• 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

里博西利联合吉西他滨治疗髓母细胞瘤。

Combination of Ribociclib and Gemcitabine for the Treatment of Medulloblastoma.

机构信息

Department of Tumor Cell Biology, St. Jude Children's Research Hospital, Memphis, Tennessee.

Department of Computational Biology, St. Jude Children's Research Hospital, Memphis, Tennessee.

出版信息

Mol Cancer Ther. 2022 Aug 2;21(8):1306-1317. doi: 10.1158/1535-7163.MCT-21-0598.

DOI:10.1158/1535-7163.MCT-21-0598
PMID:35709750
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9578677/
Abstract

Group3 (G3) medulloblastoma (MB) is one of the deadliest forms of the disease for which novel treatment is desperately needed. Here we evaluate ribociclib, a highly selective CDK4/6 inhibitor, with gemcitabine in mouse and human G3MBs. Ribociclib central nervous system (CNS) penetration was assessed by in vivo microdialysis and by IHC and gene expression studies and found to be CNS-penetrant. Tumors from mice treated with short term oral ribociclib displayed inhibited RB phosphorylation, downregulated E2F target genes, and decreased proliferation. Survival studies to determine the efficacy of ribociclib and gemcitabine combination were performed on mice intracranially implanted with luciferase-labeled mouse and human G3MBs. Treatment of mice with the combination of ribociclib and gemcitabine was well tolerated, slowed tumor progression and metastatic spread, and increased survival. Expression-based gene activity and cell state analysis investigated the effects of the combination after short- and long-term treatments. Molecular analysis of treated versus untreated tumors showed a significant decrease in the activity and expression of genes involved in cell-cycle progression and DNA damage response, and an increase in the activity and expression of genes implicated in neuronal identity and neuronal differentiation. Our findings in both mouse and human patient-derived orthotopic xenograft models suggest that ribociclib and gemcitabine combination therapy warrants further investigation as a treatment strategy for children with G3MB.

摘要

Group3(G3)髓母细胞瘤(MB)是该疾病中最致命的形式之一,迫切需要新的治疗方法。在这里,我们评估了瑞博西利(一种高度选择性的 CDK4/6 抑制剂)与吉西他滨在小鼠和人 G3MB 中的联合应用。通过体内微透析和免疫组化及基因表达研究评估了瑞博西利的中枢神经系统(CNS)穿透性,并发现其具有 CNS 穿透性。用短期口服瑞博西利治疗的小鼠肿瘤显示 RB 磷酸化受到抑制,E2F 靶基因下调,增殖减少。对颅内植入荧光素酶标记的小鼠和人 G3MB 的小鼠进行了瑞博西利和吉西他滨联合治疗的生存研究,以确定其疗效。瑞博西利和吉西他滨联合治疗的小鼠耐受性良好,肿瘤进展和转移扩散速度减慢,生存时间延长。对短期和长期治疗后的联合治疗进行基于表达的基因活性和细胞状态分析。对治疗和未治疗的肿瘤进行分子分析表明,参与细胞周期进程和 DNA 损伤反应的基因的活性和表达显著降低,而与神经元身份和神经元分化相关的基因的活性和表达增加。我们在小鼠和人源性原位异种移植模型中的发现表明,瑞博西利和吉西他滨联合治疗作为 G3MB 儿童的治疗策略值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/882b/9662921/fdbf45c23a07/1306fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/882b/9662921/e70561484f65/1306fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/882b/9662921/a733d795ed8e/1306fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/882b/9662921/e1b8c7290c0f/1306fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/882b/9662921/0fec23c42a2b/1306fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/882b/9662921/fdbf45c23a07/1306fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/882b/9662921/e70561484f65/1306fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/882b/9662921/a733d795ed8e/1306fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/882b/9662921/e1b8c7290c0f/1306fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/882b/9662921/0fec23c42a2b/1306fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/882b/9662921/fdbf45c23a07/1306fig5.jpg

相似文献

1
Combination of Ribociclib and Gemcitabine for the Treatment of Medulloblastoma.里博西利联合吉西他滨治疗髓母细胞瘤。
Mol Cancer Ther. 2022 Aug 2;21(8):1306-1317. doi: 10.1158/1535-7163.MCT-21-0598.
2
Combination of Ribociclib with BET-Bromodomain and PI3K/mTOR Inhibitors for Medulloblastoma Treatment In Vitro and In Vivo.体外和体内研究瑞波西利联合 BET 溴结构域和 PI3K/mTOR 抑制剂治疗髓母细胞瘤。
Mol Cancer Ther. 2023 Jan 3;22(1):37-51. doi: 10.1158/1535-7163.MCT-21-0896.
3
Pemetrexed and gemcitabine as combination therapy for the treatment of Group3 medulloblastoma.培美曲塞和吉西他滨联合治疗 3 组髓母细胞瘤。
Cancer Cell. 2014 Apr 14;25(4):516-29. doi: 10.1016/j.ccr.2014.02.009. Epub 2014 Mar 27.
4
CNS penetration of the CDK4/6 inhibitor ribociclib in non-tumor bearing mice and mice bearing pediatric brain tumors.在非荷瘤小鼠和荷脑瘤小鼠中 CDK4/6 抑制剂瑞博西利的中枢神经系统渗透性。
Cancer Chemother Pharmacol. 2019 Aug;84(2):447-452. doi: 10.1007/s00280-019-03864-9. Epub 2019 May 11.
5
A Phase 0 Trial of Ribociclib in Recurrent Glioblastoma Patients Incorporating a Tumor Pharmacodynamic- and Pharmacokinetic-Guided Expansion Cohort.一项纳入肿瘤药效动力学和药代动力学指导扩展队列的复发性胶质母细胞瘤患者中使用瑞博西利的 0 期临床试验。
Clin Cancer Res. 2019 Oct 1;25(19):5777-5786. doi: 10.1158/1078-0432.CCR-19-0133. Epub 2019 Jul 8.
6
Ribociclib (LEE011) suppresses cell proliferation and induces apoptosis of MDA-MB-231 by inhibiting CDK4/6-cyclin D-Rb-E2F pathway.来曲唑(LEE011)通过抑制 CDK4/6-细胞周期蛋白 D-Rb-E2F 通路抑制 MDA-MB-231 细胞增殖并诱导其凋亡。
Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):4001-4011. doi: 10.1080/21691401.2019.1670670.
7
Preclinical characterization of the CDK4/6 inhibitor LY2835219: in-vivo cell cycle-dependent/independent anti-tumor activities alone/in combination with gemcitabine.CDK4/6抑制剂LY2835219的临床前特征:单独及与吉西他滨联合应用时的体内细胞周期依赖性/非依赖性抗肿瘤活性
Invest New Drugs. 2014 Oct;32(5):825-37. doi: 10.1007/s10637-014-0120-7. Epub 2014 Jun 13.
8
Targeting MYC-driven replication stress in medulloblastoma with AZD1775 and gemcitabine.以 MYC 驱动的复制应激为靶点,联合 AZD1775 和吉西他滨治疗髓母细胞瘤。
J Neurooncol. 2020 May;147(3):531-545. doi: 10.1007/s11060-020-03457-0. Epub 2020 Mar 16.
9
Inhibition of the CDK4/6-Cyclin D-Rb Pathway by Ribociclib Augments Chemotherapy and Immunotherapy in Renal Cell Carcinoma.来曲唑联合依西美坦治疗绝经后晚期乳腺癌的疗效及安全性
Biomed Res Int. 2020 Jun 11;2020:9525207. doi: 10.1155/2020/9525207. eCollection 2020.
10
Predictors of ribociclib-mediated antitumour effects in native and sorafenib-resistant human hepatocellular carcinoma cells.预测瑞博西利在原代和索拉非尼耐药的人肝癌细胞中的抗肿瘤作用。
Cell Oncol (Dordr). 2019 Oct;42(5):705-715. doi: 10.1007/s13402-019-00458-8. Epub 2019 Jun 27.

引用本文的文献

1
FOXM1-Driven CKS1B Upregulation Promotes Pancreatic Cancer Progression and Therapeutic Resistance.FOXM1驱动的CKS1B上调促进胰腺癌进展和治疗抗性。
Int J Biol Sci. 2025 Jan 13;21(3):1047-1064. doi: 10.7150/ijbs.105289. eCollection 2025.
2
Pediatric Tumors as Disorders of Development: The Case for In Vitro Modeling Based on Human Stem Cells.儿科肿瘤作为发育障碍:基于人类干细胞的体外建模案例。
Cancer Control. 2024 Jan-Dec;31:10732748241270564. doi: 10.1177/10732748241270564.
3
Mechanistic insights into medulloblastoma relapse.

本文引用的文献

1
Clinical Outcomes and Patient-Matched Molecular Composition of Relapsed Medulloblastoma.复发性髓母细胞瘤的临床结果和患者匹配的分子成分。
J Clin Oncol. 2021 Mar 1;39(7):807-821. doi: 10.1200/JCO.20.01359. Epub 2021 Jan 27.
2
Small-molecule screen reveals synergy of cell cycle checkpoint kinase inhibitors with DNA-damaging chemotherapies in medulloblastoma.小分子筛选揭示细胞周期检查点激酶抑制剂与 DNA 损伤化疗药物在髓母细胞瘤中的协同作用。
Sci Transl Med. 2021 Jan 20;13(577). doi: 10.1126/scitranslmed.aba7401.
3
Outcomes by Clinical and Molecular Features in Children With Medulloblastoma Treated With Risk-Adapted Therapy: Results of an International Phase III Trial (SJMB03).
探讨髓母细胞瘤复发的机制研究进展
Pharmacol Ther. 2024 Aug;260:108673. doi: 10.1016/j.pharmthera.2024.108673. Epub 2024 Jun 8.
4
Group 3 medulloblastoma transcriptional networks collapse under domain specific EP300/CBP inhibition.3组髓母细胞瘤转录网络在结构域特异性EP300/CBP抑制作用下瓦解。
Nat Commun. 2024 Apr 25;15(1):3483. doi: 10.1038/s41467-024-47102-0.
5
Chemotherapy in pediatric brain tumor and the challenge of the blood-brain barrier.小儿脑肿瘤的化疗和血脑屏障的挑战。
Cancer Med. 2023 Dec;12(23):21075-21096. doi: 10.1002/cam4.6647. Epub 2023 Nov 23.
调整风险适应治疗的儿童髓母细胞瘤的临床和分子特征的结果:一项国际 III 期试验(SJMB03)的结果。
J Clin Oncol. 2021 Mar 1;39(7):822-835. doi: 10.1200/JCO.20.01372. Epub 2021 Jan 6.
4
A phase I trial of the CDK 4/6 inhibitor palbociclib in pediatric patients with progressive brain tumors: A Pediatric Brain Tumor Consortium study (PBTC-042).一项 CDK4/6 抑制剂帕博西尼在进展性脑肿瘤儿科患者中的 I 期临床试验:儿科脑瘤联盟研究(PBTC-042)。
Pediatr Blood Cancer. 2021 Apr;68(4):e28879. doi: 10.1002/pbc.28879. Epub 2021 Jan 6.
5
Functional Precision Medicine Identifies New Therapeutic Candidates for Medulloblastoma.功能精准医学鉴定出治疗髓母细胞瘤的新治疗靶点。
Cancer Res. 2020 Dec 1;80(23):5393-5407. doi: 10.1158/0008-5472.CAN-20-1655. Epub 2020 Oct 12.
6
Physiologically Based Pharmacokinetic Modeling of Central Nervous System Pharmacokinetics of CDK4/6 Inhibitors to Guide Selection of Drug and Dosing Regimen for Brain Cancer Treatment.基于生理的中枢神经系统药代动力学的 CDK4/6 抑制剂的药代动力学建模,以指导脑癌治疗的药物选择和剂量方案。
Clin Pharmacol Ther. 2021 Feb;109(2):494-506. doi: 10.1002/cpt.2021. Epub 2020 Sep 14.
7
Patient-derived orthotopic xenografts of pediatric brain tumors: a St. Jude resource.儿童脑肿瘤患者来源的原位异种移植瘤:圣裘德资源。
Acta Neuropathol. 2020 Aug;140(2):209-225. doi: 10.1007/s00401-020-02171-5. Epub 2020 Jun 10.
8
Mechanisms of Sensitivity and Resistance to CDK4/6 Inhibition.CDK4/6 抑制敏感性和耐药性的机制。
Cancer Cell. 2020 Apr 13;37(4):514-529. doi: 10.1016/j.ccell.2020.03.010.
9
Senescence-Induced Vascular Remodeling Creates Therapeutic Vulnerabilities in Pancreas Cancer.衰老诱导的血管重构在胰腺癌中产生治疗脆弱性。
Cell. 2020 Apr 16;181(2):424-441.e21. doi: 10.1016/j.cell.2020.03.008. Epub 2020 Mar 31.
10
Targeting MYC-driven replication stress in medulloblastoma with AZD1775 and gemcitabine.以 MYC 驱动的复制应激为靶点,联合 AZD1775 和吉西他滨治疗髓母细胞瘤。
J Neurooncol. 2020 May;147(3):531-545. doi: 10.1007/s11060-020-03457-0. Epub 2020 Mar 16.