Zikic Vladica, Paunovic Marija, Milovic-Kovacevic Marijana, Vucic Vesna, Ristic-Medic Danijela
Cognitive Neuroscience Department, Research and Development Institute "Life Activities Advancement Institute", 11000 Belgrade, Serbia.
Department of Speech, Language and Hearing Sciences, Institute for Experimental Phonetics and Speech Pathology, 11000 Belgrade, Serbia.
Int J Mol Sci. 2025 May 19;26(10):4867. doi: 10.3390/ijms26104867.
Epidemiological studies report inconsistent findings regarding the association between dietary polyunsaturated fatty acid (PUFA) intake and cancer risk. Genetic variations-particularly single-nucleotide polymorphisms (SNPs) in the and genes-affect PUFA metabolism, linking circulating PUFA levels to the risk of several cancers, including breast, colorectal, prostate, and pancreatic cancers. This review aimed to investigate the relationship between and gene variants and dietary intake, supplementation, or intervention with omega-3 fatty acids, gamma-linolenic acid (GLA), or their combination in cancer patients. A secondary objective was to examine genetically determined fatty acid profiles-shaped by and polymorphisms-in cancer patients without intervention and their potential association with PUFA-related cancer risk. A systematic search of the Scopus, PubMed, and Web of Science databases (up to 2024) identified 11 eligible studies out of 298 initial records. Analysis of the available literature suggests that specific genotypes influence long-chain PUFA (LC-PUFA) concentrations in blood and tissues and that altered LC-PUFA levels may contribute to cancer development. The most consistent association identified is between the rs174537 variant and altered PUFA metabolism in prostate and breast cancer. However, conclusive evidence is lacking on the impact of dietary patterns on FADS desaturase activity or expression. Only one study has examined omega-3 supplementation in relation to gene variants in prostate cancer patients, while the effects of GLA supplementation remain unexplored. Given the relative novelty of this research area and the limited number of studies, future investigations should integrate dietary PUFA intake, genetic variation in PUFA-metabolizing enzymes, and potential gene-nutrient interactions involving gene polymorphisms and PUFAs to clarify their role in cancer risk.
流行病学研究报告了饮食中多不饱和脂肪酸(PUFA)摄入量与癌症风险之间的关联,但结果并不一致。基因变异——特别是 和 基因中的单核苷酸多态性(SNP)——会影响PUFA代谢,将循环中的PUFA水平与包括乳腺癌、结直肠癌、前列腺癌和胰腺癌在内的多种癌症风险联系起来。本综述旨在研究 和 基因变异与癌症患者饮食摄入、补充或ω-3脂肪酸、γ-亚麻酸(GLA)或其组合干预之间的关系。第二个目标是检查在未进行干预的癌症患者中由 和 多态性塑造的基因决定的脂肪酸谱,以及它们与PUFA相关癌症风险的潜在关联。对Scopus、PubMed和Web of Science数据库(截至2024年)进行系统检索,在298条初始记录中确定了11项符合条件的研究。对现有文献的分析表明,特定的 基因型会影响血液和组织中长链PUFA(LC-PUFA)的浓度,而LC-PUFA水平的改变可能会促进癌症发展。确定的最一致关联是rs174537变异与前列腺癌和乳腺癌中PUFA代谢改变之间的关联。然而,关于饮食模式对FADS去饱和酶活性或表达的影响,缺乏确凿证据。只有一项研究探讨了ω-3补充剂与前列腺癌患者 基因变异的关系,而GLA补充剂的效果仍未得到探索。鉴于该研究领域相对较新且研究数量有限,未来的研究应整合饮食中PUFA的摄入量、PUFA代谢酶的基因变异以及涉及 基因多态性和PUFA的潜在基因-营养相互作用,以阐明它们在癌症风险中的作用。