Literature DB >> 26431674

Bioinformatics Prediction and In Vitro Analysis Revealed That miR-17 Targets Cyclin D1 mRNA in Triple Negative Breast Cancer Cells.

Fariba Karami1, Samira Mohammadi-Yeganeh2,3, Nairi Abedi1, Ameneh Koochaki3, Vahid Kia4, Mahdi Paryan5.   

Abstract

Breast cancer is one of the most prevalent malignancies among women worldwide. Triple negative breast cancer (TNBC) is a type of breast cancer in which estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 (HER-2) are not expressed. There is no targeted therapy for this type of cancer, and available therapies have poor therapeutic effects. Performing a preliminary research, we selected cyclin D1 (CCND1) gene of Wnt signaling pathway which is a target of miRNAs, a promising set of biomolecules in diagnosis and treatment of breast cancer. In this study using bioinformatic analyses, miR-17 was selected as it targets the 3'UTR of CCND1 gene with the highest score. Luciferase assay results also confirmed the bioinformatic prediction. Decreased expression of miR-17 in MDA-MB-231 cell line was observed using qRT-PCR method. After lentiviral transduction of miR-17 to the target cells, gene expression analysis showed decreased expression of CCND1 gene. We found miR-17 as an attractive molecule that after intensive research can probably be used as a biomarker in TNBC.
© 2015 John Wiley & Sons A/S.

Entities:  

Keywords:  CCND1 gene; luciferase assay; miRNA; quantitative real-time RT-PCR; triple negative breast cancer

Mesh:

Substances:

Year:  2015        PMID: 26431674     DOI: 10.1111/cbdd.12671

Source DB:  PubMed          Journal:  Chem Biol Drug Des        ISSN: 1747-0277            Impact factor:   2.817


  7 in total

1.  Expression of Bioinformatically Candidate miRNAs including, miR-576-5p, miR-501-3p and miR-3143, Targeting PI3K Pathway in Triple-Negative Breast Cancer.

Authors:  Razie Hadavi; Samira Mohammadi-Yeganeh; Javad Razaviyan; Ameneh Koochaki; Parviz Kokhaei; Ahmadreza Bandegi
Journal:  Galen Med J       Date:  2019-11-10

2.  Decreased MiR-17 in glioma cells increased cell viability and migration by increasing the expression of Cyclin D1, p-Akt and Akt.

Authors:  Guangwei Sun; Guozhong SiMa; Chunhui Wu; Yongzhong Fan; Yong Tan; Zhong Wang; Gang Cheng; Jie Li
Journal:  PLoS One       Date:  2018-01-19       Impact factor: 3.240

Review 3.  OncomiR-17-5p: alarm signal in cancer?

Authors:  Madhusudhan Reddy Bobbili; Robert M Mader; Johannes Grillari; Hanna Dellago
Journal:  Oncotarget       Date:  2017-07-18

4.  Investigating the inhibitory effect of miR-34a, miR-449a, miR-1827, and miR-106b on target genes including NOTCH1, c-Myc, and CCND1 in human T cell acute lymphoblastic leukemia clinical samples and cell line.

Authors:  Tohid Naderi; Samira Mohammadi-Yeganeh; Neda Mohammadi-Hezaveh; Razie Hadavi; Ahmad Gharehbaghian; Nader Vazifeh-Shiran; Vahid Fallah Azad; Mahdi Paryan
Journal:  Iran J Basic Med Sci       Date:  2020-03       Impact factor: 2.699

5.  Morusin suppresses breast cancer cell growth in vitro and in vivo through C/EBPβ and PPARγ mediated lipoapoptosis.

Authors:  Haiyan Li; Qiaoping Wang; Lihua Dong; Chuanlan Liu; Zhen Sun; Ling Gao; Xiujie Wang
Journal:  J Exp Clin Cancer Res       Date:  2015-11-04

6.  DNA methylation biomarkers for hepatocellular carcinoma.

Authors:  Guorun Fan; Yaqin Tu; Cai Chen; Haiying Sun; Chidan Wan; Xiong Cai
Journal:  Cancer Cell Int       Date:  2018-09-17       Impact factor: 5.722

7.  An integrated approach of bioinformatic prediction and in vitro analysis identified that miR-34a targets MET and AXL in triple-negative breast cancer.

Authors:  Shadan Hajalirezay Yazdi; Mahdi Paryan; Samira Mohammadi-Yeganeh
Journal:  Cell Mol Biol Lett       Date:  2018-10-24       Impact factor: 5.787

  7 in total

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