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Ki-67在寻常型银屑病中的表达及其意义

Expression and significance of Ki-67 in psoriatic lesions
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摘要 目的探讨Ki-67在寻常型银屑病发病中的作用。方法采用免疫组织化学LDP法检测了48例寻常型银屑病皮损区及20例正常人表皮中Ki-67的表达及分布特点,采用逆转录聚合酶链反应技术(RT-PCR方法)检测Ki-67的mRNA表达水平。结果寻常型银屑病皮损区Ki-67表达均较正常表皮中的表达明显增强,分布于除角质层以外的表皮各层,而正常表皮表达阴性或仅在基底层有弱阳性表达。RT-PCR检测结果表明寻常型银屑病组Ki-67的表达水平亦显著高于正常表皮。结论 Ki-67在寻常型银屑病皮损中过度表达,提示其与银屑病的表皮细胞过度增殖、分化异常有关。 Objective To investigate the effect of Ki-67 on the pathogenesis of psoriasis vulgaris lesions and to evaluate its possible significance.Methods The expression and distribution of Ki-67 were detected by immunohistochemistry in the lesions of 48 cases with psoriasis vulgaris and in the epidermis of 20 normal controls.The mRNA expression of Ki-67 was detected by RT-PCR methods.Results The expressions of Ki-67 in psoriatic epidermis were significantly higher than those in normal epidermis;they were located in all epidermal layers except horny layer.There were no or only weak positive expressions in the basal layer of normal controls.Ki-67 mRNA were markedly increased in psoriasis vulgaris.Conclusion The over expressions of Ki-67 in psoriatic epidermis suggest that it might be related to the hyperproliferation and abnormal differentiation of psoriatic keratinocytes.Ki-67 may be a novel target in preventing the process of psoriasis vulgaris.
出处 《四川医学》 CAS 2011年第2期154-156,共3页 Sichuan Medical Journal
关键词 银屑病 KI-67 psoriasis vulgaris Ki-67
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参考文献4

  • 1Duchrow M,Schluter C,Key G,et al.Cell proliferation associated nuclear antigen defined by antibody Ki-67:a new kind of cycle maintaining proteins[J].Arch Immunol Ther Exp,1995,43(2):117.
  • 2Khalid H,Shibata S,Kishikawa,et al.Immunohistochemieal analysis of progesterone receptor and Ki67 Label-ing index in astorcytic tumors[J].Cancer,1997,80(11):2133-2140.
  • 3Kawahira K.Immunohistochemical staining of proliferating cell antigen (PCNA)in malignant skin[J].Arch Derrmatol Res,1999,291:413-418.
  • 4Michaelsson G,Ahs S,Hammarstrom I,et al.Gluten-free diet in psoriasis patients with antibody gliadin results in decreased expression of tissue transglutaminase and fewer Ki67+cells in the derma[J].Acta Derm Venereol,2003,83:425-429.

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