Arachidonic acid metabolism as a novel pathogenic factor in gastrointestinal cancers
- PMID: 38963615
- DOI: 10.1007/s11010-024-05057-2
Arachidonic acid metabolism as a novel pathogenic factor in gastrointestinal cancers
Abstract
Gastrointestinal (GI) cancers are a major global health burden, representing 20% of all cancer diagnoses and 22.5% of global cancer-related deaths. Their aggressive nature and resistance to treatment pose a significant challenge, with late-stage survival rates below 15% at five years. Therefore, there is an urgent need to delve deeper into the mechanisms of gastrointestinal cancer progression and optimize treatment strategies. Increasing evidence highlights the active involvement of abnormal arachidonic acid (AA) metabolism in various cancers. AA is a fatty acid mainly metabolized into diverse bioactive compounds by three enzymes: cyclooxygenase, lipoxygenase, and cytochrome P450 enzymes. Abnormal AA metabolism and altered levels of its metabolites may play a pivotal role in the development of GI cancers. However, the underlying mechanisms remain unclear. This review highlights a unique perspective by focusing on the abnormal metabolism of AA and its involvement in GI cancers. We summarize the latest advancements in understanding AA metabolism in GI cancers, outlining changes in AA levels and their potential role in liver, colorectal, pancreatic, esophageal, gastric, and gallbladder cancers. Moreover, we also explore the potential of targeting abnormal AA metabolism for future therapies, considering the current need to explore AA metabolism in GI cancers and outlining promising avenues for further research. Ultimately, such investigations aim to improve treatment options for patients with GI cancers and pave the way for better cancer management in this area.
Keywords: Arachidonic acid; Clinical application; Colorectal cancer; Gastric cancer; Liver cancer; Pancreatic cancer.
© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Conflict of interest statement
Declarations. Competing interests: The authors declare no competing interests. Ethical approval: Not applicable. Consent to participate: Not applicable. Consent to publication: Not applicable.
Similar articles
-
Intratumoral Microbiota: Metabolic Influences and Biomarker Potential in Gastrointestinal Cancer.Biomolecules. 2024 Jul 27;14(8):917. doi: 10.3390/biom14080917. Biomolecules. 2024. PMID: 39199305 Free PMC article. Review.
-
5-Lipoxygenase: Its involvement in gastrointestinal malignancies.Crit Rev Oncol Hematol. 2018 Jul;127:50-55. doi: 10.1016/j.critrevonc.2018.05.012. Epub 2018 May 18. Crit Rev Oncol Hematol. 2018. PMID: 29891111 Review.
-
Role of cytochrome P450 in phospholipase A2- and arachidonic acid-mediated cytotoxicity.Free Radic Biol Med. 2006 Feb 1;40(3):364-75. doi: 10.1016/j.freeradbiomed.2005.10.044. Epub 2005 Nov 4. Free Radic Biol Med. 2006. PMID: 16443151 Review.
-
Arachidonic acid metabolism in health and disease.MedComm (2020). 2023 Sep 20;4(5):e363. doi: 10.1002/mco2.363. eCollection 2023 Oct. MedComm (2020). 2023. PMID: 37746665 Free PMC article. Review.
-
A Narrative Review of the Published Pre-Clinical Evaluations: Multiple Effects of Arachidonic Acid, its Metabolic Enzymes and Metabolites in Epilepsy.Mol Neurobiol. 2025 Jan;62(1):288-303. doi: 10.1007/s12035-024-04274-6. Epub 2024 Jun 6. Mol Neurobiol. 2025. PMID: 38842673 Review.
Cited by
-
Exploring causal associations between nuclear magnetic resonance biomarkers and colorectal cancer risk.Metabolomics. 2025 Aug 12;21(5):110. doi: 10.1007/s11306-025-02305-4. Metabolomics. 2025. PMID: 40794337
-
A Survey of Fatty Acid Content of the Male Reproductive System in Mice Supplemented With Arachidonic Acid.J Lipids. 2024 Dec 19;2024:3351340. doi: 10.1155/jl/3351340. eCollection 2024. J Lipids. 2024. PMID: 39734583 Free PMC article.
References
-
- Gravitz L (2014) Liver cancer. Nature 516(7529):S1 - PubMed
-
- Kim BH, Park JW (2018) Epidemiology of liver cancer in South Korea. Clin Mol Hepatol 24(1):1–9 - PubMed
-
- Stoffel EM, Brand RE, Goggins M (2023) Pancreatic cancer: changing epidemiology and new approaches to risk assessment, early detection, and prevention. Gastroenterology 164(5):752–765 - PubMed
-
- Arnold M, Abnet CC, Neale RE, Vignat J, Giovannucci EL, McGlynn KA, Bray F (2020) Global burden of 5 major types of gastrointestinal cancer. Gastroenterology 159(1):335–49.e15 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources