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Survivin磷酸化在口腔黏膜下纤维性变及其癌变组织中的表达
引用本文:周晌辉,李力力,蒋海鹰,王颖,陈顺金,吴晓珊,翦新春. Survivin磷酸化在口腔黏膜下纤维性变及其癌变组织中的表达[J]. 口腔医学, 2009, 29(2): 61-64
作者姓名:周晌辉  李力力  蒋海鹰  王颖  陈顺金  吴晓珊  翦新春
作者单位:中南大学湘雅医院口腔颌面外科,长沙,410008;中南大学肿瘤研究所分子生物室,长沙,410078;中南大学基础医学院病理学系,长沙,410013
摘    要:目的检测凋亡抑制蛋白Survivin活性形式——Survivin Thr34位磷酸化(p-Survivin)在口腔黏膜下纤维性变及其癌变组织中的表达,探讨Survivin在OSF癌变过程中的作用及意义。方法应用免疫组化SP法检测10例正常口腔黏膜组织、40例OSF组织及42例OSF癌变组织中p-Survivin的表达,并以Western Blot分析p-Survivin的表达。结果正常口腔黏膜上皮组织中无p-Survivin表达;OSF癌变组p-Survivin阳性表达率(97.6%)高于OSF组(50.0%);而OSF早、中、晚期3组间p-Survivin阳性表达率无显著性差异。Western Blot验证了免疫组化的检测结果。结论p-Survivin在OSF癌变过程中可能起促进作用,为OSF早期诊断和治疗提供理论依据。

关 键 词:Survivin  磷酸化  口腔黏膜下纤维性变  癌变

Expression of Survivin phosphorylation in carcinogenesis of oral submucous fibrosis
ZHOU Shang-hui,LI Li-li,JIANG Hai-ying,WANG Ying,CHEN Shun-jin,WU Xiao-shan,JIAN Xin-chun. Expression of Survivin phosphorylation in carcinogenesis of oral submucous fibrosis[J]. Stomatology, 2009, 29(2): 61-64
Authors:ZHOU Shang-hui  LI Li-li  JIANG Hai-ying  WANG Ying  CHEN Shun-jin  WU Xiao-shan  JIAN Xin-chun
Affiliation:ZHOU Shang-hui, LI Li-li, JIANG Hai-ying, WANG Ying, CHEN Shun-jin, WU Xiao-shan, JIAN Xin-chun. ( Department of Oral and MaxiUofacial Surgery, Xiangya Hospital, Central South University, Changsha 410008, China )
Abstract:Objective To investigate the expression of phosphorylation of Survivin on Thr34 in the tissues of oral submucous fibrosis (OSF) and oral squamous cell carcinoma (OSCC) originated from OSF, and to elucidate an important role of Survivin in the carcinogenesis of OSF. Methods The expression of Survivin Thr34 phosphorylation was examined by SP method in 10 cases of normal oral mu- cosa, 40 cases of OSF and 42 cases of OSCC originated from OSF. Western blot was used to confirm the expression of Survivin Thr34 phospho- rylation in these tissues. Results The expression of Survivin Thr34 phosphorylation was negative in normal oral mucosal epithelium. The positive staining rate of Survivin Thr34 phosphorylation in OSCC originated from OSF (97.6%) was significantly higher than that in OSF (50.0 % ) ( P 〈 0.01 ). However, the positive staining rate of Survivin Thr34 phosphorylaiton showed no significant difference among the early stage, the moderately advanced stage and the advanced stage of OSF ( P 〉 0.05). Next, Western blot analysis was used to confirm the phos- phorylation of Survivin on Thr 34 in the carcinogenesis of OSF. Conclusion The expression of Survivin Thr34 phosphorylation in the OSF and OSCC originated from OSF provided the strong evidence that Survivin might play an important role in the carcinogenesis of OSF and served as a new target for diagnosis and treatment.
Keywords:Survivin
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