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Expression of O6-methylguanine DNA methyltransferase (MGMT) and its clinical significance in gastroenteropancreatic neuroendocrine neoplasm

机译:O6-甲基鸟嘌呤DNA甲基转移酶(MGMT)在胃肠胰腺神经内分泌肿瘤中的表达及其临床意义

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摘要

O6-methylguanine-DNA methyltransferase (MGMT) is a widespread DNA repair enzyme defending against mutation caused by guanine O6-alkylating agents. Until now, we know only little about the expression of MGMT in gastroenteropancreatic neuroendocrine neoplasm (GEP-NEN). To study the expression of MGMT and its clinical significance in GEP-NEN, 174 specimens of GEP-NEN were examined, of which 152 specimens came from The First Affiliated Hospital, Sun Yat-sen University during October 1995 to November 2013, 22 specimens came from Peking Union Medical College Hospital during September 2004 to April 2010. MGMT protein was detected with EnVision immunohistochemical staining method. Clinicopathological factors were also collected and analyzed. We observed that the overall expression rate of MGMT was 83.9%. Over expression of MGMT protein was not associated with sex, age, functional status, primary tumor location, grading, classification, TNM stage and metastasis (P > 0.05). Kaplan-Meier analysis revealed that there was no significant difference in survival between MGMT-positive and MGMT-negative tumors of GEP-NEN patients (χ2 = 0.887, P = 0.346). In multivariate analyses carried out by Cox proportional hazards regression model, MGMT expression was also not an independent predictors of survival. These results demonstrated that MGMT protein was highly expressed in GEP-NEN. MGMT deficiency rate was similar in pancreatic NEN and in gastrointestinal NEN. MGMT expression was not correlated with prognosis of GEP-NEN.
机译:O 6 -甲基鸟嘌呤-DNA甲基转移酶(MGMT)是一种广泛的DNA修复酶,可抵抗鸟嘌呤O 6 -烷基化剂引起的突变。到目前为止,我们对MGMT在胃肠胰腺神经内分泌肿瘤(GEP-NEN)中的表达了解甚少。为了研究MGMT在GEP-NEN中的表达及其临床意义,共检查了174份GEP-NEN标本,其中152份来自1995年10月至2013年11月中山大学附属第一医院,22份于2004年9月至2010年4月在北京协和医院收治。采用EnVision免疫组织化学染色法检测了MGMT蛋白。还收集并分析了临床病理因素。我们观察到MGMT的总表达率为83.9%。 MGMT蛋白的过度表达与性别,年龄,功能状态,原发肿瘤位置,分级,分类,TNM分期和转移无关(P> 0.05)。 Kaplan-Meier分析显示,GEP-NEN患者的MGMT阳性和MGMT阴性肿瘤的生存率无显着差异(χ 2 = 0.887,P = 0.346)。在Cox比例风险回归模型进行的多变量分析中,MGMT表达也不是生存的独立预测因子。这些结果表明,MGMT蛋白在GEP-NEN中高表达。 MGNE缺乏率在胰腺NEN和胃肠道NEN中相似。 MGMT的表达与GEP-NEN的预后无关。

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