首页> 外文期刊>Breast cancer research and treatment. >Strigolactones: a novel class of phytohormones that inhibit the growth and survival of breast cancer cells and breast cancer stem-like enriched mammosphere cells.
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Strigolactones: a novel class of phytohormones that inhibit the growth and survival of breast cancer cells and breast cancer stem-like enriched mammosphere cells.

机译:Strigolactones:一种新的植物激素,可抑制乳腺癌细胞和富含乳腺癌干样的乳腺球细胞的生长和存活。

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摘要

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.
机译:几种天然存在的植物激素在预防和治疗各种不同类型的癌症中显示出巨大潜力。 Strigolactones(SLs)是一类在根部产生的新型植物激素,可通过抑制未分化的分生组织细胞的自我更新来调节新的地上分支。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。我们显示SL类似物能够抑制乳腺癌细胞的增殖并诱导其凋亡,但程度要小得多的“非癌”系。假定癌症复发的治疗问题被认为是由于耐药性癌症干细胞引起的,我们还测试了SL类似物抑制通常富含癌干样细胞的乳腺球培养物生长的能力。我们显示SL是乳腺细胞生长的乳腺癌细胞系自我更新和存活的有效抑制剂,即使短时间暴露也会对乳腺球的解离和细胞死亡产生不可逆的影响。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激活,并抑制PI3K / AKT激活。总而言之,这项研究表明SL可能是有前途的抗癌药物,其活性可以通过调节压力和生存信号通路来实现。

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