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本文引用的文献

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Approaches to mitochondrially mediated cancer therapy.线粒体介导的癌症治疗方法。
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Eur J Cancer. 2008 Jan;44(2):172-4. doi: 10.1016/j.ejca.2007.11.006. Epub 2007 Dec 11.
3
Desipramine induces apoptotic cell death through nonmitochondrial and mitochondrial pathways in different types of human colon carcinoma cells.地昔帕明通过非线粒体和线粒体途径在不同类型的人结肠癌细胞中诱导凋亡性细胞死亡。
Pharmacology. 2008;81(2):164-72. doi: 10.1159/000111144. Epub 2007 Nov 19.
4
Cytotoxicity of different selective serotonin reuptake inhibitors (SSRIs) against cancer cells.不同选择性5-羟色胺再摄取抑制剂(SSRI)对癌细胞的细胞毒性
J Exp Ther Oncol. 2006;6(1):23-9.
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Molecular mechanism of 'mitocan'-induced apoptosis in cancer cells epitomizes the multiple roles of reactive oxygen species and Bcl-2 family proteins.“米托坎”诱导癌细胞凋亡的分子机制体现了活性氧和Bcl-2家族蛋白的多种作用。
FEBS Lett. 2006 Oct 2;580(22):5125-9. doi: 10.1016/j.febslet.2006.05.072. Epub 2006 Jun 12.
6
15-Hydroxyprostaglandin dehydrogenase is an in vivo suppressor of colon tumorigenesis.15-羟基前列腺素脱氢酶是结肠癌发生的体内抑制因子。
Proc Natl Acad Sci U S A. 2006 Aug 8;103(32):12098-102. doi: 10.1073/pnas.0603235103. Epub 2006 Jul 31.
7
Characterization of cytotoxic actions of tricyclic antidepressants on human HT29 colon carcinoma cells.三环类抗抑郁药对人HT29结肠癌细胞的细胞毒性作用特征
Eur J Pharmacol. 2006 Jul 10;541(1-2):17-23. doi: 10.1016/j.ejphar.2006.04.053. Epub 2006 May 20.
8
Induction of the permeability transition and cytochrome c release by 15-deoxy-Delta12,14-prostaglandin J2 in mitochondria.15-脱氧-Δ12,14-前列腺素J2在线粒体中诱导通透性转换和细胞色素c释放
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9
Differential induction of apoptosis by antidepressants in glioma and neuroblastoma cell lines: evidence for p-c-Jun, cytochrome c, and caspase-3 involvement.抗抑郁药对胶质瘤和神经母细胞瘤细胞系凋亡的差异诱导作用:p-c-Jun、细胞色素c和半胱天冬酶-3参与的证据。
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Chlorimipramine: a novel anticancer agent with a mitochondrial target.氯米帕明:一种靶向线粒体的新型抗癌剂。
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用抗抑郁药战胜癌症。

Defeating cancer with antidepressants.

作者信息

Lieb J

机构信息

127 Cumberland Road, Burlington, Vermont, USA.

出版信息

Ecancermedicalscience. 2008;2:88. doi: 10.3332/ecancer.2008.88. Epub 2008 Aug 21.

DOI:10.3332/ecancer.2008.88
PMID:22275973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3234054/
Abstract

Prostaglandins are ephemeral, infinitesimal signallers self-regulating every cell in the body, including those sub-serving mood and immunity. At first, they were perceived as a master switch, but now are believed to regulate every component of cellular micro-anatomy and physiology, including those of the organelles, cytoskeleton, proteins, enzymes, nucleic acids and mitochondria. Prostaglandins are responsible, paradoxically, for cell function and dysfunction. Excessive prostaglandin synthesis depresses immune function and may induce cancer. An ideal anti-cancer agent would inhibit prostaglandins in such a manner as to shut down the pathogenesis of cancer. In this paper, I will show that antidepressants have such properties.

摘要

前列腺素是转瞬即逝、极其微小的信号分子,它们自我调节身体中的每一个细胞,包括那些与情绪和免疫相关的细胞。起初,它们被视为一个主开关,但现在人们认为它们能调节细胞微观解剖学和生理学的各个组成部分,包括细胞器、细胞骨架、蛋白质、酶、核酸和线粒体的组成部分。矛盾的是,前列腺素既负责细胞的正常功能,也会导致细胞功能紊乱。前列腺素合成过多会抑制免疫功能,并可能诱发癌症。一种理想的抗癌药物应以能够阻断癌症发病机制的方式抑制前列腺素。在本文中,我将证明抗抑郁药具有这样的特性。