A significant increase in both MCT2 and MCT4 expressions was observed from non-neoplastic (normal or adjacent) to tumour tissues (p < 0.001, for both) while a decrease was observed for MCT1 expression in the transition from normal or adjacent non-neoplastic to prostate tumour tissue (p = 0.003 and p < 0.001, respectively). Here, SLC16A1 is linked to prostate neoplasm.