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Pediatr Surg Int ; 29(3): 223-7, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23292539

RESUMO

PURPOSE: 11p13 and 11p15 loss of heterozygosity (LOH) in Wilms tumor (WT), the commonest molecular pathogenetic event in WT, shows variation in different parts of the world. The present study looked for the presence of 11p13 and 11p15 LOH as well as nephrogenic rests in WT occurring in India. METHOD: Twenty-two cases of WT were subjected to thorough pathological examination for presence of nephrogenic rests. Fresh frozen tissue was evaluated for LOH at 11p13 and 11p15, using PCR for microsatellite markers. RESULTS: Among twenty-two consecutive cases of WT, 20 were unilateral and 2 were bilateral. 6/22 showed LOH at 11p13 (27.7 %) and 1/22 showed LOH at 11p15 (4.54 %). 2/22 cases showed presence of nephrogenic rests. One of the cases with LOH at 11p13 had intralobar nephrogenic rest in the adjacent kidney. One specimen had perilobar nephrogenic rest in the adjacent kidney but did not show LOH for either 11p13 or 11p15 in the tumor. CONCLUSION: LOH at 11p13 is seen in 27.27 % of WT in India, which is similar to reports in the English language literature. LOH at 11p15 was seen in 4.54 % of WT, which is lower than that reported from Western subjects.


Assuntos
Cromossomos Humanos Par 11 , DNA de Neoplasias/genética , Neoplasias Renais/genética , Perda de Heterozigosidade , Tumor de Wilms/genética , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Masculino , Repetições de Microssatélites , Reação em Cadeia da Polimerase , Estudos Prospectivos
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