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MYCN gene amplification in patients with neuroblastic tumors

机译:神经母细胞瘤患者MYCN基因扩增

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Although neuroblastic tumors are the most prevalent solid tumors, little is known about the genetic basis underlying their progression. The prognostic role for the MYCN gene in neuroblastic tumors is irrefutable. The aim of this study is to identify the frequency of MYCN gene amplification and its relationship with clinicopathological and prognostic factors in 40 patients with neuroblastic tumors by using real-time quantitative PCR. There was significant association between the age of older than 18 months and the high number of metastasis. 83.3% of metastatic neuroblastic tumors in patients aged more than 18 months were in stage 4, while it was about 12.5% in patients aged less than 18 months. We found an amplification of MYCN in 19 out of 40 patients. Also, we found MYCN gene amplification in 64% of neuroblastoma (NB) and 8% of gangelioneuroblastoma (GNB) cases. There was a significant association between the histological type of samples with MYCN gene amplification. Neuroblastic tumors have a varied range of MYCN gene amplification depend on histopathology types. No significant associations have been found between MYCN gene amplification and tumor evaluation, CNS involvement, metastasis, stage of disease and patients outcome.
机译:尽管成神经细胞瘤是最普遍的实体瘤,但对其进展的遗传基础知之甚少。 MYCN基因在成神经细胞肿瘤中的预后作用是无可辩驳的。这项研究的目的是通过实时定量PCR来鉴定40例成神经细胞肿瘤患者中MYCN基因扩增的频率及其与临床病理和预后因素的关系。 18个月以上的年龄与高转移率之间存在显着相关性。年龄大于18个月的患者中有83.3%的转移性神经母细胞瘤处于第4阶段,而年龄小于18个月的患者中约占12.5%。我们在40例患者中的19例中发现了MYCN的扩增。此外,我们在64%的神经母细胞瘤(NB)和8%的神经节神经母细胞瘤(GNB)病例中发现MYCN基因扩增。样本的组织学类型与MYCN基因扩增之间存在显着关联。成神经细胞肿瘤具有多种MYCN基因扩增范围,具体取决于组织病理学类型。在MYCN基因扩增与肿瘤评估,中枢神经系统受累,转移,疾病阶段和患者预后之间未发现显着关联。

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