Copyright
©The Author(s) 2025.
World J Diabetes. Aug 15, 2025; 16(8): 108310
Published online Aug 15, 2025. doi: 10.4239/wjd.v16.i8.108310
Published online Aug 15, 2025. doi: 10.4239/wjd.v16.i8.108310
Figure 1 Mechanistic illustration of Ras homolog enriched in brain 1 as a central regulator of β-cell mass and its integrating function on mammalian target of rapamycin complex 1, AMP-activated protein kinase, neurogenic locus notch homolog protein 1, and hepatocyte nuclear factor 4 alpha pathways.
Ras homolog enriched in brain 1 plays a critical role in both β-cell proliferation and identity, and its dysregulation contributes to diabetes pathogenesis. Rheb1: Ras homolog enriched in brain 1; Notch1: Neurogenic locus notch homolog protein 1; MTORC1: Mammalian target of rapamycin complex 1; HNF4: Hepatocyte nuclear factor 4 alpha; MODY1: Maturity-onset diabetes of the young 1.
- Citation: Gouda MM. Rheb1 as a novel β-cell regulator connecting mTORC1, AMPK, and NOTCH1 pathways for efficient diabetes therapy. World J Diabetes 2025; 16(8): 108310
- URL: https://www.wjgnet.com/1948-9358/full/v16/i8/108310.htm
- DOI: https://dx.doi.org/10.4239/wjd.v16.i8.108310