• 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

靶向肿瘤代谢:治疗窗口开启。

Targeting cancer metabolism: a therapeutic window opens.

机构信息

Koch Institute for Integrative Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.

出版信息

Nat Rev Drug Discov. 2011 Aug 31;10(9):671-84. doi: 10.1038/nrd3504.

DOI:10.1038/nrd3504
PMID:21878982
Abstract

Genetic events in cancer activate signalling pathways that alter cell metabolism. Clinical evidence has linked cell metabolism with cancer outcomes. Together, these observations have raised interest in targeting metabolic enzymes for cancer therapy, but they have also raised concerns that these therapies would have unacceptable effects on normal cells. However, some of the first cancer therapies that were developed target the specific metabolic needs of cancer cells and remain effective agents in the clinic today. Research into how changes in cell metabolism promote tumour growth has accelerated in recent years. This has refocused efforts to target metabolic dependencies of cancer cells as a selective anticancer strategy.

摘要

癌症中的遗传事件激活了改变细胞代谢的信号通路。临床证据将细胞代谢与癌症结果联系起来。这些观察结果共同引起了人们对针对代谢酶进行癌症治疗的兴趣,但也引起了人们的担忧,即这些疗法可能对正常细胞产生不可接受的影响。然而,一些最初开发的癌症疗法针对癌细胞的特定代谢需求,并且至今仍是临床上有效的药物。近年来,关于细胞代谢变化如何促进肿瘤生长的研究进展迅速。这重新将努力集中在靶向癌细胞的代谢依赖性作为一种选择性抗癌策略上。

相似文献

1
Targeting cancer metabolism: a therapeutic window opens.靶向肿瘤代谢:治疗窗口开启。
Nat Rev Drug Discov. 2011 Aug 31;10(9):671-84. doi: 10.1038/nrd3504.
2
Clinical development of cancer therapeutics that target metabolism.针对新陈代谢的癌症治疗药物的临床开发。
QJM. 2016 Jun;109(6):367-72. doi: 10.1093/qjmed/hcv181. Epub 2015 Oct 1.
3
Targeting mitochondria in the treatment of human cancer: a coordinated attack against cancer cell energy metabolism and signalling.靶向线粒体治疗人类癌症:对癌细胞能量代谢和信号传导的协同攻击
Expert Opin Ther Targets. 2007 Aug;11(8):1055-69. doi: 10.1517/14728222.11.8.1055.
4
Altered energy metabolism in cancer: a unique opportunity for therapeutic intervention.癌症中的能量代谢改变:治疗干预的独特机会。
Cancer Biol Ther. 2013 Feb;14(2):81-9. doi: 10.4161/cbt.22958. Epub 2012 Nov 28.
5
Hypoxia, cancer metabolism and the therapeutic benefit of targeting lactate/H(+) symporters.缺氧、癌症代谢与靶向乳酸/H(+) 同向转运体的治疗益处
J Mol Med (Berl). 2016 Feb;94(2):155-71. doi: 10.1007/s00109-015-1307-x. Epub 2015 Jun 24.
6
Impairing energy metabolism in solid tumors through agents targeting oncogenic signaling pathways.通过靶向致癌信号通路的药物来破坏实体瘤中的能量代谢。
Biochem Pharmacol. 2018 May;151:114-125. doi: 10.1016/j.bcp.2018.03.006. Epub 2018 Mar 9.
7
Targeting glucose metabolism in patients with cancer.针对癌症患者的葡萄糖代谢。
Cancer. 2014 Mar 15;120(6):774-80. doi: 10.1002/cncr.28501. Epub 2013 Dec 2.
8
Emerging approaches to target tumor metabolism.靶向肿瘤代谢的新兴方法。
Curr Opin Pharmacol. 2014 Aug;17:22-9. doi: 10.1016/j.coph.2014.07.001. Epub 2014 Jul 19.
9
NAD salvage pathway in cancer metabolism and therapy.癌症代谢与治疗中的NAD挽救途径。
Pharmacol Res. 2016 Dec;114:274-283. doi: 10.1016/j.phrs.2016.10.027. Epub 2016 Nov 2.
10
Targeting mitochondria metabolism for cancer therapy.针对癌症治疗的靶向线粒体代谢。
Nat Chem Biol. 2015 Jan;11(1):9-15. doi: 10.1038/nchembio.1712.

引用本文的文献

1
Association analysis of intratumoral metabolic heterogeneity assessed by the hottest lesion based on F-FDG PET/CT with immunochemotherapy response in diffuse large B-cell lymphoma.基于F-FDG PET/CT的最热病灶评估的肿瘤内代谢异质性与弥漫性大B细胞淋巴瘤免疫化疗反应的关联分析。
Quant Imaging Med Surg. 2025 Sep 1;15(9):8096-8111. doi: 10.21037/qims-2024-2699. Epub 2025 Aug 19.
2
Metabolism and epigenetics in cancer: toward personalized treatment.癌症中的代谢与表观遗传学:迈向个性化治疗
Front Endocrinol (Lausanne). 2025 Jul 25;16:1530578. doi: 10.3389/fendo.2025.1530578. eCollection 2025.
3
Exploring the interplay between LDHA and ABCC1 in breast cancer using computational approach.

本文引用的文献

1
Phosphoglycerate dehydrogenase diverts glycolytic flux and contributes to oncogenesis.磷酸甘油酸脱氢酶改变糖酵解通量并促进肿瘤发生。
Nat Genet. 2011 Jul 31;43(9):869-74. doi: 10.1038/ng.890.
2
Functional genomics reveal that the serine synthesis pathway is essential in breast cancer.功能基因组学揭示丝氨酸合成途径在乳腺癌中是必不可少的。
Nature. 2011 Aug 18;476(7360):346-50. doi: 10.1038/nature10350.
3
Carnitine palmitoyltransferase 1C promotes cell survival and tumor growth under conditions of metabolic stress.肉毒碱棕榈酰基转移酶 1C 在代谢应激条件下促进细胞存活和肿瘤生长。
利用计算方法探索乳腺癌中LDHA与ABCC1之间的相互作用。
Discov Oncol. 2025 Aug 5;16(1):1471. doi: 10.1007/s12672-025-03354-w.
4
Single-Molecule Enzyme Activity Analysis for Illuminating Pathological Proteoforms.用于阐明病理性蛋白质异构体的单分子酶活性分析
ACS Cent Sci. 2025 Jun 17;11(7):1041-1051. doi: 10.1021/acscentsci.5c00100. eCollection 2025 Jul 23.
5
Feasibility analysis of metabolic parameters based on baseline F-FDG PET/CT to predict heterogeneity and recurrence of diffuse large B-cell lymphoma.基于基线F-FDG PET/CT代谢参数预测弥漫性大B细胞淋巴瘤异质性和复发的可行性分析
Ann Hematol. 2025 Jun 11. doi: 10.1007/s00277-025-06409-8.
6
Glycolysis-Driven Prognostic Model for Acute Myeloid Leukemia: Insights into the Immune Landscape and Drug Sensitivity.急性髓系白血病的糖酵解驱动预后模型:对免疫格局和药物敏感性的见解
Biomedicines. 2025 Mar 31;13(4):834. doi: 10.3390/biomedicines13040834.
7
GOT2: New therapeutic target in pancreatic cancer.GOT2:胰腺癌的新治疗靶点。
Genes Dis. 2024 Jul 2;12(4):101370. doi: 10.1016/j.gendis.2024.101370. eCollection 2025 Jul.
8
Construction of a programmed activation nanosystem based on intracellular hypoxia in cisplatin-resistant tumor cells for reversing cisplatin resistance.基于顺铂耐药肿瘤细胞内缺氧构建程序性激活纳米系统以逆转顺铂耐药性。
Mater Today Bio. 2025 Mar 26;32:101709. doi: 10.1016/j.mtbio.2025.101709. eCollection 2025 Jun.
9
Increasing cisplatin exposure promotes small-cell lung cancer transformation after a shift from glucose metabolism to fatty acid metabolism.在从小鼠的葡萄糖代谢转变为脂肪酸代谢后,增加顺铂暴露会促进小细胞肺癌的转化。 (注:原文中未明确说明是小鼠,根据上下文推测可能是小鼠,若不是请根据实际情况修改)
J Cancer Res Clin Oncol. 2025 Mar 28;151(3):126. doi: 10.1007/s00432-025-06164-3.
10
Targeting PI3K inhibitor resistance in breast cancer with metabolic drugs.用代谢药物靶向治疗乳腺癌中的PI3K抑制剂耐药性。
Signal Transduct Target Ther. 2025 Mar 21;10(1):92. doi: 10.1038/s41392-025-02180-4.
Genes Dev. 2011 May 15;25(10):1041-51. doi: 10.1101/gad.1987211.
4
Pyruvate carboxylase is required for glutamine-independent growth of tumor cells.丙酮酸羧化酶是肿瘤细胞谷氨酰胺非依赖性生长所必需的。
Proc Natl Acad Sci U S A. 2011 May 24;108(21):8674-9. doi: 10.1073/pnas.1016627108. Epub 2011 May 9.
5
NAMPT in regulated NAD biosynthesis and its pivotal role in human metabolism.NAMPT 在调节 NAD 生物合成及其在人体代谢中的关键作用。
Curr Med Chem. 2011;18(13):1947-61. doi: 10.2174/092986711795590101.
6
The oncometabolite 2-hydroxyglutarate inhibits histone lysine demethylases.致癌代谢物 2-羟戊二酸抑制组蛋白赖氨酸去甲基酶。
EMBO Rep. 2011 May;12(5):463-9. doi: 10.1038/embor.2011.43. Epub 2011 Apr 1.
7
Exploring the genomes of cancer cells: progress and promise.探索癌细胞的基因组:进展与前景。
Science. 2011 Mar 25;331(6024):1553-8. doi: 10.1126/science.1204040.
8
Genome-scale metabolic modeling elucidates the role of proliferative adaptation in causing the Warburg effect.基因组规模代谢建模阐明了增殖适应在导致沃伯格效应中的作用。
PLoS Comput Biol. 2011 Mar;7(3):e1002018. doi: 10.1371/journal.pcbi.1002018. Epub 2011 Mar 10.
9
Regulation of cancer cell metabolism.癌细胞代谢的调控。
Nat Rev Cancer. 2011 Feb;11(2):85-95. doi: 10.1038/nrc2981.
10
Oncometabolite 2-hydroxyglutarate is a competitive inhibitor of α-ketoglutarate-dependent dioxygenases.代谢物 2-羟基戊二酸是 α-酮戊二酸依赖性双加氧酶的竞争性抑制剂。
Cancer Cell. 2011 Jan 18;19(1):17-30. doi: 10.1016/j.ccr.2010.12.014.