• 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

相似文献

1
Serum very long-chain fatty acid-containing lipids predict response to immune checkpoint inhibitors in urological cancers.血清超长链脂肪酸脂质可预测泌尿系统癌症对免疫检查点抑制剂的反应。
Cancer Immunol Immunother. 2019 Dec;68(12):2005-2014. doi: 10.1007/s00262-019-02428-3. Epub 2019 Nov 7.
2
Imaging response assessment of immunotherapy in patients with renal cell and urothelial carcinoma.肾细胞癌和尿路上皮癌患者免疫治疗的影像反应评估
Curr Opin Urol. 2018 Jan;28(1):35-41. doi: 10.1097/MOU.0000000000000463.
3
Biomarker classification, validation, and what to look for in 2017 and beyond.生物标志物的分类、验证以及2017年及以后的关注要点。
BJU Int. 2017 May;119(5):812-814. doi: 10.1111/bju.13790. Epub 2017 Feb 20.
4
Biomarkers for immunotherapy in urological cancers.泌尿系统癌症免疫治疗的生物标志物
Curr Opin Urol. 2018 Jan;28(1):25-28. doi: 10.1097/MOU.0000000000000465.
5
Predictive Biomarkers for Checkpoint Blockade in Urothelial Cancer: A Systematic Review.预测性生物标志物在尿路上皮癌中的免疫检查点阻断:系统评价。
J Urol. 2019 Jul;202(1):49-56. doi: 10.1097/JU.0000000000000136. Epub 2019 Jun 7.
6
Recent advances in immuno-oncology and its application to urological cancers.免疫肿瘤学的最新进展及其在泌尿系统癌症中的应用。
BJU Int. 2016 Oct;118(4):506-14. doi: 10.1111/bju.13518. Epub 2016 Jun 3.
7
Current and Future Applications of Novel Immunotherapies in Urological Oncology: A Critical Review of the Literature.当前和未来新型免疫疗法在泌尿肿瘤学中的应用:文献综述的批判性评价。
Eur Urol Focus. 2018 Apr;4(3):442-454. doi: 10.1016/j.euf.2017.10.001. Epub 2017 Oct 19.
8
[Renaissance of immuno-oncology for urological tumors : Current status].[泌尿肿瘤免疫肿瘤学的复兴:现状]
Urologe A. 2016 May;55(5):621-6. doi: 10.1007/s00120-016-0107-4.
9
The landscape of immunotherapy in metastatic urothelial carcinoma.转移性尿路上皮癌的免疫治疗全景。
Curr Opin Urol. 2019 Nov;29(6):643-648. doi: 10.1097/MOU.0000000000000676.
10
A Systematic Review of Immunotherapy in Urologic Cancer: Evolving Roles for Targeting of CTLA-4, PD-1/PD-L1, and HLA-G.免疫疗法在泌尿系统肿瘤中的系统评价:CTLA-4、PD-1/PD-L1 和 HLA-G 靶向作用的不断演变。
Eur Urol. 2015 Aug;68(2):267-79. doi: 10.1016/j.eururo.2015.02.032. Epub 2015 Mar 29.

引用本文的文献

1
Immunometabolism: The role of gut-derived microbial metabolites in optimising immune response during checkpoint inhibitor therapy.免疫代谢:肠道来源的微生物代谢产物在检查点抑制剂治疗期间优化免疫反应中的作用。
Clin Transl Med. 2025 Sep;15(9):e70472. doi: 10.1002/ctm2.70472.
2
Potential biomarkers develop for predicting the prognosis of patients with esophageal squamous cell carcinoma after optimized chemoradiotherapy using serum metabolomics.利用血清代谢组学开发潜在生物标志物,用于预测食管鳞状细胞癌患者优化放化疗后的预后。
BMC Cancer. 2025 Mar 11;25(1):438. doi: 10.1186/s12885-025-13866-x.
3
Fatty acid metabolism of immune cells: a new target of tumour immunotherapy.免疫细胞的脂肪酸代谢:肿瘤免疫治疗的新靶点。
Cell Death Discov. 2024 Jan 20;10(1):39. doi: 10.1038/s41420-024-01807-9.
4
A transcriptional evaluation of the melanoma and squamous cell carcinoma TIL compartment reveals an unexpected spectrum of exhausted and functional T cells.对黑色素瘤和鳞状细胞癌肿瘤浸润淋巴细胞(TIL)区室的转录评估揭示了意想不到的耗竭型和功能型T细胞谱。
Front Oncol. 2023 Oct 30;13:1200387. doi: 10.3389/fonc.2023.1200387. eCollection 2023.
5
Cutaneous immune-related adverse events to immune checkpoint inhibitors: from underlying immunological mechanisms to multi-omics prediction.免疫检查点抑制剂相关的皮肤免疫不良反应:从潜在的免疫学机制到多组学预测。
Front Immunol. 2023 Jun 22;14:1207544. doi: 10.3389/fimmu.2023.1207544. eCollection 2023.
6
Revisiting mechanisms of resistance to immunotherapies in metastatic clear-cell renal-cell carcinoma.重新审视转移性透明细胞肾细胞癌对免疫疗法的耐药机制。
Cancer Drug Resist. 2023 May 30;6(2):314-326. doi: 10.20517/cdr.2023.09. eCollection 2023.
7
Metabolomic Profiling in Children with Celiac Disease: Beyond the Gluten-Free Diet.儿童乳糜泻的代谢组学分析:超越无麸质饮食。
Nutrients. 2023 Jun 25;15(13):2871. doi: 10.3390/nu15132871.
8
Beggars banquet: Metabolism in the tumor immune microenvironment and cancer therapy.乞丐的盛宴:肿瘤免疫微环境中的代谢与癌症治疗。
Cell Metab. 2023 Jul 11;35(7):1101-1113. doi: 10.1016/j.cmet.2023.06.003. Epub 2023 Jun 29.
9
Targeting T-cell metabolism to boost immune checkpoint inhibitor therapy.靶向 T 细胞代谢以增强免疫检查点抑制剂治疗。
Front Immunol. 2022 Dec 7;13:1046755. doi: 10.3389/fimmu.2022.1046755. eCollection 2022.
10
Renal Cell Carcinoma as a Metabolic Disease: An Update on Main Pathways, Potential Biomarkers, and Therapeutic Targets.肾细胞癌作为一种代谢疾病:主要途径、潜在生物标志物和治疗靶点的最新研究进展。
Int J Mol Sci. 2022 Nov 18;23(22):14360. doi: 10.3390/ijms232214360.

本文引用的文献

1
Lipid Metabolic Pathways Confer the Immunosuppressive Function of Myeloid-Derived Suppressor Cells in Tumor.脂质代谢通路赋予髓源性抑制细胞在肿瘤中的免疫抑制功能。
Front Immunol. 2019 Jun 19;10:1399. doi: 10.3389/fimmu.2019.01399. eCollection 2019.
2
Fatty acids distribution and content in oral squamous cell carcinoma tissue and its adjacent microenvironment.口腔鳞状细胞癌组织及其毗邻微环境中脂肪酸的分布和含量。
PLoS One. 2019 Jun 26;14(6):e0218246. doi: 10.1371/journal.pone.0218246. eCollection 2019.
3
Alteration in lipid composition differentiates breast cancer tissues: a H HRMAS NMR metabolomic study.脂质组成的改变可区分乳腺癌组织:一项 H HRMAS NMR 代谢组学研究。
Metabolomics. 2018 Sep 3;14(9):119. doi: 10.1007/s11306-018-1411-3.
4
Changes in lipids composition and metabolism in colorectal cancer: a review.结直肠癌中脂质组成和代谢的变化:综述。
Lipids Health Dis. 2019 Jan 26;18(1):29. doi: 10.1186/s12944-019-0977-8.
5
Metabolomic study of human tissue and urine in clear cell renal carcinoma by LC-HRMS and PLS-DA.基于 LC-HRMS 和 PLS-DA 的人肾透明细胞癌组织和尿液代谢组学研究。
Anal Bioanal Chem. 2018 Jun;410(16):3859-3869. doi: 10.1007/s00216-018-1059-x. Epub 2018 Apr 16.
6
The Immune Landscape of Cancer.癌症的免疫全景。
Immunity. 2018 Apr 17;48(4):812-830.e14. doi: 10.1016/j.immuni.2018.03.023. Epub 2018 Apr 5.
7
Altered metabolism distinguishes high-risk from stable carotid atherosclerotic plaques.代谢改变可区分高危与稳定颈动脉粥样硬化斑块。
Eur Heart J. 2018 Jun 21;39(24):2301-2310. doi: 10.1093/eurheartj/ehy124.
8
Tumor Mutational Burden and Response Rate to PD-1 Inhibition.肿瘤突变负荷与对PD-1抑制的反应率
N Engl J Med. 2017 Dec 21;377(25):2500-2501. doi: 10.1056/NEJMc1713444.
9
Fatty acid oxidation contributes to IL-1β secretion in M2 macrophages and promotes macrophage-mediated tumor cell migration.脂肪酸氧化有助于 M2 巨噬细胞中 IL-1β 的分泌,并促进巨噬细胞介导的肿瘤细胞迁移。
Mol Immunol. 2018 Feb;94:27-35. doi: 10.1016/j.molimm.2017.12.011. Epub 2017 Dec 15.
10
Progress and challenges of predictive biomarkers of anti PD-1/PD-L1 immunotherapy: A systematic review.抗 PD-1/PD-L1 免疫治疗预测生物标志物的研究进展与挑战:系统综述。
Cancer Lett. 2018 Feb 1;414:166-173. doi: 10.1016/j.canlet.2017.11.014. Epub 2017 Nov 16.

血清超长链脂肪酸脂质可预测泌尿系统癌症对免疫检查点抑制剂的反应。

Serum very long-chain fatty acid-containing lipids predict response to immune checkpoint inhibitors in urological cancers.

机构信息

Department of Medical Oncology, National Center for Tumor Diseases (NCT) Heidelberg, Heidelberg University Hospital, Im Neuenheimer Feld 460, 69120, Heidelberg, Germany.

Liquid Biobank, National Center for Tumor Diseases (NCT) Heidelberg, Heidelberg University Hospital, Heidelberg, Germany.

出版信息

Cancer Immunol Immunother. 2019 Dec;68(12):2005-2014. doi: 10.1007/s00262-019-02428-3. Epub 2019 Nov 7.

DOI:10.1007/s00262-019-02428-3
PMID:31701161
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11028211/
Abstract

Checkpoint inhibitors (CPI) have significantly changed the therapeutic landscape of oncology. We adopted a non-invasive metabolomic approach to understand immunotherapy response and failure in 28 urological cancer patients. In total, 134 metabolites were quantified in patient sera before the first, second, and third CPI doses. Modeling the association between metabolites and CPI response and patient characteristics revealed that one predictive metabolite class  (n = 9/10) were very long-chain fatty acid-containing lipids (VLCFA-containing lipids). The best predictive performance was achieved through a multivariate model, including age and a centroid of VLCFA-containing lipids prior to first immunotherapy (sensitivity: 0.850, specificity: 0.825, ROC: 0.935). We hypothesize that the association of VLCFA-containing lipids with CPI response is based on enhanced peroxisome signaling in T cells, which results in a switch to fatty acid catabolism. Beyond use as a novel predictive non-invasive biomarker, we envision that nutritional supplementation with VLCFA-containing lipids might serve as an immuno sensitizer.

摘要

检查点抑制剂 (CPI) 显著改变了肿瘤学的治疗格局。我们采用非侵入性代谢组学方法来理解 28 例泌尿生殖系统癌症患者的免疫治疗反应和失败。总共在患者血清中定量了 134 种代谢物,这些患者在接受第一、第二和第三次 CPI 剂量之前接受了检测。通过对代谢物与 CPI 反应和患者特征之间的关联进行建模,发现一个具有预测性的代谢物类别(n = 9/10)是含有非常长链脂肪酸的脂质(含 VLCFA 的脂质)。通过包括年龄和免疫治疗前 VLCFA 脂质质心在内的多元模型,可以实现最佳的预测性能(敏感性:0.850,特异性:0.825,ROC:0.935)。我们假设,含 VLCFA 的脂质与 CPI 反应的关联是基于 T 细胞中过氧化物酶体信号的增强,这导致脂肪酸分解代谢的转变。除了用作新型预测性非侵入性生物标志物之外,我们设想含有 VLCFA 的脂质的营养补充可能作为一种免疫敏化剂。