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汉防己甲素靶向治疗癌症耐药。

Tetrandrine for Targeting Therapy Resistance in Cancer.

机构信息

Departments of Interdisciplinary Oncology, Louisiana State University Health Sciences Center, New Orleans, LA, USA.

Southeast Louisiana Veterans Health Care System, New Orleans, LA, USA.

出版信息

Curr Top Med Chem. 2024;24(12):1035-1049. doi: 10.2174/0115680266282360240222062032.

DOI:10.2174/0115680266282360240222062032
PMID:38445699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11259026/
Abstract

During the last five decades, there has been tremendous development in our understanding of cancer biology and the development of new and novel therapeutics to target cancer. However, despite these advances, cancer remains the second leading cause of death across the globe. Most cancer deaths are attributed to the development of resistance to current therapies. There is an urgent and unmet need to address cancer therapy resistance. Tetrandrine, a bis-benzyl iso-quinoline, has shown a promising role as an anti-cancer agent. Recent work from our laboratory and others suggests that tetrandrine and its derivatives could be an excellent adjuvant to the current arsenal of anti-cancer drugs. Herein, we provide an overview of resistance mechanisms to current therapeutics and review the existing literature on the anti-cancer effects of tetrandrine and its potential use for overcoming therapy resistance in cancer.

摘要

在过去的五十年中,我们对癌症生物学的理解以及针对癌症的新型治疗方法的发展取得了巨大的进展。然而,尽管取得了这些进展,癌症仍然是全球第二大致死原因。大多数癌症死亡归因于对现有治疗方法的耐药性的发展。解决癌症治疗耐药性的需求迫在眉睫。汉防己甲素是一种双苄基异喹啉,已显示出作为抗癌剂的有前途的作用。我们实验室和其他实验室的最近工作表明,汉防己甲素及其衍生物可能是当前抗癌药物武器库的极好辅助药物。在此,我们提供了对当前治疗方法耐药机制的概述,并回顾了汉防己甲素的抗癌作用及其在克服癌症治疗耐药性方面的潜在用途的现有文献。

相似文献

1
Tetrandrine for Targeting Therapy Resistance in Cancer.汉防己甲素靶向治疗癌症耐药。
Curr Top Med Chem. 2024;24(12):1035-1049. doi: 10.2174/0115680266282360240222062032.
2
Tetrandrine Interaction with ABCB1 Reverses Multidrug Resistance in Cancer Cells Through Competition with Anti-Cancer Drugs Followed by Downregulation of ABCB1 Expression.汉防己甲素通过与抗癌药物竞争并下调 ABCB1 表达逆转癌细胞的多药耐药性。
Molecules. 2019 Nov 30;24(23):4383. doi: 10.3390/molecules24234383.
3
Tetrandrine and cancer - An overview on the molecular approach.汉防己甲素与癌症——分子方法概述。
Biomed Pharmacother. 2018 Jan;97:624-632. doi: 10.1016/j.biopha.2017.10.116. Epub 2017 Nov 6.
4
The Potential of Tetrandrine against Gliomas.汉防己甲素治疗脑胶质瘤的潜力。
Anticancer Agents Med Chem. 2010 Sep;10(7):534-42. doi: 10.2174/187152010793498609.
5
H1, a derivative of Tetrandrine, exerts anti-MDR activity by initiating intrinsic apoptosis pathway and inhibiting the activation of Erk1/2 and Akt1/2.汉防己甲素衍生物 H1 通过诱导细胞内源性凋亡途径和抑制 Erk1/2 和 Akt1/2 的激活发挥抗多药耐药作用。
Biochem Pharmacol. 2011 Dec 1;82(11):1593-603. doi: 10.1016/j.bcp.2011.08.012. Epub 2011 Aug 17.
6
Tetrandrine and fangchinoline, bisbenzylisoquinoline alkaloids from Stephania tetrandra can reverse multidrug resistance by inhibiting P-glycoprotein activity in multidrug resistant human cancer cells.汉防己甲素和汉防己乙素,从粉防己中提取的双苄基异喹啉生物碱,可通过抑制多药耐药人癌细胞中的P-糖蛋白活性来逆转多药耐药性。
Phytomedicine. 2014 Jul-Aug;21(8-9):1110-9. doi: 10.1016/j.phymed.2014.04.029. Epub 2014 May 22.
7
Tetrandrine, a Chinese plant-derived alkaloid, is a potential candidate for cancer chemotherapy.粉防己碱是一种源自中国植物的生物碱,是癌症化疗的潜在候选药物。
Oncotarget. 2016 Jun 28;7(26):40800-40815. doi: 10.18632/oncotarget.8315.
8
Autophagy and cancer: Can tetrandrine be a potent anticancer drug in the near future?自噬与癌症:汉防己甲素在不远的将来能否成为一种有效的抗癌药物?
Biomed Pharmacother. 2022 Apr;148:112727. doi: 10.1016/j.biopha.2022.112727. Epub 2022 Feb 24.
9
Design and synthesis of novel tetrandrine derivatives as potential anti-tumor agents against human hepatocellular carcinoma.新型粉防己碱衍生物作为潜在抗人肝细胞癌肿瘤药物的设计与合成
Eur J Med Chem. 2017 Feb 15;127:554-566. doi: 10.1016/j.ejmech.2017.01.008. Epub 2017 Jan 7.
10
Molecular mechanisms and therapeutic implications of tetrandrine and cepharanthine in T cell acute lymphoblastic leukemia and autoimmune diseases.汉防己甲素和粉防己碱在 T 细胞急性淋巴细胞白血病和自身免疫性疾病中的分子机制和治疗意义。
Pharmacol Ther. 2021 Jan;217:107659. doi: 10.1016/j.pharmthera.2020.107659. Epub 2020 Aug 12.

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QingGan LiDan capsules improved alcoholic liver injury by regulating liver lipid transport and oxidative stress in mice.清肝利胆胶囊通过调节小鼠肝脏脂质转运和氧化应激来改善酒精性肝损伤。
Front Pharmacol. 2025 Mar 26;16:1575280. doi: 10.3389/fphar.2025.1575280. eCollection 2025.

本文引用的文献

1
Preparation of Tetrandrine Nanocrystals by Microfluidic Method and Its In Vitro and In Vivo Evaluation.微流控法制备汉防己甲素纳米晶体及其体内外评价。
AAPS PharmSciTech. 2023 Dec 19;25(1):4. doi: 10.1208/s12249-023-02718-1.
2
MicroRNAs as important players in regulating cancer through PTEN/PI3K/AKT signalling pathways.微小 RNA 作为调节癌症的重要因子,通过 PTEN/PI3K/AKT 信号通路发挥作用。
Biochim Biophys Acta Rev Cancer. 2023 May;1878(3):188904. doi: 10.1016/j.bbcan.2023.188904. Epub 2023 May 2.
3
Blocking Autophagy by the Two-Pore Channels Antagonist Tetrandrine Improves Sorafenib-Induced Death of Hepatocellular Carcinoma Cells.
双孔通道拮抗剂粉防己碱通过阻断自噬来增强索拉非尼诱导的肝癌细胞死亡。
Toxicol In Vitro. 2023 Aug;90:105603. doi: 10.1016/j.tiv.2023.105603. Epub 2023 Apr 28.
4
Controllable release of self-assembled reduction-sensitive paclitaxel dimer prodrug and tetrandrine nanoparticles promotes synergistic therapy against multidrug-resistant cancer.自组装还原敏感紫杉醇二聚体前药和粉防己碱纳米粒的可控释放促进了多药耐药性癌症的协同治疗。
Biochim Biophys Acta Gen Subj. 2023 Jul;1867(7):130362. doi: 10.1016/j.bbagen.2023.130362. Epub 2023 Apr 7.
5
ATP-binding cassette efflux transporters and MDR in cancer.ATP结合盒转运体与癌症中的多药耐药性
Drug Discov Today. 2023 May;28(5):103537. doi: 10.1016/j.drudis.2023.103537. Epub 2023 Feb 16.
6
Targeting epigenetic regulators to overcome drug resistance in cancers.靶向表观遗传调控因子以克服癌症中的耐药性。
Signal Transduct Target Ther. 2023 Feb 17;8(1):69. doi: 10.1038/s41392-023-01341-7.
7
Tetrandrine Inhibits Cancer Stem Cell Characteristics and Epithelial to Mesenchymal Transition in Triple-Negative Breast Cancer via SOD1/ROS Signaling Pathway.粉防己碱通过SOD1/ROS信号通路抑制三阴性乳腺癌中的癌症干细胞特性和上皮-间质转化
Am J Chin Med. 2023;51(2):425-444. doi: 10.1142/S0192415X23500222. Epub 2023 Jan 20.
8
Cancer statistics, 2023.癌症统计数据,2023 年。
CA Cancer J Clin. 2023 Jan;73(1):17-48. doi: 10.3322/caac.21763.
9
Progress on structural modification of Tetrandrine with wide range of pharmacological activities.具有广泛药理活性的粉防己碱结构修饰研究进展。
Front Pharmacol. 2022 Aug 16;13:978600. doi: 10.3389/fphar.2022.978600. eCollection 2022.
10
The drug efflux pump MDR1 promotes intrinsic and acquired resistance to PROTACs in cancer cells.药物外排泵 MDR1 促进了癌细胞对 PROTAC 的固有和获得性耐药。
Sci Signal. 2022 Aug 30;15(749):eabn2707. doi: 10.1126/scisignal.abn2707.