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신 이형성증에서 PAX2 발현

PAX2 Expression in Renal Dysplasia

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초록

Abstract

Background : Renal dysplasia is the abnormal development of the kidney. The condition is usually detected in childhood along with other urinary tract anomalies, but can remain unnoticed until adulthood. It was recently reported that a PAX2 gene mutation plays a major role in the development of renal dysplasia. The aim of this study was to examine the expression of PAX2 in dysplastic kidneys of children and adults. Methods : A total of 30 cases diagnosed with renal dysplasia after a nephrectomy were examined. PAX2 expression was evaluated using immunohistochemistry. Apoptosis was detected using an Apop Tag detection kit. Results : In the dysplastic kidneys, there was strong PAX2 expression in the epithelia of the primitive ducts in both children and adults, but the degree was significantly lower in adults (p=0.007). However, the mesenchyme surrounding the primitive ducts of children showed stronger staining for the smooth muscle actin antibody and trichrome than the adults. The apoptosis index was significantly higher in the primitive duct epithelia than in the surrounding normal collecting duct epithelia (p=0.000). Conclusions : PAX2 is overexpressed in the primitive ducts of renal dysplasia, which is sustained until adulthood and is associated with increased apoptosis. However, a decrease in PAX2 expression in the dysplastic epithelia and mesenchymalcuff of adults suggest a gradual regression of the dysplastic elements with time.

참고문헌 (27)

  1. "Non-neoplastic disease of the kidney", pp.21~24 (1997), Louis: Mosby
  2. "Congenital malformation of the kidney Renal pathology with clinical and functional correlations", pp.1288~301 (1989), JB Lippincott
  3. "A familial case of multicystic dysplastic kidney", 20, pp.1245~1248 (2005)
  4. "A family study of renaldysplasia", pp.669~77
  5. "Multicystic dysplastic kidney and variable phenotype in a family with a novel deletion mutation of PAX2", 16, pp.2754~2761 (2005)
  6. "and cystic diseases of the kidney Pathology of the kidney", pp.110~21 (1992), Brown and Company
  7. "Potter EL", chicago (1972)
  8. "The pathogenesis of renal dysplasia", pp.101~3, complete and incomplete urinary obstruction
  9. "a correlation of renal dysplasia with position of ureteral orifice", pp.274~80
  10. "Differential regulation of the human Wilms tumor supressor gene (WT1) promoter by two isoforms of PAX2", 14, pp.2689~2700 (1997)
  11. "PAX2 and renal-coloboma syndrome", pp.411~432 (2003), Amsterdam: Academic Press
  12. Winyard PJ, "The PAX2 tanscription factor is expressed in cystic and hyperproliferative dysplastic epithelia in human kidney malformations", 98, pp.451~459 (1996)
  13. "Potential biological role of transforming growth factor-beta1 in human congenital kidney malformations", 157, pp.1633~1647 (2000)
  14. "Gene expression and cell turnover in human renal dysplasia", 15, pp.159~166 (2000)
  15. "Comparative in situ hybridization analysis of Pax2, Pax8, and WT1 gene transcription in human fetal kidney, and Wilms tumors", 146, pp.40~45 (1995)
  16. "The role of PAX2 in normal and abnormal development of the urinary tract", 12, pp.712~720 (1998)
  17. "Expression of Pax-2 in human renal cell carcinoma and growth inhibition by antisense oligonucleotides", 55, pp.4092~4098 (1995)
  18. "Immunohistochemical localization of Pax2 and associated proteins in the developing kidney of mice with renal hypoplasia", 49, pp.1081~1097 (2001)
  19. "Pathogenesis of human renal dysplasia an alternative scenario to the major theories", 45, pp.605~609 (2003)
  20. "Renal dysplasia: a clinicopathologic review of six cases", 31, pp.34~39 (1997)
  21. "Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +", - mutant mice, 2000, pp.9, 1~11
  22. "PAX2 suppresses apoptosis in renal collecting duct cells", 157, pp.833~842 (2000)
  23. "Evolving concepts in human renal dysplasia", 15, pp.998~1007 (2004)
  24. "Dysregulation of podocyte phenotype in idiopathic collapsing glomerulopathy and HIV-associated nephropathy", 91, pp.416~423 (2002)
  25. "Significance of early phenotypic change of glomerular podocytes detected by PAX2 in primary focal segmental glomerulosclerosis", 39, pp.475~485 (2002)
  26. "Murine Denys-Drash syndrome: evidence of podocyte de-differentiation and systemic medication of glomerulosclerosis", 12, pp.2379~2394 (2003)
  27. "WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis", 154, pp.181~192 (1999)

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