TY - JOUR
T1 - Prognostic significance of lactate/proton symporters mct1, mct4, and their chaperone CD147 expressions in urothelial carcinoma of the bladder
AU - Choi, Jung Woo
AU - Kim, Younghye
AU - Lee, Ju Han
AU - Kim, Young Sik
N1 - Funding Information:
Funding Support: This work was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (grant number: 2013 R1A1A1058146).
Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 2014
Y1 - 2014
N2 - Objective To investigate the prognostic significance of lactate/proton monocarboxylate transporters MCT1, MCT4, and their chaperone CD147 expressions in urothelial carcinoma of the bladder (UCB). Methods We examined the expressions of MCT1, MCT4, and CD147 proteins in a total of 360 cases of UCB by immunohistochemistry. The immunohistochemical expressions were quantified using an ImageJ-based analysis program. Results MCT1, MCT4, and CD147 expressions were increased in 130 (36.1%), 168 (46.7%), and 228 (63.3%) UCB cases, respectively. Most tumor cells showed diffuse membranous staining, whereas normal urothelial cells showed negative or weak staining. High levels of MCT1 expression correlated with high World Health Organization grade (P <.001), advanced tumor node metastasis (TNM) stage (P <.001), nonpapillary growth type (P <.001), and lymphatic tumor invasion (P =.010), whereas high levels of MCT4 expression did not significantly correlate with any of these variables. High CD147 expression was associated with high World Health Organization grade (P <.001), advanced tumor node metastatis stage (P <.001), and nonpapillary growth type (P =.003). Univariate analyses revealed that high MCT1 (P <.001) and CD147 (P =.029) expressions were associated with poor overall survival and that high MCT4 expression was correlated with poor recurrence-free survival (P =.036). Multivariate analyses revealed that high MCT1 and MCT4 expressions were independent prognostic factors for poor overall survival and poor recurrence-free survival, respectively, in UCB patients. Conclusion Our results indicate that increased MCT1, MCT4, and CD147 expressions have prognostic implications in UCB and suggest their roles in urothelial cancer metabolism.
AB - Objective To investigate the prognostic significance of lactate/proton monocarboxylate transporters MCT1, MCT4, and their chaperone CD147 expressions in urothelial carcinoma of the bladder (UCB). Methods We examined the expressions of MCT1, MCT4, and CD147 proteins in a total of 360 cases of UCB by immunohistochemistry. The immunohistochemical expressions were quantified using an ImageJ-based analysis program. Results MCT1, MCT4, and CD147 expressions were increased in 130 (36.1%), 168 (46.7%), and 228 (63.3%) UCB cases, respectively. Most tumor cells showed diffuse membranous staining, whereas normal urothelial cells showed negative or weak staining. High levels of MCT1 expression correlated with high World Health Organization grade (P <.001), advanced tumor node metastasis (TNM) stage (P <.001), nonpapillary growth type (P <.001), and lymphatic tumor invasion (P =.010), whereas high levels of MCT4 expression did not significantly correlate with any of these variables. High CD147 expression was associated with high World Health Organization grade (P <.001), advanced tumor node metastatis stage (P <.001), and nonpapillary growth type (P =.003). Univariate analyses revealed that high MCT1 (P <.001) and CD147 (P =.029) expressions were associated with poor overall survival and that high MCT4 expression was correlated with poor recurrence-free survival (P =.036). Multivariate analyses revealed that high MCT1 and MCT4 expressions were independent prognostic factors for poor overall survival and poor recurrence-free survival, respectively, in UCB patients. Conclusion Our results indicate that increased MCT1, MCT4, and CD147 expressions have prognostic implications in UCB and suggest their roles in urothelial cancer metabolism.
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U2 - 10.1016/j.urology.2014.03.031
DO - 10.1016/j.urology.2014.03.031
M3 - Article
C2 - 24857275
AN - SCOPUS:84903734412
SN - 0090-4295
VL - 84
SP - 245.e9-245.e15
JO - Urology
JF - Urology
IS - 1
ER -