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鉴定新型血浆代谢物谱作为肝细胞癌的诊断生物标志物。

Identification of a novel plasma metabolite panel as diagnostic biomarker for hepatocellular carcinoma.

机构信息

Department of Gastroenterology, The Second Affiliated Hospital of Chongqing Medical University, Chongqing 400010, China.

Department of Infectious Disease, The Second Affiliated Hospital of Chongqing Medical University, Chongqing 400010, China.

出版信息

Clin Chim Acta. 2023 Mar 15;543:117302. doi: 10.1016/j.cca.2023.117302. Epub 2023 Mar 20.

Abstract

BACKGROUND AND AIMS

Metabolic reprogramming is one of the hallmarks of cancer. Hepatocellular carcinoma (HCC) is one of the most lethal malignancy camcer, but the early diagnosis of HCC remains difficult. In this study, we searched for potential plasma metabolite biomarkers of HCC.

METHODS

A total of plasma samples of 104 HCC, 76 cirrhosis and 10 healthy subjects were assessed and validated through Gas chromatography-Mass spectrometry. Receiver-operating characteristic curves (ROC) combined with multivariate statistical analyses were used to assess the diagnostic performance of metabolites and combinations.

RESULTS

10 metabolites in screening cohort were significantly changed in the plasma of HCC patients. Multivariate logistic regression analysis of candidate metabolites in validation cohort showed that N-formylglycine, oxoglutaric acid, citrulline and heptaethylene glycol could distinguish HCC from cirrhosis. The combination of these four metabolites showed a better performance than AFP with the Area Under the Curve (AUC), sensitivity, specificity as 0.940, 84.00%, 97.56%, respectively. In further, the panel of N-formylglycine, heptaethylene glycol and citrulline can more effectively discriminate early stage HCC from cirrhosis than AFP (AUC: 0.835 vs. 0.634). Finally, heptaethylene glycol could significantly inhibit the proliferation, migration and invasion of HCC cells in vitro.

CONCLUSION

The combination of plasma N-formylglycine, oxoglutaric acid, citrulline, and heptaethylene glycol can be an efficient novel diagnostic biomarker for HCC.

摘要

背景与目的

代谢重编程是癌症的标志之一。肝细胞癌(HCC)是最致命的恶性肿瘤之一,但 HCC 的早期诊断仍然很困难。在本研究中,我们寻找了 HCC 的潜在血浆代谢生物标志物。

方法

共评估了 104 例 HCC、76 例肝硬化和 10 例健康受试者的血浆样本,并通过气相色谱-质谱联用进行了验证。使用受试者工作特征曲线(ROC)结合多变量统计分析来评估代谢物及其组合的诊断性能。

结果

筛选队列中的 10 种代谢物在 HCC 患者的血浆中发生了显著变化。验证队列中候选代谢物的多元逻辑回归分析表明,N-甲酰甘氨酸、草酰乙酸、瓜氨酸和七亚乙基二醇可将 HCC 与肝硬化区分开来。这四种代谢物的组合在 AUC、敏感性、特异性方面的表现优于 AFP,分别为 0.940、84.00%、97.56%。此外,N-甲酰甘氨酸、七亚乙基二醇和瓜氨酸联合检测能够更有效地将早期 HCC 与肝硬化区分开来,优于 AFP(AUC:0.835 比 0.634)。最后,七亚乙基二醇在体外可显著抑制 HCC 细胞的增殖、迁移和侵袭。

结论

血浆 N-甲酰甘氨酸、草酰乙酸、瓜氨酸和七亚乙基二醇的组合可以作为 HCC 的有效新型诊断生物标志物。

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