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机构地区:[1]首都医科大学基础医学院病理系,北京100069 [2]肿瘤侵袭和转移机制研究北京市重点实验室,北京100069
出 处:《临床与病理杂志》2017年第11期2339-2344,共6页Journal of Clinical and Pathological Research
摘 要:目的:研究N-MYC基因拷贝数在神经母细胞源性肿瘤(neuroblastic tumors,NTs)患者中的异常改变及其临床病理学意义。方法:收集483例NTs患儿肿瘤组织标本,其中包括神经母细胞瘤(neuroblastoma,NB)388例、节细胞神经母细胞瘤(ganglioneuroblastoma,GNB)89例、节细胞神经瘤(ganglioneuroma,GN)6例。运用荧光原位杂交技术(fluorescence in situ hybridization,FISH)检测N-MYC基因拷贝数改变。考察N-MYC基因拷贝数改变与临床病理学特征的关系并进行生存分析。结果:483例NTs患儿N-MYC基因扩增率为12.4%。N-MYC基因扩增均发生在NB中,而在GNB及GN中未见其扩增(P<0.05)。N-MYC基因拷贝数改变更易发生在低分化程度的NB中(P=0.01),且随着分化程度降低,N-MYC基因扩增率增加。男性患儿N-MYC基因拷贝数改变的发生率多于女性患儿(P=0.05)。患儿年龄≤18个月者N-MYC基因扩增率有低于>18个月者的趋势(P=0.092)。生存分析显示:N-MYC基因扩增组患儿生存率明显低于获得组及正常组。结论:NTs患儿N-MYC基因扩增与NTs的类型、分化程度、性别、年龄及生存密切相关。本研究为NTs患者的诊断、治疗及预后提供可靠的参考和帮助。Objective: To detect N-MYC gene copy number alterations, and to analyze their related clinicopathological implications in pediatric neuroblastic tumors(NTs). Methods: A total of 483 NT samples were obtained, including 388 neuroblastomas(NBs), 89 ganglioneuroblastomas(GNBs) and 6 ganglioneuromas(GNs). Fluorescence in situ hybridization(FISH) was used to detect numerical aberrations of N-MYC. Statistical analysis was used to study its association with clinicopathological features, as well as with the survival rate of patients. Results: Of 483 NT cases, N-MYC amplification rate was 12.4%. Gene amplification of N-MYC were found only in NB, but not in any GNB or GN case(P〈0.05). N-MYC gene amplification was more likely to occur in poorly differentiated neuroblastoma(P=0.01), the rate of which was inversely related to tumor differentiation. The N-MYC amplification rate in male patients was higher than that in female patients(P=0.05). There was a trend that the amplification rate of N-MYCgene was lower in patients ≤18 months as compared to patients 18 months, but difference was not significantly(P=0.092). The univariate survival analysis showed that the survival rate of patients with N-MYC gene amplification was significantly lower than those with N-MYC gain or normal gene status. Conclusion: N-MYC gene amplification is tightly correlated with tumor type, differentiation, gender, age and survival. Detection of abnormal N-MYC copy number would be helpful for the diagnosis and prognosis of neuroblastic tumors.
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