The expression of Toll-Like Receptors (TLRs) in testicular cancer: A case control study

被引:0
|
作者
Shapouri, Farnaz [1 ]
Saeidi, Shaghayegh [1 ]
Kakhki, Sara Ashrafi [2 ]
Pouyan, Omid [3 ]
Amirchaghmaghi, Elham [1 ,4 ]
Aflatoonian, Reza [1 ]
机构
[1] ACECR, Royan Inst Reprod Biomed, Reprod Biomed Res Ctr, Dept Endocrinol & Female Infertil, Tehran, Iran
[2] Islamic Azad Univ, Sci & Res Branch, Dept Biol, Tehran, Iran
[3] Univ Tehran Med Sci, Dept Urol, Tehran, Iran
[4] Isfahan Univ Med Sci, Fac Med, Dept Immunol, Esfahan, Iran
关键词
Toll-like Receptors (TLRs); Testicular Cancer; Innate Immunity; NF-kappa B; NF-KAPPA-B; INFLAMMATION-ASSOCIATED CANCER; GERM-CELL TUMORS; CONSTITUTIVE ACTIVATION; HELICOBACTER-PYLORI; INNATE IMMUNITY; RECOGNITION; PATHOGENS; APOPTOSIS; GROWTH;
D O I
暂无
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
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.
引用
收藏
页码:919 / 924
页数:6
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