• 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
Strategy of combining CDK4/6 inhibitors with other therapies and mechanisms of resistance.CDK4/6抑制剂与其他疗法联合的策略及耐药机制。
Int J Clin Exp Pathol. 2024 Jul 15;17(7):189-207. doi: 10.62347/HGNI4903. eCollection 2024.
2
Selective inhibition of CDK4/6: A safe and effective strategy for developing anticancer drugs.细胞周期蛋白依赖性激酶4/6的选择性抑制:一种开发抗癌药物的安全有效策略。
Acta Pharm Sin B. 2021 Jan;11(1):30-54. doi: 10.1016/j.apsb.2020.05.001. Epub 2020 May 23.
3
eIF4A Inhibitors Suppress Cell-Cycle Feedback Response and Acquired Resistance to CDK4/6 Inhibition in Cancer.eIF4A 抑制剂抑制细胞周期反馈反应和获得性 CDK4/6 抑制耐药性在癌症中。
Mol Cancer Ther. 2019 Nov;18(11):2158-2170. doi: 10.1158/1535-7163.MCT-19-0162. Epub 2019 Aug 8.
4
Resistance to cyclin-dependent kinase (CDK) 4/6 inhibitors confers cross-resistance to other CDK inhibitors but not to chemotherapeutic agents in breast cancer cells.对细胞周期蛋白依赖性激酶(CDK)4/6抑制剂的耐药性赋予了乳腺癌细胞对其他CDK抑制剂的交叉耐药性,但对化疗药物没有交叉耐药性。
Breast Cancer. 2021 Jan;28(1):206-215. doi: 10.1007/s12282-020-01150-8. Epub 2020 Aug 28.
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
A unique CDK4/6 inhibitor: Current and future therapeutic strategies of abemaciclib.一种独特的 CDK4/6 抑制剂:阿贝西利的当前和未来治疗策略。
Pharmacol Res. 2020 Jun;156:104686. doi: 10.1016/j.phrs.2020.104686. Epub 2020 Feb 14.
7
Intrinsic and acquired resistance to CDK4/6 inhibitors and potential overcoming strategies.CDK4/6 抑制剂的内在和获得性耐药及潜在克服策略。
Acta Pharmacol Sin. 2021 Feb;42(2):171-178. doi: 10.1038/s41401-020-0416-4. Epub 2020 Jun 5.
8
Upregulated PARP1 confers breast cancer resistance to CDK4/6 inhibitors via YB-1 phosphorylation.上调的PARP1通过YB-1磷酸化赋予乳腺癌对CDK4/6抑制剂的抗性。
Exp Hematol Oncol. 2023 Nov 30;12(1):100. doi: 10.1186/s40164-023-00462-7.
9
A Combination CDK4/6 and IGF1R Inhibitor Strategy for Ewing Sarcoma.CDK4/6 和 IGF1R 抑制剂联合策略治疗尤文肉瘤。
Clin Cancer Res. 2019 Feb 15;25(4):1343-1357. doi: 10.1158/1078-0432.CCR-18-0372. Epub 2018 Nov 5.
10
Combination of ZEN-3694 with CDK4/6 inhibitors reverses acquired resistance to CDK4/6 inhibitors in ER-positive breast cancer.ZEN-3694 与 CDK4/6 抑制剂联合应用可逆转 ER 阳性乳腺癌对 CDK4/6 抑制剂的获得性耐药。
Cancer Gene Ther. 2022 Jun;29(6):859-869. doi: 10.1038/s41417-021-00375-9. Epub 2021 Aug 12.

引用本文的文献

1
Ginsenoside Rg5 enhances Abemaciclib sensitivity in ER+ breast cancer by modulating cell cycle proteins via transcriptional and post-translational levels.人参皂苷Rg5通过在转录和翻译后水平调节细胞周期蛋白来增强ER+乳腺癌对阿贝西利的敏感性。
J Ginseng Res. 2025 Sep;49(5):594-603. doi: 10.1016/j.jgr.2025.06.004. Epub 2025 Jun 28.
2
Changing landscape of advanced esophageal squamous cell carcinoma: Breakthroughs in systemic therapies (Review).晚期食管鳞状细胞癌的变化格局:全身治疗的突破(综述)
Oncol Rep. 2025 Oct;54(4). doi: 10.3892/or.2025.8953. Epub 2025 Jul 19.
3
The regulatory role of CDK4/6 inhibitors in tumor immunity and the potential value of tumor immunotherapy (Review).CDK4/6抑制剂在肿瘤免疫中的调控作用及肿瘤免疫治疗的潜在价值(综述)
Int J Mol Med. 2025 Aug;56(2). doi: 10.3892/ijmm.2025.5564. Epub 2025 Jun 13.
4
Long‑term progression‑free survival in HR+/HER2+ advanced breast cancer with combination therapy with a CDK4/6 inhibitor and first‑line maintenance therapy: A case report.CDK4/6抑制剂联合治疗及一线维持治疗在HR+/HER2+晚期乳腺癌中的长期无进展生存:一例报告
Oncol Lett. 2025 Mar 10;29(5):227. doi: 10.3892/ol.2025.14973. eCollection 2025 May.

本文引用的文献

1
Novel epigenetic therapeutic strategies and targets in cancer.癌症中的新型表观遗传治疗策略与靶点
Biochim Biophys Acta Mol Basis Dis. 2022 Dec 1;1868(12):166552. doi: 10.1016/j.bbadis.2022.166552. Epub 2022 Sep 17.
2
High p16 expression and heterozygous RB1 loss are biomarkers for CDK4/6 inhibitor resistance in ER breast cancer.高 p16 表达和 RB1 杂合性缺失是 ER 型乳腺癌中 CDK4/6 抑制剂耐药的生物标志物。
Nat Commun. 2022 Sep 7;13(1):5258. doi: 10.1038/s41467-022-32828-6.
3
The spindle assembly checkpoint is a therapeutic vulnerability of CDK4/6 inhibitor-resistant ER breast cancer with mitotic aberrations.有丝分裂异常的 CDK4/6 抑制剂耐药型 ER 乳腺癌的纺锤体组装检查点是一个治疗上的弱点。
Sci Adv. 2022 Sep 9;8(36):eabq4293. doi: 10.1126/sciadv.abq4293. Epub 2022 Sep 7.
4
Evaluation of the Effect of Food on the Pharmacokinetics of SHR6390, An Oral CDK4/6 Inhibitor, in Healthy Volunteers.评价食物对健康志愿者口服 CDK4/6 抑制剂 SHR6390 药代动力学的影响。
Drugs R D. 2022 Jun;22(2):175-182. doi: 10.1007/s40268-022-00390-7. Epub 2022 May 30.
5
Targeting CDK4 and CDK6 in cancer.针对癌症中的 CDK4 和 CDK6。
Nat Rev Cancer. 2022 Jun;22(6):356-372. doi: 10.1038/s41568-022-00456-3. Epub 2022 Mar 18.
6
PROactively TACkling CDK4/6 therapy resistance.积极应对CDK4/6治疗耐药性。
Nat Cancer. 2021 Apr;2(4):372-373. doi: 10.1038/s43018-021-00193-w.
7
PROTAC targeted protein degraders: the past is prologue.PROTAC 靶向蛋白降解剂:过去是序幕。
Nat Rev Drug Discov. 2022 Mar;21(3):181-200. doi: 10.1038/s41573-021-00371-6. Epub 2022 Jan 18.
8
CDK4 and CDK6 kinases: From basic science to cancer therapy.CDK4 和 CDK6 激酶:从基础科学到癌症治疗。
Science. 2022 Jan 14;375(6577):eabc1495. doi: 10.1126/science.abc1495.
9
The Synergistic Effects of SHR6390 Combined With Pyrotinib on HER2+/HR+ Breast Cancer.SHR6390联合吡咯替尼对HER2+/HR+乳腺癌的协同作用
Front Cell Dev Biol. 2021 Dec 16;9:785796. doi: 10.3389/fcell.2021.785796. eCollection 2021.
10
KDM6B promotes activation of the oncogenic CDK4/6-pRB-E2F pathway by maintaining enhancer activity in MYCN-amplified neuroblastoma.KDM6B 通过维持 MYCN 扩增神经母细胞瘤中的增强子活性,促进致癌性 CDK4/6-pRB-E2F 通路的激活。
Nat Commun. 2021 Dec 10;12(1):7204. doi: 10.1038/s41467-021-27502-2.

CDK4/6抑制剂与其他疗法联合的策略及耐药机制。

Strategy of combining CDK4/6 inhibitors with other therapies and mechanisms of resistance.

作者信息

Xue Yingfei, Zhai Jie

机构信息

Tianjin University, School of Pharmaceutical Science and Technology (SPST) Tianjin 300072, China.

Department of Breast Surgical Oncology, Zhejiang Cancer Hospital, Institute of Basic Medicine and Cancer (IBMC), Chinese Academy of Sciences Hangzhou 310022, Zhejiang, China.

出版信息

Int J Clin Exp Pathol. 2024 Jul 15;17(7):189-207. doi: 10.62347/HGNI4903. eCollection 2024.

DOI:10.62347/HGNI4903
PMID:39114502
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11301413/
Abstract

Cell cycle-dependent protein kinase 4/6 (CDK4/6) is a crucial kinase that regulates the cell cycle, essential for cell division and proliferation. Hence, combining CDK4/6 inhibitors with other anti-tumor drugs is a pivotal clinical strategy. This strategy can efficiently inhibit the growth and division of tumor cells, reduce the side effects, and improve the quality of life of patients by reducing the dosage of combined anticancer drugs. Furthermore, the combination therapy strategy of CDK4/6 inhibitors could ameliorate the drug resistance of combined drugs and overcome the CDK4/6 resistance caused by CDK4/6 inhibitors. Various tumor treatment strategies combined with CDK4/6 inhibitors have entered the clinical trial stage, demonstrating their substantial clinical potential. This study reviews the research progress of CDK4/6 inhibitors from 2018 to 2022, the related resistance mechanism of CDK4/6 inhibitors, and the strategy of combination medication.

摘要

细胞周期蛋白依赖性激酶4/6(CDK4/6)是一种调节细胞周期的关键激酶,对细胞分裂和增殖至关重要。因此,将CDK4/6抑制剂与其他抗肿瘤药物联合使用是一种关键的临床策略。该策略可有效抑制肿瘤细胞的生长和分裂,减少副作用,并通过降低联合抗癌药物的剂量提高患者的生活质量。此外,CDK4/6抑制剂的联合治疗策略可改善联合用药的耐药性,并克服由CDK4/6抑制剂引起的CDK4/6耐药性。多种与CDK4/6抑制剂联合的肿瘤治疗策略已进入临床试验阶段,显示出其巨大的临床潜力。本研究综述了2018年至2022年CDK4/6抑制剂的研究进展、CDK4/6抑制剂的相关耐药机制以及联合用药策略。