• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于 UHPLC-MS 检测血浆代谢物预测抗 PD-1/PD-L1 抑制剂治疗肝细胞癌的效果。

Predicting effect of anti-PD-1/PD-L1 inhibitors therapy for hepatocellular carcinoma by detecting plasma metabolite based on UHPLC-MS.

机构信息

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun, China.

The Cancer Center, The First Hospital of Jilin University, Changchun, China.

出版信息

Front Immunol. 2024 Apr 18;15:1370771. doi: 10.3389/fimmu.2024.1370771. eCollection 2024.

DOI:10.3389/fimmu.2024.1370771
PMID:38707906
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11067499/
Abstract

INTRODUCTION

Anti-PD-1/PD-L1 inhibitors therapy has become a promising treatment for hepatocellular carcinoma (HCC), while the therapeutic efficacy varies significantly among effects for individual patients are significant difference. Unfortunately, specific predictive biomarkers indicating the degree of benefit for patients and thus guiding the selection of suitable candidates for immune therapy remain elusive.no specific predictive biomarkers are available indicating the degree of benefit for patients and thus screening the preferred population suitable for the immune therapy.

METHODS

Ultra-high-pressure liquid chromatography-mass spectrometry (UHPLC-MS) considered is an important method for analyzing biological samples, since it has the advantages of high rapid, high sensitivity, and high specificity. Ultra-high-pressure liquid chromatography-mass spectrometry (UHPLC-MS) has emerged as a pivotal method for analyzing biological samples due to its inherent advantages of rapidity, sensitivity, and specificity. In this study, potential metabolite biomarkers that can predict the therapeutic effect of HCC patients receiving immune therapy were identified by UHPLC-MS.

RESULTS

A partial least-squares discriminant analysis (PLS-DA) model was established using 14 glycerophospholipid metabolites mentioned above, and good prediction parameters (R2 = 0.823, Q2 = 0.615, prediction accuracy = 0.880 and p < 0.001) were obtained. The relative abundance of glycerophospholipid metabolite ions is closely related to the survival benefit of HCC patients who received immune therapy.

DISCUSSION

This study reveals that glycerophospholipid metabolites play a crucial role in predicting the efficacy of immune therapy for HCC.

摘要

简介

抗 PD-1/PD-L1 抑制剂治疗已成为治疗肝细胞癌 (HCC) 的一种有前途的方法,而其治疗效果在个体患者之间存在显著差异。不幸的是,目前仍缺乏能够指示患者获益程度并指导免疫治疗合适患者选择的特异性预测生物标志物。目前尚无特异性预测生物标志物可指示患者的获益程度,从而筛选适合免疫治疗的首选人群。

方法

超高效液相色谱-质谱联用 (UHPLC-MS) 被认为是分析生物样本的重要方法,因为它具有快速、灵敏、特异性高的优点。超高效液相色谱-质谱联用 (UHPLC-MS) 已成为分析生物样本的重要方法,因为它具有快速、灵敏、特异性高的固有优点。在这项研究中,通过 UHPLC-MS 鉴定了能够预测接受免疫治疗的 HCC 患者治疗效果的潜在代谢物生物标志物。

结果

使用上述 14 种甘油磷脂代谢物建立了偏最小二乘判别分析 (PLS-DA) 模型,获得了良好的预测参数(R2 = 0.823,Q2 = 0.615,预测准确性 = 0.880,p < 0.001)。甘油磷脂代谢物离子的相对丰度与接受免疫治疗的 HCC 患者的生存获益密切相关。

讨论

本研究表明,甘油磷脂代谢物在预测 HCC 患者免疫治疗疗效中起着至关重要的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cda/11067499/daa85be0b3f9/fimmu-15-1370771-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cda/11067499/6ebeeabe4930/fimmu-15-1370771-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cda/11067499/2e8abfb7804b/fimmu-15-1370771-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cda/11067499/75e22e9359fc/fimmu-15-1370771-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cda/11067499/daa85be0b3f9/fimmu-15-1370771-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cda/11067499/6ebeeabe4930/fimmu-15-1370771-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cda/11067499/2e8abfb7804b/fimmu-15-1370771-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cda/11067499/75e22e9359fc/fimmu-15-1370771-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cda/11067499/daa85be0b3f9/fimmu-15-1370771-g004.jpg

相似文献

1
Predicting effect of anti-PD-1/PD-L1 inhibitors therapy for hepatocellular carcinoma by detecting plasma metabolite based on UHPLC-MS.基于 UHPLC-MS 检测血浆代谢物预测抗 PD-1/PD-L1 抑制剂治疗肝细胞癌的效果。
Front Immunol. 2024 Apr 18;15:1370771. doi: 10.3389/fimmu.2024.1370771. eCollection 2024.
2
Viral status, immune microenvironment and immunological response to checkpoint inhibitors in hepatocellular carcinoma.肝癌的病毒状态、免疫微环境和免疫检查点抑制剂的免疫反应。
J Immunother Cancer. 2020 Apr;8(1). doi: 10.1136/jitc-2019-000394.
3
Detection of hepatocellular carcinoma in hepatitis C patients: biomarker discovery by LC-MS.利用 LC-MS 技术检测丙型肝炎患者的肝细胞癌:生物标志物的发现
J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Sep 1;966:154-62. doi: 10.1016/j.jchromb.2014.02.043. Epub 2014 Mar 2.
4
Association of inflammatory biomarkers with clinical outcomes in nivolumab-treated patients with advanced hepatocellular carcinoma.纳武利尤单抗治疗晚期肝细胞癌患者的炎症生物标志物与临床结局的关系。
J Hepatol. 2020 Dec;73(6):1460-1469. doi: 10.1016/j.jhep.2020.07.026. Epub 2020 Jul 22.
5
Case Report: Complete Response of Primary Massive Hepatocellular Carcinoma to Anti-Programmed Death Ligand-1 Antibody Following Progression on Anti-Programmed Death-1 Antibody.病例报告:抗程序性死亡受体-1 抗体治疗后进展,再次应用抗程序性死亡配体-1 抗体后原发性巨大肝细胞癌完全缓解。
Front Immunol. 2021 Aug 24;12:712351. doi: 10.3389/fimmu.2021.712351. eCollection 2021.
6
Phase 2 study of pembrolizumab and circulating biomarkers to predict anticancer response in advanced, unresectable hepatocellular carcinoma.帕博利珠单抗联合循环生物标志物预测不可切除晚期肝细胞癌抗肿瘤反应的 II 期研究。
Cancer. 2019 Oct 15;125(20):3603-3614. doi: 10.1002/cncr.32339. Epub 2019 Jun 28.
7
Programmed cell death protein-1 (PD-1)/programmed death-ligand-1 (PD-L1) axis in hepatocellular carcinoma: prognostic and therapeutic perspectives.肝细胞癌中的程序性细胞死亡蛋白 1(PD-1)/程序性死亡配体 1(PD-L1)轴:预后和治疗展望。
Clin Transl Oncol. 2019 Jun;21(6):702-712. doi: 10.1007/s12094-018-1975-4. Epub 2018 Nov 1.
8
Challenges of combination therapy with immune checkpoint inhibitors for hepatocellular carcinoma.免疫检查点抑制剂联合治疗肝细胞癌的挑战。
J Hepatol. 2020 Feb;72(2):307-319. doi: 10.1016/j.jhep.2019.09.025.
9
Disruption of tumour-associated macrophage trafficking by the osteopontin-induced colony-stimulating factor-1 signalling sensitises hepatocellular carcinoma to anti-PD-L1 blockade.骨桥蛋白诱导集落刺激因子 1 信号破坏肿瘤相关巨噬细胞的迁移,使肝细胞癌对抗 PD-L1 阻断敏感。
Gut. 2019 Sep;68(9):1653-1666. doi: 10.1136/gutjnl-2019-318419. Epub 2019 Mar 22.
10
Pre-treatment serum levels of soluble programmed cell death-ligand 1 predict prognosis in patients with hepatitis B-related hepatocellular carcinoma.治疗前血清可溶性程序性死亡配体 1 水平可预测乙型肝炎相关肝细胞癌患者的预后。
J Cancer Res Clin Oncol. 2019 Feb;145(2):303-312. doi: 10.1007/s00432-018-2758-6. Epub 2018 Sep 28.

本文引用的文献

1
Microbial and metabolic profiles unveil mutualistic microbe-microbe interaction in obesity-related colorectal cancer.微生物和代谢组学揭示了肥胖相关结直肠癌中互利共生的微生物-微生物相互作用。
Cell Rep Med. 2024 Mar 19;5(3):101429. doi: 10.1016/j.xcrm.2024.101429. Epub 2024 Feb 19.
2
Cholesterol-modified prognostic nutritional index (CPNI) as an effective tool for assessing the nutrition status and predicting survival in patients with breast cancer.胆固醇修饰的预后营养指数(CPNI)作为一种有效的评估乳腺癌患者营养状况和预测生存的工具。
BMC Med. 2023 Dec 21;21(1):512. doi: 10.1186/s12916-023-03225-7.
3
Mevalonate improves anti-PD-1/PD-L1 efficacy by stabilizing mRNA.
甲羟戊酸通过稳定信使核糖核酸来提高抗程序性死亡蛋白1/程序性死亡配体1的疗效。
Acta Pharm Sin B. 2023 Jun;13(6):2585-2600. doi: 10.1016/j.apsb.2023.04.002. Epub 2023 Apr 17.
4
Multi-omic Characterization of Pancreatic Ductal Adenocarcinoma Relates CXCR4 mRNA Expression Levels to Potential Clinical Targets.多组学分析胰腺导管腺癌与 CXCR4 mRNA 表达水平相关的潜在临床靶点。
Clin Cancer Res. 2022 Nov 14;28(22):4957-4967. doi: 10.1158/1078-0432.CCR-22-0275.
5
Spatially resolved proteomic profiling identifies tumor cell CD44 as a biomarker associated with sensitivity to PD-1 axis blockade in advanced non-small-cell lung cancer.空间分辨蛋白质组学分析鉴定肿瘤细胞 CD44 为与晚期非小细胞肺癌对 PD-1 轴阻断治疗敏感性相关的生物标志物。
J Immunother Cancer. 2022 Aug;10(8). doi: 10.1136/jitc-2022-004757.
6
Metabolic-Dysregulation-Based iEESI-MS Reveals Potential Biomarkers Associated with Early-Stage and Progressive Colorectal Cancer.基于代谢失调的 iEESI-MS 揭示与早期和进展期结直肠癌相关的潜在生物标志物。
Anal Chem. 2022 Aug 30;94(34):11821-11830. doi: 10.1021/acs.analchem.2c02072. Epub 2022 Aug 17.
7
Targeting Plk1 Sensitizes Pancreatic Cancer to Immune Checkpoint Therapy.靶向 Plk1 可增强胰腺癌对免疫检查点治疗的敏感性。
Cancer Res. 2022 Oct 4;82(19):3532-3548. doi: 10.1158/0008-5472.CAN-22-0018.
8
Untargeted plasma metabolomics for risk prediction of hepatocellular carcinoma: A prospective study in two Chinese cohorts.非靶向血浆代谢组学用于肝细胞癌风险预测:在中国两个队列中的前瞻性研究。
Int J Cancer. 2022 Dec 15;151(12):2144-2154. doi: 10.1002/ijc.34229. Epub 2022 Aug 17.
9
Tumor-targeted interleukin-12 synergizes with entinostat to overcome PD-1/PD-L1 blockade-resistant tumors harboring MHC-I and APM deficiencies.肿瘤靶向白细胞介素-12 与恩替诺特联合使用可克服 MHC-I 和 APM 缺陷的 PD-1/PD-L1 阻断耐药肿瘤。
J Immunother Cancer. 2022 Jun;10(6). doi: 10.1136/jitc-2022-004561.
10
Metabolomic estimation of the diagnosis of hepatocellular carcinoma based on ultrahigh performance liquid chromatography coupled with time-of-flight mass spectrometry.基于超高效液相色谱-飞行时间质谱联用技术的肝细胞癌诊断代谢组学评估
RSC Adv. 2018 Mar 6;8(17):9375-9382. doi: 10.1039/c7ra13616a. eCollection 2018 Feb 28.