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WWP1、p53在瘢痕疙瘩和正常皮肤中的差异表达及意义 被引量:3

Different expression and significance of WWP1 and p53 in keloid and normal skin
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摘要 目的探讨E3泛素连接酶WWP1、p53在人正常皮肤及瘢痕疙瘩组织中的表达差异,分析其与瘢痕疙瘩发生是否相关。方法选取临床切取的瘢痕疙瘩及正常皮肤组织标本各10例,采用免疫组织化学法和RT-PCR法分别对组织中WWP1、p53蛋白及mRNA表达情况进行检测,并通过Image-Pro Plus图像分析系统测定组织蛋白染色后累计光密度值、以β-actin为参照计算mRNA相对定量,进而比较分析两组标本中WWP1、p53表达是否有差异性。结果免疫组化染色结果提示,瘢痕疙瘩标本中p53蛋白表达明显低于正常皮肤,而WWP1蛋白沉积明显高于正常皮肤,同时p53及WWP1 mRNA RT-PCR检测证实同样结果,差异均有统计学意义(P<0.05)。结论 E3泛素连接酶WWP1及抑癌基因p53与瘢痕疙瘩的形成有相关性,可作为瘢痕疙瘩形成机制及治疗靶点研究的方向。 Objective The purpose of the study was to detect the expression of E3 ubiquitin ligase WWP1 and p53 in human normal skin and keloid tissues and its correlation with the occurrence of keloid. Methods 10 cases of keloid tissues and 10 cases of normal skin were recruited. The expressions of WWP1 and p53 in the keloid group and the controls were measured using immunohistochemical methods. And the mRNA expression of WWP1 and p53 in the two groups were detected by RT-PCR methods. We also measured integrated optical density (1OD) of the proteins by Image-Pro Plus analysis system, and calculated the relative quantity of mRNA refering to 13-actin, then made a comparative analysis of the two groups for the expressions of WWP1, p53. Results The immunohistochemical results showed that the expression of p53 protein in keloid was significantly lower compared with the controls, and WWP1 protein deposition was significantly higher than that of normal skin. The mRNA expression of p53 and WWP1 was detected by RT-PCR and confirmed the same results. All the difference was statistically significant (P 〈0.05). Conclusion E3 ubiquitin ligase WWP1 and anti oneogene p53 is related to the formation of keloid, which provides a new direction of the mechanism and new targets for the treatment of keloid.
出处 《安徽医科大学学报》 CAS 北大核心 2016年第2期247-250,共4页 Acta Universitatis Medicinalis Anhui
基金 国家自然科学基金(编号:30973124) 安徽省自然科学基金(编号:KJ2014A108)
关键词 WWP1 P53 瘢痕疙瘩 正常皮肤 WWP1 p53 keloid normal skin
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参考文献11

  • 1Nakashima M, Chung S, Takahashi A,et al. A genome-wide asso- ciation study identifies four susceptibility loci for keloid in the Jap- anese population[J]. Nat Genet,2010,42(9) :768 -71.
  • 2Cheng Q, Cao X, Yuan F, et al. Knockdown of WWP1 inhibits growth and induces apoptosis in hepatoma carcinoma ceils through the activation of caspase3 and p53 [ J ]. Biochem Biophys Res Commun, 2014,448 ( 3 ) :248 - 54.
  • 3Yeung B, Ho K C, Yang X, et al. WWP1 E3 ligase targets LATS1 for ubiquitin-mediated degradation in breast cancer ceils [ J ]. PLoS One,2013,8(4) :e61027.
  • 4汪治宇,刘荣凤,丁妍,王聪敏,李幸,王娟.泛素连接酶WWP1和Smurfs在前列腺癌组织中的表达及其与骨转移的关系[J].中国现代医学杂志,2012,22(20):66-70. 被引量:2
  • 5Cao X, Xue L, Han L,et al. WW domain-containing E3 ubiquitin protein ligase 1 ( WWP1 ) delays cellular senescence by promoting p27Kipl degradation in human diploid fibroblasts [ J]. J Biol Chem ,2011,286 (38) :33447 - 56.
  • 6Polyak K, Kato J Y, Solomon M J, et al. p27Kipl, a cyclin-Cdk inhibitor, links transforming growth factor-beta and contact inhibi- tion to cell cycle arrest[J]. Genes Dev,1994,8( 1 ) :9 -22.
  • 7Levenberg S, Yarden A, Kam Z, et al. p27 is involved in N-cad- herin-mediated contact inhibition of cell growth and S-phase entry [J]. Oncogene,1999,18(4) : 869 -76.
  • 8Teofoli P, Barduagni S, Ribuffo M, et al. Expression of Bcl-2, p53, c-jun and c-fos protooncogenes in keloids and hypertrophic scars [ J ]. J Dermatol Sci, 1999,22 ( 1 ) :31 - 7.
  • 9Laine A, Ronai Z. Regulation of p53 localization and transcription by the HECT domain E3 ligase WWP1 [ J ]. Oncogene, 2007,26 (10) :1477 -83.
  • 10Yeung B, Ho K C, Yang X. WWP1 E3 ligase targets LATS1 for ubiquitin-mediated degradation in breast cancer ceils [ J ]. PLoS One,2013,8(4) :e61027.

二级参考文献13

  • 1DATYO M, WANG XF. Ubiquitin-mediated degradation: a mech- anism for fine-tuning TGF-β signaling[J]. Cell, 2005(14), 121: 2-4.
  • 2MOGK A, SCHMIDT R, BUKAU B. The N-end rule pathway for regulated proteolysis: prokaryotic and eukaryotic stragegies[J]. Trends Cell Biol, 2007, 17(4): 165-172.
  • 3PANDIT B, GARTEL AL. Protea.some inhibitors suppress expres- sion of NPM and ARF proteins[J]. Cell Cycle, 2011, 10(22): 3827-3829.
  • 4DU JX, HAGOS EG, NANDAN MO, et al. The E3 ubiquitin ligase SMAD ubiquitination regulatory factor 2 negatively regu- lates kruppel-like factor 5 protein[J]. J of Biological Chemistry, 2011, 286(46): 40354-40364.
  • 5CAMUS S, MENENDEZ S, CHEOK CF, et al. Ubiquitin-inde- pendent degradation of p53 mediated by high-risk human papil- lomavirus protein E6[J]. Oncogene, 2007, 26(28): 4059-4070.
  • 6CHEN C, SUN X, GUO P. Ubiquitin E3 ligase WWP1 as an oncogertic factor in human prostate cancer[J]. Oncogerte, 2007, 26 (16): 2386-2394.
  • 7CHEN CS, BELLIER A, KAO CY, et al. WWPI-1 ls a novel modulator of the DAF-2 insulin-like signaling network involved in pore-forming toxin cellular defenses in caenorhabditis elegans [J]. Plos One, 2010, 5(3): e9494.
  • 8CHEN CS, SUN XD, GUO P, et al. Human kruppel-like factor 5 is a target of the E3 ubiquitin ligase WWP1 for proteolysis in epithelial cells [J]. J of Biological Chemistry, 2005, 280 (50): 41553-41561.
  • 9BOTEZATU A, GOIA-RUSANU CD, STANESCU AD, et al. WWP1, TGF beta and KLF5 gene expression levels as new possible factors involved in cervical oncogenesis[J]. Revista Ro- mana De Medicina De Laborator, 2011, 19(1-4): 47-54.
  • 10BROMBERG KD, KLUGER HM, DELAUNAY A, et al. In- creased expression of /he E3 ubiquitin ligase RNA5 is associ- ated with decreased survival in breast cancer[J]. Cancer Res,2007, 67, (17): 8172-8179.

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