• 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

耐药癌细胞中葡萄糖依赖性改变的图示。

The Illustration of Altered Glucose Dependency in Drug-Resistant Cancer Cells.

机构信息

Department of Anatomy, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.

出版信息

Int J Mol Sci. 2023 Sep 11;24(18):13928. doi: 10.3390/ijms241813928.

DOI:10.3390/ijms241813928
PMID:37762231
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10530558/
Abstract

A chemotherapeutic approach is crucial in malignancy management, which is often challenging due to the development of chemoresistance. Over time, chemo-resistant cancer cells rapidly repopulate and metastasize, increasing the recurrence rate in cancer patients. Targeting these destined cancer cells is more troublesome for clinicians, as they share biology and molecular cross-talks with normal cells. However, the recent insights into the metabolic profiles of chemo-resistant cancer cells surprisingly illustrated the activation of distinct pathways compared with chemo-sensitive or primary cancer cells. These distinct metabolic dynamics are vital and contribute to the shift from chemo-sensitivity to chemo-resistance in cancer. This review will discuss the important metabolic alterations in cancer cells that lead to drug resistance.

摘要

化疗方法在恶性肿瘤的治疗中至关重要,但由于化疗耐药性的发展,这往往具有挑战性。随着时间的推移,化疗耐药的癌细胞迅速增殖并转移,增加了癌症患者的复发率。对临床医生来说,靶向这些注定的癌细胞更加麻烦,因为它们与正常细胞具有相似的生物学和分子串扰。然而,最近对化疗耐药癌细胞代谢特征的深入研究表明,与化疗敏感或原发性癌细胞相比,这些细胞中存在明显激活的不同途径。这些不同的代谢动态是至关重要的,它们导致了癌细胞从化疗敏感性向化疗耐药性的转变。本综述将讨论导致药物耐药性的癌细胞中重要的代谢改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/27a0018fcf3e/ijms-24-13928-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/5e9b463a52bc/ijms-24-13928-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/3c27fcbceb65/ijms-24-13928-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/b6ce996ce2d8/ijms-24-13928-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/819ada938f7a/ijms-24-13928-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/9f4f30aa30ce/ijms-24-13928-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/27a0018fcf3e/ijms-24-13928-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/5e9b463a52bc/ijms-24-13928-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/3c27fcbceb65/ijms-24-13928-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/b6ce996ce2d8/ijms-24-13928-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/819ada938f7a/ijms-24-13928-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/9f4f30aa30ce/ijms-24-13928-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be9a/10530558/27a0018fcf3e/ijms-24-13928-g006.jpg

相似文献

1
The Illustration of Altered Glucose Dependency in Drug-Resistant Cancer Cells.耐药癌细胞中葡萄糖依赖性改变的图示。
Int J Mol Sci. 2023 Sep 11;24(18):13928. doi: 10.3390/ijms241813928.
2
The roles of glucose metabolic reprogramming in chemo- and radio-resistance.葡萄糖代谢重编程在化疗和放疗抵抗中的作用。
J Exp Clin Cancer Res. 2019 May 23;38(1):218. doi: 10.1186/s13046-019-1214-z.
3
Metabolic shift toward oxidative phosphorylation in docetaxel resistant prostate cancer cells.多西他赛耐药前列腺癌细胞向氧化磷酸化的代谢转变。
Oncotarget. 2016 Sep 20;7(38):61890-61904. doi: 10.18632/oncotarget.11301.
4
Mitochondrial Fuel Dependence on Glutamine Drives Chemo-Resistance in the Cancer Stem Cells of Hepatocellular Carcinoma.线粒体对谷氨酰胺的燃料依赖性驱动肝癌肿瘤干细胞的化疗耐药性。
Int J Mol Sci. 2021 Mar 24;22(7):3315. doi: 10.3390/ijms22073315.
5
Reprogramming metabolism by histone methyltransferase NSD2 drives endocrine resistance via coordinated activation of pentose phosphate pathway enzymes.组蛋白甲基转移酶NSD2对代谢进行重编程,通过磷酸戊糖途径酶的协同激活驱动内分泌抵抗。
Cancer Lett. 2016 Aug 10;378(2):69-79. doi: 10.1016/j.canlet.2016.05.004. Epub 2016 May 6.
6
Prediction of signaling cross-talks contributing to acquired drug resistance in breast cancer cells by Bayesian statistical modeling.通过贝叶斯统计建模预测乳腺癌细胞中导致获得性耐药的信号串扰。
BMC Syst Biol. 2015 Jan 20;9:2. doi: 10.1186/s12918-014-0135-x.
7
Microenvironment mediated alterations to metabolic pathways confer increased chemo-resistance in CD133+ tumor initiating cells.微环境介导的代谢途径改变赋予CD133 +肿瘤起始细胞更强的化疗抗性。
Oncotarget. 2016 Aug 30;7(35):56324-56337. doi: 10.18632/oncotarget.10838.
8
Metabolic reprogramming and redox adaptation in sorafenib-resistant leukemia cells: detected by untargeted metabolomics and stable isotope tracing analysis.索拉非尼耐药白血病细胞中的代谢重编程和氧化还原适应:通过非靶向代谢组学和稳定同位素示踪分析检测到。
Cancer Commun (Lond). 2019 Apr 4;39(1):17. doi: 10.1186/s40880-019-0362-z.
9
Identification of the specific epigenetic alterations associated with chemo-resistance via reprogramming of cancer cells.通过癌细胞重编程鉴定与化疗耐药相关的特定表观遗传改变。
Med Hypotheses. 2015 Dec;85(6):710-4. doi: 10.1016/j.mehy.2015.10.025. Epub 2015 Oct 27.
10
Linking metabolic reprogramming to therapy resistance in cancer.将代谢重编程与癌症的治疗抵抗联系起来。
Biochim Biophys Acta Rev Cancer. 2017 Aug;1868(1):1-6. doi: 10.1016/j.bbcan.2016.12.004. Epub 2017 Jan 5.

引用本文的文献

1
Exploring glycolytic enzymes in disease: potential biomarkers and therapeutic targets in neurodegeneration, cancer and parasitic infections.探索疾病中的糖酵解酶:神经退行性疾病、癌症和寄生虫感染中的潜在生物标志物及治疗靶点
Open Biol. 2025 Feb;15(2):240239. doi: 10.1098/rsob.240239. Epub 2025 Feb 5.
2
Inhibition of FBP1 expression by KMT5A through TWIST1 methylation is one of the mechanisms leading to chemoresistance in breast cancer.通过 TWIST1 甲基化抑制 FBP1 表达是导致乳腺癌化疗耐药的机制之一。
Oncol Rep. 2024 Aug;52(2). doi: 10.3892/or.2024.8769. Epub 2024 Jul 4.

本文引用的文献

1
Participation of protein metabolism in cancer progression and its potential targeting for the management of cancer.蛋白质代谢在癌症进展中的作用及其作为癌症治疗靶点的潜力。
Amino Acids. 2023 Oct;55(10):1223-1246. doi: 10.1007/s00726-023-03316-y. Epub 2023 Aug 30.
2
The regulation of amino acid metabolism in tumor cell death: from the perspective of physiological functions.氨基酸代谢调控与肿瘤细胞死亡:从生理功能角度探讨
Apoptosis. 2023 Oct;28(9-10):1304-1314. doi: 10.1007/s10495-023-01875-9. Epub 2023 Jul 31.
3
The metabolic function of pyruvate kinase M2 regulates reactive oxygen species production and microbial killing by neutrophils.
丙酮酸激酶 M2 的代谢功能调节中性粒细胞的活性氧产生和微生物杀伤。
Nat Commun. 2023 Jul 17;14(1):4280. doi: 10.1038/s41467-023-40021-6.
4
Cancer chemotherapy and beyond: Current status, drug candidates, associated risks and progress in targeted therapeutics.癌症化疗及其他:当前状况、候选药物、相关风险以及靶向治疗的进展。
Genes Dis. 2022 Mar 18;10(4):1367-1401. doi: 10.1016/j.gendis.2022.02.007. eCollection 2023 Jul.
5
Metformin and cancer hallmarks: shedding new lights on therapeutic repurposing.二甲双胍与癌症特征:为治疗用途再开发提供新的见解。
J Transl Med. 2023 Jun 21;21(1):403. doi: 10.1186/s12967-023-04263-8.
6
Signaling pathways in cancer metabolism: mechanisms and therapeutic targets.癌症代谢中的信号通路:机制和治疗靶点。
Signal Transduct Target Ther. 2023 May 10;8(1):196. doi: 10.1038/s41392-023-01442-3.
7
Metabolic reprogramming in cancer: Mechanisms and therapeutics.癌症中的代谢重编程:机制与治疗方法。
MedComm (2020). 2023 Mar 27;4(2):e218. doi: 10.1002/mco2.218. eCollection 2023 Apr.
8
How Warburg-Associated Lactic Acidosis Rewires Cancer Cell Energy Metabolism to Resist Glucose Deprivation.与沃伯格效应相关的乳酸性酸中毒如何重塑癌细胞能量代谢以抵抗葡萄糖剥夺。
Cancers (Basel). 2023 Feb 23;15(5):1417. doi: 10.3390/cancers15051417.
9
Targeting cancer-specific metabolic pathways for developing novel cancer therapeutics.靶向癌症特异性代谢途径以开发新型癌症治疗方法。
Front Immunol. 2022 Dec 22;13:955476. doi: 10.3389/fimmu.2022.955476. eCollection 2022.
10
Inhibition of TIGAR Increases Exogenous p53 and Cisplatin Combination Sensitivity in Lung Cancer Cells by Regulating Glycolytic Flux.抑制 TIGAR 通过调节糖酵解流增加肺癌细胞中外源 p53 和顺铂联合敏感性。
Int J Mol Sci. 2022 Dec 16;23(24):16034. doi: 10.3390/ijms232416034.