In silico and cheminformatics prediction with experimental validation of an adipogenesis cocktail, sorafenib with rosiglitazone for HCC dedifferentiation.

J Genet Eng Biotechnol

Biochemistry Department, Faculty of Science, Alexandria University, El-Shatbi, 21568, Alexandria, Egypt; Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC, United States.

Published: December 2024

Purpose: Hepatocellular carcinoma (HCC) resistance to sorafenib treatment and other treatment strategies causes a higher mortality rate in patients diagnosed with HCC.

Research Question: HCC often develops resistance to sorafenib treatment and other therapies, leading to increased mortality rates in diagnosed patients. Herein, we propose a combined therapeutic approach using rosiglitazone, a key factor in cellular differentiation, along with adipogenesis inducers such as dexamethasone, IBMX, and insulin. Additionally, we included sorafenib, a primary drug for liver cancer treatment, in this combination cocktail and carried out the differentiation process in the presence of sorafenib.

Results: Our study demonstrates that this combination induces the formation of adipocytes from HCC cells over several days under specific conditions and steps.

Conclusion: findings suggest that supplementing sorafenib with rosiglitazone and adipogenesis inducers may potentially transform HCC cells into adipocyte-like cells. Fat could be "the good" in the story of liver cancer alleviation, demonstrating the role of rosiglitazone.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11600669PMC
http://dx.doi.org/10.1016/j.jgeb.2024.100429DOI Listing

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