• 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
The requirement for immune infiltration and organization in the tumor microenvironment for successful immunotherapy in prostate cancer.前列腺癌免疫治疗中肿瘤微环境对免疫浸润和组织的要求。
Urol Oncol. 2019 Aug;37(8):543-555. doi: 10.1016/j.urolonc.2018.10.011. Epub 2018 Nov 13.
2
Advances in and prospects of immunotherapy for prostate cancer.前列腺癌免疫治疗的进展与展望。
Cancer Lett. 2024 Oct 1;601:217155. doi: 10.1016/j.canlet.2024.217155. Epub 2024 Aug 8.
3
Moving toward improved immune checkpoint immunotherapy for advanced prostate cancer.推进改善晚期前列腺癌的免疫检查点免疫治疗。
Int J Urol. 2024 Apr;31(4):307-324. doi: 10.1111/iju.15378. Epub 2024 Jan 2.
4
Single-Cell Analysis Reveals EP4 as a Target for Restoring T-Cell Infiltration and Sensitizing Prostate Cancer to Immunotherapy.单细胞分析揭示 EP4 是恢复 T 细胞浸润和使前列腺癌对免疫治疗敏感的靶点。
Clin Cancer Res. 2022 Feb 1;28(3):552-567. doi: 10.1158/1078-0432.CCR-21-0299. Epub 2021 Nov 5.
5
Utilizing precision medicine to modulate the prostate tumor microenvironment and enhance immunotherapy.利用精准医学调节前列腺肿瘤微环境,增强免疫治疗。
Urol Oncol. 2019 Aug;37(8):535-542. doi: 10.1016/j.urolonc.2018.11.009. Epub 2018 Nov 29.
6
How to turn up the heat on the cold immune microenvironment of metastatic prostate cancer.如何提高转移性前列腺癌的冷免疫微环境的温度。
Prostate Cancer Prostatic Dis. 2021 Sep;24(3):697-717. doi: 10.1038/s41391-021-00340-5. Epub 2021 Apr 5.
7
Immunological Complexity of the Prostate Cancer Microenvironment Influences the Response to Immunotherapy.前列腺癌微环境的免疫复杂性影响免疫治疗的反应。
Adv Exp Med Biol. 2019;1210:121-147. doi: 10.1007/978-3-030-32656-2_7.
8
Beyond immune checkpoint blockade: new approaches to targeting host-tumor interactions in prostate cancer: report from the 2014 Coffey-Holden prostate cancer academy meeting.超越免疫检查点阻断:前列腺癌中靶向宿主 - 肿瘤相互作用的新方法:2014年科菲 - 霍尔登前列腺癌学会会议报告
Prostate. 2015 Mar 1;75(4):337-47. doi: 10.1002/pros.22920. Epub 2014 Oct 30.
9
Docetaxel remodels prostate cancer immune microenvironment and enhances checkpoint inhibitor-based immunotherapy.多西他赛重塑前列腺癌免疫微环境并增强基于检查点抑制剂的免疫治疗。
Theranostics. 2022 Jun 27;12(11):4965-4979. doi: 10.7150/thno.73152. eCollection 2022.
10
The Tumor Immune Contexture of Prostate Cancer.前列腺癌的肿瘤免疫微环境。
Front Immunol. 2019 Mar 28;10:603. doi: 10.3389/fimmu.2019.00603. eCollection 2019.

引用本文的文献

1
Prostate cancer cell-derived exosomes inhibit macrophage phagocytosis through EIF3B-mediated exosomal sorting of miR-100-5p.前列腺癌细胞衍生的外泌体通过EIF3B介导的miR-100-5p外泌体分选抑制巨噬细胞吞噬作用。
Sci Rep. 2025 Jul 18;15(1):26138. doi: 10.1038/s41598-025-11799-w.
2
Integrated proteogenomic characterization of localized prostate cancer identifies biological insights and subtype-specific therapeutic strategies.局限性前列腺癌的综合蛋白质基因组特征分析揭示生物学见解和亚型特异性治疗策略。
Nat Commun. 2025 Apr 3;16(1):3189. doi: 10.1038/s41467-025-58569-w.
3
CD8 T cell-derived Fgl2 regulates immunity in a cell-autonomous manner via ligation of FcγRIIB.CD8 T 细胞衍生的 Fgl2 通过与 FcγRIIB 的结合以细胞自主的方式调节免疫。
Nat Commun. 2024 Jun 20;15(1):5280. doi: 10.1038/s41467-024-49475-8.
4
Pan-PI3K inhibition with copanlisib overcomes Treg- and M2-TAM-mediated immune suppression and promotes anti-tumor immune responses.帕纳潘利斯布抑制全 PI3K 克服 Treg 和 M2-TAM 介导的免疫抑制并促进抗肿瘤免疫反应。
Clin Exp Med. 2023 Dec;23(8):5445-5461. doi: 10.1007/s10238-023-01227-6. Epub 2023 Nov 8.
5
High expression of centromere protein A and its molecular mechanism and clinical significance in prostate cancer: A study based on data mining and immunohistochemistry.中心体蛋白 A 在前列腺癌中的高表达及其分子机制和临床意义:基于数据挖掘和免疫组织化学的研究。
IET Syst Biol. 2023 Oct;17(5):245-258. doi: 10.1049/syb2.12073. Epub 2023 Jul 24.
6
Reversal of Lactate and PD-1-mediated Macrophage Immunosuppression Controls Growth of PTEN/p53-deficient Prostate Cancer.逆转乳酸和 PD-1 介导的巨噬细胞免疫抑制控制 PTEN/p53 缺陷型前列腺癌的生长。
Clin Cancer Res. 2023 May 15;29(10):1952-1968. doi: 10.1158/1078-0432.CCR-22-3350.
7
Identification of Novel Diagnostic Biomarkers in Prostate Adenocarcinoma Based on the Stromal-Immune Score and Analysis of the WGCNA and ceRNA Network.基于基质-免疫评分和 WGCNA 及 ceRNA 网络分析鉴定前列腺腺癌中的新型诊断生物标志物。
Dis Markers. 2022 Jan 15;2022:1909196. doi: 10.1155/2022/1909196. eCollection 2022.
8
Methylation Pattern Mediated by mA Regulator and Tumor Microenvironment Invasion in Lung Adenocarcinoma.mA 调节剂介导的甲基化模式与肺腺癌肿瘤微环境浸润。
Oxid Med Cell Longev. 2022 Jan 5;2022:2930310. doi: 10.1155/2022/2930310. eCollection 2022.
9
Overcoming resistance to immune checkpoint therapy in PTEN-null prostate cancer by intermittent anti-PI3Kα/β/δ treatment.通过间歇性抗 PI3Kα/β/δ 治疗克服 PTEN 缺失型前列腺癌对免疫检查点治疗的耐药性。
Nat Commun. 2022 Jan 10;13(1):182. doi: 10.1038/s41467-021-27833-0.
10
CHALLENGES IN MANIPULATING IMMUNE SYSTEM TO TREAT PROSTATE CANCER.操纵免疫系统治疗前列腺癌所面临的挑战。
Acta Clin Croat. 2019 Nov;58(Suppl 2):76-81. doi: 10.20471/acc.2019.58.s2.13.

本文引用的文献

1
Phase III Trial of PROSTVAC in Asymptomatic or Minimally Symptomatic Metastatic Castration-Resistant Prostate Cancer.无症状或轻度症状转移性去势抵抗性前列腺癌的 PROSTVAC III 期临床试验。
J Clin Oncol. 2019 May 1;37(13):1051-1061. doi: 10.1200/JCO.18.02031. Epub 2019 Feb 28.
2
Pembrolizumab for advanced prostate adenocarcinoma: findings of the KEYNOTE-028 study.帕博利珠单抗治疗晚期前列腺腺癌:KEYNOTE-028 研究结果。
Ann Oncol. 2018 Aug 1;29(8):1807-1813. doi: 10.1093/annonc/mdy232.
3
IL-23 secreted by myeloid cells drives castration-resistant prostate cancer.髓细胞分泌的白细胞介素-23 驱动去势抵抗性前列腺癌。
Nature. 2018 Jul;559(7714):363-369. doi: 10.1038/s41586-018-0266-0. Epub 2018 Jun 27.
4
Macrophages impede CD8 T cells from reaching tumor cells and limit the efficacy of anti-PD-1 treatment.巨噬细胞阻碍 CD8 T 细胞到达肿瘤细胞,并限制抗 PD-1 治疗的效果。
Proc Natl Acad Sci U S A. 2018 Apr 24;115(17):E4041-E4050. doi: 10.1073/pnas.1720948115. Epub 2018 Apr 9.
5
Comprehensive Evaluation of Programmed Death-Ligand 1 Expression in Primary and Metastatic Prostate Cancer.前列腺癌原发灶和转移灶中程序性死亡配体 1 表达的综合评估。
Am J Pathol. 2018 Jun;188(6):1478-1485. doi: 10.1016/j.ajpath.2018.02.014. Epub 2018 Mar 22.
6
Blocking PD-1/PD-L1 in Genitourinary Malignancies: To Immunity and Beyond.阻断泌尿生殖系统恶性肿瘤中的PD-1/PD-L1:通向免疫及更远的领域
Cancer J. 2018 Jan/Feb;24(1):20-30. doi: 10.1097/PPO.0000000000000302.
7
Durable Clinical Benefit With Nivolumab Plus Ipilimumab in DNA Mismatch Repair-Deficient/Microsatellite Instability-High Metastatic Colorectal Cancer.纳武利尤单抗联合伊匹单抗治疗错配修复缺陷/微卫星高度不稳定转移性结直肠癌的持久临床获益。
J Clin Oncol. 2018 Mar 10;36(8):773-779. doi: 10.1200/JCO.2017.76.9901. Epub 2018 Jan 20.
8
High response rate to PD-1 blockade in desmoplastic melanomas.PD-1 阻断在促结缔组织增生性黑色素瘤中具有高应答率。
Nature. 2018 Jan 18;553(7688):347-350. doi: 10.1038/nature25187. Epub 2018 Jan 10.
9
Germinal Centers Determine the Prognostic Relevance of Tertiary Lymphoid Structures and Are Impaired by Corticosteroids in Lung Squamous Cell Carcinoma.生发中心决定肺鳞癌中三级淋巴结构的预后相关性,并被皮质类固醇所抑制。
Cancer Res. 2018 Mar 1;78(5):1308-1320. doi: 10.1158/0008-5472.CAN-17-1987. Epub 2017 Dec 26.
10
Checkpoint and PARP inhibitors, for whom and when.检查点抑制剂和PARP抑制剂:适用于谁以及何时使用。
Oncotarget. 2017 Sep 12;8(56):95036-95037. doi: 10.18632/oncotarget.20852. eCollection 2017 Nov 10.

前列腺癌免疫治疗中肿瘤微环境对免疫浸润和组织的要求。

The requirement for immune infiltration and organization in the tumor microenvironment for successful immunotherapy in prostate cancer.

机构信息

Department of Urology, Emory University, Atlanta, GA.

Department of Urology, Emory University, Atlanta, GA; Department of Microbiology and Immunology, Emory University, Atlanta, GA.

出版信息

Urol Oncol. 2019 Aug;37(8):543-555. doi: 10.1016/j.urolonc.2018.10.011. Epub 2018 Nov 13.

DOI:10.1016/j.urolonc.2018.10.011
PMID:30446449
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6513714/
Abstract

Immunotherapy-particularly immune checkpoint blockade-has seen great success in many tumor types. However, checkpoint-based therapies have not demonstrated high levels of success in prostate cancer, and there is much to be learned from both the successes and failures of these treatments. Here we review the evidence that composition of infiltrating immune cells in the tumor microenvironment is fundamental to the response to immunotherapy. Additionally, we discuss the emerging idea that the organization of these immune cells may also be crucial to this response. In prostate cancer, the composition and organization of the tumor immune microenvironment are preeminent topics of discussion and areas of important future investigation.

摘要

免疫疗法——尤其是免疫检查点阻断——在许多肿瘤类型中取得了巨大成功。然而,基于检查点的疗法在前列腺癌中并未显示出很高的成功率,因此从这些治疗的成功和失败中可以吸取很多经验教训。在这里,我们回顾了肿瘤微环境中浸润免疫细胞的组成对于免疫治疗反应至关重要的证据。此外,我们还讨论了一个新的观点,即这些免疫细胞的组织也可能对这种反应至关重要。在前列腺癌中,肿瘤免疫微环境的组成和组织是讨论的首要主题,也是未来重要的研究领域。