Title of article
The expression of Toll-Like Receptors (TLRs) in testicular cancer: A case control study
Author/Authors
Shapouri، Farnaz نويسنده Department of Endocrinology and Female Infertility at Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, T , , Saeidi، Shaghayegh نويسنده Department of Endocrinology and Female Infertility at Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, T , , Ashrafi Kakhki، Sara نويسنده Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran. , , Pouyan، Omid Pouyan نويسنده Department of Urology, Tehran University of Medical Sciences, Tehran, Iran , , Amirchaghmaghi، Elham نويسنده , , Aflatoonian، Mohammad Reza نويسنده ,
Issue Information
فصلنامه با شماره پیاپی سال 2013
Pages
6
From page
919
To page
924
Abstract
Background: It has been suggested that malfunction of immune system may causes testicular cancer. Recently, our understanding of innate immune system has been expanded, by discovery of “Toll-Like Receptors” (TLRs). Some studies have shown that polymorphisms of TLR2 and 4 may affect on the risk of cancer. Also, the role of TLRs 3 and 9 have been shown in apoptosis and metastasis of cancer cells in animal models.
Objective: Little information is available about the influence of innate immunity on testicular malignancy. Therefore, expression of TLRs 2, 3, 4 and 9 as main components of innate immunity has been investigated in this study.
Materials and Methods: In this case control study, TLRs gene expression was examined by RT-PCR in normal testis and testicular cancer tissues. Real time quantitative PCR (Q-PCR) analysis was used to compare the relative expression of TLRs between the samples.
Results: mRNAs of TLR 2, 3, 4 and 9 were expressed in all normal and cancer samples. Q-PCR reveals that cancer samples had stronger expression of these genes compared with normal ones.
Conclusion: It seems that the different TLRs expression in testicular cancer cells may contribute to extensive signaling pathways involved in carcinogenesis
Journal title
International Journal of Reproductive BioMedicine
Serial Year
2013
Journal title
International Journal of Reproductive BioMedicine
Record number
2391839
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