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Updated: Aug 29, 2025

Enrichment of Mammalian Tissues and Xenopus Oocytes with Cholesterol
Published on: March 25, 2020
Use of cholesterol metabolism for anti-cancer strategies
1Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Colombo, Colombo 08, Sri Lanka.
Abstract:
Irregularities in cholesterol metabolism occur in a range of human cancers. Cholesterol precursors and derivatives support tumorigenesis and weaken immune responses. Intriguing preclinical and clinical findings demonstrate that cholesterol biosynthesis inhibition achieved by targeting major events and metabolites in cholesterol metabolism is an ideal anti-tumor strategy. Investigations addressing the effects of β-hydroxy β-methylglutaryl-CoA (HMG-CoA) reductase (HMGCR), 2,3-oxidosqualene cyclase (OSC), squalene synthase (SQS), liver X receptors (LXR), and cholesterol trafficking and esterification inhibition on cancer progression have shown encouraging results. Notably, manipulation of cholesterol metabolism strengthens the function of immune cells in the tumor microenvironment (TME). In this review, I discuss the role of cholesterol metabolism in cancer progression and the latest research related to cholesterol metabolism-based anti-cancer therapies and intend to bring this stylish biochemistry topic to the Sri Lankan research landscape.
Insights
Altering cholesterol metabolism shows promise as an anti-cancer strategy. Inhibiting cholesterol biosynthesis can weaken tumors and enhance immune responses against cancer.
Area of Science:
- Biochemistry
- Oncology
- Immunology
Background:
- Cholesterol metabolism irregularities are linked to various human cancers.
- Cholesterol precursors and derivatives fuel tumor growth and suppress immune function.
- Targeting cholesterol metabolism presents a potential anti-cancer therapeutic avenue.
Purpose of the Study:
- To review the role of cholesterol metabolism in cancer progression.
- To discuss novel anti-cancer therapies targeting cholesterol metabolism.
- To highlight the impact of cholesterol metabolism manipulation on the tumor microenvironment (TME).
Main Methods:
- Review of preclinical and clinical findings on cholesterol biosynthesis inhibition.
- Examination of targets such as HMG-CoA reductase (HMGCR), 2,3-oxidosqualene cyclase (OSC), squalene synthase (SQS), and liver X receptors (LXR).
- Analysis of strategies involving cholesterol trafficking and esterification inhibition.
Main Results:
- Inhibition of cholesterol biosynthesis demonstrates anti-tumor potential.
- Targeting key enzymes and pathways in cholesterol metabolism yields encouraging results.
- Modulating cholesterol metabolism enhances immune cell function within the TME.
Conclusions:
- Cholesterol metabolism is a critical factor in cancer progression.
- Targeting cholesterol metabolism offers a promising strategy for cancer therapy.
- Further research into cholesterol metabolism-based therapies could lead to new treatments.
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