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血清核磁共振代谢组学用于鉴别血液系统恶性肿瘤。

Serum NMR metabolomics to differentiate haematologic malignancies.

作者信息

Wojtowicz Wojciech, Chachaj Angelika, Olczak Andrzej, Ząbek Adam, Piątkowska Elżbieta, Rybka Justyna, Butrym Aleksandra, Biedroń Monika, Mazur Grzegorz, Wróbel Tomasz, Szuba Andrzej, Młynarz Piotr

机构信息

Wroclaw University of Technology, Department of Bioorganic Chemistry, Wroclaw, Poland.

Wroclaw Medical University, Department of Angiology, Wroclaw, Poland.

出版信息

Oncotarget. 2018 May 11;9(36):24414-24427. doi: 10.18632/oncotarget.25311.

Abstract

Haematological malignancies are a frequently diagnosed group of neoplasms and a significant cause of cancer deaths. The successful treatment of these diseases relies on early and accurate detection. Specific small molecular compounds released by malignant cells and the simultaneous response by the organism towards the pathological state may serve as diagnostic/prognostic biomarkers or as a tool with relevance for cancer therapy management. To identify the most important metabolites required for differentiation, an H NMR metabolomics approach was applied to selected haematological malignancies. This study utilized 116 methanol serum extract samples from AML (n= 38), nHL (n= 26), CLL (n= 21) and HC (n= 31). Multivariate and univariate data analyses were performed to identify the most abundant changes among the studied groups. Complex and detailed VIP-PLS-DA models were calculated to highlight possible changes in terms of biochemical pathways and discrimination ability. Chemometric model prediction properties were validated by receiver operating characteristic (ROC) curves and statistical analysis. Two sets of eight important metabolites in HC/AML/CLL/nHL comparisons and five in AML/CLL/nHL comparisons were selected to form complex models to represent the most significant changes that occurred.

摘要

血液系统恶性肿瘤是一类经常被诊断出的肿瘤,也是癌症死亡的重要原因。这些疾病的成功治疗依赖于早期准确的检测。恶性细胞释放的特定小分子化合物以及机体对病理状态的同步反应可作为诊断/预后生物标志物,或作为与癌症治疗管理相关的工具。为了确定分化所需的最重要代谢物,采用了核磁共振氢谱代谢组学方法对选定的血液系统恶性肿瘤进行研究。本研究使用了来自急性髓系白血病(AML,n = 38)、非霍奇金淋巴瘤(nHL,n = 26)、慢性淋巴细胞白血病(CLL,n = 21)和健康对照(HC,n = 31)的116份甲醇血清提取物样本。进行了多变量和单变量数据分析,以确定研究组之间最显著的变化。计算了复杂而详细的VIP-PLS-DA模型,以突出生物化学途径和鉴别能力方面的可能变化。通过受试者工作特征(ROC)曲线和统计分析对化学计量模型预测特性进行了验证。在HC/AML/CLL/nHL比较中选择了两组共8种重要代谢物,在AML/CLL/nHL比较中选择了5种,以形成复杂模型来代表所发生的最显著变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/078d/5966245/46da7789c701/oncotarget-09-24414-g001.jpg

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