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Glycerol 3-phosphate dehydrogenases (1 and 2) in cancer and other diseases.
Oh, Sehyun; Mai, Xuan Linh; Kim, Jiwoo; de Guzman, Arvie Camille V; Lee, Ji Yun; Park, Sunghyouk.
Affiliation
  • Oh S; College of Pharmacy, Natural Products Research Institute, Seoul National University, Seoul, 08826, Korea.
  • Mai XL; Department of Cancer Biology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, 02215, USA.
  • Kim J; College of Pharmacy, Natural Products Research Institute, Seoul National University, Seoul, 08826, Korea.
  • de Guzman ACV; College of Pharmacy, Natural Products Research Institute, Seoul National University, Seoul, 08826, Korea.
  • Lee JY; College of Pharmacy, Natural Products Research Institute, Seoul National University, Seoul, 08826, Korea.
  • Park S; College of Pharmacy, Natural Products Research Institute, Seoul National University, Seoul, 08826, Korea. jiyunkr@snu.ac.kr.
Exp Mol Med ; 56(5): 1066-1079, 2024 May.
Article in En | MEDLINE | ID: mdl-38689091
ABSTRACT
The glycerol 3-phosphate shuttle (GPS) is composed of two different enzymes cytosolic NAD+-linked glycerol 3-phosphate dehydrogenase 1 (GPD1) and mitochondrial FAD-linked glycerol 3-phosphate dehydrogenase 2 (GPD2). These two enzymes work together to act as an NADH shuttle for mitochondrial bioenergetics and function as an important bridge between glucose and lipid metabolism. Since these genes were discovered in the 1960s, their abnormal expression has been described in various metabolic diseases and tumors. Nevertheless, it took a long time until scientists could investigate the causal relationship of these enzymes in those pathophysiological conditions. To date, numerous studies have explored the involvement and mechanisms of GPD1 and GPD2 in cancer and other diseases, encompassing reports of controversial and non-conventional mechanisms. In this review, we summarize and update current knowledge regarding the functions and effects of GPS to provide an overview of how the enzymes influence disease conditions. The potential and challenges of developing therapeutic strategies targeting these enzymes are also discussed.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mitochondrial Proteins / Glycerolphosphate Dehydrogenase / Neoplasms Limits: Animals / Humans Language: En Journal: Exp Mol Med Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA Year: 2024 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mitochondrial Proteins / Glycerolphosphate Dehydrogenase / Neoplasms Limits: Animals / Humans Language: En Journal: Exp Mol Med Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA Year: 2024 Document type: Article Country of publication: United States