Lysophosphatidylcholine acyltransferase 2-mediated lipid droplet production supports colorectal cancer chemoresistance
Lipid droplets (LD) accumulation correlates with colorectal cancer (CRC) relapse. Here the authors show that chemotherapy induces LD synthesis via acyltransferase LPCAT2 which, in turn, promotes chemoresistance via LD accumulation both in vitro and in vivo by blocking chemotherapy-induced ER stress.
Autor*in: |
Alexia Karen Cotte [verfasserIn] Virginie Aires [verfasserIn] Maxime Fredon [verfasserIn] Emeric Limagne [verfasserIn] Valentin Derangère [verfasserIn] Marion Thibaudin [verfasserIn] Etienne Humblin [verfasserIn] Alessandra Scagliarini [verfasserIn] Jean-Paul Pais de Barros [verfasserIn] Patrick Hillon [verfasserIn] François Ghiringhelli [verfasserIn] Dominique Delmas [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2018 |
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Übergeordnetes Werk: |
In: Nature Communications - Nature Portfolio, 2016, 9(2018), 1, Seite 16 |
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Übergeordnetes Werk: |
volume:9 ; year:2018 ; number:1 ; pages:16 |
Links: |
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DOI / URN: |
10.1038/s41467-017-02732-5 |
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Katalog-ID: |
DOAJ067524982 |
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Lysophosphatidylcholine acyltransferase 2-mediated lipid droplet production supports colorectal cancer chemoresistance |
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Lipid droplets (LD) accumulation correlates with colorectal cancer (CRC) relapse. Here the authors show that chemotherapy induces LD synthesis via acyltransferase LPCAT2 which, in turn, promotes chemoresistance via LD accumulation both in vitro and in vivo by blocking chemotherapy-induced ER stress. |
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Lipid droplets (LD) accumulation correlates with colorectal cancer (CRC) relapse. Here the authors show that chemotherapy induces LD synthesis via acyltransferase LPCAT2 which, in turn, promotes chemoresistance via LD accumulation both in vitro and in vivo by blocking chemotherapy-induced ER stress. |
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Lipid droplets (LD) accumulation correlates with colorectal cancer (CRC) relapse. Here the authors show that chemotherapy induces LD synthesis via acyltransferase LPCAT2 which, in turn, promotes chemoresistance via LD accumulation both in vitro and in vivo by blocking chemotherapy-induced ER stress. |
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