• 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

CD69 和 SBK1 可作为预测肺癌和黑色素瘤对 PD-1/PD-L1 阻断癌症免疫治疗反应的潜在标志物。

CD69 and SBK1 as potential predictors of responses to PD-1/PD-L1 blockade cancer immunotherapy in lung cancer and melanoma.

机构信息

Department of Otolaryngology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

Otorhinolaryngology Institute, Sun Yat-sen University, Guangzhou, China.

出版信息

Front Immunol. 2022 Aug 15;13:952059. doi: 10.3389/fimmu.2022.952059. eCollection 2022.

DOI:10.3389/fimmu.2022.952059
PMID:36045683
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9421049/
Abstract

BACKGROUND

PD-1/PD-L1 blockade is a promising immunotherapeutic strategy with the potential to improve the outcomes of various cancers. However, there is a critically unmet need for effective biomarkers of response to PD-1/PD-L1 blockade.

MATERIALS AND METHODS

Potential biomarkers of response to PD-1/PD-L1 blockade were obtained from the Cancer Treatment Response gene signature Database (CTR-DB). A comprehensive pan-cancer analysis was done on The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) datasets. Correlations between gene expression and infiltration by immune cells were assessed using TIMER, EPIC, MCPcounter, xCell, CIBERSORT, and quanTIseq. Immunophenoscore (IPS) was used to assess the potential application of the biomarkers to all TCGA tumors.

RESULTS

Analysis of CTR-DB data identified and as potential biomarkers of response to PD-1/PD-L1 blockade. Correlation analysis revealed that in various TCGA cancer datasets, expression level correlated positively with most immune checkpoints and tumor-infiltrating immune cells, while expression level correlated negatively with infiltrating immune cells. IPS analysis demonstrated the ability of and to predict PD-1/PD-L1 blockade responses in various cancers.

CONCLUSION

and are potential predictors of response to cancer immunotherapy using PD-1/PD-L1 blockade. These biomarkers may guide treatment decisions, leading to precise treatment and minimizing the waste of medical resources.

摘要

背景

PD-1/PD-L1 阻断是一种很有前途的免疫治疗策略,有可能改善各种癌症的预后。然而,人们迫切需要有效的 PD-1/PD-L1 阻断反应生物标志物。

材料与方法

从癌症治疗反应基因特征数据库(CTR-DB)中获得 PD-1/PD-L1 阻断反应的潜在生物标志物。在癌症基因组图谱(TCGA)和基因型组织表达(GTEx)数据集上进行了全面的泛癌分析。使用 TIMER、EPIC、MCPcounter、xCell、CIBERSORT 和 quanTIseq 评估基因表达与免疫细胞浸润之间的相关性。免疫表型评分(IPS)用于评估这些生物标志物对所有 TCGA 肿瘤的潜在应用。

结果

CTR-DB 数据分析确定 和 是 PD-1/PD-L1 阻断反应的潜在生物标志物。相关性分析显示,在各种 TCGA 癌症数据集中, 表达水平与大多数免疫检查点和肿瘤浸润免疫细胞呈正相关,而 表达水平与浸润免疫细胞呈负相关。IPS 分析表明 和 能够预测各种癌症中 PD-1/PD-L1 阻断反应。

结论

和 是 PD-1/PD-L1 阻断免疫治疗反应的潜在预测因子。这些生物标志物可以指导治疗决策,实现精准治疗,最大限度地减少医疗资源的浪费。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/5488b1e61b68/fimmu-13-952059-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/30128be13bd2/fimmu-13-952059-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/c0389eb43564/fimmu-13-952059-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/061d57b7e643/fimmu-13-952059-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/2c2bac1315a4/fimmu-13-952059-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/36347f1edb20/fimmu-13-952059-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/398da52bbc1a/fimmu-13-952059-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/5488b1e61b68/fimmu-13-952059-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/30128be13bd2/fimmu-13-952059-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/c0389eb43564/fimmu-13-952059-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/061d57b7e643/fimmu-13-952059-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/2c2bac1315a4/fimmu-13-952059-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/36347f1edb20/fimmu-13-952059-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/398da52bbc1a/fimmu-13-952059-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed10/9421049/5488b1e61b68/fimmu-13-952059-g007.jpg

相似文献

1
CD69 and SBK1 as potential predictors of responses to PD-1/PD-L1 blockade cancer immunotherapy in lung cancer and melanoma.CD69 和 SBK1 可作为预测肺癌和黑色素瘤对 PD-1/PD-L1 阻断癌症免疫治疗反应的潜在标志物。
Front Immunol. 2022 Aug 15;13:952059. doi: 10.3389/fimmu.2022.952059. eCollection 2022.
2
PD-L1 and PD-L2 expression correlated genes in non-small-cell lung cancer.非小细胞肺癌中 PD-L1 和 PD-L2 表达相关基因。
Cancer Commun (Lond). 2019 Jun 3;39(1):30. doi: 10.1186/s40880-019-0376-6.
3
The Next Immune-Checkpoint Inhibitors: PD-1/PD-L1 Blockade in Melanoma.下一代免疫检查点抑制剂:黑色素瘤中的PD-1/PD-L1阻断
Clin Ther. 2015 Apr 1;37(4):764-82. doi: 10.1016/j.clinthera.2015.02.018. Epub 2015 Mar 29.
4
Biomarkers for PD-1/PD-L1 Blockade Therapy in Non-Small-cell Lung Cancer: Is PD-L1 Expression a Good Marker for Patient Selection?非小细胞肺癌中PD-1/PD-L1阻断疗法的生物标志物:PD-L1表达是患者选择的良好标志物吗?
Clin Lung Cancer. 2016 Sep;17(5):350-361. doi: 10.1016/j.cllc.2016.03.011. Epub 2016 Apr 6.
5
A radiomics approach to assess tumour-infiltrating CD8 cells and response to anti-PD-1 or anti-PD-L1 immunotherapy: an imaging biomarker, retrospective multicohort study.一种基于放射组学的方法来评估肿瘤浸润 CD8 细胞与抗 PD-1 或抗 PD-L1 免疫治疗反应的关系:一项影像学生物标志物、回顾性多队列研究。
Lancet Oncol. 2018 Sep;19(9):1180-1191. doi: 10.1016/S1470-2045(18)30413-3. Epub 2018 Aug 14.
6
Multi-Omics Perspective Reveals the Different Patterns of Tumor Immune Microenvironment Based on Programmed Death Ligand 1 (PD-L1) Expression and Predictor of Responses to Immune Checkpoint Blockade across Pan-Cancer.多组学视角揭示基于程序性死亡配体 1(PD-L1)表达的肿瘤免疫微环境的不同模式和免疫检查点阻断反应的预测因子在泛癌中的差异。
Int J Mol Sci. 2021 May 13;22(10):5158. doi: 10.3390/ijms22105158.
7
Association of Survival and Immune-Related Biomarkers With Immunotherapy in Patients With Non-Small Cell Lung Cancer: A Meta-analysis and Individual Patient-Level Analysis.免疫治疗与非小细胞肺癌患者生存及免疫相关生物标志物的相关性:一项荟萃分析和个体患者水平分析。
JAMA Netw Open. 2019 Jul 3;2(7):e196879. doi: 10.1001/jamanetworkopen.2019.6879.
8
Molecular heterogeneity of anti-PD-1/PD-L1 immunotherapy efficacy is correlated with tumor immune microenvironment in East Asian patients with non-small cell lung cancer.抗 PD-1/PD-L1 免疫疗法疗效的分子异质性与东亚非小细胞肺癌患者的肿瘤免疫微环境相关。
Cancer Biol Med. 2020 Aug 15;17(3):768-781. doi: 10.20892/j.issn.2095-3941.2020.0121.
9
Dynamic Changes in PD-L1 Expression and Immune Infiltrates Early During Treatment Predict Response to PD-1 Blockade in Melanoma.治疗早期 PD-L1 表达和免疫浸润的动态变化可预测黑色素瘤对 PD-1 阻断的反应。
Clin Cancer Res. 2017 Sep 1;23(17):5024-5033. doi: 10.1158/1078-0432.CCR-16-0698. Epub 2017 May 16.
10
Potential Predictive Value of and Mutation Status for Response to PD-1 Blockade Immunotherapy in Lung Adenocarcinoma.在肺腺癌中, 与 突变状态对 PD-1 阻断免疫治疗反应的潜在预测价值。
Clin Cancer Res. 2017 Jun 15;23(12):3012-3024. doi: 10.1158/1078-0432.CCR-16-2554. Epub 2016 Dec 30.

引用本文的文献

1
Exploration and validation of the prognostic value of mitophagy and mitochondrial dynamics-related genes in cervical cancer.宫颈癌中线粒体自噬及线粒体动力学相关基因预后价值的探索与验证
Sci Rep. 2025 Jul 10;15(1):24950. doi: 10.1038/s41598-025-09310-6.
2
SBK3 suppresses angiotensin II-induced cardiac hypertrophy by regulating mitochondrial metabolism.SBK3通过调节线粒体代谢抑制血管紧张素II诱导的心肌肥大。
Sci Rep. 2025 Jul 2;15(1):22796. doi: 10.1038/s41598-025-05584-y.
3
The E2F1/SBK1 axis activates the Notch signaling pathway to accelerate the malignant progression of breast cancer.

本文引用的文献

1
The status of tumor mutational burden and immunotherapy.肿瘤突变负荷与免疫治疗的现状。
Nat Cancer. 2022 Jun;3(6):652-656. doi: 10.1038/s43018-022-00382-1.
2
Tumour-infiltrating B cells: immunological mechanisms, clinical impact and therapeutic opportunities.肿瘤浸润 B 细胞:免疫机制、临床影响和治疗机会。
Nat Rev Cancer. 2022 Jul;22(7):414-430. doi: 10.1038/s41568-022-00466-1. Epub 2022 Apr 7.
3
Pembrolizumab versus placebo as adjuvant therapy in completely resected stage IIB or IIC melanoma (KEYNOTE-716): a randomised, double-blind, phase 3 trial.
E2F1/SBK1轴激活Notch信号通路以加速乳腺癌的恶性进展。
Naunyn Schmiedebergs Arch Pharmacol. 2025 May 27. doi: 10.1007/s00210-025-04251-3.
4
Asthma-derived genetic signature predicts lung cancer prognosis: a multi-scale omics investigation.哮喘衍生的基因特征预测肺癌预后:一项多尺度组学研究。
J Thorac Dis. 2025 Mar 31;17(3):1400-1423. doi: 10.21037/jtd-24-1697. Epub 2025 Mar 26.
5
The CLEC3B inhibits cellular proliferation and metastasis of cholangiocarcinoma through Wnt/β-catenin pathway.CLEC3B 通过 Wnt/β-catenin 通路抑制胆管癌的细胞增殖和转移。
PeerJ. 2024 Nov 13;12:e18497. doi: 10.7717/peerj.18497. eCollection 2024.
6
CTR-DB 2.0: an updated cancer clinical transcriptome resource, expanding primary drug resistance and newly adding acquired resistance datasets and enhancing the discovery and validation of predictive biomarkers.CTR-DB 2.0:一个更新的癌症临床转录组资源,扩展了原发性耐药性并新增了获得性耐药性数据集,增强了预测性生物标志物的发现与验证。
Nucleic Acids Res. 2025 Jan 6;53(D1):D1335-D1347. doi: 10.1093/nar/gkae993.
7
Identification of Key Genes Mediated by N6-Methyladenosine Methyltransferase METTL3 in Ischemic Stroke via Bioinformatics Analysis and Experiments.通过生物信息学分析和实验鉴定N6-甲基腺苷甲基转移酶METTL3介导的缺血性中风关键基因
Mol Biotechnol. 2025 Jan;67(1):160-174. doi: 10.1007/s12033-023-00991-w. Epub 2023 Dec 22.
8
In-depth single-cell and bulk-RNA sequencing developed a NETosis-related gene signature affects non-small-cell lung cancer prognosis and tumor microenvironment: results from over 3,000 patients.深度单细胞和批量RNA测序揭示的一种与NETosis相关的基因特征影响非小细胞肺癌的预后和肿瘤微环境:来自3000多名患者的结果
Front Oncol. 2023 Oct 19;13:1282335. doi: 10.3389/fonc.2023.1282335. eCollection 2023.
9
Single-cell mass cytometric analysis of peripheral immunity and multiplex plasma marker profiling of non-small cell lung cancer patients receiving PD-1 targeting immune checkpoint inhibitors in comparison with platinum-based chemotherapy.单细胞质量细胞分析外周免疫和非小细胞肺癌患者接受 PD-1 靶向免疫检查点抑制剂与铂类化疗的多重血浆标志物分析。
Front Immunol. 2023 Oct 13;14:1243233. doi: 10.3389/fimmu.2023.1243233. eCollection 2023.
10
Construction and validation of a novel prognostic model of neutrophil‑related genes signature of lung adenocarcinoma.构建和验证一种新型的肺腺癌中性粒细胞相关基因特征的预后模型。
Sci Rep. 2023 Oct 25;13(1):18226. doi: 10.1038/s41598-023-45289-8.
帕博利珠单抗对比安慰剂作为完全切除的IIB期或IIC期黑色素瘤辅助治疗(KEYNOTE-716):一项随机、双盲、3期试验
Lancet. 2022 Apr 30;399(10336):1718-1729. doi: 10.1016/S0140-6736(22)00562-1. Epub 2022 Apr 1.
4
Src homology 3 domain binding kinase 1 protects against hepatic steatosis and insulin resistance through the Nur77-FGF21 pathway.Src同源3结构域结合激酶1通过Nur77-FGF21途径预防肝脂肪变性和胰岛素抵抗。
Hepatology. 2023 Jan 1;77(1):213-229. doi: 10.1002/hep.32501. Epub 2022 Apr 22.
5
mA Regulator-Mediated Methylation Modification Patterns and Characterisation of Tumour Microenvironment Infiltration in Non-Small Cell Lung Cancer.mA调节因子介导的非小细胞肺癌甲基化修饰模式及肿瘤微环境浸润特征
J Inflamm Res. 2022 Mar 23;15:1969-1989. doi: 10.2147/JIR.S356841. eCollection 2022.
6
Pembrolizumab Alone or With Chemotherapy for Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma in KEYNOTE-048: Subgroup Analysis by Programmed Death Ligand-1 Combined Positive Score.帕博利珠单抗单药或联合化疗治疗复发/转移性头颈部鳞状细胞癌的 KEYNOTE-048 研究:程序性死亡配体-1 联合阳性评分的亚组分析。
J Clin Oncol. 2022 Jul 20;40(21):2321-2332. doi: 10.1200/JCO.21.02198. Epub 2022 Mar 25.
7
Immune Landscape and an RBM38-Associated Immune Prognostic Model with Laboratory Verification in Malignant Melanoma.恶性黑色素瘤的免疫图谱及基于RBM38的免疫预后模型与实验室验证
Cancers (Basel). 2022 Mar 21;14(6):1590. doi: 10.3390/cancers14061590.
8
Circulating Immune Bioenergetic, Metabolic, and Genetic Signatures Predict Melanoma Patients' Response to Anti-PD-1 Immune Checkpoint Blockade.循环免疫生物能量学、代谢和遗传特征可预测黑色素瘤患者对抗 PD-1 免疫检查点阻断的反应。
Clin Cancer Res. 2022 Mar 15;28(6):1192-1202. doi: 10.1158/1078-0432.CCR-21-3114.
9
Challenges and opportunities in the PD1/PDL1 inhibitor clinical trial landscape.PD1/PDL1抑制剂临床试验领域的挑战与机遇
Nat Rev Drug Discov. 2022 Jul;21(7):482-483. doi: 10.1038/d41573-022-00030-4.
10
Intestinal Akkermansia muciniphila predicts clinical response to PD-1 blockade in patients with advanced non-small-cell lung cancer.肠道阿克曼氏菌预测晚期非小细胞肺癌患者对 PD-1 阻断治疗的临床反应。
Nat Med. 2022 Feb;28(2):315-324. doi: 10.1038/s41591-021-01655-5. Epub 2022 Feb 3.