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[口腔鳞状细胞癌中的p53-p21(waf1)通路与中心体扩增]

[The p53-p21(waf1) pathway and centrosome amplification in oral squamous cell carcinomas].

作者信息

Cai Yang, Liu Yong-fa, Yang Hong, Lu Hong

机构信息

Department of Stomatology, Guiyang Medical College, Guiyang 550004, China.

出版信息

Zhonghua Kou Qiang Yi Xue Za Zhi. 2009 Jun;44(6):332-5.

Abstract

OBJECTIVE

To elucidate the possible role of p53-p21(waf1) pathway for centrosome amplification in oral squamous cell carcinoma (OSCC).

METHODS

Formalin-fixed, paraffin-embedded tissues of 8 cases of normal oral epithelium tissues and 27 cases of OSCC tissues were examined for the expression of p21(waf1) and mutated p53 proteins by flow cytometry and immunohistochemistry, and centrosome status was investigated by indirect immunofluorescence double staining with antibodies to centrosome protein gamma-tubulin and cytokeratin. The correlation between p21(waf1), p53 and centrosome amplification in OSCC was statistically analyzed by SPSS 12.0.

RESULTS

All normal oral epithelium tissues showed normal centrosomes (1-2 centrosomes per cell)in epithelium cells, while 21 out of 27 cases (78%) of OSCC showed the evidence of centrosome amplification characterized by supernumerary centrosomes ( >2 centrosomes per cell) in a fraction of tumor cells. The quantity of p21(waf1) protein was lower in OSCC with centrosome amplification [(0.878 +/- 0.081)] than that in OSCC without centrosome amplification [(0.952 +/- 0.018), t = 3.838, P < 0.01], and negative correlations were found between the quantity of p21(waf1) protein and the degree of centrosome amplification (r = -0.472, P < 0.05), as well as the positive staining of p53 (r = -0.491, P < 0.01).

CONCLUSIONS

p53-p21(waf1) pathway might involve in centrosome duplication cycle in OSCC. Down-regulated p21(waf1) protein, via p53 transactivation-dependent mechanism, was likely a contributing factor towards centrosome amplification in OSCC.

摘要

目的

阐明p53-p21(waf1)通路在口腔鳞状细胞癌(OSCC)中心体扩增中可能发挥的作用。

方法

采用流式细胞术和免疫组织化学法检测8例正常口腔上皮组织和27例OSCC组织中p21(waf1)和突变型p53蛋白的表达,并通过用抗中心体蛋白γ-微管蛋白和细胞角蛋白的抗体进行间接免疫荧光双重染色来研究中心体状态。使用SPSS 12.0对OSCC中p21(waf1)、p53与中心体扩增之间的相关性进行统计学分析。

结果

所有正常口腔上皮组织的上皮细胞均显示正常中心体(每个细胞1-2个中心体),而27例OSCC中有21例(78%)显示出中心体扩增的证据,其特征为部分肿瘤细胞中存在多余中心体(每个细胞>2个中心体)。中心体扩增的OSCC中p21(waf1)蛋白量[(0.878±0.081)]低于无中心体扩增的OSCC[(0.952±0.018),t = 3.838,P < 0.01],并且发现p21(waf1)蛋白量与中心体扩增程度(r = -0.472,P < 0.05)以及p53阳性染色(r = -0.491,P < 0.01)之间呈负相关。

结论

p53-p21(waf1)通路可能参与OSCC的中心体复制周期。通过p53反式激活依赖性机制下调的p21(waf1)蛋白可能是OSCC中心体扩增的一个促成因素。

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