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P27^(kipl)和ki-67蛋白在病理性瘢痕组织中的表达和意义 被引量:1

Expression and significance of P27^(kipl) and ki-67 protein in pathological scar
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摘要 目的:研究病理性瘢痕组织中P27kipl和ki-67蛋白的表达情况及其相互关系,探讨他们在瘢痕形成中的作用及机制。方法:应用免疫组化SP法检测正常皮肤、成熟瘢痕、增生性瘢痕和瘢痕疙瘩组织中P27kipl、ki-67蛋白的表达并进行统计学分析。结果:病理性瘢痕组织中P27kipl蛋白表达显著低于正常皮肤、成熟瘢痕(P=0.036);ki-67蛋白在病理性瘢痕组织中的表达显著高于正常皮肤、成熟瘢痕(P<0.000);病理性瘢痕组织中P27kipl的表达与ki-67蛋白表达呈负相关(P<0.000)。结论:P27kipl蛋白表达的下降及ki-67的表达升高可能与病理性瘢痕的形成有关。 Objective To study the expression of P27kjpl and ki-67 in the pathological scars and their reaction-ship and to investigate its role and its possible mechanism in the pathogenesis of abnormal scars. Methods Immunohistochemiscal technique was performered to detect the expression and distribution of P27kjpl and ki-67 protein in hypertrophic scar (42cases), keloid (18cases), normal scar (40 cases) and normal skin (50cases),statistics was used to analyze the data. Results The positive rate of P27kjpl and ki-67 protein expression were remarkably significant in comparison between normal scar and abnormal scar (P〈0.05). In pathological scar the protein of P27kjpl and ki-67 showed a strong inverse correlation (P〈0.000). Conclusion Low expression of P27kjpl and high expression of ki-67 may play an important role in the proliferation of fibroblasts and in the pathogenesis of pathological scar.
出处 《中国美容医学》 CAS 2008年第10期1477-1479,共3页 Chinese Journal of Aesthetic Medicine
基金 福建省自然科学基金资助项目(项目编号:C0410027)
关键词 P27KIPL蛋白 KI-67蛋白 增生性瘢痕 瘢痕疙瘩 P27kjpl protein ki-67 protein hypertrophic scar keloid
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  • 1Haverstock BD. Hypertrophic scars and keloids [J]. Clin Pediatr Med Surg,2001,18(1):147.
  • 2陈伟,付小兵,孙同柱,孙晓庆,盛志勇.增生性瘢痕组织中转化生长因子-β异构体与受体含量变化及对瘢痕形成的影响[J].中国修复重建外科杂志,2002,16(4):252-255. 被引量:24
  • 3Yang G,Ayala G ,Marzo AD, et al. Elevated Skp2 protein expression in human prostate cancer, association with loss of the cyclin-dependent kinase inhibitor p27 and PTEN and with reduced recurrence-freesurviveal[J]. Clin Res,2002,8:3419-3426.
  • 4张玉霞,喻伦银,刘铭球.细胞周期调控研究进展[J].国外医学(遗传学分册),2001,24(5):262-266. 被引量:29
  • 5Polyak K,Kato J ,Solomon M, et al. P27^kip1, a cyclin-CDK inhibitor, links transforming growth factor-B and contact inhibition to cell cycle arrest [J]. Genes Dev,1994,8:9.
  • 6Fero ML,Randel E, Gurley KE, et al .The murine gene P27^kip1 is haplo insufficient for tumour suppression[J]. Nature, 1998,396:177-180.
  • 7Slaven HB, Iversen OE, Akslen LA. Prognostic significance of an-giognesis and ki-67, p53 and p21 expression: a population-based endometrial carcinoma study[J]. J Clin Oncol, 1999,17:1382.
  • 8Vlach J, Hennecke S, Amati B. Phosphorylation-dependent degradation of the cyclin-dependent kinase inhibitor P27^kip1[J]. EMBO J,1997,16(17): 5334.
  • 9Lloya RV, Enckson LA, Jin L,et al. P27^kip1 :A Multifunctional Cyclin-Dependent Kinase Inhibitor with Prognostic Significance in Hu-man Cancers[J]. Am J Pathol,1999,154(2):313.

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