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川陈皮素:癌症治疗中的老药新用。

Toosendanin: upgrade of an old agent in cancer treatment.

机构信息

Shanghai Frontiers Science Center for Chinese Medicine Chemical Biology; Institute of Interdisciplinary Integrative Medicine Research and Shuguang Hospital; Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.

Shanghai Frontiers Science Center for Chinese Medicine Chemical Biology; Institute of Interdisciplinary Integrative Medicine Research and Shuguang Hospital; Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.

出版信息

Chin J Nat Med. 2024 Oct;22(10):887-899. doi: 10.1016/S1875-5364(24)60693-X.

DOI:10.1016/S1875-5364(24)60693-X
PMID:39428181
Abstract

Toosendanin (TSN), a tetracyclic triterpenoid derived from Melia toosendan and M. azedarach, demonstrates broad application prospects in cancer treatment. Although previously employed as a pesticide, recent studies have revealed its potential therapeutic value in treating various types of cancer. TSN exerts an anticancer effect via mechanisms including proliferation inhibition, apoptosis induction, migration suppression, and angiogenesis inhibition. However, TSN's toxicity, particularly its hepatotoxicity, significantly limits its therapeutic application. This review explored the dual nature of TSN, evaluating both its anticancer potential and toxicological risks, emphasizing the importance of balancing these aspects in therapeutic applications. Furthermore, we investigated the incorporation of TSN into novel therapeutic strategies, such as Proteolysis-targeting chimeras (PROTAC) technology and nanotechnology-based drug delivery systems (DDS), which enhance treatment efficacy while mitigating toxicity in normal tissues.

摘要

川楝素(TSN)是从川楝和苦楝中提取的四环三萜类化合物,在癌症治疗方面具有广泛的应用前景。虽然它曾被用作农药,但最近的研究表明,它在治疗多种类型的癌症方面具有潜在的治疗价值。TSN 通过抑制增殖、诱导凋亡、抑制迁移和抑制血管生成等机制发挥抗癌作用。然而,TSN 的毒性,特别是其肝毒性,极大地限制了其治疗应用。本综述探讨了 TSN 的双重性质,评估了其抗癌潜力和毒理学风险,强调了在治疗应用中平衡这两方面的重要性。此外,我们研究了将 TSN 纳入新型治疗策略,如蛋白水解靶向嵌合体(PROTAC)技术和基于纳米技术的药物传递系统(DDS),这些策略可以提高治疗效果,同时减轻正常组织的毒性。

相似文献

1
Toosendanin: upgrade of an old agent in cancer treatment.川陈皮素:癌症治疗中的老药新用。
Chin J Nat Med. 2024 Oct;22(10):887-899. doi: 10.1016/S1875-5364(24)60693-X.
2
Anti-cancer effect of toosendanin and its underlying mechanisms.川楝素的抗癌作用及其潜在机制。
J Asian Nat Prod Res. 2019 Mar;21(3):270-283. doi: 10.1080/10286020.2018.1451516. Epub 2018 Apr 9.
3
Toosendanin inhibits hepatocellular carcinoma cells by inducing mitochondria-dependent apoptosis.川陈皮素通过诱导线粒体依赖性细胞凋亡抑制肝癌细胞。
Planta Med. 2010 Sep;76(13):1447-53. doi: 10.1055/s-0029-1240902. Epub 2010 Feb 15.
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Toosendanin induces apoptosis of MKN‑45 human gastric cancer cells partly through miR‑23a‑3p‑mediated downregulation of BCL2.川陈皮素通过 miR-23a-3p 介导的 BCL2 下调部分诱导 MKN-45 人胃癌细胞凋亡。
Mol Med Rep. 2020 Sep;22(3):1793-1802. doi: 10.3892/mmr.2020.11263. Epub 2020 Jun 22.
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Anticancer effects of crude extract from Melia toosendan Sieb. et Zucc on hepatocellular carcinoma in vitro and in vivo.川楝子粗提物对肝癌的体内外抗癌作用
Chin J Integr Med. 2016 May;22(5):362-9. doi: 10.1007/s11655-015-2084-7. Epub 2015 Sep 17.
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Toosendanin induces apoptosis through suppression of JNK signaling pathway in HL-60 cells.川楝素通过抑制 JNK 信号通路诱导 HL-60 细胞凋亡。
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Toosendanin and isotoosendanin suppress triple-negative breast cancer growth via inducing necrosis, apoptosis and autophagy.川陈皮素和异川陈皮素通过诱导坏死、凋亡和自噬来抑制三阴性乳腺癌的生长。
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Natural product toosendanin reverses the resistance of human breast cancer cells to adriamycin as a novel PI3K inhibitor.天然产物川陈皮素作为一种新型的 PI3K 抑制剂逆转人乳腺癌细胞对阿霉素的耐药性。
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Therapeutic potential of toosendanin: Novel applications of an old ascaris repellent as a drug candidate.苦楝素的治疗潜力:一种古老驱虫药作为候选药物的新应用。
Biomed Pharmacother. 2023 Nov;167:115541. doi: 10.1016/j.biopha.2023.115541. Epub 2023 Sep 20.
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Biological effects of toosendanin, a triterpenoid extracted from Chinese traditional medicine.川楝素(一种从中药中提取的三萜类化合物)的生物学效应
Prog Neurobiol. 2007 May;82(1):1-10. doi: 10.1016/j.pneurobio.2007.02.002. Epub 2007 Feb 15.

引用本文的文献

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Toosendanin induces ferroptosis in gastrointestinal stromal tumor cells through the regulation of the NCOA4 ferritinophagy pathway: implications for tumor proliferation, migration, and invasion.川楝素通过调节NCOA4铁自噬途径诱导胃肠道间质瘤细胞发生铁死亡:对肿瘤增殖、迁移和侵袭的影响
J Gastrointest Oncol. 2025 Jun 30;16(3):853-864. doi: 10.21037/jgo-2024-1002. Epub 2025 Jun 26.
2
Yuanhuacine suppresses head and neck cancer growth by promoting ASCT2 degradation and inhibiting glutamine uptake.芫花酯甲通过促进ASCT2降解和抑制谷氨酰胺摄取来抑制头颈癌生长。
Acta Pharmacol Sin. 2025 May 15. doi: 10.1038/s41401-025-01562-2.
3
Natural products target programmed cell death signaling mechanisms to treat colorectal cancer.
天然产物靶向程序性细胞死亡信号传导机制以治疗结直肠癌。
Front Pharmacol. 2025 Apr 24;16:1565332. doi: 10.3389/fphar.2025.1565332. eCollection 2025.