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MiR-2861作为肺癌干细胞的生物标志物并调控HDAC5-ERK系统基因。

MiR-2861 Behaves as a Biomarker of Lung Cancer Stem Cells and Regulates the HDAC5-ERK System Genes.

作者信息

Zhao Mengya, Li Lin, Zhou Jundong, Cui Xueyuan, Tian Qingmei, Jin Yaqing, Zhu Yimin

机构信息

1 CAS Key Laboratory of Nano-Bio Interface, Suzhou Institute of Nano-Tech and Nano-Bionics , Chinese Academy of Sciences, Suzhou, China .

2 College of Life Sciences, Shanghai University , Shanghai, China .

出版信息

Cell Reprogram. 2018 Apr;20(2):99-106. doi: 10.1089/cell.2017.0045. Epub 2018 Mar 13.

Abstract

Cancer stem cells (CSCs) are responsible for cancer initiating, recurrence, and drug resistance. Discovery of novel biomarkers for CSCs is helpful for early diagnosis and prognosis. Lung cancer stem cells (LCSCs) were closely related to the occurrence and development of lung cancer. In our study, the important role of miR-2861 in maintaining the stemness of LCSCs was investigated. The LCSC differentiation model was established through introducing serum into the medium of H460 spheres. miR-2861 expression was significantly higher in LCSCs no matter compared to the differentiation cells or normal cells. HDAC5 expression was positively correlated with miR-2861 in LCSCs, and knockdown of miR-2861 decreased the expression of HDAC5, which implied that HDAC5 may be involved in the differentiation of LCSCs mediated by miR-2861. The role of HDAC5 in the regulation of LCSC differentiation was further verified by the inhibitory effect of LMK-235 on the phosphorylation of ERK1/2, which was recognized as the regulator of CSC differentiation. Our study provided a better understanding of miR-2861 and HDAC5 axis in maintaining the stemness of LCSCs and laid a foundation for molecular targeted therapy.

摘要

癌症干细胞(CSCs)负责癌症的起始、复发和耐药性。发现CSCs的新型生物标志物有助于早期诊断和预后。肺癌干细胞(LCSCs)与肺癌的发生和发展密切相关。在我们的研究中,研究了miR-2861在维持LCSCs干性中的重要作用。通过向H460球体培养基中添加血清建立LCSC分化模型。无论与分化细胞还是正常细胞相比,LCSCs中miR-2861的表达均显著更高。LCSCs中HDAC5的表达与miR-2861呈正相关,敲低miR-2861会降低HDAC5的表达,这意味着HDAC5可能参与了miR-2861介导的LCSCs分化。ERK1/2的磷酸化被认为是CSC分化的调节因子,LMK-235对其具有抑制作用,进一步证实了HDAC5在调节LCSC分化中的作用。我们的研究为更好地理解miR-2861和HDAC5轴在维持LCSCs干性方面提供了依据,并为分子靶向治疗奠定了基础。

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