» Articles » PMID: 36798663

The Role of FOXA Family Transcription Factors in Glucolipid Metabolism and NAFLD

Overview
Specialty Endocrinology
Date 2023 Feb 17
PMID 36798663
Authors
Affiliations
Soon will be listed here.
Abstract

Abnormal glucose metabolism and lipid metabolism are common pathological processes in many metabolic diseases, such as nonalcoholic fatty liver disease (NAFLD). Many studies have shown that the forkhead box (FOX) protein subfamily FOXA has a role in regulating glucolipid metabolism and is closely related to hepatic steatosis and NAFLD. FOXA exhibits a wide range of functions ranging from the initiation steps of metabolism such as the development of the corresponding metabolic organs and the differentiation of cells, to multiple pathways of glucolipid metabolism, to end-of-life problems of metabolism such as age-related obesity. The purpose of this article is to review and discuss the currently known targets and signal transduction pathways of FOXA in glucolipid metabolism. To provide more experimental evidence and basis for further research and clinical application of FOXA in the regulation of glucolipid metabolism and the prevention and treatment of NAFLD.

Citing Articles

Novel Therapeutic Target for ALI/ARDS: Forkhead Box Transcription Factors.

Zhu X, Meng L, Xu L, Hua Y, Feng J Lung. 2024; 202(5):513-522.

PMID: 39259274 DOI: 10.1007/s00408-024-00740-z.


Exploring the Pathogenesis of Autoimmune Liver Diseases from the Heterogeneity of Target Cells.

Qiu Z, Huang L, Wang X, Wang Z, Li X, Feng B J Clin Transl Hepatol. 2024; 12(7):659-666.

PMID: 38993508 PMC: 11233981. DOI: 10.14218/JCTH.2023.00531.


An integrated analysis of the anticarcinogenic role of forkhead box protein 1 in oesophageal squamous cell carcinoma.

Ye G, Pan G, Zhu X, Li N, Liu H, Geng G J Cell Mol Med. 2024; 28(8):e18294.

PMID: 38652109 PMC: 11037412. DOI: 10.1111/jcmm.18294.


FOXA1 and FOXA2: the regulatory mechanisms and therapeutic implications in cancer.

Liu N, Wang A, Xue M, Zhu X, Liu Y, Chen M Cell Death Discov. 2024; 10(1):172.

PMID: 38605023 PMC: 11009302. DOI: 10.1038/s41420-024-01936-1.


Peroxisome proliferator-activated receptor gamma coactivator-1 (PGC-1) family in physiological and pathophysiological process and diseases.

Qian L, Zhu Y, Deng C, Liang Z, Chen J, Chen Y Signal Transduct Target Ther. 2024; 9(1):50.

PMID: 38424050 PMC: 10904817. DOI: 10.1038/s41392-024-01756-w.


References
1.
Balsalobre A, Drouin J . Pioneer factors as master regulators of the epigenome and cell fate. Nat Rev Mol Cell Biol. 2022; 23(7):449-464. DOI: 10.1038/s41580-022-00464-z. View

2.
Hannenhalli S, Kaestner K . The evolution of Fox genes and their role in development and disease. Nat Rev Genet. 2009; 10(4):233-40. PMC: 2733165. DOI: 10.1038/nrg2523. View

3.
Vatamaniuk M, Gupta R, Lantz K, Doliba N, Matschinsky F, Kaestner K . Foxa1-deficient mice exhibit impaired insulin secretion due to uncoupled oxidative phosphorylation. Diabetes. 2006; 55(10):2730-6. DOI: 10.2337/db05-0470. View

4.
Gao B, Xie W, Wu X, Wang L, Guo J . Functionally analyzing the important roles of hepatocyte nuclear factor 3 (FoxA) in tumorigenesis. Biochim Biophys Acta Rev Cancer. 2020; 1873(2):188365. DOI: 10.1016/j.bbcan.2020.188365. View

5.
Khalifa O, Al-Akl N, Errafii K, Arredouani A . Exendin-4 alleviates steatosis in an in vitro cell model by lowering FABP1 and FOXA1 expression via the Wnt/-catenin signaling pathway. Sci Rep. 2022; 12(1):2226. PMC: 8828858. DOI: 10.1038/s41598-022-06143-5. View