Expression of TLR4/MyD88 in CRC
Wang, EL University of Tokushima|Kanazawa Medical University
Qian, ZR University of Tokushima
Nakasono, M University of Tokushima|Tsurugi Municipal Handa-Hospital
Tanahashi, T University of Tokushima
Yoshimoto, Katsuhiko University of Tokushima Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Bando, Yoshimi University of Tokushima Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Kudo, E University of Tokushima
Shimada, Mitsuo University of Tokushima Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Sano, Toshiaki University of Tokushima Tokushima University Educator and Researcher Directory KAKEN Search Researchers
BACKGROUND: The Toll-like receptor (TLR) 4 signalling pathway has been shown to have oncogenic effects in vitro and in vivo. To demonstrate the role of TLR4 signalling in colon tumourigenesis, we examined the expression of TLR4 and myeloid differentiation factor 88 (MyD88) in colorectal cancer (CRC).
METHODS: The expression of TLR4 and MyD88 in 108 CRC samples, 15 adenomas, and 15 normal mucosae was evaluated by immunohistochemistry, and the correlations between their immunoscores and clinicopathological variables, including disease-free survival (DFS) and overall survival (OS), were analysed.
RESULTS: Compared with normal mucosae and adenomas, 20% cancers displayed high expression of TLR4, and 23% cancers showed high expression of MyD88. The high expression of TLR4 and MyD88 was significantly correlated with liver metastasis (P=0.0001, P=0.0054). In univariate analysis, the high expression of TLR4 was significantly associated with shorter OS (hazard ratio (HR): 2.17; 95% confidence interval (95% CI): 1.15–4.07; P=0.015). The high expression of MyD88 expression was significantly associated with poor DFS and OS (HR: 2.33; 95% CI: 1.31–4.13; P=0.0038 and HR: 3.03; 95% CI: 1.67–5.48; P=0.0002). The high combined expression of TLR4 and MyD88 was also significantly associated with poor DFS and OS (HR: 2.25; 95% CI: 1.27–3.99; P=0.0053 and HR: 2.97; 95% CI: 1.64–5.38; P=0.0003). Multivariate analysis showed that high expressions of TLR4 (OS: adjusted HR: 1.88; 95% CI: 0.99–3.55; P=0.0298) and MyD88 (DFS: adjusted HR: 1.93; 95% CI: 1.01–3.67; P=0.0441; OS: adjusted HR: 2.25; 95% CI: 1.17–4.33; P=0.0112) were independent prognostic factors of OS. Furthermore, high co-expression of TLR4/MyD88 was strongly associated with both poor DFS and OS.
CONCLUSION: Our findings suggest that high expression of TLR4 and MyD88 is associated with liver metastasis and is an independent predictor of poor prognosis in patients with CRC.
British Journal of Cancer
This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License(http://creativecommons.org/licenses/by-nc-sa/3.0/).
|DOI (Published Version)|
|URL ( Publisher's Version )|
bjc_102_5_908.pdf 1020 KB