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Jean-Christophe Stehle

Researcher at University of Lausanne

Publications -  30
Citations -  3379

Jean-Christophe Stehle is an academic researcher from University of Lausanne. The author has contributed to research in topics: Cancer & Stem cell. The author has an hindex of 24, co-authored 30 publications receiving 3109 citations. Previous affiliations of Jean-Christophe Stehle include University Hospital of Lausanne.

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EZH2 Is Essential for Glioblastoma Cancer Stem Cell Maintenance

TL;DR: It is shown that targeted pharmacologic disruption of EZH2 by the S-adenosylhomocysteine hydrolase inhibitor 3-deazaneplanocin A (DZNep), or its specific downregulation by short hairpin RNA (shRNA), strongly impairs GBM cancer stem cell (CSC) self-renewal in vitro and tumor-initiating capacity in vivo.
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Malarial hemozoin is a Nalp3 inflammasome activating danger signal.

TL;DR: It is found that hemozoin acts as a proinflammatory danger signal that activates the Nalp3 inflammasome, causing the release of IL-1β in mice infected with Plasmodium berghei sporozoites.
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EWS-FLI-1 Expression Triggers a Ewing's Sarcoma Initiation Program in Primary Human Mesenchymal Stem Cells

TL;DR: This article showed that expression of EWS-FLI-1 fusion protein in human mesenchymal stem cells (hMSC) is not only stably maintained without inhibiting proliferation but also induces a gene expression profile bearing striking similarity to that of Ewing's sarcoma, including genes that are among the highest ESFT discriminators.
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Identification of Cancer Stem Cells in Ewing's Sarcoma

TL;DR: These observations provide the first identification of ESFT cancer stem cells and demonstration of their MSC properties, a critical step towards a better biological understanding and rational therapeutic targeting of these tumors.
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EWS-FLI-1 modulates miRNA145 and SOX2 expression to initiate mesenchymal stem cell reprogramming toward Ewing sarcoma cancer stem cells

TL;DR: Insight is provided for the first time into the mechanisms whereby a single oncogene can reprogram primary cells to display a CSC phenotype and the common target gene, SOX2, in addition to miRNA145 itself, is identified as key players in ESFT cell differentiation and tumorigenicity.