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  1. Cancer Biotherapy & Radiopharmaceuticals
  2. Year: 2014 Volume: 29
  3. Year: 2014 Volume: 29 Issue: 8
  4. si-RNA-Mediated Silencing of ADRBK1 Gene Attenuates Breast Cancer Cell Proliferation.
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Year: 2017 Volume: 32
Year: 2016 Volume: 31
Year: 2015 Volume: 30
Year: 2014 Volume: 29
Year: 2014 Volume: 29 Issue: 10
Year: 2014 Volume: 29 Issue: 9
Year: 2014 Volume: 29 Issue: 8
Pretargeted Radioimmunotherapy of Prostate Cancer with an Anti-TROP-2×Anti-HSG Bispecific Antibody and a $^{177}Lu-Labeled$ Peptide
si-RNA-Mediated Silencing of ADRBK1 Gene Attenuates Breast Cancer Cell Proliferation.
Year: 2014 Volume: 29 Issue: 7
Year: 2014 Volume: 29 Issue: 6
Year: 2014 Volume: 29 Issue: 5
Year: 2014 Volume: 29 Issue: 4
Year: 2014 Volume: 29 Issue: 3
Year: 2014 Volume: 29 Issue: 2
Year: 2014 Volume: 29 Issue: 1
Year: 2013 Volume: 28
Year: 2012 Volume: 27
Year: 2011 Volume: 26
Year: 2010 Volume: 25
Year: 2009 Volume: 24
Year: 2008 Volume: 23
Year: 2007 Volume: 22
Year: 2006 Volume: 21

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si-RNA-Mediated Silencing of ADRBK1 Gene Attenuates Breast Cancer Cell Proliferation.

Content Provider World Health Organization (WHO)-Global Index Medicus
Author Zhang, Chen Chen, Xianzhen Li, Yongxin Himaya, S. W. A. Wu, Jie Shi, Xiujuan Liu, Xiaoqing Kim, Sekwon
Description Country affiliation: China Author Affiliation: Zhang C ( 1 Shanghai Tenth People's Hospital, Tongji University School of Medicine , Shanghai, China .)
Abstract Abstract Breast cancer is the most prominent cause of cancer-related deaths among women worldwide. It has been found that genetic mutations play distinct roles in the onset and progression of breast cancer. Androgenic, beta, receptor kinase 1 (ADRBK1) has been reported to possess oncogenic characteristics vital for cancer cell viability. This study was designed to investigate the effects of small interference RNA (si-RNA)-mediated ADRBK1 knockdown on breast cancer cell growth in vitro. High-expression levels of ADRBK1 were observed in all tested breast cancer cell lines (MDA-MB-231, MCF-7, T-47D, and BT-474). ADRBK1 si-RNA was delivered to breast cancer cells using lentivirus delivery system. Depletion of ADRBK1 significantly attenuated the cell viability and colony-formation ability. Flow cytometry analysis further demonstrated that ADRBK1 silencing led to MDA-MB-231 cell arrest in the G0/G1 phase. Collectively, these results indicate that knockdown of ADRBK1 gene has detrimental effects on breast cancer cell growth, which may be a potential therapeutic approach for the treatment of breast cancer.
File Format HTM / HTML
ISSN 10849785
e-ISSN 15578852
DOI 10.1089/cbr.2014.1653
Journal Cancer Biotherapy & Radiopharmaceuticals
Issue Number 8
Volume Number 29
Language English
Publisher Mary Ann Liebert, Inc.
Publisher Date 2014-10-01
Publisher Place United States
Access Restriction Open
Subject Keyword Discipline Pharmacology Discipline Oncology Breast Neoplasms Therapy G-protein-coupled Receptor Kinase 2 Genetics Rna, Small Interfering Administration & Dosage Apoptosis Enzymology Cell Growth Processes Cell Line, Tumor Deficiency Metabolism Gene Expression Regulation, Neoplastic Gene Knockdown Techniques Gene Silencing Mcf-7 Cells Transfection Research Support, Non-u.s. Gov't
Content Type Text
Resource Type Article
Subject Radiology, Nuclear Medicine and Imaging Cancer Research Pharmacology Oncology
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