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本文引用的文献

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Cytotoxic triterpene diglycosides from the sea cucumber Stichopus horrens.来自糙海参的细胞毒性三萜二糖苷。
Bioorg Med Chem Lett. 2017 Jul 1;27(13):2939-2942. doi: 10.1016/j.bmcl.2017.05.003. Epub 2017 May 6.
2
The marine triterpene glycoside frondoside A induces p53-independent apoptosis and inhibits autophagy in urothelial carcinoma cells.海洋三萜糖苷 frondoside A 诱导尿路上皮癌细胞发生 p53 非依赖性细胞凋亡并抑制自噬。
BMC Cancer. 2017 Feb 1;17(1):93. doi: 10.1186/s12885-017-3085-z.
3
The Cytotoxicity of Dacarbazine Potentiated by Sea Cucumber Saponin in Resistant B16F10 Melanoma Cells through Apoptosis Induction.海参皂苷增强达卡巴嗪对耐药B16F10黑色素瘤细胞的细胞毒性并诱导其凋亡
Avicenna J Med Biotechnol. 2016 Jul-Sep;8(3):112-9.
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Pharmacokinetics in Mouse and Comparative Effects of Frondosides in Pancreatic Cancer.小鼠体内药代动力学及海参叶苷对胰腺癌的比较作用
Mar Drugs. 2016 Jun 17;14(6):115. doi: 10.3390/md14060115.
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Apoptosis inducing capacity of Holothuria arenicola in CT26 colon carcinoma cells in vitro and in vivo.沙参海胆对CT26结肠癌细胞在体外和体内的凋亡诱导能力。
Iran J Basic Med Sci. 2016 Apr;19(4):358-65.
6
Selective Toxicity of Persian Gulf Sea Cucumber (Holothuria parva) and Sponge (Haliclona oculata) Methanolic Extracts on Liver Mitochondria Isolated from an Animal Model of Hepatocellular Carcinoma.波斯湾海参(Holothuria parva)和海绵(Haliclona oculata)甲醇提取物对从肝细胞癌动物模型分离的肝线粒体的选择性毒性。
Hepat Mon. 2015 Dec 27;15(12):e33073. doi: 10.5812/hepatmon.33073. eCollection 2015 Dec.
7
Marine Non-Glycosaminoglycan Sulfated Glycans as Potential Pharmaceuticals.海洋非糖胺聚糖硫酸化聚糖作为潜在药物
Pharmaceuticals (Basel). 2015 Dec 10;8(4):848-64. doi: 10.3390/ph8040848.
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Marine Drugs Regulating Apoptosis Induced by Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand (TRAIL).海洋药物对肿瘤坏死因子相关凋亡诱导配体(TRAIL)诱导的细胞凋亡的调控作用
Mar Drugs. 2015 Nov 13;13(11):6884-909. doi: 10.3390/md13116884.
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Marine Compounds and Cancer: Where Do We Stand?海洋化合物与癌症:我们目前的进展如何?
Mar Drugs. 2015 Sep;13(9):5657-65. doi: 10.3390/md13095657. Epub 2015 Sep 2.
10
Characterization of apoptosis and autophagy through Bcl-2 and Beclin-1 immunoexpression in gestational trophoblastic disease.通过Bcl-2和Beclin-1免疫表达对妊娠滋养细胞疾病中的细胞凋亡和自噬进行特征分析。
Iran J Reprod Med. 2015 Jul;13(7):413-20.

海参来源化合物诱导癌细胞死亡的机制。

Mechanisms of cancer cell killing by sea cucumber-derived compounds.

机构信息

Faculty of Medicine, Universitas Kristen Maranatha (Maranatha Christian University), Jl. Prof. Drg. Suria Sumantri MPH No. 65, Bandung, 40164, Indonesia.

Biology Department, Faculty of Mathematics and Natural Sciences, The University of Brawijaya, Jl. Veteran, Malang, 65145, Indonesia.

出版信息

Invest New Drugs. 2017 Dec;35(6):820-826. doi: 10.1007/s10637-017-0505-5. Epub 2017 Sep 18.

DOI:10.1007/s10637-017-0505-5
PMID:28920157
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5694523/
Abstract

The aim of cancer therapy is to specifically eradicate tumor cells while causing minimal damage to normal tissues and minimal side-effects. Because of this, the use of natural substances with low toxicity is a good option. Sea cucumbers are one of many potential marine animals that contain valuable nutrients and medicinal properties. The medicinal value of sea cucumbers is attributed to the presence of bioactive agents with promising biological and pharmacological properties that include cytotoxic activity, induction of apoptosis, cell cycle arrest, inhibition of tumor growth, anti-metastatic and anti-angiogenic properties, and inhibition of drug resistance. This review discusses the mechanisms of cancer cell death induced by sea cucumber-derived compounds with regard to exploring the potential use of these marine natural products for cancer therapy.

摘要

癌症治疗的目的是特异性地消灭肿瘤细胞,同时对正常组织造成最小的损伤和最小的副作用。因此,使用毒性低的天然物质是一个很好的选择。海参是许多具有潜在药用价值的海洋动物之一,含有有价值的营养物质和药用特性。海参的药用价值归因于存在具有有前途的生物和药理特性的生物活性物质,包括细胞毒性活性、诱导细胞凋亡、细胞周期停滞、抑制肿瘤生长、抗转移和抗血管生成特性以及抑制耐药性。本综述讨论了海参衍生化合物诱导癌细胞死亡的机制,以期探索这些海洋天然产物在癌症治疗中的潜在用途。