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先天性尿道下裂阴茎皮肤细胞雌雄激素受体表达及胞核内的聚集 被引量:4

Androgen and Estrogen Receptors in Prepuce of Children with Hypospadias
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摘要 目的:探索先天性尿道下裂与阴茎皮肤细胞雄激素受体(AR)、雌激素受体(ER)的表达及细胞核内的聚集的关系。方法:通过受体的放射配基结合分析,对28例不同程度的先天性尿道下裂患儿外生殖器皮肤细胞内的AR、ER的表达及细胞内的分布进行了测定。结果:实验显示尿道下裂患儿外生殖器皮肤细胞内及胞核内AR量较正常对照减少(P<0.01),尿道下裂的严重程度与细胞内及细胞核内的AR量无关(P>0.05)。细胞内总ER与正常无显著性差异(P>0.05),胞核内ER量较正常对照减少(P<0.05)。结论:AR异常是先天性尿道下裂的原因之一,先天性尿道下裂也属于雄激素不敏感综合征的范畴。 Objective: To study the relationship between androgen receptors(AR) and estrogen receptors(ER) in cells and nuclei of prepuce in patients with hypospadias and the severity of hypospadias. Methods: AR and ER expression and its distribution in the preputial cells of 28 cases with different types of hypospadias were examined by radioligand binding assay(RBA). Results: The total cellular and nuclear AR concentrations in prepuce of hypospadias patients were lower than those of control group (P<0.01). There was no correlation between the severity of hypospadias and the cellular and nuclear levels of AR (P>0.05). There was no statistically significant difference in cellular ER between the hypospadias patients and the control group (P>0.05). The nuclear ER in hypospadias patients was lower than that of control (P<0.05). Conclusions: Abnormality of AR is a contributing factor in the pathogenesis of hypospadias. Hypospadias may be a manifestation of androgen insensibility syndrome. Reduced level of nuclear ER may be a secondary change.
出处 《中华小儿外科杂志》 CSCD 1998年第5期275-278,共4页 Chinese Journal of Pediatric Surgery
关键词 尿道下裂 雄激素 受体 阴茎 儿童 Hypospadias Androgen insensitivity syndrome Androgen receptor Estrogen receptor
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参考文献3

  • 1吴何明,中华小儿外科杂志,1995年,16卷,138页
  • 2郭畹华,细胞生物学杂志,1993年,216页
  • 3Chan L,Pediatric Endocrinology,1989年

同被引文献35

  • 1崔毓桂.雄激素受体的结构和功能[J].国外医学(计划生育分册),1994,13(4):201-205. 被引量:3
  • 2蒋学武,陈绍基,王光义,黄鲁刚,姚先莹.先天性尿道下裂阴茎雄激素受体的研究[J].中华小儿外科杂志,1995,16(3):141-142. 被引量:7
  • 3唐耘熳,黄进,陈绍基,黄鲁刚,王明和.小儿先天性无尿道下裂阴茎下曲畸形的解剖特点及诊治[J].中国修复重建外科杂志,2006,20(3):217-219. 被引量:8
  • 4Kalfa N,Philibert P,Sultan C.Is hypospadias a genetic,endocrine orenvironmental disease,or still an unexplained malformation?Int J An-drol,2009,32(3):187-197.
  • 5Kalfa N,Philibert P,Baskin LS,et al.Hypospadias:interactions be-tween environment and genetics.Mol Cell Endocrinol,2011,335(2):89-95.
  • 6Vottero A,Minari R,Viani I,et al.Evidence for epigenetic abnormali-ties of the androgen receptor gene in foreskin from children with hy-pospadias.J Clin Endocrinol Metab,2011,96(12):E1953-1962.
  • 7Kojima Y,Kohri K,Hayashi Y.Genetic pathway of external genitaliaformation and molecular etiology of hypospadias.J Pediatr Urol,2010,6(4):346-354.
  • 8Yong W,Yang Z,Periyasamy S,et al.Essential role for Co-chaperoneFkbp52 but not Fkbp51 in androgen receptor-mediated signaling andphysiology.J Biol Chem,2007,282(7):5026-5036.
  • 9Beleza-Meireles A,Barbaro M,Wedell A,et al.Studies of a co-chaper-one of the androgen receptor,FKBP52,as candidate for hypospadias.Reprod Biol Endocrinol,2007,5:8.
  • 10Bentvelsen FM,Brinkmann AO,van der Linden JE,et al.Decreasedimmunoreactive androgen receptor levels are not the cause of isolatedhypospadias.Br J Urol,1995,76(3):384-388.

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