RETRACTED: MiR-16-5p inhibits breast cancer by reducing AKT3 to restrain NF-κB pathway (Retracted article. See vol. 42, 2022)

被引:52
作者
Ruan, Liwei [1 ]
Qian, Xiaojun [1 ]
机构
[1] Zhejiang Univ, Shaoxing Hosp, Shaoxing Peoples Hosp, Dept Breast & Thyroid Surg, Shaoxing 312000, Peoples R China
关键词
CELL-PROLIFERATION; THYROID-CANCER; MIRNAS; MIGRATION; EXPRESSION; MICRORNAS; PROMOTES; TARGETS; ROLES;
D O I
10.1042/BSR20191611
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
Background: Breast cancer endangers the life of women and has become the major cause of deaths among them. MiRNAs are found to exert a regulatory effect on the migration, proliferation and apoptosis of breast cancer cells. This research aims at investigating the miR-16-5p expression and its effect on the pathogenesis of breast cancer. Methods: Their clinical data were analyzed with qRT-PCR. CCK8, EdU and Transwell was performed to explore the function of miR-16-5p in cell migration and proliferation of breast cancer cells. Dual-luciferase reporter assay, immunohistochemistry and Western blotting were carried out to explore the relation between miR-16-5p and AKT3. Results: It was discovered that miR-16-5p was lowly expressed in breast cancer patients. Meanwhile, breast cancer patients with under-expressed miR-16-5p had a lower survival rate than those with highly expressed miR-16-5p. Furthermore, decreased miR-16-5p in cell and animal models enhanced migration and proliferation of breast cancer cells, stimulated cell cycle and reduced cell apoptosis. Finally, we found miR-16-5p restrained the NF-kappa B pathway and decreased AKT3 gene, thereby suppressing the breast cancer development. Conclusion: It can be seen that miR-16-5p exhibits a low expression in breast cancer tissues, which can inhibit breast cancer by restraining the NF-kappa B pathway and elevating reducing AKT3.
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页数:10
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共 38 条
[1]   Awareness and current knowledge of breast cancer [J].
Akram, Muhammad ;
Iqbal, Mehwish ;
Daniyal, Muhammad ;
Khan, Asmat Ullah .
BIOLOGICAL RESEARCH, 2017, 50
[2]   miRNA profiling identifies deregulated miRNAs associated with osteosarcoma development and time to metastasis in two large cohorts [J].
Andersen, Gitte B. ;
Knudsen, Alice ;
Hager, Henrik ;
Hansen, Lise L. ;
Tost, Jorg .
MOLECULAR ONCOLOGY, 2018, 12 (01) :114-131
[3]   SNHG16 contributes to breast cancer cell migration by competitively binding miR-98 with E2F5 [J].
Cai, Chang ;
Huo, Qiang ;
Wang, Xiaolong ;
Chen, Bing ;
Yang, Qifeng .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2017, 485 (02) :272-278
[4]   miRNA and Methylation: A Multifaceted Liaison [J].
Chhabra, Ravindresh .
CHEMBIOCHEM, 2015, 16 (02) :195-203
[5]   MicroRNAs in Cancer [J].
Di Leva, Gianpiero ;
Garofalo, Michela ;
Croce, Carlo M. .
ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 9, 2014, 9 :287-314
[6]   miR-424 targets AKT3 and PSAT1 and has a tumor-suppressive role in human colorectal cancer [J].
Fang, Yifeng ;
Liang, Xiao ;
Xu, Junfen ;
Cai, Xiujun .
CANCER MANAGEMENT AND RESEARCH, 2018, 10 :6537-6547
[7]   Breast Cancer Survivorship: Where Are We Today? [J].
Ganz, Patricia A. ;
Goodwin, Pamela J. .
IMPROVING OUTCOMES FOR BREAST CANCER SURVIVORS: PERSPECTIVES ON RESEARCH CHALLENGES AND OPPORTUNITIES, 2015, 862 :1-8
[8]  
Ghoncheh Mahshid, 2016, Asian Pac J Cancer Prev, V17, P43
[9]   Shared principles in NF-κB signaling [J].
Hayden, Matthew S. ;
Ghosh, Sankar .
CELL, 2008, 132 (03) :344-362
[10]   Triangle of AKT2, miRNA, and Tumorigenesis in Different Cancers [J].
Honardoost, Maryam ;
Rad, Seyed Mohammad Ali Hosseini .
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 2018, 185 (02) :524-540