• 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

Panobinostat induces CD38 upregulation and augments the antimyeloma efficacy of daratumumab.

作者信息

García-Guerrero Estefanía, Gogishvili Tea, Danhof Sophia, Schreder Martin, Pallaud Celine, Pérez-Simón Jose Antonio, Einsele Hermann, Hudecek Michael

机构信息

Medizinische Klinik und Poliklinik II, Universitätsklinikum Würzburg, Würzburg, Germany.

Instituto de Biomedicina de Sevilla, Hospital Universitario Virgen del Rocío/Consejo Superior de Investigaciones Científicas/Universidad de Sevilla, Seville, Spain; and.

出版信息

Blood. 2017 Jun 22;129(25):3386-3388. doi: 10.1182/blood-2017-03-770776. Epub 2017 May 5.

DOI:10.1182/blood-2017-03-770776
PMID:28476749
Abstract
摘要

相似文献

1
Panobinostat induces CD38 upregulation and augments the antimyeloma efficacy of daratumumab.帕比司他可诱导CD38上调,并增强达雷妥尤单抗的抗骨髓瘤疗效。
Blood. 2017 Jun 22;129(25):3386-3388. doi: 10.1182/blood-2017-03-770776. Epub 2017 May 5.
2
Upregulation of CD38 expression on multiple myeloma cells by novel HDAC6 inhibitors is a class effect and augments the efficacy of daratumumab.新型 HDAC6 抑制剂上调多发性骨髓瘤细胞 CD38 表达属类效应,并增强达雷妥尤单抗的疗效。
Leukemia. 2021 Jan;35(1):201-214. doi: 10.1038/s41375-020-0840-y. Epub 2020 Apr 29.
3
Tinostamustine (EDO-S101), an Alkylating Deacetylase Inhibitor, Enhances the Efficacy of Daratumumab in Multiple Myeloma by Upregulation of CD38 and NKG2D Ligands.替努司他滨(EDO-S101),一种烷化脱乙酰酶抑制剂,通过上调 CD38 和 NKG2D 配体增强达雷妥尤单抗在多发性骨髓瘤中的疗效。
Int J Mol Sci. 2024 Apr 26;25(9):4718. doi: 10.3390/ijms25094718.
4
Class 1 HDAC and HDAC6 inhibition inversely regulates CD38 induction in myeloma cells via interferon-α and ATRA.1类组蛋白去乙酰化酶(HDAC)和HDAC6抑制通过干扰素-α和全反式维甲酸(ATRA)反向调节骨髓瘤细胞中CD38的诱导。
Br J Haematol. 2019 Jun;185(5):969-974. doi: 10.1111/bjh.15673. Epub 2018 Nov 26.
5
Molecular dynamics of targeting CD38 in multiple myeloma.靶向多发性骨髓瘤 CD38 的分子动力学。
Br J Haematol. 2021 May;193(3):581-591. doi: 10.1111/bjh.17329. Epub 2021 Feb 11.
6
Synergistic targeting of Sp1, a critical transcription factor for myeloma cell growth and survival, by panobinostat and proteasome inhibitors.帕比司他和蛋白酶体抑制剂对Sp1(骨髓瘤细胞生长和存活的关键转录因子)的协同靶向作用。
Oncotarget. 2016 Nov 29;7(48):79064-79075. doi: 10.18632/oncotarget.12594.
7
Panobinostat for the Treatment of Multiple Myeloma.泊马度胺治疗多发性骨髓瘤。
Clin Cancer Res. 2015 Nov 1;21(21):4767-73. doi: 10.1158/1078-0432.CCR-15-0530. Epub 2015 Sep 11.
8
Deacetylase inhibitors: an advance in myeloma therapy?去乙酰化酶抑制剂:骨髓瘤治疗的新进展?
Expert Rev Hematol. 2017 Mar;10(3):229-237. doi: 10.1080/17474086.2017.1280388. Epub 2017 Feb 1.
9
Effects of Histone Deacetylase Inhibitor Panobinostat (LBH589) on Bone Marrow Mononuclear Cells of Relapsed or Refractory Multiple Myeloma Patients and Its Mechanisms.组蛋白去乙酰化酶抑制剂帕比司他(LBH589)对复发或难治性多发性骨髓瘤患者骨髓单个核细胞的影响及其机制。
Med Sci Monit. 2017 Oct 29;23:5150-5157. doi: 10.12659/msm.904232.
10
New insights into the treatment of multiple myeloma with histone deacetylase inhibitors.新型组蛋白去乙酰化酶抑制剂在多发性骨髓瘤治疗中的新认识
Curr Pharm Des. 2013;19(4):734-44.

引用本文的文献

1
Functional multiomics reveals genetic and pharmacologic regulation of surface CD38 in multiple myeloma.功能多组学揭示了多发性骨髓瘤中表面CD38的遗传和药理调控。
Blood Neoplasia. 2024 Jun 10;1(3):100025. doi: 10.1016/j.bneo.2024.100025. eCollection 2024 Sep.
2
CD38 in the pathobiology of cutaneous T-cell lymphoma and the potential for combination therapeutic intervention.CD38在皮肤T细胞淋巴瘤病理生物学中的作用及联合治疗干预的潜力
Leukemia. 2025 May;39(5):1146-1156. doi: 10.1038/s41375-025-02551-4. Epub 2025 Mar 8.
3
Monoclonal anti-CD38 therapy in human myeloma: retrospects and prospects.
人骨髓瘤中的单克隆抗CD38疗法:回顾与展望。
Front Immunol. 2025 Feb 12;16:1519300. doi: 10.3389/fimmu.2025.1519300. eCollection 2025.
4
Tinostamustine (EDO-S101), an Alkylating Deacetylase Inhibitor, Enhances the Efficacy of Daratumumab in Multiple Myeloma by Upregulation of CD38 and NKG2D Ligands.替努司他滨(EDO-S101),一种烷化脱乙酰酶抑制剂,通过上调 CD38 和 NKG2D 配体增强达雷妥尤单抗在多发性骨髓瘤中的疗效。
Int J Mol Sci. 2024 Apr 26;25(9):4718. doi: 10.3390/ijms25094718.
5
Exploring the role of histone deacetylase and histone deacetylase inhibitors in the context of multiple myeloma: mechanisms, therapeutic implications, and future perspectives.探索组蛋白去乙酰化酶及组蛋白去乙酰化酶抑制剂在多发性骨髓瘤中的作用:作用机制、治疗意义及未来展望
Exp Hematol Oncol. 2024 Apr 23;13(1):45. doi: 10.1186/s40164-024-00507-5.
6
Epigenetic regulation of CD38/CD48 by KDM6A mediates NK cell response in multiple myeloma.组蛋白赖氨酸去甲基化酶 6A 通过调控 CD38/CD48 介导多发性骨髓瘤中自然杀伤细胞的反应。
Nat Commun. 2024 Feb 14;15(1):1367. doi: 10.1038/s41467-024-45561-z.
7
EZH2 targeting induces CD38 upregulation and response to anti-CD38 immunotherapies in multiple myeloma.靶向EZH2可诱导多发性骨髓瘤中CD38上调并增强对抗CD38免疫疗法的反应。
Leukemia. 2023 Sep;37(9):1925-1928. doi: 10.1038/s41375-023-01983-0. Epub 2023 Aug 2.
8
Cytokine receptor IL27RA is an NF-κB-responsive gene involved in CD38 upregulation in multiple myeloma.细胞因子受体 IL27RA 是一种 NF-κB 反应性基因,参与多发性骨髓瘤中 CD38 的上调。
Blood Adv. 2023 Aug 8;7(15):3874-3890. doi: 10.1182/bloodadvances.2022009044.
9
CD38-Induced Metabolic Dysfunction Primes Multiple Myeloma Cells for NAD-Lowering Agents.CD38诱导的代谢功能障碍使多发性骨髓瘤细胞对降低NAD的药物敏感。
Antioxidants (Basel). 2023 Feb 15;12(2):494. doi: 10.3390/antiox12020494.
10
Advances in the molecular characterization of multiple myeloma and mechanism of therapeutic resistance.多发性骨髓瘤的分子特征及治疗耐药机制的研究进展
Front Oncol. 2022 Oct 27;12:1020011. doi: 10.3389/fonc.2022.1020011. eCollection 2022.