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Targeting the lipid metabolic reprogramming of tumor-associated macrophages: A novel insight into cancer immunotherapy.

Authors :
Li L
Ma SR
Yu ZL
Source :
Cellular oncology (Dordrecht) [Cell Oncol (Dordr)] 2024 Apr; Vol. 47 (2), pp. 415-428. Date of Electronic Publication: 2023 Sep 30.
Publication Year :
2024

Abstract

Background: Tumor-associated macrophages, as the major immunocytes in solid tumors, show divided loyalty and remarkable plasticity in tumorigenesis. Once the M2-to-M1 repolarization is achieved, they could be switched from the supporters for tumor development into the guardians for host immunity. Meanwhile, Lipid metabolic reprogramming is demonstrated to be one of the most important hallmarks of tumor-associated macrophages, which plays a decisive role in regulating their phenotypes and functions to promote tumorigenesis and immunotherapy resistance. Therefore, targeting the lipid metabolism of TAMs may provide a new direction for anti-tumor strategies.<br />Conclusion: In this review, we first summarized the origins, classifications and general lipid metabolic process of TAMs. Then we discussed the currently available drugs and interventions that target lipid metabolic disorders of TAMs, including those targeting lipid uptake, efflux, lipolysis, FAO and lipid peroxidation. Besides, based on the recent research status, we summarized the present challenges for this cancer immunotherapy, including the precise drug delivery system, the lipid metabolic heterogeneity, and the intricate lipid metabolic interactions in the TME, and we also proposed corresponding possible solutions. Collectively, we hope this review will give researchers a better understanding of the lipid metabolism of TAMs and lead to the development of corresponding anti-tumor therapies in the future.<br /> (© 2023. Springer Nature Switzerland AG.)

Details

Language :
English
ISSN :
2211-3436
Volume :
47
Issue :
2
Database :
MEDLINE
Journal :
Cellular oncology (Dordrecht)
Publication Type :
Academic Journal
Accession number :
37776422
Full Text :
https://doi.org/10.1007/s13402-023-00881-y