• 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

化疗和 CDK4/6 抑制剂在癌症治疗中的应用:时机至关重要。

Chemotherapy and CDK4/6 Inhibition in Cancer Treatment: Timing Is Everything.

机构信息

Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Department of Genetics, Blavantik Institute, Harvard Medical School, Boston, MA 02115, USA.

Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Department of Genetics, Blavantik Institute, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Cancer Cell. 2020 Mar 16;37(3):265-267. doi: 10.1016/j.ccell.2020.02.007.

DOI:10.1016/j.ccell.2020.02.007
PMID:32183946
Abstract

Chemotherapy remains the main treatment option for patients with several tumor types. In this issue of Cancer Cell, Salvador-Barbero et al. demonstrate that treatment with CDK4/6 inhibitors after application of taxanes (or other chemotherapeutic compounds) strongly potentiates the anti-tumor effect due to repression of DNA repair machinery.

摘要

化疗仍然是多种肿瘤类型患者的主要治疗选择。在本期《癌细胞》杂志上,Salvador-Barbero 等人证明,在应用紫杉烷(或其他化疗药物)后使用 CDK4/6 抑制剂治疗,由于抑制了 DNA 修复机制,可显著增强抗肿瘤作用。

相似文献

1
Chemotherapy and CDK4/6 Inhibition in Cancer Treatment: Timing Is Everything.化疗和 CDK4/6 抑制剂在癌症治疗中的应用:时机至关重要。
Cancer Cell. 2020 Mar 16;37(3):265-267. doi: 10.1016/j.ccell.2020.02.007.
2
Selective impact of CDK4/6 suppression on patient-derived models of pancreatic cancer.CDK4/6抑制对胰腺癌患者来源模型的选择性影响。
Oncotarget. 2015 Jun 30;6(18):15788-801. doi: 10.18632/oncotarget.3819.
3
Cell cycle plasticity driven by MTOR signaling: integral resistance to CDK4/6 inhibition in patient-derived models of pancreatic cancer.由 MTOR 信号驱动的细胞周期可塑性:胰腺癌患者来源模型中对 CDK4/6 抑制的整体耐药性。
Oncogene. 2019 May;38(18):3355-3370. doi: 10.1038/s41388-018-0650-0. Epub 2019 Jan 29.
4
CDK4/6 Therapeutic Intervention and Viable Alternative to Taxanes in CRPC.CDK4/6治疗干预及在去势抵抗性前列腺癌中作为紫杉烷类药物的可行替代方案
Mol Cancer Res. 2017 Jun;15(6):660-669. doi: 10.1158/1541-7786.MCR-17-0028. Epub 2017 Feb 16.
5
Elacestrant (RAD1901) exhibits anti-tumor activity in multiple ER+ breast cancer models resistant to CDK4/6 inhibitors.Elacestrant(RAD1901)在多种对 CDK4/6 抑制剂耐药的 ER+ 乳腺癌模型中表现出抗肿瘤活性。
Breast Cancer Res. 2019 Dec 18;21(1):146. doi: 10.1186/s13058-019-1230-0.
6
E2F Reporting Reveals Efficacious Schedules of MEK1/2-CDK4/6 Targeting and mTOR-S6 Resistance Mechanisms.E2F 报告揭示了 MEK1/2-CDK4/6 靶向和 mTOR-S6 耐药机制的有效方案。
Cancer Discov. 2018 May;8(5):568-581. doi: 10.1158/2159-8290.CD-17-0699. Epub 2018 Mar 1.
7
Preclinical development of G1T38: A novel, potent and selective inhibitor of cyclin dependent kinases 4/6 for use as an oral antineoplastic in patients with CDK4/6 sensitive tumors.G1T38的临床前开发:一种新型、强效且选择性的细胞周期蛋白依赖性激酶4/6抑制剂,用于治疗对CDK4/6敏感肿瘤的患者的口服抗肿瘤药。
Oncotarget. 2017 Jun 27;8(26):42343-42358. doi: 10.18632/oncotarget.16216.
8
Attenuation of the retinoblastoma pathway in pancreatic neuroendocrine tumors due to increased cdk4/cdk6.由于 CDK4/CDK6 的增加,导致胰腺神经内分泌肿瘤中视网膜母细胞瘤通路的衰减。
Clin Cancer Res. 2012 Sep 1;18(17):4612-20. doi: 10.1158/1078-0432.CCR-11-3264. Epub 2012 Jul 3.
9
Ribociclib, a Cdk4/Cdk6 kinase inhibitor, enhances glucocorticoid sensitivity in B-acute lymphoblastic leukemia (B-All).瑞博西利,一种 CDK4/CDK6 激酶抑制剂,可增强急性 B 淋巴细胞白血病(B-ALL)对糖皮质激素的敏感性。
Biochem Pharmacol. 2018 Jul;153:230-241. doi: 10.1016/j.bcp.2018.01.050. Epub 2018 Feb 3.
10
Loss of MutL Disrupts CHK2-Dependent Cell-Cycle Control through CDK4/6 to Promote Intrinsic Endocrine Therapy Resistance in Primary Breast Cancer.MutL 缺失通过 CDK4/6 破坏 CHK2 依赖性细胞周期控制,从而促进原发性乳腺癌的内在内分泌治疗耐药性。
Cancer Discov. 2017 Oct;7(10):1168-1183. doi: 10.1158/2159-8290.CD-16-1179. Epub 2017 Aug 11.

引用本文的文献

1
Prioritization of novel agents for further investigation in pediatric non-rhabdomyosarcoma soft tissue sarcomas: A report from the Children's Oncology Group.儿童非横纹肌肉瘤软组织肉瘤中进一步研究新型药物的优先级排序:来自儿童肿瘤协作组的报告
Eur J Cancer. 2025 Aug 26;226:115600. doi: 10.1016/j.ejca.2025.115600. Epub 2025 Jul 6.
2
Rationale for combination of paclitaxel and CDK4/6 inhibitor in ovarian cancer therapy - non-mitotic mechanisms of paclitaxel.紫杉醇与CDK4/6抑制剂联合用于卵巢癌治疗的理论依据——紫杉醇的非有丝分裂机制
Front Oncol. 2022 Sep 15;12:907520. doi: 10.3389/fonc.2022.907520. eCollection 2022.
3
Clinical Utility of CDK4/6 Inhibitors in Sarcoma: Successes and Future Challenges.
CDK4/6 抑制剂在肉瘤中的临床应用:成功与未来挑战。
JCO Precis Oncol. 2022 Feb;6:e2100211. doi: 10.1200/PO.21.00211.
4
Therapeutic evaluation of palbociclib and its compatibility with other chemotherapies for primary and recurrent nasopharyngeal carcinoma.帕博西尼治疗初发性和复发性鼻咽癌的疗效评价及其与其他化疗药物的相容性。
J Exp Clin Cancer Res. 2020 Nov 26;39(1):262. doi: 10.1186/s13046-020-01763-z.
5
Targeting CDK9: A novel biomarker in the treatment of endometrial cancer.靶向 CDK9:子宫内膜癌治疗的新生物标志物。
Oncol Rep. 2020 Nov;44(5):1929-1938. doi: 10.3892/or.2020.7746. Epub 2020 Sep 1.
6
CDKs in Sarcoma: Mediators of Disease and Emerging Therapeutic Targets.肉瘤中的 CDK :疾病的介质和新兴的治疗靶点。
Int J Mol Sci. 2020 Apr 24;21(8):3018. doi: 10.3390/ijms21083018.