Evaluation of MiR-1908-3p as a novel serum biomarker for breast cancer and analysis its oncogenic function and target genes

被引:15
作者
Zhu, Youzhi [1 ]
Wang, Qingshui [2 ,3 ]
Xia, Yun [2 ]
Xiong, Xiaoxue [2 ]
Weng, Shuyun [2 ]
Ni, Huizhen [2 ]
Ye, Yan [2 ]
Chen, Ling [1 ]
Lin, Junyu [1 ]
Chen, Yajuan [2 ]
Niu, Haitao [2 ]
Chen, Xiangjin [1 ]
Lin, Yao [2 ]
机构
[1] Fujian Med Univ, Dept Thyroid & Breast Surg, Affiliated Hosp 1, Fuzhou, Peoples R China
[2] Fujian Normal Univ, Key Lab OptoElect Sci & Technol Med, Minist Educ, Coll Life Sci, Fuzhou, Peoples R China
[3] Ningde Normal Univ, Engn Technol Res Ctr Characterist Med Plants Fuji, Ningde, Peoples R China
关键词
Breast cancer; miR-1908-3p; Proliferation; Migration; Invasion; MICRORNA; CELLS; PROLIFERATION; APOPTOSIS; PROGNOSIS;
D O I
10.1186/s12885-020-07125-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundBreast cancer is one of the most common tumors for women globally. Various miRNAs have been reported to play a crucial role in breast cancer, however the clinical significance of miR-1908-3p in breast cancer remains unclear. The present study aimed to explore the role of miR-1908-3p in breast cancer.MethodsThe expression of miR-1908-3p was detected in 50 pairs of breast cancer tissues and adjacent normal tissues, 60 breast cancer patient serum and 60 healthy volunteer serum. The functional roles of miR-1908-3p in breast cancer cells such as proliferation, migration and invasion were evaluated using CCK8, SRB, wound healing and transwell chambers. In addition, bioinformatics tools were used to identify potential targets of miR-1908-3p.ResultsThe results showed that the expression of miR-1908-3p were increased in breast cancer tissues and serum compared with normal breast tissues and serum of healthy volunteers respectively. Furthermore, the young breast cancer patients and HER2-positive patients had a higher level of tissues' miR-1908-3p than elder breast cancer patients and HER2-negative patients, respectively. The young breast cancer patients had a higher level of serum miR-1908-3p than elder breast cancer patients, ROC analysis suggested that miR-1908-3p had the potential as a promising serum diagnostic biomarker of breast cancer. Up-regulation of miR-1908-3p promoted the cells proliferation, migration and invasion while knockdown of miR-1908-3p inhibited these processes in breast cancer cell MCF-7 and MDA-MB-231. The potential target genes of miR-1908-3p in breast cancer included ID4, LTBP4, GPM6B, RGMA, EFCAB1, ALX4, OSR1 and PPARA. Higher expression of these eight genes correlated with a better prognosis for breast cancer patients.ConclusionsThese results suggest that miR-1908-3p may exert its oncogenic functions via suppression of these eight genes in breast cancer.
引用
收藏
页数:12
相关论文
共 34 条
[1]   Predicting effective microRNA target sites in mammalian mRNAs [J].
Agarwal, Vikram ;
Bell, George W. ;
Nam, Jin-Wu ;
Bartel, David P. .
ELIFE, 2015, 4
[2]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[3]   RETRACTED: Long non-coding RNA LINC00467 regulates hepatocellular carcinoma progression by modulating miR-9-5p/ PPARA expression (Retracted Article) [J].
Cai, Kerui ;
Li, Tieling ;
Guo, Ling ;
Guo, Haifeng ;
Zhu, Wei ;
Yan, Lei ;
Li, Fujuan .
OPEN BIOLOGY, 2019, 9 (09)
[4]   Altered Circulating miRNA Expression Profile in Pregestational and Gestational Obesity [J].
Carreras-Badosa, Gemma ;
Bonmati, Alexandra ;
Ortega, Francisco-Jose ;
Mercader, Josep-Maria ;
Guindo-Martinez, Marta ;
Torrents, David ;
Prats-Puig, Anna ;
Martinez-Calcerrada, Jose-Maria ;
Platero-Gutierrez, Estibaliz ;
De Zegher, Francis ;
Ibanez, Lourdes ;
Fernandez-Real, Jose-Manuel ;
Lopez-Bermejo, Abel ;
Bassols, Judit .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2015, 100 (11) :E1446-E1456
[5]   miR-1908 as a novel prognosis marker of glioma via promoting malignant phenotype and modulating SPRY4/RAF1 axis [J].
Chai, Zhi ;
Fan, Huijie ;
Li, Yanyan ;
Song, Lijuan ;
Jin, Xiaoming ;
Yu, Jiezhong ;
Li, Yanhua ;
Ma, Cungen ;
Zhou, Ran .
ONCOLOGY REPORTS, 2017, 38 (05) :2717-2726
[6]   ID4: a new player in the cancer arena [J].
Dell'Orso, Stefania ;
Ganci, Federica ;
Strano, Sabrina ;
Blandino, Giovanni ;
Fontemaggi, Giulia .
ONCOTARGET, 2010, 1 (01) :48-58
[7]   Weak seed-pairing stability and high target-site abundance decrease the proficiency of lsy-6 and other microRNAs [J].
Garcia, David M. ;
Baek, Daehyun ;
Shin, Chanseok ;
Bell, George W. ;
Grimson, Andrew ;
Bartel, David P. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2011, 18 (10) :1139-U75
[8]   MicroRNA targeting specificity in mammals: Determinants beyond seed pairing [J].
Grimson, Andrew ;
Farh, Kyle Kai-How ;
Johnston, Wendy K. ;
Garrett-Engele, Philip ;
Lim, Lee P. ;
Bartel, David P. .
MOLECULAR CELL, 2007, 27 (01) :91-105
[9]   Effect of OSW-1 on microRNA expression profiles of hepatoma cells and functions of novel microRNAs [J].
Jin, Ji-Chun ;
Jin, Xing-Lin ;
Zhang, Xian ;
Piao, Ying-Shi ;
Liu, Shuang-Ping .
MOLECULAR MEDICINE REPORTS, 2013, 7 (06) :1831-1837
[10]   WP1130 Enhances TRAIL-Induced Apoptosis through USP9X-Dependent miR-708-Mediated Downregulation of c-FLIP [J].
Kim, Seok ;
Woo, Seon Min ;
Min, Kyoung-jin ;
Seo, Seung Un ;
Lee, Tae-Jin ;
Kubatka, Peter ;
Kim, Dong Eun ;
Kwon, Taeg Kyu .
CANCERS, 2019, 11 (03)