Is Irisin an Anticarcinogenic Peptide?

Prostate cancer is the most common type of cancer in males. There has been currently no therapy to cure various types of cancer, and hence, studies aiming to develop cancer treatment are important and have been ongoing. Irisin is a hormone, which regulates body weight and metabolism, including insul...

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Main Authors: Suat Tekin, Yavuz Erden, Suleyman Sandal, Bayram Yilmaz
Format: Article
Language:English
Published: Society of TURAZ AKADEMI 2015-06-01
Series:Medicine Science
Subjects:
PC3
Online Access:http://www.ejmanager.com/fulltextpdf.php?mno=171454
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spelling doaj-8954ef2b62ab49b19c667fa429dc532f2020-11-25T00:17:17ZengSociety of TURAZ AKADEMI Medicine Science2147-06342015-06-014221728010.5455/medscience.2014.03.8210171454Is Irisin an Anticarcinogenic Peptide?Suat Tekin0Yavuz ErdenSuleyman SandalBayram YilmazDepartment of Physiology, Inonu University, Faculty of Medicine, Malatya, Turkey Department of Physiology, Yeditepe University, Faculty of Medicine, Istanbul, TurkeyProstate cancer is the most common type of cancer in males. There has been currently no therapy to cure various types of cancer, and hence, studies aiming to develop cancer treatment are important and have been ongoing. Irisin is a hormone, which regulates body weight and metabolism, including insulin resistance and is thought to have beneficial effects on the properties of antiobesytetic. It is known that obesity is a risk factor in the development of cancer and at the present time, the effects of peptides on cancer thay may reduce obesity have been investigated. This study was carried out to investigate whether there is a role of irisin on human prostate cancer cell viability. In the present study, 0.1, 1, 10 and 100 nM concentrations of irisin were separately applied to human prostate cancer cells with androgen receptor positive (LNCaP) and androgen receptor negative (DU-145, PC3). Effects of irisin on prostate cancer cells were determined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. At the end of study, all concentrations of irisin reduced the viability of all three prostate cell types, but only 10 and 100 nM concentrations of the irisin caused a significant decrease (p [Med-Science 2015; 4(2.000): 2172-80]http://www.ejmanager.com/fulltextpdf.php?mno=171454IrisinLNCaPDU-145PC3cell viability
collection DOAJ
language English
format Article
sources DOAJ
author Suat Tekin
Yavuz Erden
Suleyman Sandal
Bayram Yilmaz
spellingShingle Suat Tekin
Yavuz Erden
Suleyman Sandal
Bayram Yilmaz
Is Irisin an Anticarcinogenic Peptide?
Medicine Science
Irisin
LNCaP
DU-145
PC3
cell viability
author_facet Suat Tekin
Yavuz Erden
Suleyman Sandal
Bayram Yilmaz
author_sort Suat Tekin
title Is Irisin an Anticarcinogenic Peptide?
title_short Is Irisin an Anticarcinogenic Peptide?
title_full Is Irisin an Anticarcinogenic Peptide?
title_fullStr Is Irisin an Anticarcinogenic Peptide?
title_full_unstemmed Is Irisin an Anticarcinogenic Peptide?
title_sort is irisin an anticarcinogenic peptide?
publisher Society of TURAZ AKADEMI
series Medicine Science
issn 2147-0634
publishDate 2015-06-01
description Prostate cancer is the most common type of cancer in males. There has been currently no therapy to cure various types of cancer, and hence, studies aiming to develop cancer treatment are important and have been ongoing. Irisin is a hormone, which regulates body weight and metabolism, including insulin resistance and is thought to have beneficial effects on the properties of antiobesytetic. It is known that obesity is a risk factor in the development of cancer and at the present time, the effects of peptides on cancer thay may reduce obesity have been investigated. This study was carried out to investigate whether there is a role of irisin on human prostate cancer cell viability. In the present study, 0.1, 1, 10 and 100 nM concentrations of irisin were separately applied to human prostate cancer cells with androgen receptor positive (LNCaP) and androgen receptor negative (DU-145, PC3). Effects of irisin on prostate cancer cells were determined using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. At the end of study, all concentrations of irisin reduced the viability of all three prostate cell types, but only 10 and 100 nM concentrations of the irisin caused a significant decrease (p [Med-Science 2015; 4(2.000): 2172-80]
topic Irisin
LNCaP
DU-145
PC3
cell viability
url http://www.ejmanager.com/fulltextpdf.php?mno=171454
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