首页> 美国卫生研究院文献>Journal of Dental Research Dental Clinics Dental Prospects >Immunohistochemichal Assessment of the CrkII Proto-oncogene Expression in Common Malignant Salivary Gland Tumors and Pleomorphic Adenoma
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Immunohistochemichal Assessment of the CrkII Proto-oncogene Expression in Common Malignant Salivary Gland Tumors and Pleomorphic Adenoma

机译:免疫组织化学评估常见恶性涎腺肿瘤和多形性腺瘤中CrkII原癌基因的表达

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摘要

>Background and aims. Various morphologies are seen in different salivary gland tumorsor within an individual tumor, and the lesions show divers biological behaviors. Experimental results support the hypothesis that increased CrkII proto-oncogene is associated with cytokine-induced tumor initiation and progression by altering cell motility signaling pathway. The aim of this study was to assess the CrkII expression in common malignant salivary gland tumors and pleomorphic ade-noma.>Materials and methods. Immunohistochemical analysis of CrkII expression was performed on paraffin blocks of 64 car-cinomas of salivary glands, 10 pleomorphic adenomas, and 10 normal salivary glands. Biopsies were subjected to immu-nostaining with EnVision detection system using monoclonal anti-CrkII. Evaluation of immunoreactivity of CrkII was based on the immunoreaction intensity and percentage of stained tumor cells which were scored semi-quantitatively on a scale with four grades 0 to 3. Kruskal-wallis test and additional Mann-Whitney statistical test were used for analysis of CrkII expression levels.>Results. Increased expression of CrkII was seen (P=0.005) in malignant tumors including: mucoepidermoid carcinoma, adenoid cystic carcinoma, and carcinoma ex pleomorphic adenoma, but CrkII expression in acinic cell carcinoma was weak. CrkII expression in pleomorphic adenoma was weak or negative. A weak staining was sparsely seen in normal acinar serous cell.>Conclusion. Increased expression of CrkII and its higher intensity of staining in tumors with more aggressive biologic behavior in carcinomas of salivary gland is consistent with a role for this proto-oncogene in salivary gland tumorigenesis and cancer progression.
机译:>背景和目标。在不同的唾液腺肿瘤中或单个肿瘤内可见多种形态,并且病变表现出多种生物学行为。实验结果支持这样的假说:增加的CrkII原癌基因与细胞因子诱导的肿瘤的发生和发展通过改变细胞运动信号通路有关。这项研究的目的是评估CrkII在常见的恶性涎腺肿瘤和多形性腺瘤中的表达。>材料和方法。免疫组化分析了CrkII在64例癌的石蜡块中的表达。唾液腺,10个多形腺瘤和10个正常唾液腺。使用单克隆抗CrkII,通过EnVision检测系统对活检标本进行免疫染色。 CrkII免疫反应性的评估是基于免疫反应强度和染色肿瘤细胞的百分比进行的,该肿瘤细胞的染色以4级至3级进行半定量评分。使用Kruskal-wallis检验和其他Mann-Whitney统计检验来分析CrkII表达水平。>结果。在包括粘液表皮样癌,腺样囊性癌和多形性腺瘤在内的恶性肿瘤中,CrkII的表达增加(P = 0.005),但在腺癌细胞中CrkII的表达较弱。 CrkII在多形性腺瘤中的表达弱或阴性。在正常的腺泡浆液细胞中稀疏地观察到弱染色。>结论。在唾液腺癌中,CrkII的表达增加且其染色强度更高,生物学行为更具侵袭性,这与此一致原癌基因在唾液腺肿瘤发生和癌症进展中的作用。

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