Title of article :
Effect of Toll-Like Receptor 3 Agonists on the Functionality and Metastatic Properties of Breast Cancer Cell Model
Author/Authors :
Alizadeh, Nastaran Department of Immunology - School of Medicineb - Tehran University of Medical Sciences, Tehran , Amiri, Mohammad Mehdi Department of Pathobiology - School of Public Health - Tehran University of Medical Sciences, Tehran , Salek Moghadam, Alireza Department of Immunology - School of Medicineb - Tehran University of Medical Sciences, Tehran , Zarnani, Amir Hassan AlirezaDepartment of Immunology - School of Medicineb - Tehran University of Medical Sciences, Tehran , Saadat, Farshid Department of Immunology - School of Medicine - Guilan University of Medical Sciences, Rasht , Safavifar, Farnaz Endocrinology and Metabolism Research Center - Endocrinology and Metabolism Research Institute - Tehran University of Medical Sciences, Tehran , Berahmeh, Azar Endocrinology and Metabolism Research Center - Endocrinology and Metabolism Research Institute - Tehran University of Medical Sciences, Tehran , Khorramizadeh, Mohammad Reza Endocrinology and Metabolism Research Center - Endocrinology and Metabolism Research Institute - Tehran University of Medical Sciences, Tehran
Pages :
7
From page :
161
To page :
167
Abstract :
There exists compelling evidence that Toll-like receptor 3 (TLR3) agonists can directly affect human cancer cells. The aim of this study was to investigate anti-cancer effects of TLR3 agonist in human breast cell line. We assessed potential effects of poly (A:U) on human breast cell line (MDA-MB-231) on a dose-response and time-course basis. Human breast cell line MDA-MB-231 was treated with different concentrations of poly (A:U) and lipopolysaccharide (LPS). Then, the following assays were performed on the treated cells: dose-response and time-course cytotoxicity using colorimetric method; matrix metalloproteinase-2 (MMP-2) activity using gelatin zymography method; apoptosis using annexin-v flowcytometry method; and relative expression of TLR3 and MMP-2 mRNA using reverse transcriptase polymerase chain reaction (RT-PCR) method. Following treatments, doseresponse and time-course cytotoxicity using a colorimetric method, (MMP-2) activity (using gelatin zymography), apoptosis (using annexin-v flowcytometry method) assays and expression of TLR3 and MMP-2 genes (using PCR method) were performed. Cytotoxicity and flowcytometry analysis of poly (A:U) showed that poly (A:U) do not have any cytotoxic and apoptotic effects in different concentrations used. MMP-2 activity analysis showed significant decrease in higher concentrations (50 and 100 μg/ ml) between treated and untreated cells. Moreover, poly A:U treated cells demonstrated decreased expression of MMP-2 gene in higher concentrations. Collectively, our data indicated that human breast cancer cell line (MDA-MB-231) was highly responsive to poly (A:U). The antimetastatic effect of direct poly (A:U) and TLR3 interactions in MDA-MB-231 cells could provide new approaches in malignant tumor therapeutic strategy.
Keywords :
MDA-MB-231 , MMP-2 , Poly (A:U) , TLR3
Journal title :
Astroparticle Physics
Serial Year :
2013
Record number :
2479245
Link To Document :
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