• 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

FBXO38 驱动 PD-1 降解。

FBXO38 Drives PD-1 to Destruction.

机构信息

Department of Microbiology, The University of Chicago, Chicago, IL 60637, USA.

Department of Microbiology, The University of Chicago, Chicago, IL 60637, USA.

出版信息

Trends Immunol. 2019 Feb;40(2):81-83. doi: 10.1016/j.it.2018.12.005. Epub 2019 Jan 1.

DOI:10.1016/j.it.2018.12.005
PMID:30609969
Abstract

Aberrant expression of T cell-resident programmed cell death protein-1 (PD-1) is known to promote tumor progression. A recent study (Nature 2018;564:130-135) has now identified the E3 ubiquitin ligase FBXO38 as a crucial regulator of PD-1 protein turnover in T cells, providing a novel mechanism for potential use in cancer immunotherapy.

摘要

已知 T 细胞驻留程序性细胞死亡蛋白-1(PD-1)的异常表达可促进肿瘤进展。最近的一项研究(《自然》2018 年;564:130-135)现已确定 E3 泛素连接酶 FBXO38 是 T 细胞中 PD-1 蛋白降解的关键调节因子,为癌症免疫治疗的潜在应用提供了新的机制。

相似文献

1
FBXO38 Drives PD-1 to Destruction.FBXO38 驱动 PD-1 降解。
Trends Immunol. 2019 Feb;40(2):81-83. doi: 10.1016/j.it.2018.12.005. Epub 2019 Jan 1.
2
FBXO38 mediates PD-1 ubiquitination and regulates anti-tumour immunity of T cells.FBXO38 介导 PD-1 泛素化并调节 T 细胞的抗肿瘤免疫。
Nature. 2018 Dec;564(7734):130-135. doi: 10.1038/s41586-018-0756-0. Epub 2018 Nov 28.
3
UFL1 ablation in T cells suppresses PD-1 UFMylation to enhance anti-tumor immunity.T细胞中UFL1的缺失抑制PD-1的UFMylation以增强抗肿瘤免疫。
Mol Cell. 2024 Mar 21;84(6):1120-1138.e8. doi: 10.1016/j.molcel.2024.01.024. Epub 2024 Feb 19.
4
T-cell infiltration and clonality correlate with programmed cell death protein 1 and programmed death-ligand 1 expression in patients with soft tissue sarcomas.T细胞浸润和克隆性与软组织肉瘤患者程序性细胞死亡蛋白1和程序性死亡配体1的表达相关。
Cancer. 2017 Sep 1;123(17):3291-3304. doi: 10.1002/cncr.30726. Epub 2017 May 2.
5
Potential biomarker for checkpoint blockade immunotherapy and treatment strategy.用于检查点阻断免疫疗法的潜在生物标志物及治疗策略。
Tumour Biol. 2016 Apr;37(4):4251-61. doi: 10.1007/s13277-016-4812-9. Epub 2016 Jan 16.
6
Phosphatidylserine-targeting antibodies augment the anti-tumorigenic activity of anti-PD-1 therapy by enhancing immune activation and downregulating pro-oncogenic factors induced by T-cell checkpoint inhibition in murine triple-negative breast cancers.靶向磷脂酰丝氨酸的抗体通过增强免疫激活和下调小鼠三阴性乳腺癌中由T细胞检查点抑制诱导的促癌因子,增强抗PD-1疗法的抗肿瘤活性。
Breast Cancer Res. 2016 May 11;18(1):50. doi: 10.1186/s13058-016-0708-2.
7
Landscape of PD-1/PD-L1 Regulation and Targeted Immunotherapy.PD-1/PD-L1调节与靶向免疫治疗的全景
Chin Med Sci J. 2018 Sep 20;33(3):174-182. doi: 10.24920/21804.
8
Programmed cell death 1-directed immunotherapy for enhancing T-cell function.程序性细胞死亡蛋白1导向的免疫疗法以增强T细胞功能。
Cold Spring Harb Symp Quant Biol. 2013;78:239-47. doi: 10.1101/sqb.2013.78.019869.
9
The PD-1, PD-L1 expression and CD3+ T cell infiltration in relation to outcome in advanced gastric signet-ring cell carcinoma, representing a potential biomarker for immunotherapy.PD-1、PD-L1表达及CD3+ T细胞浸润与晚期胃印戒细胞癌预后的关系,是免疫治疗的潜在生物标志物。
Oncotarget. 2017 Jun 13;8(24):38850-38862. doi: 10.18632/oncotarget.16407.
10
The Roles of microRNAs in Regulating the Expression of PD-1/PD-L1 Immune Checkpoint.microRNAs 在调控 PD-1/PD-L1 免疫检查点表达中的作用
Int J Mol Sci. 2017 Nov 27;18(12):2540. doi: 10.3390/ijms18122540.

引用本文的文献

1
Mitophagy: A Potential Therapeutic Target for Tuberculosis Immunotherapy.线粒体自噬:结核病免疫治疗的潜在治疗靶点。
Immunotargets Ther. 2025 Jul 22;14:773-786. doi: 10.2147/ITT.S518628. eCollection 2025.
2
Targeting PD-1 post-translational modifications for improving cancer immunotherapy.靶向程序性死亡受体1(PD-1)的翻译后修饰以改善癌症免疫治疗
Cell Insight. 2025 Apr 10;4(3):100248. doi: 10.1016/j.cellin.2025.100248. eCollection 2025 Jun.
3
Ubiquitination of Immune System and Cancer Therapy.免疫系统的泛素化与癌症治疗。
Adv Exp Med Biol. 2024;1466:35-45. doi: 10.1007/978-981-97-7288-9_3.
4
The ubiquitin-proteasome system in the tumor immune microenvironment: a key force in combination therapy.肿瘤免疫微环境中的泛素-蛋白酶体系统:联合治疗的关键力量。
Front Immunol. 2024 Sep 9;15:1436174. doi: 10.3389/fimmu.2024.1436174. eCollection 2024.
5
Strategic advancement of E3 ubiquitin ligase in the management of hepatocellular carcinoma.E3 泛素连接酶在肝细胞癌治疗中的策略性推进。
Med Oncol. 2024 Jun 18;41(7):178. doi: 10.1007/s12032-024-02411-8.
6
CRISPR screening identifies the deubiquitylase ATXN3 as a PD-L1-positive regulator for tumor immune evasion.CRISPR 筛选鉴定去泛素化酶 ATXN3 为 PD-L1 阳性肿瘤免疫逃逸的调节因子。
J Clin Invest. 2023 Dec 1;133(23):e167728. doi: 10.1172/JCI167728.
7
Cognitive Skills and DNA Methylation Are Correlating in Healthy and Novice College Students Practicing Preksha Dhyāna Meditation.在健康的新手大学生中,认知技能与DNA甲基化在练习内观禅修时存在关联。
Brain Sci. 2023 Aug 17;13(8):1214. doi: 10.3390/brainsci13081214.
8
Application and Effectiveness of Chinese Medicine in Regulating Immune Checkpoint Pathways.中药调节免疫检查点通路的应用与效果。
Chin J Integr Med. 2023 Nov;29(11):1045-1056. doi: 10.1007/s11655-023-3743-8. Epub 2023 Aug 15.
9
Exploiting E3 ubiquitin ligases to reeducate the tumor microenvironment for cancer therapy.利用E3泛素连接酶重塑肿瘤微环境以进行癌症治疗。
Exp Hematol Oncol. 2023 Mar 30;12(1):34. doi: 10.1186/s40164-023-00394-2.
10
Lysosomes in T Cell Immunity and Aging.T细胞免疫与衰老中的溶酶体
Front Aging. 2021 Dec 9;2:809539. doi: 10.3389/fragi.2021.809539. eCollection 2021.