001     275343
005     20240229154939.0
024 7 _ |a 10.1038/s42255-023-00781-3
|2 doi
024 7 _ |a pmid:37024754
|2 pmid
024 7 _ |a altmetric:145110678
|2 altmetric
037 _ _ |a DKFZ-2023-00712
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Talwar, Deepti
|0 P:(DE-He78)290f7b71b45035214574625eccde4d08
|b 0
|e First author
|u dkfz
245 _ _ |a The GAPDH redox switch safeguards reductive capacity and enables survival of stressed tumour cells.
260 _ _ |a [London]
|c 2023
|b Springer Nature
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1692022207_20937
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
500 _ _ |a DKFZ-ZMBH Alliance / 2023 Apr;5(4):660-676 / #EA:A160#LA:A160#
520 _ _ |a Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) is known to contain an active-site cysteine residue undergoing oxidation in response to hydrogen peroxide, leading to rapid inactivation of the enzyme. Here we show that human and mouse cells expressing a GAPDH mutant lacking this redox switch retain catalytic activity but are unable to stimulate the oxidative pentose phosphate pathway and enhance their reductive capacity. Specifically, we find that anchorage-independent growth of cells and spheroids is limited by an elevation of endogenous peroxide levels and is largely dependent on a functional GAPDH redox switch. Likewise, tumour growth in vivo is limited by peroxide stress and suppressed when the GAPDH redox switch is disabled in tumour cells. The induction of additional intratumoural oxidative stress by chemo- or radiotherapy synergized with the deactivation of the GAPDH redox switch. Mice lacking the GAPDH redox switch exhibit altered fatty acid metabolism in kidney and heart, apparently in compensation for the lack of the redox switch. Together, our findings demonstrate the physiological and pathophysiological relevance of oxidative GAPDH inactivation in mammals.
536 _ _ |a 311 - Zellbiologie und Tumorbiologie (POF4-311)
|0 G:(DE-HGF)POF4-311
|c POF4-311
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: inrepo02.dkfz.de
700 1 _ |a Miller, Colin Gregory
|0 P:(DE-He78)eb748bd61964bae06c38c8893b52bcfd
|b 1
|e First author
|u dkfz
700 1 _ |a Grossmann, Justus
|0 0009-0002-7094-1888
|b 2
700 1 _ |a Szyrwiel, Lukasz
|0 0000-0003-1983-2950
|b 3
700 1 _ |a Schwecke, Torsten
|b 4
700 1 _ |a Demichev, Vadim
|b 5
700 1 _ |a Mikecin Drazic, Ana-Matea
|0 P:(DE-He78)7497b1427e6dd93688642d946fbaee12
|b 6
700 1 _ |a Mayakonda, Anand
|0 P:(DE-HGF)0
|b 7
700 1 _ |a Lutsik, Pavlo
|0 P:(DE-He78)ff1677c63392be9b31a1c8d23db7c9dc
|b 8
|u dkfz
700 1 _ |a Veith, Carmen
|0 P:(DE-He78)7583d0eaa7d0cc360d4aabfc85dd00cd
|b 9
700 1 _ |a Milsom, Michael
|0 P:(DE-He78)7b613cadb8c16ce178713e15b85d982c
|b 10
|u dkfz
700 1 _ |a Müller-Decker, Karin
|0 P:(DE-He78)799d978330dff449f8244947929a4518
|b 11
|u dkfz
700 1 _ |a Mülleder, Michael
|0 0000-0001-9792-3861
|b 12
700 1 _ |a Ralser, Markus
|0 0000-0001-9535-7413
|b 13
700 1 _ |a Dick, Tobias
|0 P:(DE-He78)7f55a0ed8b021080de00960cc73768fb
|b 14
|e Last author
|u dkfz
773 _ _ |a 10.1038/s42255-023-00781-3
|0 PERI:(DE-600)2933873-6
|n 4
|p 660-676
|t Nature metabolism
|v 5
|y 2023
|x 2522-5812
909 C O |p VDB
|o oai:inrepo02.dkfz.de:275343
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 0
|6 P:(DE-He78)290f7b71b45035214574625eccde4d08
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 1
|6 P:(DE-He78)eb748bd61964bae06c38c8893b52bcfd
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 6
|6 P:(DE-He78)7497b1427e6dd93688642d946fbaee12
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 7
|6 P:(DE-HGF)0
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 8
|6 P:(DE-He78)ff1677c63392be9b31a1c8d23db7c9dc
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 9
|6 P:(DE-He78)7583d0eaa7d0cc360d4aabfc85dd00cd
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 10
|6 P:(DE-He78)7b613cadb8c16ce178713e15b85d982c
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 11
|6 P:(DE-He78)799d978330dff449f8244947929a4518
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 14
|6 P:(DE-He78)7f55a0ed8b021080de00960cc73768fb
913 1 _ |a DE-HGF
|b Gesundheit
|l Krebsforschung
|1 G:(DE-HGF)POF4-310
|0 G:(DE-HGF)POF4-311
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Zellbiologie und Tumorbiologie
|x 0
914 1 _ |y 2023
915 _ _ |a DEAL Nature
|0 StatID:(DE-HGF)3003
|2 StatID
|d 2023-03-31
|w ger
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1190
|2 StatID
|b Biological Abstracts
|d 2023-03-31
915 _ _ |a WoS
|0 StatID:(DE-HGF)0113
|2 StatID
|b Science Citation Index Expanded
|d 2023-03-31
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2023-03-31
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b NAT METAB : 2022
|d 2023-08-19
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2023-08-19
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2023-08-19
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2023-08-19
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
|d 2023-08-19
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2023-08-19
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
|d 2023-08-19
915 _ _ |a IF >= 20
|0 StatID:(DE-HGF)9920
|2 StatID
|b NAT METAB : 2022
|d 2023-08-19
920 2 _ |0 I:(DE-He78)A160-20160331
|k A160
|l A160 Redoxregulation
|x 0
920 1 _ |0 I:(DE-He78)A160-20160331
|k A160
|l A160 Redoxregulation
|x 0
920 1 _ |0 I:(DE-He78)A012-20160331
|k A012
|l A012 Experimentelle Hämatologie
|x 1
920 1 _ |0 I:(DE-He78)B370-20160331
|k B370
|l Epigenomik
|x 2
920 1 _ |0 I:(DE-He78)W420-20160331
|k W420
|l Gruppe Müller-Decker
|x 3
920 0 _ |0 I:(DE-He78)A160-20160331
|k A160
|l A160 Redoxregulation
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)A160-20160331
980 _ _ |a I:(DE-He78)A012-20160331
980 _ _ |a I:(DE-He78)B370-20160331
980 _ _ |a I:(DE-He78)W420-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21