Prognostic significance of lactate/proton symporters mct1, mct4, and their chaperone CD147 expressions in urothelial carcinoma of the bladder

Jung Woo Choi, Younghye Kim, Ju Han Lee, Young Sik Kim

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    49 Citations (Scopus)

    Abstract

    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.

    Original languageEnglish
    Pages (from-to)245.e9-245.e15
    JournalUrology
    Volume84
    Issue number1
    DOIs
    Publication statusPublished - 2014

    ASJC Scopus subject areas

    • Urology

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