| Literature DB >> 31462712 |
David Dimmock1,2, Ayelet Erez3, Shiran Rabinovich4, Alon Silberman4, Lital Adler4, Shani Agron4, Smadar Levin-Zaidman5, Amir Bahat4, Ziv Porat6, Efrat Ben-Zeev7, Inbal Geva7, Maxim Itkin8, Sergey Malitsky8, Adam Buchaklian1, Daniel Helbling1.
Abstract
Citrin, encoded by SLC25A13 gene, is an inner mitochondrial transporter that is part of the malate-aspartate shuttle, which regulates the NAD+/NADH ratio between the cytosol and mitochondria. Citrullinemia type II (CTLN-II) is an inherited disorder caused by germline mutations in SLC25A13, manifesting clinically in growth failure that can be alleviated by dietary restriction of carbohydrates. The association of citrin with glycolysis and NAD+/NADH ratio led us to hypothesize that it may play a role in carcinogenesis. Indeed, we find that citrin is upregulated in multiple cancer types and is essential for supplementing NAD+ for glycolysis and NADH for oxidative phosphorylation. Consequently, citrin deficiency associates with autophagy, whereas its overexpression in cancer cells increases energy production and cancer invasion. Furthermore, based on the human deleterious mutations in citrin, we found a potential inhibitor of citrin that restricts cancerous phenotypes in cells. Collectively, our findings suggest that targeting citrin may be of benefit for cancer therapy.Entities:
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Year: 2019 PMID: 31462712 DOI: 10.1038/s41388-019-0976-2
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867