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KLRC3, a Natural Killer receptor gene, is a key factor involved in glioblastoma tumourigenesis and aggressiveness
Glioblastoma is the most lethal brain tumour with a poor prognosis. Cancer stem cells (CSC) were proposed to be the most aggressive cells allowing brain tumour recurrence and aggressiveness. Current challenge is to determine CSC signature to characterize these cells and to develop new therapeutics....
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5264145/ https://www.ncbi.nlm.nih.gov/pubmed/27641066 http://dx.doi.org/10.1111/jcmm.12960 |
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author | Cheray, Mathilde Bessette, Barbara Lacroix, Aurélie Mélin, Carole Jawhari, Soha Pinet, Sandra Deluche, Elise Clavère, Pierre Durand, Karine Sanchez‐Prieto, Ricardo Jauberteau, Marie‐Odile Battu, Serge Lalloué, Fabrice |
author_facet | Cheray, Mathilde Bessette, Barbara Lacroix, Aurélie Mélin, Carole Jawhari, Soha Pinet, Sandra Deluche, Elise Clavère, Pierre Durand, Karine Sanchez‐Prieto, Ricardo Jauberteau, Marie‐Odile Battu, Serge Lalloué, Fabrice |
author_sort | Cheray, Mathilde |
collection | PubMed |
description | Glioblastoma is the most lethal brain tumour with a poor prognosis. Cancer stem cells (CSC) were proposed to be the most aggressive cells allowing brain tumour recurrence and aggressiveness. Current challenge is to determine CSC signature to characterize these cells and to develop new therapeutics. In a previous work, we achieved a screening of glycosylation‐related genes to characterize specific genes involved in CSC maintenance. Three genes named CHI3L1,KLRC3 and PRUNE2 were found overexpressed in glioblastoma undifferentiated cells (related to CSC) compared to the differentiated ones. The comparison of their roles suggest that KLRC3 gene coding for NKG2E, a protein initially identified in NK cells, is more important than both two other genes in glioblastomas aggressiveness. Indeed, KLRC3 silencing decreased self‐renewal capacity, invasion, proliferation, radioresistance and tumourigenicity of U87‐MG glioblastoma cell line. For the first time we report that KLRC3 gene expression is linked to glioblastoma aggressiveness and could be a new potential therapeutic target to attenuate glioblastoma. |
format | Online Article Text |
id | pubmed-5264145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52641452017-02-01 KLRC3, a Natural Killer receptor gene, is a key factor involved in glioblastoma tumourigenesis and aggressiveness Cheray, Mathilde Bessette, Barbara Lacroix, Aurélie Mélin, Carole Jawhari, Soha Pinet, Sandra Deluche, Elise Clavère, Pierre Durand, Karine Sanchez‐Prieto, Ricardo Jauberteau, Marie‐Odile Battu, Serge Lalloué, Fabrice J Cell Mol Med Original Articles Glioblastoma is the most lethal brain tumour with a poor prognosis. Cancer stem cells (CSC) were proposed to be the most aggressive cells allowing brain tumour recurrence and aggressiveness. Current challenge is to determine CSC signature to characterize these cells and to develop new therapeutics. In a previous work, we achieved a screening of glycosylation‐related genes to characterize specific genes involved in CSC maintenance. Three genes named CHI3L1,KLRC3 and PRUNE2 were found overexpressed in glioblastoma undifferentiated cells (related to CSC) compared to the differentiated ones. The comparison of their roles suggest that KLRC3 gene coding for NKG2E, a protein initially identified in NK cells, is more important than both two other genes in glioblastomas aggressiveness. Indeed, KLRC3 silencing decreased self‐renewal capacity, invasion, proliferation, radioresistance and tumourigenicity of U87‐MG glioblastoma cell line. For the first time we report that KLRC3 gene expression is linked to glioblastoma aggressiveness and could be a new potential therapeutic target to attenuate glioblastoma. John Wiley and Sons Inc. 2016-09-19 2017-02 /pmc/articles/PMC5264145/ /pubmed/27641066 http://dx.doi.org/10.1111/jcmm.12960 Text en © 2016 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Cheray, Mathilde Bessette, Barbara Lacroix, Aurélie Mélin, Carole Jawhari, Soha Pinet, Sandra Deluche, Elise Clavère, Pierre Durand, Karine Sanchez‐Prieto, Ricardo Jauberteau, Marie‐Odile Battu, Serge Lalloué, Fabrice KLRC3, a Natural Killer receptor gene, is a key factor involved in glioblastoma tumourigenesis and aggressiveness |
title |
KLRC3, a Natural Killer receptor gene, is a key factor involved in glioblastoma tumourigenesis and aggressiveness |
title_full |
KLRC3, a Natural Killer receptor gene, is a key factor involved in glioblastoma tumourigenesis and aggressiveness |
title_fullStr |
KLRC3, a Natural Killer receptor gene, is a key factor involved in glioblastoma tumourigenesis and aggressiveness |
title_full_unstemmed |
KLRC3, a Natural Killer receptor gene, is a key factor involved in glioblastoma tumourigenesis and aggressiveness |
title_short |
KLRC3, a Natural Killer receptor gene, is a key factor involved in glioblastoma tumourigenesis and aggressiveness |
title_sort | klrc3, a natural killer receptor gene, is a key factor involved in glioblastoma tumourigenesis and aggressiveness |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5264145/ https://www.ncbi.nlm.nih.gov/pubmed/27641066 http://dx.doi.org/10.1111/jcmm.12960 |
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