• 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

抑制CHK2与DNA复制对癌细胞生长的协同作用。

Synergistic effect of inhibiting CHK2 and DNA replication on cancer cell growth.

作者信息

Coquel Flavie, Ho Sing-Zong, Tsai Keng-Chang, Yang Chun-Yen, Aze Antoine, Devin Julie, Chang Ting-Hsiang, Kong-Hap Marie, Bioteau Audrey, Moreaux Jerome, Maiorano Domenico, Pourquier Philippe, Yang Wen-Chin, Lin Yea-Lih, Pasero Philippe

机构信息

Institut de Génétique Humaine, Univ. de Montpellier, CNRS, Montpellier, France.

'Maintenance of Genome Integrity during DNA replication' laboratory, équipe labélisée Ligue contre le Cancer, Montpellier, France.

出版信息

Elife. 2025 Jan 31;13:RP104718. doi: 10.7554/eLife.104718.

DOI:10.7554/eLife.104718
PMID:39887032
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11785374/
Abstract

Cancer cells display high levels of oncogene-induced replication stress (RS) and rely on DNA damage checkpoint for viability. This feature is exploited by cancer therapies to either increase RS to unbearable levels or inhibit checkpoint kinases involved in the DNA damage response. Thus far, treatments that combine these two strategies have shown promise but also have severe adverse effects. To identify novel, better-tolerated anticancer combinations, we screened a collection of plant extracts and found two natural compounds from the plant, , that synergistically inhibit cancer cell proliferation. Bakuchiol inhibited DNA replication and activated the checkpoint kinase CHK1 by targeting DNA polymerases. Isobavachalcone interfered with DNA double-strand break repair by inhibiting the checkpoint kinase CHK2 and DNA end resection. The combination of bakuchiol and isobavachalcone synergistically inhibited cancer cell proliferation in vitro. Importantly, it also prevented tumor development in xenografted NOD/SCID mice. The synergistic effect of inhibiting DNA replication and CHK2 signaling identifies a vulnerability of cancer cells that might be exploited by using clinically approved inhibitors in novel combination therapies.

摘要

癌细胞表现出高水平的癌基因诱导的复制应激(RS),并依赖DNA损伤检查点来维持生存能力。癌症治疗利用这一特性,要么将RS增加到无法承受的水平,要么抑制参与DNA损伤反应的检查点激酶。到目前为止,结合这两种策略的治疗方法已显示出前景,但也有严重的副作用。为了确定新的、耐受性更好的抗癌组合,我们筛选了一组植物提取物,从该植物中发现了两种天然化合物,它们协同抑制癌细胞增殖。补骨脂酚通过靶向DNA聚合酶抑制DNA复制并激活检查点激酶CHK1。异补骨脂查尔酮通过抑制检查点激酶CHK2和DNA末端切除来干扰DNA双链断裂修复。补骨脂酚和异补骨脂查尔酮的组合在体外协同抑制癌细胞增殖。重要的是,它还能预防NOD/SCID异种移植小鼠的肿瘤发展。抑制DNA复制和CHK2信号传导的协同效应确定了癌细胞的一个弱点,在新的联合疗法中使用临床批准的抑制剂可能会利用这一弱点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/e2b91eadb579/elife-104718-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/c6378aab6eab/elife-104718-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/21de78b07afa/elife-104718-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/f6694141d9d3/elife-104718-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/7dec82b1e297/elife-104718-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/5337e2248487/elife-104718-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/588f1831339b/elife-104718-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/c3354e24a7fe/elife-104718-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/d45d0b4b5794/elife-104718-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/82e3eea13d05/elife-104718-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/c756c177a2b4/elife-104718-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/b9a1c48681f8/elife-104718-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/c8dcc287deda/elife-104718-fig6-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/a531784adbdc/elife-104718-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/cd08bb9793ab/elife-104718-fig7-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/e2b91eadb579/elife-104718-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/c6378aab6eab/elife-104718-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/21de78b07afa/elife-104718-fig1-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/f6694141d9d3/elife-104718-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/7dec82b1e297/elife-104718-fig2-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/5337e2248487/elife-104718-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/588f1831339b/elife-104718-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/c3354e24a7fe/elife-104718-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/d45d0b4b5794/elife-104718-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/82e3eea13d05/elife-104718-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/c756c177a2b4/elife-104718-fig5-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/b9a1c48681f8/elife-104718-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/c8dcc287deda/elife-104718-fig6-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/a531784adbdc/elife-104718-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/cd08bb9793ab/elife-104718-fig7-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2607/11785374/e2b91eadb579/elife-104718-fig8.jpg

相似文献

1
Synergistic effect of inhibiting CHK2 and DNA replication on cancer cell growth.抑制CHK2与DNA复制对癌细胞生长的协同作用。
Elife. 2025 Jan 31;13:RP104718. doi: 10.7554/eLife.104718.
2
Targeting the replication checkpoint using SCH 900776, a potent and functionally selective CHK1 inhibitor identified via high content screening.通过高通量筛选鉴定出一种有效的、功能选择性的 CHK1 抑制剂 SCH 900776,该抑制剂可靶向复制检查点。
Mol Cancer Ther. 2011 Apr;10(4):591-602. doi: 10.1158/1535-7163.MCT-10-0928. Epub 2011 Feb 14.
3
Acetyl-macrocalin B suppresses tumor growth in esophageal squamous cell carcinoma and exhibits synergistic anti-cancer effects with the Chk1/2 inhibitor AZD7762.乙酰-巨姜辣素 B 抑制食管鳞癌细胞生长,并与 Chk1/2 抑制剂 AZD7762 具有协同抗癌作用。
Toxicol Appl Pharmacol. 2019 Feb 15;365:71-83. doi: 10.1016/j.taap.2019.01.005. Epub 2019 Jan 8.
4
Far-infrared irradiation inhibits breast cancer cell proliferation independently of DNA damage through increased nuclear Ca/calmodulin binding modulated-activation of checkpoint kinase 2.远红外线辐射通过增加核钙/钙调蛋白结合调节检查点激酶 2 的激活来抑制乳腺癌细胞增殖,而不依赖于 DNA 损伤。
J Photochem Photobiol B. 2021 Jun;219:112188. doi: 10.1016/j.jphotobiol.2021.112188. Epub 2021 Apr 20.
5
Checkpoint kinase inhibitor AZD7762 strongly sensitises urothelial carcinoma cells to gemcitabine.检查点激酶抑制剂AZD7762可使尿路上皮癌细胞对吉西他滨高度敏感。
J Exp Clin Cancer Res. 2017 Jan 3;36(1):1. doi: 10.1186/s13046-016-0473-1.
6
Investigation into the Neuroprotective and Therapeutic Potential of Plant-Derived Chk2 Inhibitors.探究植物源性 Chk2 抑制剂的神经保护和治疗潜力。
Int J Mol Sci. 2024 Jul 15;25(14):7725. doi: 10.3390/ijms25147725.
7
Re-purposing clinical kinase inhibitors to enhance chemosensitivity by overriding checkpoints.重新利用临床激酶抑制剂,通过绕过检查点来增强化疗敏感性。
Cell Cycle. 2014;13(14):2172-91. doi: 10.4161/cc.29214. Epub 2014 Jun 23.
8
Combined Targeting of G9a and Checkpoint Kinase 1 Synergistically Inhibits Pancreatic Cancer Cell Growth by Replication Fork Collapse.组蛋白甲基转移酶 G9a 和细胞周期检查点激酶 1 的联合靶向通过复制叉崩溃协同抑制胰腺癌细胞生长。
Mol Cancer Res. 2020 Mar;18(3):448-462. doi: 10.1158/1541-7786.MCR-19-0490. Epub 2019 Dec 10.
9
Prexasertib, a checkpoint kinase inhibitor: from preclinical data to clinical development.普雷沙替尼,一种检查点激酶抑制剂:从临床前数据到临床开发。
Cancer Chemother Pharmacol. 2020 Jan;85(1):9-20. doi: 10.1007/s00280-019-03950-y. Epub 2019 Sep 11.
10
Part II: New candidates of pyrazole-benzimidazole conjugates as checkpoint kinase 2 (Chk2) inhibitors.第二部分:作为细胞周期检查点激酶 2(Chk2)抑制剂的吡唑并苯并咪唑化合物的新候选物。
Eur J Med Chem. 2018 Jan 20;144:859-873. doi: 10.1016/j.ejmech.2017.12.023. Epub 2017 Dec 8.

本文引用的文献

1
Isobavachalcone, a natural sirtuin 2 inhibitor, exhibits anti-triple-negative breast cancer efficacy in vitro and in vivo.异甘草素是一种天然的 SIRT2 抑制剂,在体外和体内均表现出抗三阴性乳腺癌的功效。
Phytother Res. 2024 Apr;38(4):1815-1829. doi: 10.1002/ptr.8143. Epub 2024 Feb 13.
2
Bakuchiol, a natural constituent and its pharmacological benefits.补骨脂酚,一种天然成分及其药理学益处。
F1000Res. 2023 Nov 7;12:29. doi: 10.12688/f1000research.129072.2. eCollection 2023.
3
The multifaceted functions of homologous recombination in dealing with replication-associated DNA damages.
同源重组在应对复制相关 DNA 损伤方面的多效性功能。
DNA Repair (Amst). 2023 Sep;129:103548. doi: 10.1016/j.dnarep.2023.103548. Epub 2023 Aug 1.
4
Isobavachalcone Induces Multiple Cell Death in Human Triple-Negative Breast Cancer MDA-MB-231 Cells.异甘草素诱导人三阴性乳腺癌 MDA-MB-231 细胞发生多种细胞死亡。
Molecules. 2022 Oct 11;27(20):6787. doi: 10.3390/molecules27206787.
5
A superior loading control for the cellular thermal shift assay.一种用于细胞热转移分析的优越加载控制。
Sci Rep. 2022 Apr 23;12(1):6672. doi: 10.1038/s41598-022-10653-7.
6
A phase IA dose-escalation study of PHI-101, a new checkpoint kinase 2 inhibitor, for platinum-resistant recurrent ovarian cancer.PHI-101(一种新型细胞周期检查点激酶 2 抑制剂)治疗铂类耐药复发性卵巢癌的 I 期剂量递增研究。
BMC Cancer. 2022 Jan 3;22(1):28. doi: 10.1186/s12885-021-09138-z.
7
DNA End Resection: Mechanism and Control.DNA 末端切除:机制与调控。
Annu Rev Genet. 2021 Nov 23;55:285-307. doi: 10.1146/annurev-genet-071719-020312.
8
Replication stress: from chromatin to immunity and beyond.复制压力:从染色质到免疫及其他。
Curr Opin Genet Dev. 2021 Dec;71:136-142. doi: 10.1016/j.gde.2021.08.004. Epub 2021 Aug 26.
9
Targeting the DNA damage response in immuno-oncology: developments and opportunities.靶向免疫肿瘤学中的 DNA 损伤反应:进展与机遇。
Nat Rev Cancer. 2021 Nov;21(11):701-717. doi: 10.1038/s41568-021-00386-6. Epub 2021 Aug 10.
10
The Replication Stress Response on a Narrow Path Between Genomic Instability and Inflammation.基因组不稳定与炎症之间狭窄路径上的复制应激反应
Front Cell Dev Biol. 2021 Jun 25;9:702584. doi: 10.3389/fcell.2021.702584. eCollection 2021.