Al 
mucosa (NM), microadenoma (MA) and colorectal carcinoma (CRC). * p,0.05 vs normal colorectal mucosa. doi:10.1371/journal.pone.0054488.tThPOK in Colorectal CarcinogenesisFigure 4. Colocalization analysis. Quantitative analysis of co-expression levels by Manders coefficient in normal mucosa (NM), microadenomas (MA), and colorectal cancer (CRC), analyzing the ratio between ThPOK/CD4 (panel A), ThPOK/CD8 (panel 
B), and ThPOK/CD56 (panelC). *P,0,05 vs NM; { P,0,05 vs CRC. Panel D: Normalized co-expression levels in normal mucosa (NM), microadenomas (MA), and colorectal cancer (CRC), between ThPOK and CD4 (white bars), ThPOK and CD8 (black bars), and ThPOK and CD56 (gray bars). *P,0,05 vs CD4; { P,0,05 vs CD56. doi:10.1371/journal.pone.0054488.Clavulanic acid potassium salt manufacturer gcolorectal lesions, suggesting its involvement since the earliest phases of immune system remodelling in the colorectal neoplastic microenvironment. By morphological analysis with immunofluorescence coupled with confocal microscopy, we AN-3199 web observed changes in the immunological pattern during neoplastic progression. In normal mucosa there was a predominance of CD56+ cells, and a lower infiltration of T lymphocytes (both helper and cytotoxic), associated with lower levels of ThPOK. In microadenomas, we observed both a decrease of CD56+ cells and an increase of CD8+ T cells, paralleled by a relevant increase of ThPOK immunostaining. Finally, in carcinomas, the presence of CD56+ cells was scarce, with a prevalence of CD8+ T cells together with an increase of ThPOK labeling. Many studies have analyzed the presence/amount of helper and cytotoxic T cells in colorectal carcinomas, but only few evaluated changes during colorectal cancer development, since normal mucosa and microadenomas. In addition, data on quantification of lymphocyte populations in colorectal carcinogenesis are currently elusive. It has been demonstrated that the increased expression of genes specific for cytotoxic T lymphocytes, as CD8a, granzyme B, or perforin was related to the absence of early metastatic invasion ofcolorectal cancer, and it could also improve patient survival [37,38]. At the moment, data are not available regarding a tumourspecific activation of CD8+ T cells, but it has been demonstrated a tumour-induced inhibition of CD8+ T cells, related to tumour stage. There are at least three mechanisms to account for a disfunction of CD8+ cells: i) cytotoxic T lymphocytes may be inactive, as revealed by the low levels of cytotoxic 1662274 markers, ii) cytotoxic T lymphocytes may be apoptotic, iii) cytotoxic T lymphocytes may be immature [39?4]. ThPOK was initially considered a regulator of CD4+ lineage. Further experiments have shown its activation not only in CD4+ lymphocytes, but also in peripheral CD8+ cells [45]. These data are consistent with the hypothesis that ThPOK is important in maintaining the CD4+ phenotype in physiological conditions, as in normal mucosa this protein is mostly expressed in CD4+ cells. Foxp3 is 10457188 a master regulator of a class of immunosuppressive T cell, that has a central role in cancer progression. Our studies failed to find a correlation between foxp3 and ThPOK, but as reported by others works [46,47], an increase of foxp3+ cells during colorectal cancer progression was evident. However, the novelty as well as the main finding of the present work is the observation that ThPOK becomes prevalent in CD8+ThPOK in Colorectal CarcinogenesisFigure 5. Foxp3, GZMB and RUNX3 fluorescence levels. Fluorescence levels of Fo.Al mucosa (NM), microadenoma (MA) and colorectal carcinoma (CRC). * p,0.05 vs normal colorectal mucosa. doi:10.1371/journal.pone.0054488.tThPOK in Colorectal CarcinogenesisFigure 4. Colocalization analysis. Quantitative analysis of co-expression levels by Manders coefficient in normal mucosa (NM), microadenomas (MA), and colorectal cancer (CRC), analyzing the ratio between ThPOK/CD4 (panel A), ThPOK/CD8 (panel B), and ThPOK/CD56 (panelC). *P,0,05 vs NM; { P,0,05 vs CRC. Panel D: Normalized co-expression levels in normal mucosa (NM), microadenomas (MA), and colorectal cancer (CRC), between ThPOK and CD4 (white bars), ThPOK and CD8 (black bars), and ThPOK and CD56 (gray bars). *P,0,05 vs CD4; { P,0,05 vs CD56. doi:10.1371/journal.pone.0054488.gcolorectal lesions, suggesting its involvement since the earliest phases of immune system remodelling in the colorectal neoplastic microenvironment. By morphological analysis with immunofluorescence coupled with confocal microscopy, we observed changes in the immunological pattern during neoplastic progression. In normal mucosa there was a predominance of CD56+ cells, and a lower infiltration of T lymphocytes (both helper and cytotoxic), associated with lower levels of ThPOK. In microadenomas, we observed both a decrease of CD56+ cells and an increase of CD8+ T cells, paralleled by a relevant increase of ThPOK immunostaining. Finally, in carcinomas, the presence of CD56+ cells was scarce, with a prevalence of CD8+ T cells together with an increase of ThPOK labeling. Many studies have analyzed the presence/amount of helper and cytotoxic T cells in colorectal carcinomas, but only few evaluated changes during colorectal cancer development, since normal mucosa and microadenomas. In addition, data on quantification of lymphocyte populations in colorectal carcinogenesis are currently elusive. It has been demonstrated that the increased expression of genes specific for cytotoxic T lymphocytes, as CD8a, granzyme B, or perforin was related to the absence of early metastatic invasion ofcolorectal cancer, and it could also improve patient survival [37,38]. At the moment, data are not available regarding a tumourspecific activation of CD8+ T cells, but it has been demonstrated a tumour-induced inhibition of CD8+ T cells, related to tumour stage. There are at least three mechanisms to account for a disfunction of CD8+ cells: i) cytotoxic T lymphocytes may be inactive, as revealed by the low levels of cytotoxic 1662274 markers, ii) cytotoxic T lymphocytes may be apoptotic, iii) cytotoxic T lymphocytes may be immature [39?4]. ThPOK was initially considered a regulator of CD4+ lineage. Further experiments have shown its activation not only in CD4+ lymphocytes, but also in peripheral CD8+ cells [45]. These data are consistent with the hypothesis that ThPOK is important in maintaining the CD4+ phenotype in physiological conditions, as in normal mucosa this protein is mostly expressed in CD4+ cells. Foxp3 is 10457188 a master regulator of a class of immunosuppressive T cell, that has a central role in cancer progression. Our studies failed to find a correlation between foxp3 and ThPOK, but as reported by others works [46,47], an increase of foxp3+ cells during colorectal cancer progression was evident. However, the novelty as well as the main finding of the present work is the observation that ThPOK becomes prevalent in CD8+ThPOK in Colorectal CarcinogenesisFigure 5. Foxp3, GZMB and RUNX3 fluorescence levels. Fluorescence levels of Fo.
