SIRT3, a metabolic target linked to ataxia-telangiectasia mutated (ATM) gene deficiency in diffuse large B-cell lymphoma View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2020-12-03

AUTHORS

Kavita Bhalla, Sausan Jaber, Kayla Reagan, Arielle Hamburg, Karen F. Underwood, Aditya Jhajharia, Maninder Singh, Binny Bhandary, Shambhu Bhat, Nahid M. Nanaji, Ruching Hisa, Carrie McCracken, Heather Huot Creasy, Rena G. Lapidus, Tami Kingsbury, Dirk Mayer, Brian Polster, Ronald B. Gartenhaus

ABSTRACT

Inactivation of Ataxia-telangiectasia mutated (ATM) gene results in an increased risk to develop cancer. We show that ATM deficiency in diffuse large B-cell lymphoma (DLBCL) significantly induce mitochondrial deacetylase sirtuin-3 (SIRT3) activity, disrupted mitochondrial structure, decreased mitochondrial respiration, and compromised TCA flux compared with DLBCL cells expressing wild type (WT)-ATM. This corresponded to enrichment of glutamate receptor and glutamine pathways in ATM deficient background compared to WT-ATM DLBCL cells. ATM−/− DLBCL cells have decreased apoptosis in contrast to radiosensitive non-cancerous A-T cells. In vivo studies using gain and loss of SIRT3 expression showed that SIRT3 promotes growth of ATM CRISPR knockout DLBCL xenografts compared to wild-type ATM control xenografts. Importantly, screening of DLBCL patient samples identified SIRT3 as a putative therapeutic target, and validated an inverse relationship between ATM and SIRT3 expression. Our data predicts SIRT3 as an important therapeutic target for DLBCL patients with ATM null phenotype. More... »

PAGES

21159

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/s41598-020-78193-6

DOI

http://dx.doi.org/10.1038/s41598-020-78193-6

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1132950925

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/33273545


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RDF/XML is a standard XML format for linked data.

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