首页> 外文期刊>Cancer: A Journal of the American Cancer Society >Distinctive expression of the polycomb group proteins Bmi1 polycomb ring finger oncogene and enhancer of zeste homolog 2 in nonsmall cell lung cancers and their clinical and clinicopathologic significance.
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Distinctive expression of the polycomb group proteins Bmi1 polycomb ring finger oncogene and enhancer of zeste homolog 2 in nonsmall cell lung cancers and their clinical and clinicopathologic significance.

机译:非小细胞肺癌中polycomb组蛋白Bmi1 polycomb无名指癌基因和zeste同源物2增强子的独特表达及其临床和临床病理意义。

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BACKGROUND: The polycomb group genes Bmi1 polycomb ring finger oncogene (Bmi1) and enhancer of zeste homolog 2 (EZH2) function as transcriptional repressors involved in gene silencing and in the malignant transformation and biologic aggressiveness of several human carcinomas. In the current study, the authors evaluated Bmi1 and EZH2 protein expression in specimens of human nonsmall cell lung cancer (NSCLC). METHODS: The authors conducted an immunohistochemical assessment of 157 surgically resected NSCLCs to evaluate the correlation between Bmi1 and EZH2 expression and various features, including clinical, clinicopathologic, and biologic characteristics. RESULTS: Normal bronchial epithelia revealed abundant expression of Bmi1 and sporadic expression of EZH2. Patients who had high EZH2 expression in tumor cells had a poorer prognosis than patients who had low EZH2 expression in tumor cells all pathologic stages of NSCLC (P = .001) and in pathologic stage I NSCLC (P = .006). Multivariate analysis revealed that high EZH2 expression was a independent, unfavorable prognostic factor in patients with pathologic stage I disease (P = .048). High EZH2 expression was correlated significantly with nonadenocarcinoma histology (P = .001), moderate and poor differentiation (P = .001), advanced pathologic tumor classification (P = .02), and high Ki-67 and cyclin E labeling indices (P < .001). Bmi1 expression, in contrast, was not a significant prognostic factor and was not correlated with any clinicopathologic factors other than early pathologic tumor classification. CONCLUSIONS: Bmi1 and EZH2 had characteristic and distinctive expression in NSCLCs. High EZH2 expression was correlated with tumor aggressiveness and may provide a novel prognostic marker for NSCLCs.
机译:背景:polycomb组基因Bmi1聚梳无名指癌基因(Bmi1)和zeste同源2增强子(EZH2)充当转录抑制因子,参与基因沉默以及几种人类癌症的恶性转化和生物学侵袭性。在当前的研究中,作者评估了人类非小细胞肺癌(NSCLC)标本中Bmi1和EZH2蛋白的表达。方法:作者对157例手术切除的NSCLC进行了免疫组织化学评估,以评估Bmi1和EZH2表达与各种特征之间的相关性,包括临床,临床病理和生物学特征。结果:正常支气管上皮细胞显示Bmi1大量表达和EZH2偶发表达。在所有NSCLC病理分期(P = .001)和病理I期NSCLC(P = .006)中,肿瘤细胞中EZH2表达高的患者的预后要差于肿瘤细胞中EZH2表达低的患者。多变量分析显示,高EZH2表达是病理性I期疾病患者的独立,不利的预后因素(P = .048)。高EZH2表达与非腺癌组织学(P = .001),中度和差分化(P = .001),晚期肿瘤分类(P = .02)和高Ki-67和cyclin E标记指数(P显着相关) <.001)。相比之下,Bmi1表达不是重要的预后因素,除早期病理肿瘤分类外,与任何临床病理因素均不相关。结论:Bmi1和EZH2在非小细胞肺癌中具有特征性和独特表达。 EZH2高表达与肿瘤的侵袭性有关,可能为NSCLCs提供一种新的预后标志物。

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