• 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

精准医学凸显了小儿、青少年和青年肉瘤中CDK4/6细胞周期调节通路的失调。

Precision Medicine Highlights Dysregulation of the CDK4/6 Cell Cycle Regulatory Pathway in Pediatric, Adolescents and Young Adult Sarcomas.

作者信息

Barghi Farinaz, Shannon Harlan E, Saadatzadeh M Reza, Bailey Barbara J, Riyahi Niknam, Bijangi-Vishehsaraei Khadijeh, Just Marissa, Ferguson Michael J, Pandya Pankita H, Pollok Karen E

机构信息

Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, USA.

Department of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.

出版信息

Cancers (Basel). 2022 Jul 25;14(15):3611. doi: 10.3390/cancers14153611.

DOI:10.3390/cancers14153611
PMID:35892870
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9331212/
Abstract

Despite improved therapeutic and clinical outcomes for patients with localized diseases, outcomes for pediatric and AYA sarcoma patients with high-grade or aggressive disease are still relatively poor. With advancements in next generation sequencing (NGS), precision medicine now provides a strategy to improve outcomes in patients with aggressive disease by identifying biomarkers of therapeutic sensitivity or resistance. The integration of NGS into clinical decision making not only increases the accuracy of diagnosis and prognosis, but also has the potential to identify effective and less toxic therapies for pediatric and AYA sarcomas. Genome and transcriptome profiling have detected dysregulation of the CDK4/6 cell cycle regulatory pathway in subpopulations of pediatric and AYA OS, RMS, and EWS. In these patients, the inhibition of CDK4/6 represents a promising precision medicine-guided therapy. There is a critical need, however, to identify novel and promising combination therapies to fight the development of resistance to CDK4/6 inhibition. In this review, we offer rationale and perspective on the promise and challenges of this therapeutic approach.

摘要

尽管局部疾病患者的治疗和临床结果有所改善,但患有高级别或侵袭性疾病的儿科和青少年及年轻成人肉瘤患者的结果仍然相对较差。随着下一代测序(NGS)技术的进步,精准医学现在提供了一种策略,通过识别治疗敏感性或耐药性的生物标志物来改善侵袭性疾病患者的治疗结果。将NGS整合到临床决策中不仅提高了诊断和预后的准确性,还有潜力为儿科和青少年及年轻成人肉瘤识别有效且毒性较小的治疗方法。基因组和转录组分析已在儿科和青少年及年轻成人骨肉瘤、横纹肌肉瘤和尤文肉瘤亚群中检测到细胞周期蛋白依赖性激酶4/6(CDK4/6)细胞周期调节通路的失调。在这些患者中,抑制CDK4/6代表了一种有前景的精准医学指导治疗方法。然而,迫切需要识别新的、有前景的联合治疗方法,以对抗对CDK4/6抑制产生的耐药性。在这篇综述中,我们对这种治疗方法的前景和挑战提供了理论依据和观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d6/9331212/f629b59bd120/cancers-14-03611-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d6/9331212/f629b59bd120/cancers-14-03611-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d6/9331212/f629b59bd120/cancers-14-03611-g001.jpg

相似文献

1
Precision Medicine Highlights Dysregulation of the CDK4/6 Cell Cycle Regulatory Pathway in Pediatric, Adolescents and Young Adult Sarcomas.精准医学凸显了小儿、青少年和青年肉瘤中CDK4/6细胞周期调节通路的失调。
Cancers (Basel). 2022 Jul 25;14(15):3611. doi: 10.3390/cancers14153611.
2
Integration of genomic copy number variations and chemotherapy-response biomarkers in pediatric sarcoma.基因组拷贝数变异与儿童肉瘤化疗反应生物标志物的整合。
BMC Med Genomics. 2019 Jan 31;12(Suppl 1):23. doi: 10.1186/s12920-018-0456-5.
3
Functional, chemical genomic, and super-enhancer screening identify sensitivity to cyclin D1/CDK4 pathway inhibition in Ewing sarcoma.功能、化学基因组学和超级增强子筛选确定尤因肉瘤对细胞周期蛋白D1/细胞周期蛋白依赖性激酶4通路抑制的敏感性。
Oncotarget. 2015 Oct 6;6(30):30178-93. doi: 10.18632/oncotarget.4903.
4
Integrative Multi-OMICs Identifies Therapeutic Response Biomarkers and Confirms Fidelity of Clinically Annotated, Serially Passaged Patient-Derived Xenografts Established from Primary and Metastatic Pediatric and AYA Solid Tumors.整合多组学技术鉴定治疗反应生物标志物,并确认从原发性和转移性儿科及青年成人实体瘤建立的临床注释、连续传代的患者来源异种移植模型的保真度。
Cancers (Basel). 2022 Dec 30;15(1):259. doi: 10.3390/cancers15010259.
5
Impact of locus of care on outcomes in adolescents and young adults with osteosarcoma and Ewing sarcoma treated at pediatric versus adult cancer centers: An IMPACT cohort study.医疗机构对青少年和年轻成骨肉瘤和尤因肉瘤患者结局的影响:一项 IMPACT 队列研究。
Pediatr Blood Cancer. 2022 Apr;69(4):e29458. doi: 10.1002/pbc.29458. Epub 2022 Jan 14.
6
Disparity in Outcomes for Adolescent and Young Adult Patients Diagnosed With Pediatric Solid Tumors Across 4 Decades.40年间被诊断为儿童实体瘤的青少年和青年患者的预后差异。
Am J Clin Oncol. 2018 May;41(5):471-475. doi: 10.1097/COC.0000000000000304.
7
Advances in the Management of Pediatric Sarcomas.儿科肉瘤的治疗进展。
Curr Oncol Rep. 2020 Nov 16;23(1):3. doi: 10.1007/s11912-020-00995-8.
8
CDK4 Amplification Reduces Sensitivity to CDK4/6 Inhibition in Fusion-Positive Rhabdomyosarcoma.细胞周期蛋白依赖性激酶4(CDK4)扩增降低了融合阳性横纹肌肉瘤对CDK4/6抑制的敏感性。
Clin Cancer Res. 2015 Nov 1;21(21):4947-59. doi: 10.1158/1078-0432.CCR-14-2955. Epub 2015 Mar 25.
9
Target actionability review to evaluate CDK4/6 as a therapeutic target in paediatric solid and brain tumours.针对儿童实体瘤和脑肿瘤,进行目标可操作性评估以评估 CDK4/6 作为治疗靶点的潜力。
Eur J Cancer. 2022 Jul;170:196-208. doi: 10.1016/j.ejca.2022.04.028. Epub 2022 Jun 4.
10
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.

引用本文的文献

1
Harnessing the immune responses: a new frontier in Ewing sarcoma treatment.利用免疫反应:尤因肉瘤治疗的新前沿。
Med Oncol. 2025 Jun 27;42(8):291. doi: 10.1007/s12032-025-02848-5.
2
Molecular Targets in Alveolar Rhabdomyosarcoma: A Narrative Review of Progress and Pitfalls.肺泡横纹肌肉瘤的分子靶点:进展与陷阱的叙述性综述
Int J Mol Sci. 2025 May 28;26(11):5204. doi: 10.3390/ijms26115204.
3
Whole-Exome Analysis and Osteosarcoma: A Game Still Open.全外显子组分析与骨肉瘤:游戏仍在继续。

本文引用的文献

1
Concerning FDA approval of trilaciclib (Cosela) in extensive-stage small-cell lung cancer.关于美国食品药品监督管理局(FDA)批准曲拉西利(Cosela)用于广泛期小细胞肺癌的情况。
Transl Oncol. 2021 Nov;14(11):101206. doi: 10.1016/j.tranon.2021.101206. Epub 2021 Aug 19.
2
Clinical and Pharmacologic Differences of CDK4/6 Inhibitors in Breast Cancer.CDK4/6抑制剂在乳腺癌中的临床及药理学差异
Front Oncol. 2021 Jul 12;11:693104. doi: 10.3389/fonc.2021.693104. eCollection 2021.
3
Breast Cancer Resistance to Cyclin-Dependent Kinases 4/6 Inhibitors: Intricacy of the Molecular Mechanisms.
Int J Mol Sci. 2024 Dec 20;25(24):13657. doi: 10.3390/ijms252413657.
4
Panobinostat Synergizes with Chemotherapeutic Agents and Improves Efficacy of Standard-of-Care Chemotherapy Combinations in Ewing Sarcoma Cells.帕比司他与化疗药物协同作用,提高尤因肉瘤细胞中标准护理化疗组合的疗效。
Cancers (Basel). 2024 Oct 23;16(21):3565. doi: 10.3390/cancers16213565.
5
Molecular-guided therapy for the treatment of patients with relapsed and refractory childhood cancers: a Beat Childhood Cancer Research Consortium trial.分子制导疗法治疗复发和难治性儿童癌症患者:Beat 儿童癌症研究联盟试验。
Genome Med. 2024 Feb 12;16(1):28. doi: 10.1186/s13073-024-01297-5.
6
Drugging Hijacked Kinase Pathways in Pediatric Oncology: Opportunities and Current Scenario.靶向小儿肿瘤学中被劫持的激酶信号通路:机遇与现状
Pharmaceutics. 2023 Feb 16;15(2):664. doi: 10.3390/pharmaceutics15020664.
7
Integrative Multi-OMICs Identifies Therapeutic Response Biomarkers and Confirms Fidelity of Clinically Annotated, Serially Passaged Patient-Derived Xenografts Established from Primary and Metastatic Pediatric and AYA Solid Tumors.整合多组学技术鉴定治疗反应生物标志物,并确认从原发性和转移性儿科及青年成人实体瘤建立的临床注释、连续传代的患者来源异种移植模型的保真度。
Cancers (Basel). 2022 Dec 30;15(1):259. doi: 10.3390/cancers15010259.
乳腺癌对细胞周期蛋白依赖性激酶4/6抑制剂的耐药性:分子机制的复杂性
Front Oncol. 2021 May 26;11:651541. doi: 10.3389/fonc.2021.651541. eCollection 2021.
4
Clinical CDK4/6 inhibitors induce selective and immediate dissociation of p21 from cyclin D-CDK4 to inhibit CDK2.临床 CDK4/6 抑制剂诱导 p21 从 cyclin D-CDK4 中选择性且即刻解离,从而抑制 CDK2。
Nat Commun. 2021 Jun 7;12(1):3356. doi: 10.1038/s41467-021-23612-z.
5
CDK inhibitors in cancer therapy, an overview of recent development.癌症治疗中的细胞周期蛋白依赖性激酶(CDK)抑制剂——近期进展综述
Am J Cancer Res. 2021 May 15;11(5):1913-1935. eCollection 2021.
6
Efficacy and safety of regorafenib in patients with metastatic or locally advanced chondrosarcoma: Results of a non-comparative, randomised, double-blind, placebo controlled, multicentre phase II study.regorafenib 治疗转移性或局部晚期软骨肉瘤患者的疗效和安全性:一项非比较、随机、双盲、安慰剂对照、多中心 II 期研究结果。
Eur J Cancer. 2021 Jun;150:108-118. doi: 10.1016/j.ejca.2021.03.039. Epub 2021 Apr 22.
7
Effects of Trilaciclib on Chemotherapy-Induced Myelosuppression and Patient-Reported Outcomes in Patients with Extensive-Stage Small Cell Lung Cancer: Pooled Results from Three Phase II Randomized, Double-Blind, Placebo-Controlled Studies.特立西利布对广泛期小细胞肺癌患者化疗引起的骨髓抑制和患者报告结局的影响:来自三项 II 期随机、双盲、安慰剂对照研究的汇总结果。
Clin Lung Cancer. 2021 Sep;22(5):449-460. doi: 10.1016/j.cllc.2021.03.010. Epub 2021 Mar 26.
8
A phase 1 study of dalpiciclib, a cyclin-dependent kinase 4/6 inhibitor in Chinese patients with advanced breast cancer.一项在中国晚期乳腺癌患者中开展的细胞周期蛋白依赖性激酶4/6抑制剂dalpiciclib的1期研究。
Biomark Res. 2021 Apr 12;9(1):24. doi: 10.1186/s40364-021-00271-2.
9
The next horizon in precision oncology: Proteogenomics to inform cancer diagnosis and treatment.精准肿瘤学的下一个前沿领域:蛋白质基因组学助力癌症诊断与治疗
Cell. 2021 Apr 1;184(7):1661-1670. doi: 10.1016/j.cell.2021.02.055.
10
New Insights into CDK Regulators: Novel Opportunities for Cancer Therapy.CDK 调节剂的新见解:癌症治疗的新机遇。
Trends Cell Biol. 2021 May;31(5):331-344. doi: 10.1016/j.tcb.2021.01.010. Epub 2021 Mar 3.