PGRMC1-dependent lipophagy promotes ferroptosis in paclitaxel-tolerant persister cancer cells

Condensed abstract Paclitaxel-tolerant persister cancer cells (PCC) had PGRMC1 upregulation related to increased free fatty acids, lipid droplets, and fatty acid oxidation. PGRMC1 expression substantially increased ferroptosis by xCT inhibition via lipophagy and tubulin detyrosination, whereas PGRMC...

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Main Authors: Ji Hyeon You, Jaewang Lee, Jong-Lyel Roh
Format: Article
Language:English
Published: BMC 2021-11-01
Series:Journal of Experimental & Clinical Cancer Research
Subjects:
Online Access:https://doi.org/10.1186/s13046-021-02168-2
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author Ji Hyeon You
Jaewang Lee
Jong-Lyel Roh
author_facet Ji Hyeon You
Jaewang Lee
Jong-Lyel Roh
author_sort Ji Hyeon You
collection DOAJ
description Condensed abstract Paclitaxel-tolerant persister cancer cells (PCC) had PGRMC1 upregulation related to increased free fatty acids, lipid droplets, and fatty acid oxidation. PGRMC1 expression substantially increased ferroptosis by xCT inhibition via lipophagy and tubulin detyrosination, whereas PGRMC1 silencing decreased ferroptosis: this suggests that PGRMC1 expression promotes ferroptosis in PCC.
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spelling doaj.art-41933309701f4eca826b9aecb9d2a8b12022-12-22T04:03:53ZengBMCJournal of Experimental & Clinical Cancer Research1756-99662021-11-0140111810.1186/s13046-021-02168-2PGRMC1-dependent lipophagy promotes ferroptosis in paclitaxel-tolerant persister cancer cellsJi Hyeon You0Jaewang Lee1Jong-Lyel Roh2Department of Otorhinolaryngology-Head and Neck Surgery, CHA Bundang Medical Center, CHA University School of MedicineDepartment of Otorhinolaryngology-Head and Neck Surgery, CHA Bundang Medical Center, CHA University School of MedicineDepartment of Otorhinolaryngology-Head and Neck Surgery, CHA Bundang Medical Center, CHA University School of MedicineCondensed abstract Paclitaxel-tolerant persister cancer cells (PCC) had PGRMC1 upregulation related to increased free fatty acids, lipid droplets, and fatty acid oxidation. PGRMC1 expression substantially increased ferroptosis by xCT inhibition via lipophagy and tubulin detyrosination, whereas PGRMC1 silencing decreased ferroptosis: this suggests that PGRMC1 expression promotes ferroptosis in PCC.https://doi.org/10.1186/s13046-021-02168-2Progesterone receptor membrane component 1FerroptosisFatty acid oxidationLipophagyTubulin detyrosination
spellingShingle Ji Hyeon You
Jaewang Lee
Jong-Lyel Roh
PGRMC1-dependent lipophagy promotes ferroptosis in paclitaxel-tolerant persister cancer cells
Journal of Experimental & Clinical Cancer Research
Progesterone receptor membrane component 1
Ferroptosis
Fatty acid oxidation
Lipophagy
Tubulin detyrosination
title PGRMC1-dependent lipophagy promotes ferroptosis in paclitaxel-tolerant persister cancer cells
title_full PGRMC1-dependent lipophagy promotes ferroptosis in paclitaxel-tolerant persister cancer cells
title_fullStr PGRMC1-dependent lipophagy promotes ferroptosis in paclitaxel-tolerant persister cancer cells
title_full_unstemmed PGRMC1-dependent lipophagy promotes ferroptosis in paclitaxel-tolerant persister cancer cells
title_short PGRMC1-dependent lipophagy promotes ferroptosis in paclitaxel-tolerant persister cancer cells
title_sort pgrmc1 dependent lipophagy promotes ferroptosis in paclitaxel tolerant persister cancer cells
topic Progesterone receptor membrane component 1
Ferroptosis
Fatty acid oxidation
Lipophagy
Tubulin detyrosination
url https://doi.org/10.1186/s13046-021-02168-2
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AT jonglyelroh pgrmc1dependentlipophagypromotesferroptosisinpaclitaxeltolerantpersistercancercells