Oncology Department, Jianhu Hospital Affiliated to Nantong University, Jianhu, Jiangsu 224700, P.R. China.
Thoracic Surgery Department, Sheyang People's Hospital, Sheyang, Jiangsu 224300, P.R. China.
Mol Med Rep. 2020 Jan;21(1):35-42. doi: 10.3892/mmr.2019.10836. Epub 2019 Nov 20.
Dysregulation of microRNAs (miRNAs) is involved in the pathogenesis of esophageal cancer. miRNA (miR)‑542‑3p is a tumor suppressor in multiple types of cancer. However, whether and how miR‑542‑3p contributes to the progression of esophageal cancer remains unknown, and this is the aim of the present study. In the current study, decreased expression of miR‑542‑3p was detected in tumor tissues compared with normal tissues from patients with esophageal cancer, and miR‑542‑3p expression was negatively correlated with mRNA expression levels of ovarian tumor domain‑containing ubiquitin aldehyde‑binding protein 1 (OTUB1) in tumor tissues from patients with esophageal cancer. In KYSE150 human esophageal squamous cell carcinoma cells, overexpression of miR‑542‑3p significantly decreased OTUB1 at mRNA and protein levels, whereas downregulation of miR‑542‑3p significantly increased OTUB1 expression. Using a dual‑luciferase assay, OTUB1 was validated to be a target gene of miR‑542‑3p in KYSE150 cells. Functionally, miR‑542‑3p significantly inhibited the migration and invasion of KYSE150 cells by repression of OTUB1 expression. These results demonstrated that miR‑542‑3p may promote the metastasis of esophageal cancer cells, and indicated that miR‑542‑3p may be a treatment target for esophageal cancer.
microRNAs (miRNAs) 的失调参与了食管癌的发病机制。miRNA (miR)-542-3p 在多种类型的癌症中是一种肿瘤抑制因子。然而,miR-542-3p 是否以及如何促进食管癌的进展尚不清楚,这也是本研究的目的。在本研究中,与食管癌患者的正常组织相比,肿瘤组织中检测到 miR-542-3p 的表达降低,并且食管癌患者肿瘤组织中 miR-542-3p 的表达与卵巢肿瘤结构域包含的泛素醛结合蛋白 1 (OTUB1) 的 mRNA 表达水平呈负相关。在 KYSE150 人食管鳞癌细胞中,miR-542-3p 的过表达显著降低了 OTUB1 的 mRNA 和蛋白水平,而 miR-542-3p 的下调显著增加了 OTUB1 的表达。通过双荧光素酶报告基因实验,验证了 OTUB1 是 KYSE150 细胞中 miR-542-3p 的靶基因。功能上,通过抑制 OTUB1 的表达,miR-542-3p 显著抑制了 KYSE150 细胞的迁移和侵袭。这些结果表明 miR-542-3p 可能促进食管癌细胞的转移,并表明 miR-542-3p 可能是食管癌的治疗靶点。