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Virchows Arch ; 448(5): 584-90, 2006 May.
Article in English | MEDLINE | ID: mdl-16525826

ABSTRACT

The present study was carried out in order to examine molecular alterations of extracellular matrix (ECM), associated with cell-cell communication in conventional (clear-cell) renal cell carcinomas (cRCCs) influenced by persistent long-term, low-dose ionizing radiation (IR) exposure to patients living more than 19 years after the Chernobyl accident in Cesium 137 (137Cs)-contaminated areas of Ukraine. The ECM major components such as fibronectin, laminin, E-cadherin/beta-catenin complexes and p53 tumor suppressor gene protein, and transforming growth factor beta 1 (TGF-beta1) were immunohistochemically (IHC) evaluated in cRCCs from 59 Ukrainian patients, which represented 18 patients living in non-contaminated areas and 41 patients from 137Cs-contaminated areas. In contrast, a control group of 19 Spanish patients with analogue tumors were also investigated. For IHC evaluation, a tissue microarray technique was used. Decrease or loss and abnormal distribution of fibronectin, laminin, E-cadherin/beta-catenin complexes accompanied by elevated levels of p53 and TGF-beta1 were detected in the Ukrainian cRCCs from 137Cs-contaminated areas with statistically significant differences. Thus, our study suggests that chronic long-term, low-dose IR exposure might result in global remodeling of ECM components of the cRCCs with disruption in peri-epithelial stroma and epithelial basement membranes.


Subject(s)
Carcinoma, Renal Cell/pathology , Chernobyl Nuclear Accident , Extracellular Matrix/radiation effects , Kidney Neoplasms/pathology , Adolescent , Adult , Aged , Aged, 80 and over , Cadherins/radiation effects , Carcinoma, Renal Cell/metabolism , Female , Fibronectins/radiation effects , Gene Expression/radiation effects , Humans , Immunohistochemistry , Kidney Neoplasms/metabolism , Laminin/radiation effects , Male , Middle Aged , Neoplasm Staging , Radiation Effects , Time Factors , Transforming Growth Factor beta/radiation effects , Tumor Suppressor Protein p53/radiation effects
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