Tumor suppressor RARRES1 links tubulin deglutamylation to mitochondrial metabolism and cell survival.

PTM tubulin RARRES1 drug resistance metabolic reprogramming retinoic acid signaling

Journal

Oncotarget
ISSN: 1949-2553
Titre abrégé: Oncotarget
Pays: United States
ID NLM: 101532965

Informations de publication

Date de publication:
26 Feb 2019
Historique:
received: 09 10 2018
accepted: 04 12 2018
entrez: 23 3 2019
pubmed: 23 3 2019
medline: 23 3 2019
Statut: epublish

Résumé

RARRES1, a retinoic acid regulated carboxypeptidase inhibitor associated with fatty acid metabolism, stem cell differentiation and tumorigenesis is among the most commonly methylated loci in multiple cancers but has no known mechanism of action. Here we show that RARRES1 interaction with cytoplasmic carboxypeptidase 2 (CCP2) inhibits tubulin deglutamylation, which in turn regulates the mitochondrial voltage dependent anion channel (VDAC1), mitochondrial membrane potential, AMPK activation, energy balance and metabolically reprograms cells and zebrafish to a more energetic and anabolic phenotype. Depletion of

Identifiants

pubmed: 30899431
doi: 10.18632/oncotarget.26600
pii: 26600
pmc: PMC6422194
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1606-1624

Subventions

Organisme : NCI NIH HHS
ID : P30 CA051008
Pays : United States
Organisme : NCATS NIH HHS
ID : TL1 TR001431
Pays : United States

Commentaires et corrections

Type : ErratumIn

Déclaration de conflit d'intérêts

CONFLICTS OF INTEREST The authors declare that they have no conflicts of interest with the contents of this article.

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Auteurs

Sara Maimouni (S)

Department of Biochemical, Molecular and Cellular Biology, Georgetown University, Washington, DC, USA.

Mi-Hye Lee (MH)

Department of Oncology, Georgetown-Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.

You-Me Sung (YM)

Department of Oncology, Georgetown-Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.

Michael Hall (M)

Department of Oncology, Georgetown-Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.

Arpita Roy (A)

University of the District of Columbia, Washington, DC, USA.

Chokri Ouaari (C)

Department of Oncology, Georgetown-Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
University of the District of Columbia, Washington, DC, USA.

Yoo-Seok Hwang (YS)

Cancer & Developmental Biology Laboratory, National Cancer Institute-Frederick, Frederick, MD, USA.

Justin Spivak (J)

Department of Oncology, Georgetown-Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.

Eric Glasgow (E)

Department of Oncology, Georgetown-Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.

Matthew Swift (M)

Department of Oncology, Georgetown-Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.

Jay Patel (J)

Department of Oncology, Georgetown-Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.

Amrita Cheema (A)

Department of Oncology, Georgetown-Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.

Deepak Kumar (D)

University of the District of Columbia, Washington, DC, USA.

Stephen Byers (S)

Department of Oncology, Georgetown-Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Department of Biochemical, Molecular and Cellular Biology, Georgetown University, Washington, DC, USA.

Classifications MeSH