AI Article Synopsis

  • Clear cell renal cell carcinomas (ccRCCs) are aggressive kidney cancers, prompting research into biomarkers for better diagnosis and treatment; this study examined caspase-8, phosphorylated p38 MAPK (p-p38), and bcl-2 protein in relation to 27 ccRCC patients' clinical outcomes.
  • *The study used immunohistochemistry to analyze tissue samples, finding that higher levels of caspase-8 and bcl-2 were linked to lower tumor grades and better survival chances, whereas higher p-p38 levels were associated with higher tumor grades.
  • *Overall, the research highlights the potential prognostic significance of caspase-8 and shows how p-p38 varies with tumor grades,

Article Abstract

Background: Clear cell renal cell carcinomas (ccRCCs) constitute the most common renal carcinomas, characterized by a relatively aggressive clinical course. Thus, scientific research is targeting towards the identification of immunohistochemical and molecular markers that could be useful regarding diagnosis, appropriate therapy and prediction of prognosis. In the present study we assessed and correlated the expression of caspase-8, phosphorylated p38 mitogen-activated protein kinase (p-p38) and bcl-2 protein with histopathological features and clinical outcome of 27 patients with ccRCCs.

Method: Immunohistochemistry in formalin-fixed and paraffin-embedded tissue sections was performed. The associations among various features were assessed utilizing statistical analysis.

Results: We found that increased expression of cytoplasmic caspase-8 and bcl-2 protein was strongly associated with low Fuhrman's grade of carcinomas (p = 0.019 and p = 0.041, respectively). On the other hand, increased p-p38 expression was significantly related to high Fuhrman's grade (p = 0.006). Moreover, high bcl-2 expression was correlated with low pathological stage of ccRCCs (p = 0.026). Increased expression of cytoplasmic caspase-8 as well as low-grade tumors (grade 1 and 2) implied a greater probability of patients' survival, in univariate statistical analysis (p = 0.037 and p = 0.019, respectively). Neither p-p38 nor bcl-2 expression was significantly linked to patients' survival. There were not emerged statistically significant associations among caspase-8, p-p38 kinase and bcl-2 protein.

Conclusion: For the first time the prognostic impact of caspase-8 and p-p38 was studied in a series of ccRCCs, using immunohistochemistry in formalin-fixed and paraffin-embedded tissue sections. The suggestive relationship of caspase-8 with patients' clinical outcome, as well as the role of p-p38 within different grade categories, mandates further studies in larger cohorts of RCCs.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2649896PMC
http://dx.doi.org/10.1186/1746-1596-4-7DOI Listing

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