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The role of cholesterol metabolism in lung cancer.

Authors :
Xiu W
Liu X
Hu K
Zhang Q
Shi H
Source :
Oncology research [Oncol Res] 2024 Sep 18; Vol. 32 (10), pp. 1613-1621. Date of Electronic Publication: 2024 Sep 18 (Print Publication: 2024).
Publication Year :
2024

Abstract

Elevated serum cholesterol metabolism is associated with a reduced risk of lung cancer. Disrupted cholesterol metabolism is evident in both lung cancer patients and tumor cells. Inhibiting tumor cell cholesterol uptake or biosynthesis pathways, through the modulation of receptors and enzymes such as liver X receptor and sterol-regulatory element binding protein 2, effectively restrains lung tumor growth. Similarly, promoting cholesterol excretion yields comparable effects. Cholesterol metabolites, including oxysterols and isoprenoids, play a crucial role in regulating cholesterol metabolism within tumor cells, consequently impacting cancer progression. In lung cancer patients, both the cholesterol levels in the tumor microenvironment and within tumor cells significantly influence cell growth, proliferation, and metastasis. The effects of cholesterol metabolism are further mediated by the reprogramming of immune cells such as T cells, B cells, macrophages, myeloid-derived suppressor cells, among others. Ongoing research is investigating drugs targeting cholesterol metabolism for clinical treatments. Statins, targeting the cholesterol biosynthesis pathway, are widely employed in lung cancer treatment, either as standalone agents or in combination with other drugs. Additionally, drugs focusing on cholesterol transportation have shown promise as effective therapies for lung cancer. In this review, we summarized current research regarding the rule of cholesterol metabolism and therapeutic advances in lung cancer.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (© 2024 The Authors.)

Details

Language :
English
ISSN :
1555-3906
Volume :
32
Issue :
10
Database :
MEDLINE
Journal :
Oncology research
Publication Type :
Academic Journal
Accession number :
39308527
Full Text :
https://doi.org/10.32604/or.2024.047933