• 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

靶向调控程序性细胞死亡的激酶:乳腺癌的一种新治疗策略。

Targeting kinases that regulate programmed cell death: a new therapeutic strategy for breast cancer.

作者信息

Hong Yun, He Jun, Deng Dan, Liu Qinyue, Zu Xuyu, Shen Yingying

机构信息

Cancer Research Institute, The First Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, Hunan, 421001, PR China.

Department of Clinical Laboratory Medicine, Institution of Microbiology and Infectious Diseases, Hunan Province Clinical Research Center for Accurate Diagnosis and Treatment of High-Incidence Sexually Transmitted Diseases, The First Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, Hunan, China.

出版信息

J Transl Med. 2025 Apr 14;23(1):439. doi: 10.1186/s12967-025-06367-9.

DOI:10.1186/s12967-025-06367-9
PMID:40229646
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11995514/
Abstract

Breast cancer is one of the most prevalent malignant tumors among women and ranks as the second leading cause of cancer-related deaths in females, primarily due to delays in diagnosis and shortcomings in treatment strategies. Consequently, there is a pressing need to identify reliable therapeutic targets and strategies. In recent years, the identification of effective biomarkers-particularly novel molecular therapeutic targets-has become a focal point in breast cancer research, aimed at predicting disease aggressiveness and monitoring treatment responses. Simultaneously, advancements in understanding the molecular mechanisms underlying cellular programmed death have opened new avenues for targeting kinase-regulated programmed cell death as a viable therapeutic strategy. This review summarizes the latest research progress regarding kinase-regulated programmed death (including apoptosis, pyroptosis, autophagy, necroptosis, and ferroptosis) in breast cancer treatment. It covers the key kinases involved in this mechanism, their roles in the onset and progression of breast cancer, and strategies for modulating these kinases through pharmacological interventions.

摘要

乳腺癌是女性中最常见的恶性肿瘤之一,是女性癌症相关死亡的第二大主要原因,主要是由于诊断延迟和治疗策略的不足。因此,迫切需要确定可靠的治疗靶点和策略。近年来,识别有效的生物标志物,特别是新型分子治疗靶点,已成为乳腺癌研究的重点,旨在预测疾病的侵袭性并监测治疗反应。同时,对细胞程序性死亡潜在分子机制的理解进展,为将激酶调节的程序性细胞死亡作为一种可行的治疗策略开辟了新途径。本综述总结了乳腺癌治疗中激酶调节的程序性死亡(包括细胞凋亡、焦亡、自噬、坏死性凋亡和铁死亡)的最新研究进展。它涵盖了参与这一机制的关键激酶、它们在乳腺癌发生和发展中的作用,以及通过药物干预调节这些激酶的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffeb/11995514/82cdbd2a3ced/12967_2025_6367_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffeb/11995514/660edb5a67d2/12967_2025_6367_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffeb/11995514/257e51773997/12967_2025_6367_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffeb/11995514/f21bb54fd47b/12967_2025_6367_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffeb/11995514/e2b17e2582d6/12967_2025_6367_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffeb/11995514/36ee937f1163/12967_2025_6367_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffeb/11995514/82cdbd2a3ced/12967_2025_6367_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffeb/11995514/660edb5a67d2/12967_2025_6367_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffeb/11995514/257e51773997/12967_2025_6367_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffeb/11995514/f21bb54fd47b/12967_2025_6367_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffeb/11995514/e2b17e2582d6/12967_2025_6367_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffeb/11995514/36ee937f1163/12967_2025_6367_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffeb/11995514/82cdbd2a3ced/12967_2025_6367_Fig6_HTML.jpg

相似文献

1
Targeting kinases that regulate programmed cell death: a new therapeutic strategy for breast cancer.靶向调控程序性细胞死亡的激酶:乳腺癌的一种新治疗策略。
J Transl Med. 2025 Apr 14;23(1):439. doi: 10.1186/s12967-025-06367-9.
2
Cell Death: Mechanisms and Potential Targets in Breast Cancer Therapy.细胞死亡:乳腺癌治疗中的机制和潜在靶点。
Int J Mol Sci. 2024 Sep 7;25(17):9703. doi: 10.3390/ijms25179703.
3
Regulated lytic cell death in breast cancer.乳腺癌中的调控性细胞死亡。
Cell Biol Int. 2022 Jan;46(1):12-33. doi: 10.1002/cbin.11705. Epub 2021 Oct 4.
4
Targeting regulated cell death (RCD) with small-molecule compounds in triple-negative breast cancer: a revisited perspective from molecular mechanisms to targeted therapies.用小分子化合物靶向三阴性乳腺癌中的调控细胞死亡(RCD):从分子机制到靶向治疗的再思考视角。
J Hematol Oncol. 2022 Apr 12;15(1):44. doi: 10.1186/s13045-022-01260-0.
5
Selected Flavonols Targeting Cell Death Pathways in Cancer Therapy: The Latest Achievements in Research on Apoptosis, Autophagy, Necroptosis, Pyroptosis, Ferroptosis, and Cuproptosis.癌症治疗中靶向细胞死亡途径的选定黄酮醇:细胞凋亡、自噬、坏死性凋亡、焦亡、铁死亡和铜死亡研究的最新成果
Nutrients. 2024 Apr 18;16(8):1201. doi: 10.3390/nu16081201.
6
PANoptosis: a potential new target for programmed cell death in breast cancer treatment and prognosis.PANoptosis:乳腺癌治疗和预后中程序性细胞死亡的潜在新靶点。
Apoptosis. 2024 Apr;29(3-4):277-288. doi: 10.1007/s10495-023-01904-7. Epub 2023 Nov 24.
7
Emerging role of necroptosis, pyroptosis, and ferroptosis in breast cancer: New dawn for overcoming therapy resistance.细胞焦亡、铁死亡和细胞坏死在乳腺癌中的新作用:克服治疗耐药性的新曙光。
Neoplasia. 2024 Sep;55:101017. doi: 10.1016/j.neo.2024.101017. Epub 2024 Jun 14.
8
Crosstalk between autophagy and other forms of programmed cell death.自噬与其他形式的程序性细胞死亡之间的相互作用。
Eur J Pharmacol. 2025 May 15;995:177414. doi: 10.1016/j.ejphar.2025.177414. Epub 2025 Feb 20.
9
The evolving landscape of protein kinases in breast cancer: clinical implications.乳腺癌中不断变化的蛋白激酶全景:临床意义。
Cancer Treat Rev. 2013 Feb;39(1):68-76. doi: 10.1016/j.ctrv.2012.05.004. Epub 2012 Jun 15.
10
Small Molecules Targeting Programmed Cell Death in Breast Cancer Cells.小分子靶向乳腺癌细胞程序性细胞死亡。
Int J Mol Sci. 2021 Sep 8;22(18):9722. doi: 10.3390/ijms22189722.

引用本文的文献

1
bFGF Knockdown Inhibits mTOR Signaling by Suppressing Caveolin-1 and Aggravates Cognitive Damage After Arterial Ischemic Brain Injury in Juvenile Rats.碱性成纤维细胞生长因子基因敲低通过抑制小窝蛋白-1抑制mTOR信号传导并加重幼鼠动脉缺血性脑损伤后的认知损害。
Mol Neurobiol. 2025 Jun 11. doi: 10.1007/s12035-025-05108-9.

本文引用的文献

1
Transcriptomic analysis revealed potential regulatory biomarkers and repurposable drugs for breast cancer treatment.转录组分析揭示了潜在的乳腺癌治疗调控生物标志物和可再利用药物。
Cancer Rep (Hoboken). 2024 May;7(5):e2009. doi: 10.1002/cnr2.2009.
2
A review on structure-function mechanism and signaling pathway of serine/threonine protein PIM kinases as a therapeutic target.丝氨酸/苏氨酸蛋白PIM激酶作为治疗靶点的结构-功能机制及信号通路综述
Int J Biol Macromol. 2024 Jun;270(Pt 1):132030. doi: 10.1016/j.ijbiomac.2024.132030. Epub 2024 May 3.
3
Iron affects the sphere-forming ability of ovarian cancer cells in non-adherent culture conditions.
铁在非贴壁培养条件下会影响卵巢癌细胞的成球能力。
Front Cell Dev Biol. 2023 Nov 14;11:1272667. doi: 10.3389/fcell.2023.1272667. eCollection 2023.
4
Cantharidin induces apoptosis of human triple negative breast cancer cells through mir-607-mediated downregulation of EGFR.斑蝥素通过 mir-607 介导的 EGFR 下调诱导人三阴性乳腺癌细胞凋亡。
J Transl Med. 2023 Sep 5;21(1):597. doi: 10.1186/s12967-023-04483-y.
5
TAM family kinases as therapeutic targets at the interface of cancer and immunity.酪氨酸激酶家族作为癌症与免疫交叉领域的治疗靶点。
Nat Rev Clin Oncol. 2023 Nov;20(11):755-779. doi: 10.1038/s41571-023-00813-7. Epub 2023 Sep 4.
6
Cell death, therapeutics, and the immune response in cancer.细胞死亡、治疗学与癌症中的免疫反应。
Trends Cancer. 2023 May;9(5):381-396. doi: 10.1016/j.trecan.2023.02.001. Epub 2023 Feb 24.
7
Copper-dependent autophagic degradation of GPX4 drives ferroptosis.铜依赖的自噬性 GPX4 降解驱动铁死亡。
Autophagy. 2023 Jul;19(7):1982-1996. doi: 10.1080/15548627.2023.2165323. Epub 2023 Jan 12.
8
TMEM164 is a new determinant of autophagy-dependent ferroptosis.TMEM164 是自噬依赖性铁死亡的一个新决定因素。
Autophagy. 2023 Mar;19(3):945-956. doi: 10.1080/15548627.2022.2111635. Epub 2022 Aug 22.
9
N6-methyladenosine regulated FGFR4 attenuates ferroptotic cell death in recalcitrant HER2-positive breast cancer.N6-甲基腺苷调节 FGFR4 减轻难治性 HER2 阳性乳腺癌中的铁死亡细胞死亡。
Nat Commun. 2022 May 13;13(1):2672. doi: 10.1038/s41467-022-30217-7.
10
Lipogenesis mediated by OGR1 regulates metabolic adaptation to acid stress in cancer cells via autophagy.OGR1 介导的脂生成通过自噬调节癌细胞对酸应激的代谢适应。
Cell Rep. 2022 May 10;39(6):110796. doi: 10.1016/j.celrep.2022.110796.