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成釉细胞瘤和牙源性角化囊性瘤中Bcl-2蛋白免疫组化显示的研究

Study of immunohistochemical demonstration of Bcl-2 protein in ameloblastoma and keratocystic odontogenic tumor.

作者信息

Sindura Cs, Babu Chaitanya, Mysorekar Vijaya, Kumar Vinod

机构信息

Department of Oral Pathology, Srinivas Institute of Dental Science, Mangalore, Karnataka, India.

出版信息

J Oral Maxillofac Pathol. 2013 May;17(2):176-80. doi: 10.4103/0973-029X.119750.

Abstract

BACKGROUND

The Bcl-2 (B-cell lymphoma) gene product also known as apoptotic inhibitor is expressed in many normal and tumor tissues. This Bcl-2 gene protects the cell by blocking postmitotic differentiation from apoptosis, thus maintaining the stem cell pool.

OBJECTIVE

To study the expression of Bcl-2 protein in ameloblastoma and keratocystic odontogenic tumor (KCOT) to determine their apoptotic behaviors and to analyze biological nature of KCOT, which has higher proliferative potential and aggressive clinical behavior like odontogenic tumors.

MATERIALS AND METHODS

Formalin-fixed paraffin sections of ameloblastoma (n = 20) and KCOT (n = 20) are considered for immunohistochemical analysis using monoclonal antibody against antihuman Bcl-2 oncoprotein. Lymphomas (n = 3) were used as controls.

STATISTICAL ANALYSIS

The statistical analysis was performed using software package of social science version 16. The data were analyzed using Chi-square test and Student's t test. In all the above tests, P < 0.05 was accepted as statistically significant.

RESULTS

The positive ratio of Bcl-2 was 85% (17/20) in ameloblastoma, 85% (17/20) in KCOT and 100% (3/3) in lymphomas. Bcl-2 was expressed in peripheral cells and few scattered cells of stellate reticulum in ameloblastoma. KCOT showed strong positivity for Bcl-2 mainly in the basal layer.

INTERPRETATION AND CONCLUSION

The present study demonstrates the aggressive nature of KCOT and intrinsic growth potential of its lining epithelium. This study clearly demonstrates that KCOT like ameloblastoma demonstrates aggressive clinical and noticeable invasive behavior. Therefore, it is now considered as no longer a developmental cyst but as odontogenic tumor.

摘要

背景

Bcl-2(B细胞淋巴瘤)基因产物也被称为凋亡抑制因子,在许多正常组织和肿瘤组织中均有表达。该Bcl-2基因通过阻止有丝分裂后细胞分化凋亡来保护细胞,从而维持干细胞池。

目的

研究Bcl-2蛋白在成釉细胞瘤和牙源性角化囊性瘤(KCOT)中的表达,以确定它们的凋亡行为,并分析KCOT的生物学特性,其具有较高的增殖潜能以及与牙源性肿瘤相似的侵袭性临床行为。

材料与方法

采用抗人Bcl-2癌蛋白单克隆抗体,对成釉细胞瘤(n = 20)和KCOT(n = 20)的福尔马林固定石蜡切片进行免疫组织化学分析。以淋巴瘤(n = 3)作为对照。

统计学分析

使用社会科学统计软件包16进行统计学分析。采用卡方检验和学生t检验分析数据。在上述所有检验中,P < 0.05被认为具有统计学意义。

结果

Bcl-2在成釉细胞瘤中的阳性率为85%(17/20),在KCOT中为85%(17/20),在淋巴瘤中为100%(3/3)。Bcl-2在成釉细胞瘤的周边细胞及星网状层少数散在细胞中表达。KCOT中Bcl-2主要在基底层呈强阳性。

解读与结论

本研究证实了KCOT的侵袭性本质及其衬里上皮的内在生长潜能。本研究清楚地表明,KCOT与成釉细胞瘤一样具有侵袭性临床行为和明显的侵袭性。因此,现在认为它不再是发育性囊肿,而是牙源性肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b207/3830222/b7ff8d819012/JOMFP-17-176-g001.jpg

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