide an overview of the signaling functions of IL-17RD and review the evidence for its involvement in cancer.
topic IL-17RD
cancer
tumor suppressor
MAPK signaling
inflammation
url https://www.frontiersin.org/articles/10.3389/fonc.2021.656004/full
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