MicroRNA-137 Inhibits Cancer Progression by Targeting Del-1 in Triple-Negative Breast Cancer Cells

被引:25
|
作者
Lee, Soo Jung [1 ]
Jeong, Jae-Hwan [2 ]
Kang, Seung Hee [2 ]
Kang, Jieun [2 ]
Kim, Eun Ae [2 ]
Lee, Jeeyeon [3 ]
Jung, Jin Hyang [3 ]
Park, Ho Yong [3 ,4 ]
Chae, Yee Soo [1 ]
机构
[1] Kyungpook Natl Univ, Chilgok Hosp, Sch Med, Dept Oncol Hematol, Daegu 41404, South Korea
[2] Kyungpook Natl Univ, Sch Med, Cell & Matrix Res Inst, Daegu 41944, South Korea
[3] Kyungpook Natl Univ, Chilgok Hosp, Sch Med, Dept Breast & Thyroid Surg, Daegu 41404, South Korea
[4] Kyungpook Natl Univ, Joint Inst Regenerat Med, Daegu 41944, South Korea
基金
新加坡国家研究基金会;
关键词
biomarker; Del-1; developmental endothelial locus-1; miR-137; triple-negative breast cancer; DEVELOPMENTAL ENDOTHELIAL LOCUS-1; TUMOR-SUPPRESSOR; EXTRACELLULAR VESICLES; IDENTIFICATION; PROLIFERATION; TRANSCRIPTION; EXPRESSION; CARCINOMA; EDIL3;
D O I
10.3390/ijms20246162
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) can be used to target a variety of human malignancy by targeting their oncogenes or tumor suppressor genes. The developmental endothelial locus-1 (Del-1) might be under miRNA regulation. This study investigated microRNA-137 (miR-137) function and Del-1 expression in triple-negative breast cancer (TNBC) cells and tissues. Del-1 mRNA and miRNA-137 levels were determined via qRT-PCR in breast cancer cells (MDA-MB-231, MCF7, SK-BR3, and T-47D) and tissues from 30 patients with TNBC. The effects of miR-137 on cell proliferation, migration, and invasion were determined using MTT assays, wound healing, and Matrigel transwell assays. The luciferase reporter assay revealed direct binding of miR-137 to the 3'-UTR of Del-1. miR-137 inhibited cell proliferation, migration, and invasion of MDA-MB-231 cells. Among the 30 TNBC specimens, miR-137 was downregulated and Del-1 level in plasma was significantly elevated relative to normal controls. It is concluded that miR-137 regulates Del-1 expression in TNBC by directly binding to the Del-1 gene and cancer progression. The results implicate miR-137 as a new therapeutic biomarker for patients with TNBC.
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页数:14
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