• 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 Vascular Disrupting Agent CA4P Improves the Antitumor Efficacy of CAR-T Cells in Preclinical Models of Solid Human Tumors.血管破坏剂 CA4P 提高了 CAR-T 细胞在实体人肿瘤临床前模型中的抗肿瘤疗效。
Mol Ther. 2020 Jan 8;28(1):75-88. doi: 10.1016/j.ymthe.2019.10.010. Epub 2019 Oct 18.
2
Effective Targeting of TAG72 Peritoneal Ovarian Tumors via Regional Delivery of CAR-Engineered T Cells.通过区域递送 CAR 工程化 T 细胞靶向 TAG72 腹膜卵巢肿瘤。
Front Immunol. 2018 Nov 19;9:2268. doi: 10.3389/fimmu.2018.02268. eCollection 2018.
3
Enhancement of the antitumor effect of HER2-directed CAR-T cells through blocking epithelial-mesenchymal transition in tumor cells.通过阻断肿瘤细胞中的上皮-间充质转化来增强 HER2 靶向 CAR-T 细胞的抗肿瘤作用。
FASEB J. 2020 Aug;34(8):11185-11199. doi: 10.1096/fj.202000080RR. Epub 2020 Jul 9.
4
rhIL-7-hyFc, a long-acting interleukin-7, improves efficacy of CAR-T cell therapy in solid tumors.rhIL-7-hyFc,一种长效白细胞介素-7,可提高 CAR-T 细胞疗法在实体瘤中的疗效。
J Immunother Cancer. 2024 Jul 23;12(7):e008989. doi: 10.1136/jitc-2024-008989.
5
Chimeric cytokine receptor enhancing PSMA-CAR-T cell-mediated prostate cancer regression.嵌合细胞因子受体增强 PSMA-CAR-T 细胞介导的前列腺癌消退。
Cancer Biol Ther. 2020 Jun 2;21(6):570-580. doi: 10.1080/15384047.2020.1739952. Epub 2020 Mar 25.
6
Off-the-shelf Vδ1 gamma delta T cells engineered with glypican-3 (GPC-3)-specific chimeric antigen receptor (CAR) and soluble IL-15 display robust antitumor efficacy against hepatocellular carcinoma.现货即用型 Vδ1 γδ T 细胞经 GPC-3 特异性嵌合抗原受体(CAR)和可溶性 IL-15 修饰后,显示出针对肝细胞癌的强大抗肿瘤疗效。
J Immunother Cancer. 2021 Dec;9(12). doi: 10.1136/jitc-2021-003441.
7
Chimeric Antigen Receptor-modified T Cells Repressed Solid Tumors and Their Relapse in an Established Patient-derived Colon Carcinoma Xenograft Model.嵌合抗原受体修饰的 T 细胞抑制实体瘤及其在建立的患者来源结肠癌细胞异种移植模型中的复发。
J Immunother. 2019 Feb/Mar;42(2):33-42. doi: 10.1097/CJI.0000000000000251.
8
PLAP -CAR T cells mediate high specific cytotoxicity against colon cancer cells.PLAP-CAR T 细胞对结肠癌细胞具有高特异性细胞毒性。
Front Biosci (Landmark Ed). 2020 Jun 1;25(9):1765-1786. doi: 10.2741/4877.
9
Antitumor efficacy of chimeric antigen receptor T cells against EGFRvIII-expressing glioblastoma in C57BL/6 mice.嵌合抗原受体 T 细胞对 C57BL/6 小鼠 EGFRvIII 表达型脑胶质瘤的抗肿瘤疗效。
Biomed Pharmacother. 2019 May;113:108734. doi: 10.1016/j.biopha.2019.108734. Epub 2019 Mar 5.
10
CD27 enhances the killing effect of CAR T cells targeting trophoblast cell surface antigen 2 in the treatment of solid tumors.CD27增强靶向滋养层细胞表面抗原2的嵌合抗原受体T细胞在实体瘤治疗中的杀伤作用。
Cancer Immunol Immunother. 2021 Jul;70(7):2059-2071. doi: 10.1007/s00262-020-02838-8. Epub 2021 Jan 13.

引用本文的文献

1
Expanding Immunotherapy Beyond CAR T Cells: Engineering Diverse Immune Cells to Target Solid Tumors.将免疫疗法扩展至CAR-T细胞之外:改造多种免疫细胞以靶向实体瘤
Cancers (Basel). 2025 Sep 5;17(17):2917. doi: 10.3390/cancers17172917.
2
In vivo CAR-T cell therapy: New breakthroughs for cell-based tumor immunotherapy.体内CAR-T细胞疗法:基于细胞的肿瘤免疫疗法的新突破。
Hum Vaccin Immunother. 2025 Dec;21(1):2558403. doi: 10.1080/21645515.2025.2558403. Epub 2025 Sep 11.
3
Delivery-Graded Programmable Micelles Achieve Enhanced Tumor Starvation through Combined Glutamine Deprivation and Angiogenesis Inhibition.递送分级可编程胶束通过联合谷氨酰胺剥夺和血管生成抑制实现增强的肿瘤饥饿疗法。
Research (Wash D C). 2025 Sep 5;5:0858. doi: 10.34133/research.0858. eCollection 2025.
4
Adoptive cell therapy in colorectal cancer: Advances in chimeric antigen receptor T cells.结直肠癌中的过继性细胞疗法:嵌合抗原受体T细胞的进展
World J Gastrointest Oncol. 2025 Jul 15;17(7):106723. doi: 10.4251/wjgo.v17.i7.106723.
5
Exosomes: a double-edged sword in cancer immunotherapy.外泌体:癌症免疫治疗中的双刃剑。
MedComm (2020). 2025 Feb 17;6(3):e70095. doi: 10.1002/mco2.70095. eCollection 2025 Mar.
6
Advances in CAR T cell therapy: antigen selection, modifications, and current trials for solid tumors.嵌合抗原受体T细胞疗法的进展:抗原选择、修饰及实体瘤的当前试验
Front Immunol. 2025 Jan 6;15:1489827. doi: 10.3389/fimmu.2024.1489827. eCollection 2024.
7
C118P Suppresses Gastric Cancer Growth via Promoting Autophagy-Lysosomal Degradation of RAB1A.C118P通过促进RAB1A的自噬-溶酶体降解来抑制胃癌生长。
Pharmaceutics. 2024 Dec 21;16(12):1620. doi: 10.3390/pharmaceutics16121620.
8
Hybrid model of tumor growth, angiogenesis and immune response yields strategies to improve antiangiogenic therapy.肿瘤生长、血管生成和免疫反应的混合模型产生了改善抗血管生成治疗的策略。
NPJ Biol Phys Mech. 2024;1(1):4. doi: 10.1038/s44341-024-00002-2. Epub 2024 Dec 2.
9
Revolutionizing Cancer Treatment: Unveiling the Power of CAR T-cell Therapy.变革癌症治疗:揭示CAR-T细胞疗法的力量。
Curr Pharm Des. 2025;31(13):1020-1036. doi: 10.2174/0113816128336391241107112957.
10
Oncolytic virus and CAR-T cell therapy in solid tumors.溶瘤病毒与 CAR-T 细胞疗法治疗实体瘤
Front Immunol. 2024 Oct 30;15:1455163. doi: 10.3389/fimmu.2024.1455163. eCollection 2024.

本文引用的文献

1
CAR T Cells for Solid Tumors: New Strategies for Finding, Infiltrating, and Surviving in the Tumor Microenvironment.实体瘤的嵌合抗原受体 T 细胞:在肿瘤微环境中寻找、浸润和存活的新策略。
Front Immunol. 2019 Feb 5;10:128. doi: 10.3389/fimmu.2019.00128. eCollection 2019.
2
LAYN Is a Prognostic Biomarker and Correlated With Immune Infiltrates in Gastric and Colon Cancers.LAYN 是胃癌和结肠癌的预后生物标志物,并与免疫浸润相关。
Front Immunol. 2019 Jan 29;10:6. doi: 10.3389/fimmu.2019.00006. eCollection 2019.
3
Chimeric Antigen Receptor-modified T Cells Repressed Solid Tumors and Their Relapse in an Established Patient-derived Colon Carcinoma Xenograft Model.嵌合抗原受体修饰的 T 细胞抑制实体瘤及其在建立的患者来源结肠癌细胞异种移植模型中的复发。
J Immunother. 2019 Feb/Mar;42(2):33-42. doi: 10.1097/CJI.0000000000000251.
4
Engineered T lymphocytes eliminate lung metastases in models of pancreatic cancer.工程化T淋巴细胞可消除胰腺癌模型中的肺转移。
Oncotarget. 2018 Jan 10;9(17):13694-13705. doi: 10.18632/oncotarget.24122. eCollection 2018 Mar 2.
5
The market for chimeric antigen receptor T cell therapies.嵌合抗原受体T细胞疗法的市场。
Nat Rev Drug Discov. 2018 Mar;17(3):161-162. doi: 10.1038/nrd.2017.266. Epub 2018 Jan 29.
6
Chimeric Antigen Receptors T Cell Therapy in Solid Tumor: Challenges and Clinical Applications.实体瘤中的嵌合抗原受体T细胞疗法:挑战与临床应用
Front Immunol. 2017 Dec 22;8:1850. doi: 10.3389/fimmu.2017.01850. eCollection 2017.
7
Constitutive Signaling from an Engineered IL7 Receptor Promotes Durable Tumor Elimination by Tumor-Redirected T Cells.工程化 IL7 受体的组成性信号转导促进肿瘤导向 T 细胞持久消除肿瘤。
Cancer Discov. 2017 Nov;7(11):1238-1247. doi: 10.1158/2159-8290.CD-17-0538. Epub 2017 Aug 22.
8
Clinical development of CAR T cells-challenges and opportunities in translating innovative treatment concepts.CAR T 细胞的临床开发——转化创新治疗理念的挑战与机遇。
EMBO Mol Med. 2017 Sep;9(9):1183-1197. doi: 10.15252/emmm.201607485.
9
PD-L1 induced by IFN-γ from tumor-associated macrophages via the JAK/STAT3 and PI3K/AKT signaling pathways promoted progression of lung cancer.肿瘤相关巨噬细胞产生的 IFN-γ 通过 JAK/STAT3 和 PI3K/AKT 信号通路诱导的 PD-L1 促进了肺癌的进展。
Int J Clin Oncol. 2017 Dec;22(6):1026-1033. doi: 10.1007/s10147-017-1161-7. Epub 2017 Jul 26.
10
Improving homing in T cell therapy.提高 T 细胞疗法的归巢效率。
Cytokine Growth Factor Rev. 2017 Aug;36:107-116. doi: 10.1016/j.cytogfr.2017.06.009. Epub 2017 Jun 23.

血管破坏剂 CA4P 提高了 CAR-T 细胞在实体人肿瘤临床前模型中的抗肿瘤疗效。

The Vascular Disrupting Agent CA4P Improves the Antitumor Efficacy of CAR-T Cells in Preclinical Models of Solid Human Tumors.

机构信息

Department of Cell Biology and Stem Cell Research Center, School of Basic Medical Sciences, State Key Laboratory of Natural and Biomimetic Drugs, Peking University Health Science Center, Peking University, Beijing 100191, China.

Department of Cell Biology and Stem Cell Research Center, School of Basic Medical Sciences, State Key Laboratory of Natural and Biomimetic Drugs, Peking University Health Science Center, Peking University, Beijing 100191, China.

出版信息

Mol Ther. 2020 Jan 8;28(1):75-88. doi: 10.1016/j.ymthe.2019.10.010. Epub 2019 Oct 18.

DOI:10.1016/j.ymthe.2019.10.010
PMID:31672285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6953963/
Abstract

Chimeric antigen receptor (CAR) T cell therapy remains relatively ineffective against solid tumors due to inadequate infiltration and in vivo expansion of CAR-T cells. Unlike hematological malignancies, solid tumors have vascular barriers that hinder CAR-T cells from reaching the tumor site. Here, we demonstrated that combretastatin A-4 phosphate (CA4P), a vascular disrupting agent (VDA), can significantly improve the infiltration ability of CAR-T cells in solid tumors as evidenced by elevated levels of IFN-γ. Moreover, combined treatment with CA4P and CAR-T cells greatly increased the therapeutic efficiency of the CAR-T cells in subcutaneous ovarian cancer mouse xenograft models and patient-derived xenograft (PDX) models of colon and ovarian carcinoma. Our findings highlight CA4P as an effective antitumor agent candidate for combination with CAR-T cells in clinical applications to treat solid tumors.

摘要

嵌合抗原受体 (CAR) T 细胞疗法对实体瘤的疗效相对较差,这是由于 CAR-T 细胞在体内的浸润和扩增不足所致。与血液恶性肿瘤不同,实体瘤具有血管屏障,阻碍 CAR-T 细胞到达肿瘤部位。在这里,我们证明了 combretastatin A-4 磷酸盐 (CA4P),一种血管破坏剂 (VDA),可以显著提高 CAR-T 细胞在实体瘤中的浸润能力,这一点可以从 IFN-γ水平的升高得到证明。此外,CA4P 与 CAR-T 细胞联合治疗大大提高了 CAR-T 细胞在皮下卵巢癌小鼠异种移植模型和结肠癌和卵巢癌患者来源异种移植 (PDX) 模型中的治疗效率。我们的研究结果强调了 CA4P 作为一种有效的抗肿瘤候选药物,可与 CAR-T 细胞联合应用于临床治疗实体瘤。