• 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

胃癌顺铂耐药的机制及相关 microRNAs。

Mechanism of cisplatin resistance in gastric cancer and associated microRNAs.

机构信息

Key Laboratory of Cancer Cellular and Molecular Pathology in Hunan Province, Cancer Research Institute of Hengyang Medical School, University of South China, 28 Changsheng Road, Hengyang, 421001, Hunan Province, People's Republic of China.

Department of Pathology, People's Hospital of Shaoyang County, Hengyang, Hunan Province, People's Republic of China.

出版信息

Cancer Chemother Pharmacol. 2023 Nov;92(5):329-340. doi: 10.1007/s00280-023-04572-1. Epub 2023 Aug 3.

DOI:10.1007/s00280-023-04572-1
PMID:37535106
Abstract

Gastric cancer (GC) is a common malignant tumor with high morbidity and mortality rates that seriously affects human health worldwide. Although surgery is currently the preferred clinical treatment for GC, chemotherapy remains the first choice for perioperative treatment, adjuvant therapy, and palliative care for patients with advanced GC. Cisplatin (DDP) is an antineoplastic agent that has been used clinically for decades, and it is the first-line chemotherapy for many solid tumors. However, the therapeutic efficacy of DDP is often limited by resistance and the complexity of its resistance mechanisms, which involve multiple proteins and signaling pathways. It is well documented that a variety of microRNAs (miRNAs) differentially expressed in DDP-resistant GC cells play important roles in regulating or reversing DDP resistance via various pathways. In this review, we first provide an introduction to the cytotoxicity and major resistance mechanisms of DDP in GC and then discuss the role and mechanism of miRNAs in regulating the DDP resistance process in GC cells. This work demonstrates the potential of relevant miRNAs to become diagnostic and prognostic biomarkers for gastric cancer and targets of action to enhance chemosensitivity and provides directions for future research.

摘要

胃癌(GC)是一种常见的恶性肿瘤,发病率和死亡率都很高,严重影响着全球人类的健康。尽管手术目前是 GC 的首选临床治疗方法,但化疗仍然是 GC 围手术期治疗、辅助治疗和晚期 GC 姑息治疗的首选。顺铂(DDP)是一种抗癌药物,已在临床上使用了几十年,是许多实体瘤的一线化疗药物。然而,DDP 的治疗效果往往受到耐药性的限制,其耐药机制复杂,涉及多种蛋白质和信号通路。有大量文献报道,DDP 耐药 GC 细胞中差异表达的多种 microRNAs(miRNAs)通过多种途径在调节或逆转 DDP 耐药中发挥重要作用。在本综述中,我们首先介绍了 DDP 在 GC 中的细胞毒性和主要耐药机制,然后讨论了 miRNAs 在调节 GC 细胞中 DDP 耐药过程中的作用和机制。这项工作证明了相关 miRNAs 作为胃癌诊断和预后生物标志物以及增强化疗敏感性的作用靶点的潜力,并为未来的研究提供了方向。

相似文献

1
Mechanism of cisplatin resistance in gastric cancer and associated microRNAs.胃癌顺铂耐药的机制及相关 microRNAs。
Cancer Chemother Pharmacol. 2023 Nov;92(5):329-340. doi: 10.1007/s00280-023-04572-1. Epub 2023 Aug 3.
2
MiR-223 promotes the cisplatin resistance of human gastric cancer cells via regulating cell cycle by targeting FBXW7.微小RNA-223通过靶向F-box蛋白7调控细胞周期促进人胃癌细胞的顺铂耐药性。
J Exp Clin Cancer Res. 2015 Mar 26;34(1):28. doi: 10.1186/s13046-015-0145-6.
3
miR-21 modulates cisplatin resistance of gastric cancer cells by inhibiting autophagy via the PI3K/Akt/mTOR pathway.miR-21 通过抑制自噬来调节胃癌细胞对顺铂的耐药性,其作用机制是通过 PI3K/Akt/mTOR 通路。
Anticancer Drugs. 2020 Apr;31(4):385-393. doi: 10.1097/CAD.0000000000000886.
4
Knockdown of long non-coding RNA HOTAIR inhibits cisplatin resistance of gastric cancer cells through inhibiting the PI3K/Akt and Wnt/β-catenin signaling pathways by up-regulating miR-34a.敲低长链非编码 RNA HOTAIR 通过上调 miR-34a 抑制 PI3K/Akt 和 Wnt/β-catenin 信号通路抑制胃癌细胞顺铂耐药。
Int J Biol Macromol. 2018 Feb;107(Pt B):2620-2629. doi: 10.1016/j.ijbiomac.2017.10.154. Epub 2017 Oct 26.
5
miR-1271 regulates cisplatin resistance of human gastric cancer cell lines by targeting IGF1R, IRS1, mTOR, and BCL2.微小RNA-1271通过靶向胰岛素样生长因子1受体(IGF1R)、胰岛素受体底物1(IRS1)、雷帕霉素靶蛋白(mTOR)和B细胞淋巴瘤2(BCL2)来调节人胃癌细胞系的顺铂耐药性。
Anticancer Agents Med Chem. 2014;14(6):884-91. doi: 10.2174/1871520614666140528161318.
6
miR-20a induces cisplatin resistance of a human gastric cancer cell line via targeting CYLD.微小RNA-20a通过靶向CYLD诱导人胃癌细胞系产生顺铂耐药性。
Mol Med Rep. 2016 Aug;14(2):1742-50. doi: 10.3892/mmr.2016.5413. Epub 2016 Jun 21.
7
MicroRNA-206 facilitates gastric cancer cell apoptosis and suppresses cisplatin resistance by targeting MAPK2 signaling pathway.MicroRNA-206 通过靶向 MAPK2 信号通路促进胃癌细胞凋亡并抑制顺铂耐药性。
Eur Rev Med Pharmacol Sci. 2019 Jan;23(1):171-180. doi: 10.26355/eurrev_201901_16761.
8
Linc00852 from cisplatin-resistant gastric cancer cell-derived exosomes regulates COMMD7 to promote cisplatin resistance of recipient cells through microRNA-514a-5p.顺铂耐药胃癌细胞来源的外泌体中的 Linc00852 通过 microRNA-514a-5p 调控 COMMD7 促进受体细胞的顺铂耐药性。
Cell Biol Toxicol. 2023 Apr;39(2):483-496. doi: 10.1007/s10565-021-09685-y. Epub 2022 Jan 28.
9
Targeted Regulation of FoxO3a by miR-372 to Mediate Gastric Carcinoma Cell Apoptosis and DDP Drug Resistance.miR-372对FoxO3a的靶向调控介导胃癌细胞凋亡及顺铂耐药
Cancer Biother Radiopharm. 2020 Dec;35(10):753-759. doi: 10.1089/cbr.2019.3299. Epub 2020 May 5.
10
Let-7b attenuates cisplatin resistance and tumor growth in gastric cancer by targeting AURKB.Let-7b 通过靶向 AURKB 来减弱胃癌中的顺铂耐药性和肿瘤生长。
Cancer Gene Ther. 2018 Dec;25(11-12):300-308. doi: 10.1038/s41417-018-0048-8. Epub 2018 Sep 20.

引用本文的文献

1
Carnosic acid enhances cisplatin sensitivity and suppresses gastric cancer progression via the TP53/SLC7A11/ALOX12 axis.肌醇六磷酸通过TP53/SLC7A11/ALOX12轴增强顺铂敏感性并抑制胃癌进展。
Hereditas. 2025 Jul 23;162(1):139. doi: 10.1186/s41065-025-00508-2.
2
A state-of-the-art view: G-quadruplex-targeting for platinum complexes' treatment of tumors.前沿观点:铂配合物靶向G-四链体用于肿瘤治疗
RSC Chem Biol. 2025 Apr 29. doi: 10.1039/d5cb00024f.
3
Miltirone enhances the chemosensitivity of gastric cancer cells to cisplatin by suppressing the PI3K/AKT signaling pathway.

本文引用的文献

1
CircRNA: A new class of targets for gastric cancer drug resistance therapy.环状 RNA:胃癌耐药治疗的新靶点。
Pathol Oncol Res. 2023 Mar 30;29:1611033. doi: 10.3389/pore.2023.1611033. eCollection 2023.
2
Role of IL-6/STAT3 Axis in Resistance to Cisplatin in Gastric Cancers.白细胞介素-6/信号转导与转录激活因子3轴在胃癌顺铂耐药中的作用
Biomedicines. 2023 Feb 24;11(3):694. doi: 10.3390/biomedicines11030694.
3
Inhibition of EP2 receptor suppresses tumor growth and chemoresistance of gastric cancer.抑制EP2受体可抑制胃癌的肿瘤生长和化疗耐药性。
米替罗宁通过抑制PI3K/AKT信号通路增强胃癌细胞对顺铂的化疗敏感性。
Front Pharmacol. 2025 Apr 7;16:1553791. doi: 10.3389/fphar.2025.1553791. eCollection 2025.
4
Exosomal miR‑3681‑3p from M2‑polarized macrophages confers cisplatin resistance to gastric cancer cells by targeting MLH1.来自M2极化巨噬细胞的外泌体miR-3681-3p通过靶向MLH1赋予胃癌细胞顺铂抗性。
Mol Med Rep. 2025 Apr;31(4). doi: 10.3892/mmr.2025.13459. Epub 2025 Feb 21.
5
Patient-derived tumor xenograft animal model of gastric cancer in precision chemotherapy.用于精准化疗的胃癌患者来源肿瘤异种移植动物模型
Naunyn Schmiedebergs Arch Pharmacol. 2025 Feb 19. doi: 10.1007/s00210-025-03903-8.
6
Non-coding RNA in the Regulation of Gastric Cancer Tumorigenesis: Focus on microRNAs and Exosomal microRNAs.非编码RNA在胃癌肿瘤发生调控中的作用:聚焦于微小RNA和外泌体微小RNA
Int J Mol Cell Med. 2024;13(4):417-435. doi: 10.22088/IJMCM.BUMS.13.4.417.
7
Ginsenoside RG3 Synergizes With STING Agonist to Reverse Cisplatin Resistance in Gastric Cancer.人参皂苷RG3与STING激动剂协同作用逆转胃癌顺铂耐药性。
Food Sci Nutr. 2025 Jan 20;13(1):e4744. doi: 10.1002/fsn3.4744. eCollection 2025 Jan.
8
Synergistic effects of dihydroartemisinin and cisplatin on inducing ferroptosis in gastric cancer through GPX4 inhibition.双氢青蒿素和顺铂通过抑制GPX4对胃癌诱导铁死亡的协同作用。
Gastric Cancer. 2025 Mar;28(2):187-210. doi: 10.1007/s10120-024-01574-7. Epub 2024 Dec 29.
9
Silencing HEATR1 Rescues Cisplatin Resistance of Non-small Cell Lung Cancer by Inducing Ferroptosis the p53/SAT1/ALOX15 Axis.沉默HEATR1通过诱导铁死亡及p53/SAT1/ALOX15轴挽救非小细胞肺癌的顺铂耐药性
Curr Cancer Drug Targets. 2025;25(4):345-356. doi: 10.2174/0115680096284068240506095417.
10
METTL5 promotes gastric cancer progression sphingomyelin metabolism.METTL5通过鞘磷脂代谢促进胃癌进展。
World J Gastrointest Oncol. 2024 May 15;16(5):1925-1946. doi: 10.4251/wjgo.v16.i5.1925.
Am J Cancer Res. 2022 Oct 15;12(10):4680-4692. eCollection 2022.
4
Cancer multidrug-resistance reversal by ABCB1 inhibition: A recent update.通过抑制ABCB1逆转癌症多药耐药性:最新进展
Eur J Med Chem. 2022 Sep 5;239:114542. doi: 10.1016/j.ejmech.2022.114542. Epub 2022 Jun 17.
5
M A demethylase fat mass and obesity-associated protein regulates cisplatin resistance of gastric cancer by modulating autophagy activation through ULK1.M A 去甲基化酶脂肪量和肥胖相关蛋白通过调节 ULK1 来调节自噬激活从而调控胃癌对顺铂的耐药性。
Cancer Sci. 2022 Sep;113(9):3085-3096. doi: 10.1111/cas.15469. Epub 2022 Jul 7.
6
Exosome-transmitted miR-769-5p confers cisplatin resistance and progression in gastric cancer by targeting CASP9 and promoting the ubiquitination degradation of p53.外泌体传递的 miR-769-5p 通过靶向 CASP9 并促进 p53 的泛素化降解赋予胃癌顺铂耐药性和进展。
Clin Transl Med. 2022 May;12(5):e780. doi: 10.1002/ctm2.780.
7
Breast Cancer Stem-Like Cells in Drug Resistance: A Review of Mechanisms and Novel Therapeutic Strategies to Overcome Drug Resistance.耐药性乳腺癌干细胞样细胞:克服耐药性的机制及新型治疗策略综述
Front Oncol. 2022 Mar 21;12:856974. doi: 10.3389/fonc.2022.856974. eCollection 2022.
8
Functional role of the SLC7A11-AS1/xCT axis in the development of gastric cancer cisplatin-resistance by a GSH-dependent mechanism.SLC7A11-AS1/xCT轴通过谷胱甘肽依赖性机制在胃癌顺铂耐药发生中的功能作用
Free Radic Biol Med. 2022 May 1;184:53-65. doi: 10.1016/j.freeradbiomed.2022.03.026. Epub 2022 Mar 31.
9
Clinical significance of FBXW7 loss of function in human cancers.FBXW7 功能丧失在人类癌症中的临床意义。
Mol Cancer. 2022 Mar 26;21(1):87. doi: 10.1186/s12943-022-01548-2.
10
Immunotherapy in Gastric Cancer.胃癌的免疫治疗。
Curr Oncol. 2022 Mar 2;29(3):1559-1574. doi: 10.3390/curroncol29030131.