C and F show sections of CCRCC. Mc: Malpighian corpuscle, dt: distal tubule, pt: proximal tubule, cd: collecting duct, bv: blood vessel, tt: tumor tissue, nt: normal tissue. Scale bars: 300 μm, scale bars

inset: 150 μm. 3.2 Increased levels of galectin-3 in CCRCC-tumor tissues To monitor the expression pattern of galectin-3, equal protein amounts of tissue homogenates from normal, intermediate or tumor were analyzed by immunoblots together with the polypeptides GAPDH or α-tubulin and epithelial β-catenin, E-cadherin and villin. Most of the immunoblots showed an increase in galectin-3 staining in tumor versus normal this website samples (Figure 2A), while the intensities of E-cadherin and villin were decreased in the tumor. The staining of galectin-3, E-cadherin or villin in the intermediate Veliparib supplier tissues fluctuates between the basic values for normal or tumor tissues. For densitometric quantification the suitability of α-tubulin as a reference protein in comparison to β-catenin or GAPDH was assessed (additional file 1A). In agreement with published data CCRCC tumor tissues revealed reduced mean values of β-catenin [17], whereas the amount of GAPDH was increased [18]. For α-tubulin no tendency between normal and tumor tissues could be observed. Therefore, α-tubulin was used as a reference protein for normalization of the densitometric data from

galectin-3, E-cadherin, Clomifene or villin in additional file 1B. Furthermore, the data were normalized to the sum (Figure 2B, C). Both calculations demonstrated an increase in galectin-3 and a decrease in E-cadherin or villin in most of the tumor samples

with p-values below 0,001 according to Student’s T-test. To conclude, galectin-3 expression was significantly increased in a majority of 79% of the CCRCC-patients during tumor development. As summarized in Table 1, clinicopathological parameters, including age, sex, histological grade and metastasis, were well balanced between the groups. However, none of the patients with low galectin-3 levels had developed metastases at the time of nephrectomy, thus pointing to a correlation between galectin-3 expression and tumor malignancy as had been recently published for gastric cancer [19, 20]. Figure 2 Immunoblot analysis of galectin-3, E-cadherin, and villin in normal kidney, intermediate and tumor tissues as well as RC-124 and RCC-FG1 cells. A, Protein contents in homogenates from tissue samples of 39 patients were measured. Equal protein amounts were separated by SDS-PAGE followed by immunoblot analysis with anti-galectin-3, -E-cadherin or -villin. One representative blot is depicted. B, Anlotinib Quantitative immunoblot analysis of galectin-3, villin and E-cadherin in normal and tumor tissue. C, Relative variation of galectin-3, villin and E-cadherin in CCRCC to the corresponding normal tissue of each patient.