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The influence of miR-34a expression on stemness and cytotoxic susceptibility of breast cancer stem cells

机译:miR-34a表达对乳腺癌干细胞的干性和细胞毒性敏感性的影响

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In this study, we investigate the effect of miR-34a expression and biological characteristics of breast cancer stem cells (BCSCs). The mammospheres were formed from murine breast cancer cell line 4T1 and regarded as murine BCSCs. Identification of stemness molecules and cloning experiments validate the biological characteristics of BCSCs we have established. We showed that miR-34a, as a tumor suppressor, could separately reduce the stemness of BCSCs and activate the cytotoxic susceptibility of BCSCs to natural killer (NK) cells in vitro via down regulating the expression of Notch1 signaling molecules. Moreover, miR-34a could completely restrain established mice breast tumor xenografts in vivo in the NOD/SCID mice that have functional NK cells at a normal level, whereas it was less effective in NOD/SCID/ CD122/IL-2R mice that do not have functional NK cells. We conclude that miR-34a is a crucial, dual tumor suppressor and BCSCs-targeting immunotherapeutic agent and has shown efficacy in the treatment of murine breast cancer. The results also suggest that impaired NK cells could contribute to the resistance to therapies.
机译:在这项研究中,我们调查了miR-34a表达的影响以及乳腺癌干细胞(BCSCs)的生物学特性。乳球由鼠乳腺癌细胞系4T1形成,被视为鼠BCSC。茎分子的鉴定和克隆实验验证了我们已经建立的BCSC的生物学特性。我们表明,miR-34a作为一种肿瘤抑制因子,可以通过下调Notch1信号分子的表达来单独降低BCSC的干性并激活BCSC对自然杀伤(NK)细胞的细胞毒性敏感性。此外,miR-34a可以完全抑制体内功能正常的NK细胞的NOD / SCID小鼠体内已建立的小鼠乳腺肿瘤异种移植,而在不具有此功能的NOD / SCID / CD122 / IL-2R小鼠中效果较差具有功能性NK细胞。我们得出的结论是,miR-34a是至关重要的双重肿瘤抑制因子和BCSCs靶向免疫治疗剂,并已显示出对鼠类乳腺癌的治疗功效。结果还表明受损的NK细胞可能有助于抵抗治疗。

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