首页> 外文期刊>Journal of Nanjing Medical University >Expression of CyclinD1/Bcl-1 and p27/Kipl in Gliomas: Their Correlation with Pathological Grade and Prognosis
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Expression of CyclinD1/Bcl-1 and p27/Kipl in Gliomas: Their Correlation with Pathological Grade and Prognosis

机译:胶质瘤中CyclinD1 / Bcl-1和p27 / Kipl的表达及其与病理分级和预后的关系

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Objective: To study cyclinD1/bcl-1 and p27/kip1 expression in gliomas and their correlation with pathological grade and prognosis. Methods: Immunohistochemical technique was used to detect the cyclinD1/bcl-1 and p27/kip1 expression in 48 human brain glioma tissues of different malignant grades, and 12 normal non-neoplastic tissues collected from internal decompression. The data were analyzed quantitatively by the image system and also correlated retrospectively with the patients' clinical characteristics. Results: The immunohistochemical reaction for cyclinD1/bcl-1 and p27/kip1 was confined to the nuclei. The abnormal positive expression rates of both cyclinD1/bcl-1 and p27/kip1 in gliomas were found higher than that in non-neoplastic tissues(P < 0.05). The number and staining intensity of cyclinD1/bcl-1 positive nuclei increased with malignant grades (P < 0.05). On the contrary, the positive nuclei of p27/kip1 expression decreased in number and staining intensity with malignant grades(P < 0.05). Higher expression of cyclinD1/bcl-1 or/and lower expression of p27/kip1 were associated with poor prognosis(P <0.05). Conclusion: The abnormal expression of both cyclinD1/bcl-1 and p27/kip1 might be closely related to the occurrence and development of gliomas and they might have synergistic effect. These data suggest that both cyclinD1/bcl-1 expression and p27/kip1 expression can act as an independent prognostic factor.
机译:目的:研究cyclinD1 / bcl-1和p27 / kip1在脑胶质瘤中的表达及其与病理分级和预后的关系。方法:采用免疫组织化学技术检测48例恶性程度不同的人脑神经胶质瘤组织和12例从内部减压收集的正常非肿瘤组织中cyclinD1 / bcl-1和p27 / kip1的表达。通过图像系统对数据进行定量分析,并与患者的临床特征进行回顾性关联。结果:cyclinD1 / bcl-1和p27 / kip1的免疫组织化学反应仅限于细胞核。胶质瘤中cyclinD1 / bcl-1和p27 / kip1的阳性表达率均高于非肿瘤组织(P <0.05)。 cyclinD1 / bcl-1阳性细胞核的数目和染色强度随恶性程度的增加而增加(P <0.05)。相反,p27 / kip1表达阳性细胞的数目和染色强度随恶性程度的降低而降低(P <0.05)。 cyclinD1 / bcl-1的高表达或p27 / kip1的低表达与预后不良相关(P <0.05)。结论:cyclinD1 / bcl-1和p27 / kip1的异常表达可能与神经胶质瘤的发生和发展密切相关,可能具有协同作用。这些数据表明,cyclinD1 / bcl-1表达和p27 / kip1表达均可作为独立的预后因素。

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