Survive and proliferate in a hostile microenvironment and is a critical determinant of the tumor progression. [36] Indeed we demonstrated that re-expressed and agonist-activated MR reduced VEGFA mRNA buy KDM5A-IN-1 Salmon calcitonin price expression in colon order KDM5A-IN-1 cancer cells even when maximally activated by their exposure to lower oxygen concentration or CoCl2 treatment.Figure 5. VEGFA mRNA induction during hypoxic response of HCT116 cells. Real-time PCR analysis of VEGFA mRNA induction in wild type HCT116 cells exposed to the indicated times of hypoxia (A) and in pchMR-transfected HCT116 cells exposed to normoxia, hypoxia or CoCl2 treatment (B). In panel A, PHCCC web values of VEGFA mRNA expression for each sample were compared to that of time 0, set as 1. In panel B, values of VEGF mRNA expression of pchMR-transfected cells exposed to hypoxia or 
CoCl2 treatment were compared to that of pchMRtransfected control cells exposed to normoxia, set as 1. Results are expressed as Mean6SEM (n = 3?). * p,0.05 ANOVA followed by Bonferroni t-test. doi:10.1371/journal.pone.0059410.gFigure 6. Hypoxia-induced VEGFA mRNA expression is decreased by MR activation in 
HCT116 cells. Real-time PCR analysis of VEGFA mRNA induction in (A) pchMR-transfected HCT116 cells treated with 3 nM aldosterone in the presence or in the absence of 1 mM spironolactone and exposed to CoCl2 treatment or hypoxia and (B) pchMR- or pcDNA3-transfected HCT116 cells cultured with 10 FCS alone under normoxic and hypoxic culture conditions. In panel A, values of VEGFA mRNA expression for each sample were compared to those of unstimulated pchMR-transfected control cells, set as 1. In panel B, values of VEGF mRNA expression of serum-activated pchMRtransfected cells were compared to those of pcDNA3-transfected control cells, set as 1. 
Results are expressed as Mean6SEM (n = 3?). *p,0.05 vs pchMR-transfected control cells or pcDNA3-transfected cells, ANOVA followed by Bonferroni t-test or Student t-test when appropriate. doi:10.1371/journal.pone.0059410.gMR Activity Attenuates VEGF/KDR Pathways in CRCFigure 7. MR activation decreases KDR expression levels in HCT116 cells. Effects of aldosterone (A) or serum (B) on KDR mRNA levels. Cell culture and treatments conditions were as in figure 4, or figure 6 panel B-Normoxia, respectively. Analyses of KDR mRNA levels were performed by Real-time PCR and results (n = 5) are given as in Fig 5. *p,0.05 vs pchMR-transfected control cells or pcDNA3transfected cells, ANOVA followed by Bonferroni t-test or Student ttest 15755315 when appropriate. doi:10.1371/journal.pone.0059410.gIn addition, our findings that, in MR-transfected colon cancer cells, KDR expression was significantly decreased by MR activation indicated that activated MR can inhibit also the expression of the receptor 2 of VEGFA, thus strengthening the hypothesis of a causal relationship between MR underexpression and KDR overexpression found in CRC by Di Fabio and collaborators. [22] On the basis of their results, these authors hypothesized that MR underexpression may play a role in the proangiogenic switch of the tumor through the enhancement of KDR expression. Here we suggest mechanistic insights on the role of increased KDR in promoting colorectal tumorigenesis, other than supporting angiogenesis. Indeed, it has been shown that VEGFA binds to KDR expressed on colon cancer cells and, through activation of specific KDR downstream signaling pathways, leads to a late induction of HIF-1a, which in turn mediates an autocrine production of VEGFA. Thi.Survive and proliferate in a hostile microenvironment and is a critical determinant of the tumor progression. [36] Indeed we demonstrated that re-expressed and agonist-activated MR reduced VEGFA mRNA expression in colon cancer cells even when maximally activated by their exposure to lower oxygen concentration or CoCl2 treatment.Figure 5. VEGFA mRNA induction during hypoxic response of HCT116 cells. Real-time PCR analysis of VEGFA mRNA induction in wild type HCT116 cells exposed to the indicated times of hypoxia (A) and in pchMR-transfected HCT116 cells exposed to normoxia, hypoxia or CoCl2 treatment (B). In panel A, values of VEGFA mRNA expression for each sample were compared to that of time 0, set as 1. In panel B, values of VEGF mRNA expression of pchMR-transfected cells exposed to hypoxia or CoCl2 treatment were compared to that of pchMRtransfected control cells exposed to normoxia, set as 1. Results are expressed as Mean6SEM (n = 3?). * p,0.05 ANOVA followed by Bonferroni t-test. doi:10.1371/journal.pone.0059410.gFigure 6. Hypoxia-induced VEGFA mRNA expression is decreased by MR activation in HCT116 cells. Real-time PCR analysis of VEGFA mRNA induction in (A) pchMR-transfected HCT116 cells treated with 3 nM aldosterone in the presence or in the absence of 1 mM spironolactone and exposed to CoCl2 treatment or hypoxia and (B) pchMR- or pcDNA3-transfected HCT116 cells cultured with 10 FCS alone under normoxic and hypoxic culture conditions. In panel A, values of VEGFA mRNA expression for each sample were compared to those of unstimulated pchMR-transfected control cells, set as 1. In panel B, values of VEGF mRNA expression of serum-activated pchMRtransfected cells were compared to those of pcDNA3-transfected control cells, set as 1. Results are expressed as Mean6SEM (n = 3?). *p,0.05 vs pchMR-transfected control cells or pcDNA3-transfected cells, ANOVA followed by Bonferroni t-test or Student t-test when appropriate. doi:10.1371/journal.pone.0059410.gMR Activity Attenuates VEGF/KDR Pathways in CRCFigure 7. MR activation decreases KDR expression levels in HCT116 cells. Effects of aldosterone (A) or serum (B) on KDR mRNA levels. Cell culture and treatments conditions were as in figure 4, or figure 6 panel B-Normoxia, respectively. Analyses of KDR mRNA levels were performed by Real-time PCR and results (n = 5) are given as in Fig 5. *p,0.05 vs pchMR-transfected control cells or pcDNA3transfected cells, ANOVA followed by Bonferroni t-test or Student ttest 15755315 when appropriate. doi:10.1371/journal.pone.0059410.gIn addition, our findings that, in MR-transfected colon cancer cells, KDR expression was significantly decreased by MR activation indicated that activated MR can inhibit also the expression of the receptor 2 of VEGFA, thus strengthening the hypothesis of a causal relationship between MR underexpression and KDR overexpression found in CRC by Di Fabio and collaborators. [22] On the basis of their results, these authors hypothesized that MR underexpression may play a role in the proangiogenic switch of the tumor through the enhancement of KDR expression. Here we suggest mechanistic insights on the role of increased KDR in promoting colorectal tumorigenesis, other than supporting angiogenesis. Indeed, it has been shown that VEGFA binds to KDR expressed on colon cancer cells and, through activation of specific KDR downstream signaling pathways, leads to a late induction of HIF-1a, which in turn mediates an autocrine production of VEGFA. Thi.Survive and proliferate in a hostile microenvironment and is a critical determinant of the tumor progression. [36] Indeed we demonstrated that re-expressed and agonist-activated MR reduced VEGFA mRNA expression in colon cancer cells even when maximally activated by their exposure to lower oxygen concentration or CoCl2 treatment.Figure 5. VEGFA mRNA induction during hypoxic response of HCT116 cells. Real-time PCR analysis of VEGFA mRNA induction in wild type HCT116 cells exposed to the indicated times of hypoxia (A) and in pchMR-transfected HCT116 cells exposed to normoxia, hypoxia or CoCl2 treatment (B). In panel A, values of VEGFA mRNA expression for each sample were compared to that of time 0, set as 1. In panel B, values of VEGF mRNA expression of pchMR-transfected cells exposed to hypoxia or CoCl2 treatment were compared to that of pchMRtransfected control cells exposed to normoxia, set as 1. Results are expressed as Mean6SEM (n = 3?). * p,0.05 ANOVA followed by Bonferroni t-test. doi:10.1371/journal.pone.0059410.gFigure 6. Hypoxia-induced VEGFA mRNA expression is decreased by MR activation in HCT116 cells. Real-time PCR analysis of VEGFA mRNA induction in (A) pchMR-transfected HCT116 cells treated with 3 nM aldosterone in the presence or in the absence of 1 mM spironolactone and exposed to CoCl2 treatment or hypoxia and (B) pchMR- or pcDNA3-transfected HCT116 cells cultured with 10 FCS alone under normoxic and hypoxic culture conditions. In panel A, values of VEGFA mRNA expression for each sample were 
compared to those of unstimulated pchMR-transfected control cells, set as 1. In panel B, values of VEGF mRNA expression of serum-activated pchMRtransfected cells were compared to those of pcDNA3-transfected control cells, set as 1. Results are expressed as Mean6SEM (n = 3?). *p,0.05 vs pchMR-transfected control cells or pcDNA3-transfected cells, ANOVA followed by Bonferroni t-test or Student t-test when appropriate. doi:10.1371/journal.pone.0059410.gMR Activity Attenuates VEGF/KDR Pathways in CRCFigure 7. MR activation decreases KDR expression levels in HCT116 cells. Effects of aldosterone (A) or serum (B) on KDR mRNA levels. Cell culture and treatments conditions were as in figure 4, or figure 6 panel B-Normoxia, respectively. Analyses of KDR mRNA levels were performed by Real-time PCR and results (n = 5) are given as in Fig 5. *p,0.05 vs pchMR-transfected control cells or pcDNA3transfected cells, ANOVA followed by Bonferroni t-test or Student ttest 15755315 when appropriate. doi:10.1371/journal.pone.0059410.gIn addition, our findings that, in MR-transfected colon cancer cells, KDR expression was significantly decreased by MR activation indicated that activated MR can inhibit also the expression of the receptor 2 of VEGFA, thus strengthening the hypothesis of a causal relationship between MR underexpression and KDR overexpression found in CRC by Di Fabio and collaborators. [22] On the basis of their results, these authors hypothesized that MR underexpression may play a role in the proangiogenic switch of the tumor through the enhancement of KDR expression. Here we suggest mechanistic insights on the role of increased KDR in promoting colorectal tumorigenesis, other than supporting angiogenesis. Indeed, it has been shown that VEGFA binds to KDR expressed on colon cancer cells and, through activation of specific KDR downstream signaling pathways, leads to a late induction of HIF-1a, which in turn mediates an autocrine production of VEGFA. Thi.Survive and proliferate in a hostile microenvironment and is a critical determinant of the tumor progression. [36] Indeed we demonstrated that re-expressed and agonist-activated MR reduced VEGFA mRNA expression in colon cancer cells even when maximally activated by their exposure to lower oxygen concentration or CoCl2 treatment.Figure 5. VEGFA mRNA induction during hypoxic response of HCT116 cells. Real-time PCR analysis of VEGFA mRNA induction in wild type HCT116 cells exposed to the indicated times of hypoxia (A) and in pchMR-transfected HCT116 cells exposed to normoxia, hypoxia or CoCl2 treatment (B). In panel A, values of VEGFA mRNA expression for each sample were compared to that of time 0, set as 1. In panel B, values of VEGF mRNA expression of pchMR-transfected cells exposed to hypoxia or CoCl2 treatment were compared to that of pchMRtransfected control cells exposed to normoxia, set as 1. Results are expressed as Mean6SEM (n = 3?). * p,0.05 ANOVA followed by Bonferroni t-test. doi:10.1371/journal.pone.0059410.gFigure 6. Hypoxia-induced VEGFA mRNA expression is decreased by MR activation in HCT116 cells. Real-time PCR analysis of VEGFA mRNA induction in (A) pchMR-transfected HCT116 cells treated with 3 nM aldosterone in the presence or in the absence of 1 mM spironolactone and exposed to CoCl2 treatment or hypoxia and (B) pchMR- or pcDNA3-transfected HCT116 cells cultured with 10 FCS alone under normoxic and hypoxic culture conditions. In panel A, values of VEGFA mRNA expression for each sample were compared to those of unstimulated pchMR-transfected control cells, set as 1. In panel B, values of VEGF mRNA expression of serum-activated pchMRtransfected cells were compared to those of pcDNA3-transfected control cells, set as 1. Results are expressed as Mean6SEM (n = 3?). *p,0.05 vs pchMR-transfected control cells or pcDNA3-transfected cells, ANOVA followed by Bonferroni t-test or Student t-test when appropriate. doi:10.1371/journal.pone.0059410.gMR Activity Attenuates VEGF/KDR Pathways in CRCFigure 7. MR activation decreases KDR expression levels in HCT116 cells. Effects of aldosterone (A) or serum (B) on KDR mRNA levels. Cell culture and treatments conditions were as in figure 4, or figure 6 panel B-Normoxia, respectively. Analyses of KDR mRNA levels were performed by Real-time PCR and results (n = 5) are given as in Fig 5. *p,0.05 vs pchMR-transfected control cells or pcDNA3transfected cells, ANOVA followed by Bonferroni t-test or Student ttest 15755315 when appropriate. doi:10.1371/journal.pone.0059410.gIn addition, our findings that, in MR-transfected colon cancer cells, KDR expression was significantly decreased by MR activation indicated that activated MR can inhibit also the expression of the receptor 2 of VEGFA, thus strengthening the hypothesis of a causal relationship between MR underexpression and KDR overexpression found in CRC by Di Fabio and collaborators. [22] On the basis of their results, these authors hypothesized that MR underexpression may play a role in the proangiogenic switch of the tumor through the enhancement of KDR expression. Here we suggest mechanistic insights on the role of increased KDR in promoting colorectal tumorigenesis, other than supporting angiogenesis. Indeed, it has been shown that VEGFA binds to KDR expressed on colon cancer cells and, through activation of specific KDR downstream signaling pathways, leads to a late induction of HIF-1a, which in turn mediates an autocrine production of VEGFA. Thi.
