The high expression of miR-31 in lung adenocarcinoma inhibits the malignancy of lung adenocarcinoma tumor stem cells

Ran Xu; Tianhua Liu; Ling Zuo; Dongqing Guo; Guancheng Ye; Jingjing Jiang; Xue Yu; Shujing Zhang; Chunying Hou

doi:10.1016/j.bbrep.2021.101122

The high expression of miR-31 in lung adenocarcinoma inhibits the malignancy of lung adenocarcinoma tumor stem cells

Biochem Biophys Rep. 2021 Aug 30:28:101122. doi: 10.1016/j.bbrep.2021.101122. eCollection 2021 Dec.

Authors

Ran Xu¹, Tianhua Liu², Ling Zuo³, Dongqing Guo³, Guancheng Ye², Jingjing Jiang⁴, Xue Yu², Shujing Zhang², Chunying Hou²

Affiliations

¹ School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
² School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
³ School of Life Science, Beijing University of Chinese Medicine, Beijing, China.
⁴ School of the Humanities, Beijing University of Chinese Medicine, Beijing, China.

Abstract

Therapies for lung adenocarcinoma (LUAD) are mainly limited by drug resistance, metastasis or recurrence related to cancer stem cells (CSCs) with high proliferation and self-renewing. This research validated that miR-31 was over-expressed in LUAD by the analysis of generous clinical samples data. And the results of clinical data analysis showed that high expression of miR-31 was more common in patients with worse prognosis. The genes differentially expressed in LUAD tissues compared with normal tissues and A549CD133⁺ cells (LUAD CSCs) compared with A549 cells were separately screened from Gene Expression Profiling Interactive Analysis and GEO datasets. The target genes that may play a role in the regulation of lung adenocarcinoma was screened by comparison between the differential genes and the target genes of miR-31. The functional enrichment analysis of GO Biological Processes showed that the expression of target genes related to cell proliferation was increased, while the expression of target genes related to cell invasion and metastasis was decreased in LUAD tissues and A549CD133⁺ cells. The results suggested that miR-31 may have a significant inhibitory effect on the differentiation, invasion, metastasis and adhesion of LUAD CSCs, which was verified in vivo and in vitro experiments. Knock down of miR-31 accelerated xenograft tumor growth and liver metastasis in vivo. Likewise, the carcinogenicity, invasion and metastasis of A549CD133⁺ CSCs were promoted after miR-31 knockdown. The study validated that miR-31 was up regulated in LUAD and its expression may affect the survival time of patients with lung adenocarcinoma, which indicated that miR-31 may have potential value for diagnosis and prognosis of LUAD. However, the inhibitory effect of miR-31 on tumorigenesis, invasion and metastasis of lung adenocarcinoma CSCs suggested its complexity in the regulation of lung adenocarcinoma, which may be related to its extensive regulation of various target genes.

Keywords: CSCs; LUAD; Metastasis; MiR-31; Tumorigenesis.