Chistyakov Dmitry V, Guryleva Mariia V, Stepanova Elena S, Makarenkova Lyubov M, Ptitsyna Elena V, Goriainov Sergei V, Nikolskaya Arina I, Astakhova Alina A, Klimenko Anna S, Bezborodova Olga A, Rasskazova Elena A, Potanina Olga G, Abramovich Rimma A, Nemtsova Elena R, Sergeeva Marina G
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119992 Moscow, Russia.
Faculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, 119234 Moscow, Russia.
Cancers (Basel). 2022 Apr 18;14(8):2041. doi: 10.3390/cancers14082041.
The involvement of oxylipins, metabolites of polyunsaturated fatty acids, in cancer pathogenesis was known long ago, but only the development of the high-throughput methods get the opportunity to study oxylipins on a system level. The study aimed to elucidate alterations in oxylipin metabolism as characteristics of breast cancer patients. We compared the ultra-high-performance liquid chromatography-mass spectrometry (UPLC-MS/MS) oxylipin profile signatures in the blood plasma of 152 healthy volunteers (HC) and 169 patients with different stages of breast cancer (BC). To integrate lipidomics, transcriptomics, and genomics data, we analyzed a transcriptome of 10 open database datasets obtained from tissues and blood cells of BC patients and SNP data for 33 genes related to oxylipin metabolism. We identified 18 oxylipins, metabolites of omega-3 or omega-6 polyunsaturated fatty acids, that were differentially expressed between BCvsHC patients, including anandamide, prostaglandins and hydroxydocosahexaenoic acids. DEGs analysis of tissue and blood samples from BC patients revealed that 19 genes for oxylipin biosynthesis change their expression level, with CYP2C19, PTGS2, HPGD, and FAAH included in the list of DEGs in the analysis of transcriptomes and the list of SNPs associated with BC. Results allow us to suppose that oxylipin signatures reflect the organism's level of response to the disease. Our data regarding changes in oxylipins at the system level show that oxylipin profiles can be used to evaluate the early stages of breast cancer.
很久以前就知道氧化脂质(多不饱和脂肪酸的代谢产物)参与癌症发病机制,但只有高通量方法的发展才使人们有机会在系统水平上研究氧化脂质。本研究旨在阐明氧化脂质代谢的改变作为乳腺癌患者的特征。我们比较了152名健康志愿者(HC)和169名不同阶段乳腺癌(BC)患者血浆中的超高效液相色谱-质谱联用(UPLC-MS/MS)氧化脂质谱特征。为了整合脂质组学、转录组学和基因组学数据,我们分析了从BC患者的组织和血细胞中获得的10个开放数据库数据集的转录组以及33个与氧化脂质代谢相关基因的单核苷酸多态性(SNP)数据。我们鉴定出18种氧化脂质,即ω-3或ω-6多不饱和脂肪酸的代谢产物,在BC与HC患者之间差异表达,包括花生四烯乙醇胺、前列腺素和羟基二十二碳六烯酸。对BC患者的组织和血液样本进行的差异表达基因(DEG)分析表明,19个氧化脂质生物合成基因的表达水平发生了变化,其中CYP2C19、PTGS2、HPGD和FAAH包含在转录组分析的DEG列表以及与BC相关的SNP列表中。结果使我们推测氧化脂质特征反映了机体对疾病的反应水平。我们在系统水平上关于氧化脂质变化的数据表明,氧化脂质谱可用于评估乳腺癌的早期阶段。