• 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

凋亡蛋白抑制剂拮抗剂揭示了一种新型的、基于免疫反应的 T 细胞淋巴瘤治疗方法。

Antagonism of inhibitors of apoptosis proteins reveals a novel, immune response-based therapeutic approach for T-cell lymphoma.

机构信息

Astex Pharmaceuticals, Cambridge, UK; and.

Astex Pharmaceuticals, Inc., Pleasanton, CA.

出版信息

Blood Adv. 2021 Oct 26;5(20):4003-4016. doi: 10.1182/bloodadvances.2020003955.

DOI:10.1182/bloodadvances.2020003955
PMID:34474469
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8945623/
Abstract

Tolinapant (ASTX660) is a potent, nonpeptidomimetic antagonist of cellular inhibitor of apoptosis proteins 1 and 2 (cIAP1/2) and X-linked IAP, which is currently being evaluated in a phase 2 study in T-cell lymphoma (TCL) patients. Tolinapant has demonstrated evidence of single-agent clinical activity in relapsed/refractory peripheral TCL and cutaneous TCL. To investigate the mechanism of action underlying the single-agent activity observed in the clinic, we have used a comprehensive translational approach integrating in vitro and in vivo models of TCL confirmed by data from human tumor biopsies. Here, we show that tolinapant acts as an efficacious immunomodulatory molecule capable of inducing complete tumor regression in a syngeneic model of TCL exclusively in the presence of an intact immune system. These findings were confirmed in samples from our ongoing clinical study showing that tolinapant treatment can induce changes in gene expression and cytokine profile consistent with immune modulation. Mechanistically, we show that tolinapant can activate both the adaptive and the innate arms of the immune system through the induction of immunogenic forms of cell death. In summary, we describe a novel role for IAP antagonists as immunomodulatory molecules capable of promoting a robust antitumor immune response in TCL.

摘要

托利那泮(ASTX660)是一种有效的、非肽模拟物的细胞凋亡抑制蛋白 1 和 2(cIAP1/2)和 X 连锁凋亡抑制蛋白的拮抗剂,目前正在 T 细胞淋巴瘤(TCL)患者的 2 期研究中进行评估。托利那泮在复发/难治性外周 TCL 和皮肤 TCL 中表现出单药临床活性的证据。为了研究在临床观察到的单药活性的作用机制,我们使用了综合转化方法,整合了经体外和体内 TCL 模型证实的数据,这些模型来自人类肿瘤活检。在这里,我们表明,托利那泮作为一种有效的免疫调节分子,能够在一个完整的免疫系统存在的情况下,在一个 TCL 的同种异体模型中诱导完全的肿瘤消退。这些发现得到了我们正在进行的临床研究中样本的证实,表明托利那泮治疗可以诱导基因表达和细胞因子谱的变化,与免疫调节一致。从机制上讲,我们表明,托利那泮可以通过诱导免疫原性细胞死亡的形式,激活适应性和先天免疫系统。总之,我们描述了一种新型的 IAP 拮抗剂作为免疫调节分子,能够在 TCL 中促进强烈的抗肿瘤免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/4bfeed091045/advancesADV2020003955f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/4c906cbb1ae5/advancesADV2020003955absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/a0f8be090efc/advancesADV2020003955f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/ced052e4fe1d/advancesADV2020003955f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/a2f479b1d997/advancesADV2020003955f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/8c9ee46c78ec/advancesADV2020003955f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/2cbfe3e55915/advancesADV2020003955f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/fb19e70e1dbe/advancesADV2020003955f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/4bfeed091045/advancesADV2020003955f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/4c906cbb1ae5/advancesADV2020003955absf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/a0f8be090efc/advancesADV2020003955f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/ced052e4fe1d/advancesADV2020003955f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/a2f479b1d997/advancesADV2020003955f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/8c9ee46c78ec/advancesADV2020003955f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/2cbfe3e55915/advancesADV2020003955f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/fb19e70e1dbe/advancesADV2020003955f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e52/8945623/4bfeed091045/advancesADV2020003955f7.jpg

相似文献

1
Antagonism of inhibitors of apoptosis proteins reveals a novel, immune response-based therapeutic approach for T-cell lymphoma.凋亡蛋白抑制剂拮抗剂揭示了一种新型的、基于免疫反应的 T 细胞淋巴瘤治疗方法。
Blood Adv. 2021 Oct 26;5(20):4003-4016. doi: 10.1182/bloodadvances.2020003955.
2
Epigenetic Priming by Hypomethylation Enhances the Immunogenic Potential of Tolinapant in T-cell Lymphoma.低甲基化的表观遗传引发增强了 Tolinapant 在 T 细胞淋巴瘤中的免疫原性潜力。
Cancer Res Commun. 2024 Jun 6;4(6):1441-1453. doi: 10.1158/2767-9764.CRC-23-0415.
3
Clinical Positioning of the IAP Antagonist Tolinapant (ASTX660) in Colorectal Cancer.IAP 拮抗剂托利那肽(ASTX660)在结直肠癌中的临床定位。
Mol Cancer Ther. 2021 Sep;20(9):1627-1639. doi: 10.1158/1535-7163.MCT-20-1050. Epub 2021 Aug 13.
4
The non-peptidomimetic IAP antagonist ASTX660 sensitizes colorectal cancer cells for extrinsic apoptosis.非肽拟似物 IAP 拮抗剂 ASTX660 增敏结直肠癌细胞发生外在细胞凋亡。
FEBS Open Bio. 2021 Mar;11(3):714-723. doi: 10.1002/2211-5463.13096. Epub 2021 Feb 19.
5
ASTX660, an antagonist of cIAP1/2 and XIAP, increases antigen processing machinery and can enhance radiation-induced immunogenic cell death in preclinical models of head and neck cancer.ASTX660是一种cIAP1/2和XIAP的拮抗剂,可增强抗原加工机制,并能在头颈癌临床前模型中增强辐射诱导的免疫原性细胞死亡。
Oncoimmunology. 2020 Jan 9;9(1):1710398. doi: 10.1080/2162402X.2019.1710398. eCollection 2020.
6
Novel smac mimetic ASTX660 (Tolinapant) and TNF-α synergistically induce necroptosis in bladder cancer cells in vitro upon apoptosis inhibition.新型 SMAC 模拟物 ASTX660(Tolinapant)与 TNF-α 协同抑制细胞凋亡时诱导膀胱癌细胞发生体外坏死性凋亡。
Biochem Biophys Res Commun. 2022 Apr 30;602:8-14. doi: 10.1016/j.bbrc.2022.02.053. Epub 2022 Feb 16.
7
Next-generation hypomethylating agent SGI-110 primes acute myeloid leukemia cells to IAP antagonist by activating extrinsic and intrinsic apoptosis pathways.新一代去甲基化剂 SGI-110 通过激活外在和内在凋亡途径使急性髓细胞白血病细胞对 IAP 拮抗剂敏化。
Cell Death Differ. 2020 Jun;27(6):1878-1895. doi: 10.1038/s41418-019-0465-8. Epub 2019 Dec 12.
8
A Phase I Study of ASTX660, an Antagonist of Inhibitors of Apoptosis Proteins, in Adults with Advanced Cancers or Lymphoma.ASTX660(一种凋亡蛋白抑制剂拮抗剂)治疗晚期癌症或淋巴瘤成人患者的 I 期临床研究。
Clin Cancer Res. 2020 Jun 15;26(12):2819-2826. doi: 10.1158/1078-0432.CCR-19-1430. Epub 2020 Jan 3.
9
Dual Antagonist of cIAP/XIAP ASTX660 Sensitizes HPV and HPV Head and Neck Cancers to TNFα, TRAIL, and Radiation Therapy.cIAP/XIAP 双重拮抗剂 ASTX660 增敏 HPV 和 HPV 头颈部癌症对 TNFα、TRAIL 和放射治疗的敏感性。
Clin Cancer Res. 2019 Nov 1;25(21):6463-6474. doi: 10.1158/1078-0432.CCR-18-3802. Epub 2019 Jul 2.
10
ASTX660, a Novel Non-peptidomimetic Antagonist of cIAP1/2 and XIAP, Potently Induces TNFα-Dependent Apoptosis in Cancer Cell Lines and Inhibits Tumor Growth.ASTX660,一种新型的 cIAP1/2 和 XIAP 的非肽模拟物拮抗剂,可强效诱导肿瘤细胞系中 TNFα 依赖性凋亡并抑制肿瘤生长。
Mol Cancer Ther. 2018 Jul;17(7):1381-1391. doi: 10.1158/1535-7163.MCT-17-0848. Epub 2018 Apr 25.

引用本文的文献

1
Epigenetic Priming by Hypomethylation Enhances the Immunogenic Potential of Tolinapant in T-cell Lymphoma.低甲基化的表观遗传引发增强了 Tolinapant 在 T 细胞淋巴瘤中的免疫原性潜力。
Cancer Res Commun. 2024 Jun 6;4(6):1441-1453. doi: 10.1158/2767-9764.CRC-23-0415.

本文引用的文献

1
A Critical Role for Fas-Mediated Off-Target Tumor Killing in T-cell Immunotherapy.Fas 介导体外肿瘤杀伤在 T 细胞免疫治疗中的关键作用。
Cancer Discov. 2021 Mar;11(3):599-613. doi: 10.1158/2159-8290.CD-20-0756. Epub 2020 Dec 17.
2
TNFR2 is required for RIP1-dependent cell death in human leukemia.TNFR2是人类白血病中RIP1依赖性细胞死亡所必需的。
Blood Adv. 2020 Oct 13;4(19):4823-4833. doi: 10.1182/bloodadvances.2019000796.
3
Peripheral T cell lymphomas: from the bench to the clinic.外周 T 细胞淋巴瘤:从基础到临床。
Nat Rev Cancer. 2020 Jun;20(6):323-342. doi: 10.1038/s41568-020-0247-0. Epub 2020 Apr 6.
4
Discovery of New Immune Checkpoints: Family Grows Up.新免疫检查点的发现:家族壮大。
Adv Exp Med Biol. 2020;1248:61-82. doi: 10.1007/978-981-15-3266-5_4.
5
ASTX660, an antagonist of cIAP1/2 and XIAP, increases antigen processing machinery and can enhance radiation-induced immunogenic cell death in preclinical models of head and neck cancer.ASTX660是一种cIAP1/2和XIAP的拮抗剂,可增强抗原加工机制,并能在头颈癌临床前模型中增强辐射诱导的免疫原性细胞死亡。
Oncoimmunology. 2020 Jan 9;9(1):1710398. doi: 10.1080/2162402X.2019.1710398. eCollection 2020.
6
The Immuno-Modulatory Effects of Inhibitor of Apoptosis Protein Antagonists in Cancer Immunotherapy.凋亡蛋白抑制剂在癌症免疫治疗中的免疫调节作用。
Cells. 2020 Jan 14;9(1):207. doi: 10.3390/cells9010207.
7
Top 10 Challenges in Cancer Immunotherapy.癌症免疫疗法的十大挑战。
Immunity. 2020 Jan 14;52(1):17-35. doi: 10.1016/j.immuni.2019.12.011.
8
A Phase I Study of ASTX660, an Antagonist of Inhibitors of Apoptosis Proteins, in Adults with Advanced Cancers or Lymphoma.ASTX660(一种凋亡蛋白抑制剂拮抗剂)治疗晚期癌症或淋巴瘤成人患者的 I 期临床研究。
Clin Cancer Res. 2020 Jun 15;26(12):2819-2826. doi: 10.1158/1078-0432.CCR-19-1430. Epub 2020 Jan 3.
9
Integrated drug profiling and CRISPR screening identify essential pathways for CAR T-cell cytotoxicity.整合药物分析和 CRISPR 筛选鉴定 CAR T 细胞细胞毒性的必需途径。
Blood. 2020 Feb 27;135(9):597-609. doi: 10.1182/blood.2019002121.
10
The Diversification of Cell Death and Immunity: Memento Mori.细胞死亡与免疫的多样化:记住死亡。
Mol Cell. 2019 Oct 17;76(2):232-242. doi: 10.1016/j.molcel.2019.09.006. Epub 2019 Oct 2.