Molecular mechanisms of RAB24 in vesicle traffic, lipid accumulation and cell-cell adhesion

Description of the granted funding

RAB24 is a small GTP-binding protein known to function in autophagy, an intracellular recycling pathway. RAB24 is important for health. It supports the survival of neurons, and mutations in RAB24 cause ataxia, lack of coordination of muscle movements, in dogs. RAB24 promotes malignancy of liver cancer, and its overexpression enhances liver fat accumulation. RAB24 facilitates cancer cell survival by decreasing cell death, promoting growth and increasing cell motility. This project will elucidate the molecular mechanisms that mediate the effects of RAB24 in neurons and hepatocytes. We will screen for proteins that interact with RAB24 and investigate the molecular mechanisms they use to regulate RAB24. The results have potential to open possibilities for the development of new treatments for neurodegeneration, cancer and fatty liver disease.
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Starting year

2022

End year

2026

Granted funding

Eeva-Liisa Eskelinen Orcid -palvelun logo
499 979 €

Funder

Research Council of Finland

Funding instrument

Academy projects

Other information

Funding decision number

351215

Fields of science

Biochemistry, cell and molecular biology

Research fields

Solu- ja molekyylibiologia

Identified topics

molecular biology, biochemistry