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独脚金内酯:一类新型植物激素,可抑制乳腺癌细胞和富含乳腺癌干细胞样的球体细胞的生长和存活。

Strigolactones: a novel class of phytohormones that inhibit the growth and survival of breast cancer cells and breast cancer stem-like enriched mammosphere cells.

机构信息

Department of Human Science, Georgetown University, St. Mary's Hall Rm 260, Washington, DC 20007, USA.

出版信息

Breast Cancer Res Treat. 2012 Aug;134(3):1041-55. doi: 10.1007/s10549-012-1992-x. Epub 2012 Mar 29.

DOI:10.1007/s10549-012-1992-x
PMID:22476848
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3706105/
Abstract

Several naturally occurring phytohormones have shown enormous potential in the prevention and treatment of variety of different type of cancers. Strigolactones (SLs) are a novel class of plant hormones produced in roots and regulate new above ground shoot branching, by inhibiting self-renewal of undifferentiated meristem cells. Here, we study the effects of six synthetic SL analogs on breast cancer cell lines growth and survival. We show that SL analogs are able to inhibit proliferation and induce apoptosis of breast cancer cells but to a much lesser extent "non-cancer" lines. Given the therapeutic problem of cancer recurrence which is hypothesized to be due to drug resistant cancer stem cells, we also tested the ability of SL analogs to inhibit the growth of mammosphere cultures that are typically enriched with cancer stem-like cells. We show that SLs are potent inhibitors of self-renewal and survival of breast cancer cell lines grown as mammospheres and even a short exposure leads to irreversible effects on mammosphere dissociation and cell death. Immunoblot analysis revealed that SLs analogs induce activation of the stress response mediated by both P38 and JNK1/2 MAPK modules and inhibits PI3K/AKT activation. Taken together this study indicates that SLs may be promising anticancer agents whose activities may be achieved through modulation of stress and survival signaling pathways.

摘要

几种天然存在的植物激素在预防和治疗多种不同类型的癌症方面显示出巨大的潜力。独脚金内酯(SLs)是一类新型的植物激素,在根部分泌,通过抑制未分化的分生细胞的自我更新来调节地上新的分枝。在这里,我们研究了六种合成 SL 类似物对乳腺癌细胞系生长和存活的影响。我们表明,SL 类似物能够抑制乳腺癌细胞的增殖并诱导其凋亡,但对“非癌细胞系”的作用要小得多。鉴于癌症复发的治疗问题,据推测这是由于耐药性的癌症干细胞引起的,我们还测试了 SL 类似物抑制通常富含癌症干细胞样细胞的乳腺球体培养物生长的能力。我们表明,SLs 是乳腺癌细胞系作为乳腺球体生长的自我更新和存活的有效抑制剂,即使短时间暴露也会导致乳腺球体解离和细胞死亡的不可逆影响。免疫印迹分析显示,SLs 类似物诱导由 P38 和 JNK1/2 MAPK 模块介导的应激反应的激活,并抑制 PI3K/AKT 的激活。总之,这项研究表明,SLs 可能是有前途的抗癌药物,其活性可能通过调节应激和存活信号通路来实现。

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Breast Cancer Res Treat. 2012 Aug;134(3):1041-55. doi: 10.1007/s10549-012-1992-x. Epub 2012 Mar 29.
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Activation and function of the MAPKs and their substrates, the MAPK-activated protein kinases.
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Front Mol Biosci. 2023 Oct 26;10:1242935. doi: 10.3389/fmolb.2023.1242935. eCollection 2023.
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Comput Struct Biotechnol J. 2023 Jan 25;21:1092-1101. doi: 10.1016/j.csbj.2023.01.032. eCollection 2023.
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