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基于磁共振波谱的代谢组学生物标志物用于早期人类肺癌的分型、分期和生存估计。

Magnetic Resonance Spectroscopy-based Metabolomic Biomarkers for Typing, Staging, and Survival Estimation of Early-Stage Human Lung Cancer.

机构信息

Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, 02114, USA.

Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, 02114, USA.

出版信息

Sci Rep. 2019 Jul 16;9(1):10319. doi: 10.1038/s41598-019-46643-5.

Abstract

Low-dose CT has shown promise in detecting early stage lung cancer. However, concerns about the adverse health effects of radiation and high cost prevent its use as a population-wide screening tool. Effective and feasible screening methods to triage suspicious patients to CT are needed. We investigated human lung cancer metabolomics from 93 paired tissue-serum samples with magnetic resonance spectroscopy and identified tissue and serum metabolomic markers that can differentiate cancer types and stages. Most interestingly, we identified serum metabolomic profiles that can predict patient overall survival for all cases (p = 0.0076), and more importantly for Stage I cases alone (n = 58, p = 0.0100), a prediction which is significant for treatment strategies but currently cannot be achieved by any clinical method. Prolonged survival is associated with relative overexpression of glutamine, valine, and glycine, and relative suppression of glutamate and lipids in serum.

摘要

低剂量 CT 已显示出在早期肺癌检测方面的应用前景。然而,由于对辐射的不良健康影响和高成本的担忧,它不能作为一种广泛应用于人群的筛查工具。需要有效的和可行的筛选方法来对疑似患者进行 CT 分诊。我们通过磁共振波谱法对 93 对组织-血清样本进行了人类肺癌代谢组学研究,确定了可以区分癌症类型和阶段的组织和血清代谢标志物。最有趣的是,我们确定了血清代谢组学图谱,这些图谱可以预测所有病例(p=0.0076)的患者总生存率,对于仅 I 期病例(n=58,p=0.0100)的预测更具价值,这对治疗策略具有重要意义,但目前任何临床方法都无法实现。延长的生存与血清中谷氨酰胺、缬氨酸和甘氨酸的相对过表达以及谷氨酸和脂质的相对抑制有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9a8/6635503/c4171be17087/41598_2019_46643_Fig1_HTML.jpg

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