Bissan Aboubacar Dit Tietie, Michel Mathieu, Dieu Xavier, Bocca Cinzia, Amegonou Awo Emmanuela Hilda, Sidibe Fatoumata Matokoma, Ly Madani, Koné Bocary Sidi, Barry Nènè Oumou Kesso, Dembélé Kletigui Casimir, Cissé Bakary, Kouriba Bourèma, Simard Gilles, Mirebeau-Prunier Delphine, Chao de la Barca Juan Manuel, Ouzzif Zahra, Reynier Pascal
Faculty of Medicine and Pharmacy, Mohammed V University of Rabat, Rabat, Morocco.
Biochemistry, Metabolic and Molecular Unit, Faculty of Medicine and Pharmacy of Rabat, Rabat, Morocco.
Sci Rep. 2025 Aug 12;15(1):29603. doi: 10.1038/s41598-025-13475-5.
In this study, we conducted a targeted quantitative metabolomic analysis of 630 metabolites in the plasma of 78 West African patients at the time of breast cancer diagnosis and prior to any treatment. Most of these patients were at an advanced stage of the disease. The data were compared with those of 79 healthy controls using a combination of several machine learning approaches and statistical analyses. The predictive models obtained with the machine learning algorithms were comparable, with the best AUC of 0.878 obtained with ridge logistic regression using Boruta feature selection. The most consistently identified discriminating metabolites across univariate analyses with Benjamini-Hochberg correction, OPLS-DA analyses, and the best machine learning approach were thirteen, out of a total of 63 discriminating metabolites identified cumulatively by the three approaches. This signature highlights several key biological processes, including oxidative stress, disrupted neurotransmitter profiles, altered nitric oxide and xanthine oxidase metabolism, and impaired energy metabolism. The involvement of new metabolites significantly deregulated in breast cancer, such as asymmetric dimethylarginine and hexosylceramides, have also been identified. The identified metabolomic signature provides a comprehensive and global view of the blood biochemical phenotype associated with advanced breast cancer at the time of diagnosis.
在本研究中,我们对78名西非乳腺癌患者在确诊时且未接受任何治疗前的血浆中的630种代谢物进行了靶向定量代谢组学分析。这些患者大多处于疾病晚期。我们使用多种机器学习方法和统计分析相结合的方式,将这些数据与79名健康对照者的数据进行了比较。通过机器学习算法获得的预测模型具有可比性,使用Boruta特征选择的岭逻辑回归获得的最佳AUC为0.878。在采用Benjamini-Hochberg校正的单变量分析、OPLS-DA分析以及最佳机器学习方法中,最一致鉴定出的具有鉴别作用的代谢物共有13种,这是三种方法累计鉴定出的63种具有鉴别作用的代谢物中的一部分。该特征突出了几个关键的生物学过程,包括氧化应激、神经递质谱紊乱、一氧化氮和黄嘌呤氧化酶代谢改变以及能量代谢受损。我们还发现了在乳腺癌中显著失调的新代谢物,如不对称二甲基精氨酸和己糖神经酰胺。所鉴定出的代谢组学特征提供了与晚期乳腺癌诊断时相关的血液生化表型的全面整体视图。