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微小RNA-196b的过表达通过调控同源框A9促进复发性上皮性卵巢癌癌细胞的侵袭性。

Overexpression of microRNA-196b Accelerates Invasiveness of Cancer Cells in Recurrent Epithelial Ovarian Cancer Through Regulation of Homeobox A9.

作者信息

Chong Gun Oh, Jeon Hyo-Sung, Han Hyung Soo, Son Ji Woong, Lee Yoon Hee, Hong Dae Gy, Park Hong Jun, Lee Yoon Soon, Cho Young Lae

机构信息

Department of Obstetrics and Gynecology, School of Medicine, Kyungpook National University Hospital, Daegu, Republic of Korea.

Mmonitor. Inc., Daegu, Republic of Korea

出版信息

Cancer Genomics Proteomics. 2017 Mar-Apr;14(2):137-141. doi: 10.21873/cgp.20026.

Abstract

BACKGROUND/AIM: Although microRNAs (miRNAs) are known to influence messenger RNA post-transcriptional control and contribute to human tumorigenesis, little is known about the differences in miRNA expression between primary and recurrent epithelial ovarian cancer (EOC). The purpose of this study was to assess the differential miRNA expression between primary and recurrent EOC and to investigate whether miR-196b could regulate the expression of the Homeobox A9 (HOXA9) gene, and thus affect the invasiveness of cancer cells in recurrent EOC.

MATERIALS AND METHODS

Microarrays were used to generate the expression profiles of 6658 miRNAs from samples of 10 patients with EOC. miRNA expression patterns were compared between primary and recurrent EOC. Aberrantly expressed miRNA, associated genes, and invasion activities were validated by a luciferase assay and an in vitro invasion assay.

RESULTS

miRNA microarray analysis identified 33 overexpressed miRNAs (including miR-196b) and 18 under expressed miRNAs in recurrent EOC from 6658 human miRNAs. HOXA9 expression was inversely correlated with miR-196b levels in recurrent EOC. We noted that miR-196b induced ovarian cancer cell invasiveness in recurrent EOC by an in vitro invasion assay.

CONCLUSION

Overexpression of miR-196b may contribute to invasion activities in recurrent EOC by regulating the HOXA9 gene. Moreover, miR-196b can be a potential biomarker in recurrent EOC.

摘要

背景/目的:尽管已知微小RNA(miRNA)会影响信使核糖核酸的转录后调控并参与人类肿瘤发生过程,但对于原发性和复发性上皮性卵巢癌(EOC)之间miRNA表达的差异却知之甚少。本研究的目的是评估原发性和复发性EOC之间miRNA表达的差异,并研究miR-196b是否能够调节同源盒A9(HOXA9)基因的表达,进而影响复发性EOC中癌细胞的侵袭性。

材料与方法

使用微阵列分析10例EOC患者样本中6658种miRNA的表达谱。比较原发性和复发性EOC之间的miRNA表达模式。通过荧光素酶测定和体外侵袭试验验证异常表达的miRNA、相关基因及侵袭活性。

结果

miRNA微阵列分析从6658种人类miRNA中鉴定出复发性EOC中33种过表达的miRNA(包括miR-196b)和18种低表达的miRNA。在复发性EOC中,HOXA9的表达与miR-196b水平呈负相关。我们通过体外侵袭试验发现,miR-196b可诱导复发性EOC中的卵巢癌细胞侵袭。

结论

miR-196b的过表达可能通过调控HOXA9基因促进复发性EOC中的侵袭活性。此外,miR-196b可能成为复发性EOC的潜在生物标志物。

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