首页> 外文期刊>Oncology letters. >Association between miR-212-3p and SOX11, and the effects of miR-212-3p on cell proliferation and migration in mantle cell lymphoma
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Association between miR-212-3p and SOX11, and the effects of miR-212-3p on cell proliferation and migration in mantle cell lymphoma

机译:miR-212-3p与SOX11的关联,以及miR-212-3p对套细胞淋巴瘤细胞增殖和迁移的影响

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摘要

To the best of our knowledge, the effect of miR-212-3p on sex-determining region Y-box 11 (SOX11) expression has not been previously investigated and how this effect affects cell proliferation and migration in lymphoma remains unclear. The present study aimed to assess the association between microRNA-212-3p (miR-212-3p) and SOX11, and the effects of miR-212-3p on cell proliferation and migration in mantle cell lymphoma. Cancer tissue and corresponding paracancerous tissue samples were collected from 65 patients with mantle cell lymphoma. The mRNA expression levels of miR-212-3p and SOX11 were analyzed using quantitative PCR, and SOX11 protein expression was determined using western blotting. Following transfection, the miR-212-3p mimic group exhibited a significantly lower SOX11 mRNA and protein expression than the miR-NC group. After 48-72 h of transfection, cell proliferation in the miR-212-3p mimic group was significantly lower than that in the miR-NC group. Furthermore, the miR-212-3p mimic group exhibited significantly lower cell invasion and significantly higher apoptosis than the miR-NC group. The current results suggested that miR-212-3p inhibited lymphoma cell proliferation and migration, and promoted their apoptosis by specifically regulating SOX11. Therefore, miR-212-3p may serve as a novel therapeutic target and marker for lymphoma.
机译:据我们所知,miR-212-3p 对性别决定区 Y-box 11 (SOX11) 表达的影响以前尚未研究过,这种影响如何影响淋巴瘤的细胞增殖和迁移仍不清楚。本研究旨在评估microRNA-212-3p(miR-212-3p)与SOX11的相关性,以及miR-212-3p对套细胞淋巴瘤细胞增殖和迁移的影响。从 65 例套细胞淋巴瘤患者中收集癌组织和相应的癌旁组织样本。采用定量PCR法检测miR-212-3p和SOX11的mRNA表达水平,Western blotting法检测SOX11蛋白表达。转染后,miR-212-3p 模拟物组的 SOX11 mRNA 和蛋白表达显著低于 miR-NC 组。转染48-72 h后,miR-212-3p模拟物组的细胞增殖率显著低于miR-NC组。此外,与miR-NC组相比,miR-212-3p模拟组的细胞侵袭率显著降低,细胞凋亡显著升高。目前的结果表明,miR-212-3p抑制淋巴瘤细胞的增殖和迁移,并通过特异性调控SOX11促进其凋亡。因此,miR-212-3p可以作为淋巴瘤的新型治疗靶点和标志物。

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