COKU, Jorida, David M BOOTH, Jan ŠKODA, Madison C PEDROTTY, Jennifer VOGEL, Kangning LIU, Annette VU, Erica L CARPENTER, Jamie C YE, Michelle A CHEN, Peter DUNBAR, Elizabeth SCADDEN, Taekyung D YUN, Eiko NAKAMARU-OGISO, Estela AREA-GOMEZ, Yimei LI, Kelly C GOLDSMITH, C Patrick REYNOLDS, Gyorgy HAJNOCZKY a Michael D HOGARTY. Reduced ER–mitochondria connectivity promotes neuroblastoma multidrug resistance. EMBO Journal. Hoboken: Wiley, 2022, roč. 41, č. 8, s. 1-20. ISSN 0261-4189. Dostupné z: https://dx.doi.org/10.15252/embj.2021108272.
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Základní údaje
Originální název Reduced ER–mitochondria connectivity promotes neuroblastoma multidrug resistance
Autoři COKU, Jorida, David M BOOTH, Jan ŠKODA (203 Česká republika, domácí), Madison C PEDROTTY, Jennifer VOGEL, Kangning LIU, Annette VU, Erica L CARPENTER, Jamie C YE, Michelle A CHEN, Peter DUNBAR, Elizabeth SCADDEN, Taekyung D YUN, Eiko NAKAMARU-OGISO, Estela AREA-GOMEZ, Yimei LI, Kelly C GOLDSMITH, C Patrick REYNOLDS, Gyorgy HAJNOCZKY a Michael D HOGARTY (garant).
Vydání EMBO Journal, Hoboken, Wiley, 2022, 0261-4189.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30204 Oncology
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 11.400
Kód RIV RIV/00216224:14310/22:00125550
Organizační jednotka Přírodovědecká fakulta
Doi http://dx.doi.org/10.15252/embj.2021108272
UT WoS 000760798100001
Klíčová slova anglicky ceramides; inter-organelle contacts; mitochondria-associated membranes; multidrug resistance; sphingolipids
Štítky rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Marie Šípková, DiS., učo 437722. Změněno: 3. 6. 2022 13:45.
Anotace
Most cancer deaths result from progression of therapy resistant disease, yet our understanding of this phenotype is limited. Cancer therapies generate stress signals that act upon mitochondria to initiate apoptosis. Mitochondria isolated from neuroblastoma cells were exposed to tBid or Bim, death effectors activated by therapeutic stress. Multidrug-resistant tumor cells obtained from children at relapse had markedly attenuated Bak and Bax oligomerization and cytochrome c release (surrogates for apoptotic commitment) in comparison with patient-matched tumor cells obtained at diagnosis. Electron microscopy identified reduced ER-mitochondria-associated membranes (MAMs; ER-mitochondria contacts, ERMCs) in therapy-resistant cells, and genetically or biochemically reducing MAMs in therapy-sensitive tumors phenocopied resistance. MAMs serve as platforms to transfer Ca2+ and bioactive lipids to mitochondria. Reduced Ca2+ transfer was found in some but not all resistant cells, and inhibiting transfer did not attenuate apoptotic signaling. In contrast, reduced ceramide synthesis and transfer was common to resistant cells and its inhibition induced stress resistance. We identify ER-mitochondria-associated membranes as physiologic regulators of apoptosis via ceramide transfer and uncover a previously unrecognized mechanism for cancer multidrug resistance.
Návaznosti
GJ20-00987Y, projekt VaVNázev: Mitochondriální dynamika a autofagie: Chybějící článek mezi dediferenciací a vznikem rezistence u solidních nádorů dětského věku
Investor: Grantová agentura ČR, Mitochondrial dynamics and autophagy: A missing link between dedifferentiation and development of resistance in pediatric solid tumors
VytisknoutZobrazeno: 1. 9. 2024 01:46