Decreased expression of Toll-like receptor 4 and 5 during progression of prostate transformation in transgenic adenocarcinoma of mouse prostate mice.
10.4142/jvs.2015.16.3.281
- Author:
Ju Hee HAN
1
;
Jong Hwan PARK
;
Bo Yeon KIM
;
Seo Na CHANG
;
Tae Hyoun KIM
;
Jae Hak PARK
;
Dong Jae KIM
Author Information
1. Laboratory Animal Medicine, BK21 PLUS Program for Creative Veterinary Science Research, Research Institute for Veterinary Science and College of Veterinary Medicine, Seoul National University, Seoul 151-742, Korea. pjhak@snu.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
prostate cancer;
Toll-like receptor 4;
Toll-like receptor 5;
transgenic adenocarcinoma of mouse prostate
- MeSH:
Adenocarcinoma/etiology/*genetics;
Animals;
Cell Transformation, Neoplastic;
Disease Progression;
*Gene Expression Regulation, Neoplastic;
Humans;
Male;
Mice;
Mice, Inbred C57BL;
Mice, Transgenic;
Prostatic Neoplasms/etiology/*genetics;
Toll-Like Receptor 4/*genetics/metabolism;
Toll-Like Receptor 5/*genetics/metabolism
- From:Journal of Veterinary Science
2015;16(3):281-287
- CountryRepublic of Korea
- Language:English
-
Abstract:
Chronic inflammation has been considered an important risk factor for development of prostate cancer. Toll-like receptors (TLRs) recognize microbial moieties or endogenous molecules and play an important role in the triggering and promotion of inflammation. In this study, we examined whether expression of TLR4 and TLR5 was associated with progression of prostate transformation in the transgenic adenocarcinoma of mouse prostate (TRAMP) model. The expression of TLR4 and TLR5 was evaluated by immunohistochemisty in formalin-fixed paraffin-embedded prostate tissue from wild-type (WT) and TRAMP mice. Normal prostate tissue from WT mice showed strong expression of TLR4 and TLR5. However, TLR4 expression in the prostate tissue from TRAMP mice gradually decreased as pathologic grade became more aggressive. TLR5 expression in the prostate tissue from TRAMP mice also decreased in low-grade prostate intraepithelial neoplasia (PIN), high-grade PIN and poorly differentiated adenocarcinoma. Overall, our results suggest that decreased expression of TLR4 and TLR5 may contribute to prostate tumorigenesis.