Abstract

Clear cell renal cell carcinoma (ccRCC) is a common malignant kidney tumor, the pathogenesis of which remains unclear. The aim of the present study was to investigate whether caspase-10, matrix metalloproteinase-9 (MMP-9) and total laminin (LM) were involved into the pathogenesis of ccRCC. The levels of caspase-10, MMP-9 and total LM were analyzed by ELISA in tumor tissues and adjacent non-malignant tissues of 27 patients with ccRCC. The results revealed that caspase-10 levels in the tumor tissues were significantly higher than those in the adjacent non-malignant tissues (P<0.05). The MMP-9 levels in the tumor tissues were significantly lower than those in adjacent non-malignant tissues (P<0.01). The total LM levels in tumor tissues revealed no statistical difference with those in the adjacent non-malignant tissues (P=0.757). Additionally, caspase-10 levels were positively correlated with MMP-9 levels (P<0.001), but negatively correlated with total LM levels (P<0.05) in tumor tissues. Correlation analyses with clinical data of patients with ccRCC, revealed that caspase-10 levels (P<0.05) and MMP-9 levels (P<0.001) in tumor tissues were positively correlated with tumor grades of ccRCC, whereas total LM levels were positively correlated with tumor size (P<0.05). The results of the present study suggested that interactions between caspase-10, MMP-9 and LM are likely involved in the pathogenesis of ccRCC. A deeper understanding of the correlation between caspase-10, MMP-9 and LM would aid the clarification of pathogenesis of ccRCC.

Highlights

  • Renal cell carcinoma (RCC) is the most common kidney tumor, accounting for almost 3% of all human malignancies; 70‐80% of RCC cases are clear cell RCC [1,2,3]

  • Caspase‐10, matrix metalloproteinase‐9 (MMP‐9) and total LM levels in tumor and adjacent non‐malignant tissue from 27 patients with clear cell RCC (ccRCC) were detected by ELISA

  • Statistical analysis indicated that caspase‐10 levels were positively correlated with Matrix metalloproteinases (MMPs)‐9 levels (P

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Summary

Introduction

Renal cell carcinoma (RCC) is the most common kidney tumor, accounting for almost 3% of all human malignancies; 70‐80% of RCC cases are clear cell RCC (ccRCC) [1,2,3]. Alteration of the apoptotic pathway is essential for tumor development; analysis of the expression levels of caspases in tumor tissues is necessary for a deeper understanding of tumor biology. CDNA microarrays revealed that caspase‐10 was downregulated in gastric carcinoma, compared with adjacent non‐cancerous tissue [7]. Resistance to drug‐inducing apoptosis in RCC cell lines is considered to be QIAN et al: CASPASE-10, MMP-9 AND LM IN ccRCC correlated with downregulation of caspase‐10 [8]. It remains unclear whether caspase‐10 is involved in tumor development, in RCC

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