期刊文献+

创面修复中C-myc原癌基因表达变化的观察 被引量:2

Observation of C-myc proto-oncogene expression during the clinical wound healing
下载PDF
导出
摘要 目的:观测创面修复中C-myc原癌基因的表达变化,探讨C-myc原癌基因表达变化在创面修复中的作用。方法:应用原位杂交方法对临床患者断层供皮区创面愈合中C-myc原癌基因表达变化进行了动态观察,并进行了半定量分析。结果:临床创面愈合中C-myc原癌基因有明显的规律性的表达变化,伤后4d时,C-myc原癌基因在创面内有明显的表达,表达强度+~。伤后10d时,C-myc原癌基因在创面内表达较伤后4d时增强,除分布在创面浅层的成纤维细胞胞浆和创缘上皮基底细胞胞浆以外,尚可见分布在血管内皮细胞和皮肤附属上皮细胞中,创面的中层和深层也可见有表达,多较密集分布,表达强度~。伤后16d时,C-myc原癌基因在创面内表达的强度较伤后10d时明显减弱,表达强度接近伤后4d时的水平,表达强度+。结论:C-myc原癌基因表达与临床创面修复的过程有明显相关,C-myc原癌基因表达变化参与了临床创面修复过程,合理调控其表达变化有助于临床创面修复。 A IM:To detect the changes of C-myc proto-oncogene expression and to ex-plore its roles during the clinical wound healing.METHODS:Dynamic observation and se miquanti tative analysis were ex-amined in 22patients during the wound healin g of splitting skin donor using the in situ hybridization method.RESULTS:In cl inical wound healing,changes o f C-myc proto-oncogene ex-pression were obser ved obviously.C-myc proto-oncogene expressed more ob-viously at 10day(str ength of-)than at 4day(strength of +-)after wound.At 10day,C-m yc expression was observed in vascular en-dothelial cells and dermal epithelial cells,in middle and deep layer of wound,and in also superficial layer of fibr oblast cytoplasm and basal ce lls on the wound margins,most of whose distributi on was denseness.C-myc pro-to-oncogene expression at 16day(strength of + )was decreased compared with that at 10day,and was close to th at at 4day.C-myc proto-oncogene expression wa s obviously correlated with the clinical wound healing.The changes of its expression take part i n the clinica l wound healing process.It i s helpful for the clinical wound healing to reason ably control the
出处 《中国临床康复》 CSCD 2004年第2期266-267,T005,共3页 Chinese Journal of Clinical Rehabilitation
  • 相关文献

参考文献6

二级参考文献44

  • 1程飚,付小兵,盛志勇.有关创面愈合中信号调控机制的新认识[J].中国组织工程研究与临床康复,2001,10(24):72-73. 被引量:10
  • 2屈纪富,程天民,郝利.参与皮肤伤口愈合的细胞及其作用的研究进展[J].中国组织工程研究与临床康复,2001,10(24):74-75. 被引量:56
  • 3李小静 孟刚 宁金龙.瘢痕微血管构筑对瘢痕形成、发展及临床防治的基础研究[J].现代康复,2001,5(1):44-5.
  • 4MARTIN P.Wound healing aiming for perfect skin regeneration[J]. Science, 1997, 276(4): 75-81.
  • 5NUGENT MA, IOZZO RV. Fibroblast growth factor 2[J]. Int J Biochem & Cell Biology,2000,32(2):115-120.
  • 6LORENZ HP.TGF beta isoform and receptor expression during scarless wound repair[J]. J Craniofac Surg,2001,12(4):387-388.
  • 7HSU M,PELED ZM,CHIN GS,et al.Ontogeny of expression of transforming growth factor beta 1 (TGF beta 1),TGF beta 3,and TGF beta receptors I and II in fetal rat fibroblasts and skin[J]. Plast Reconstr Surg, 2001,107(7):1787-1794.
  • 8BROWN DL,KAO WWY,GREENHALGH.Apoptosis down regulates inflammation under the advancing epithelial wound edge:delayed pat terns in diabetes and improvement with topical growth factors[J]. Surgery,1997, 121(4): 372-380.
  • 9SOO C,SHAW WW,ZHANG X.et al.Differential expression of matrix metalloproteinase and their tissue derived inhibitors in cutaneous wound repair[J]. Plast Reconstr Surg,2000,105(2):638-647.
  • 10CHIN GS, LIU W,PELED Z, et al. Differential expression of transforming growth factor beta receptors I and II and activation of Smad 3 in keloid fibroblasts[J]. Plast Reconstr Surg, 2001, 108(2):423-429.

共引文献179

同被引文献35

  • 1谷廷敏,牛星焘,陈东明.创面愈合过程中EGF基因表达变化的研究[J].中国修复重建外科杂志,1996,10(3):133-135. 被引量:10
  • 2胡国刚 陈泉克.亚硒酸钠对MNNG和MNU诱导离体V79细胞姐妹染色单体互换(SCE)频率的影响[J].中华肿瘤杂志,1985,7(1):22-25.
  • 3刘秋燕,黄胜利,陈焕朝,等.亚硒酸钠对正常肝及肝癌细胞依赖于的蛋白激酶同工酶的作用[J].中华肿瘤杂志,1985,7(5):343.
  • 4安捷,陈泉光,高福正,等.亚硒酸钠对MNN G诱导小儿包皮成纤维细胞遗传物质损伤的影响[J].中华肿瘤杂志,1988,10(3):180.
  • 5[12]Hartwig A. Current aspects in metal genotoxicity. Biometals 1995; 8(1): 3-11
  • 6[13]Hartwig A, Mullenders LH, Schlepegrell R, et al. Nickel(Ⅱ) interferes with the incision step in nucleotide excision repair in mammalian cells. Cancer Res 1994; 54(15):4045-51
  • 7[14]Nagaoka M, Kuwahara J, Sugiura Y. Alteration of DNA binding specificity by nickel(Ⅱ) substitution in three zinc(Ⅱ) fingers of transcription factor spl. Biochem Biophys Res Commun 1993; 194:1515 -20
  • 8[15]Predki PF , Sarkar B. Effect of replacement of "zinc finger" zinc on estrogen receptor DNA interactions. J Biol Chem 1992; 267 (9): 5842 - 6
  • 9[16]Van WR, Welters M, Souren JE, et al. Serum-stimulated cell cycle progression and stress protein synthesis in C3H10T1/2 fibroblasts treated with sodium arsenite. J Cell Physiol 1993; 155 (2): 265 -72
  • 10[18]Chesters JK, Petrie L, Vint H. Specificity and timing of the zinc(Ⅱ) requirement for DNA synthesis by 3T3 cells. Exp Cell Res 1989; 184(2):499 -508

引证文献2

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部