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[儿童实体瘤发生与进展中的癌基因与抑癌基因]

[Oncogenes and suppressor genes in the genesis and progression of solid tumors in children].

作者信息

Tonini G P, Mazzocco K, Scaruffi P

机构信息

Laboratorio Scientifico di Oncologia, Istituto Scientifico G. Gaslini, Genova, Italia.

出版信息

Pediatr Med Chir. 1994 May-Jun;16(3):203-9.

PMID:7971441
Abstract

Molecular and genetic analyses of tumor cell show that cellular oncogenes and suppressor genes are involved in neoplastic transformation. In pediatric tumors oncogenes as N-myc play an important role in the tumor progression. In retinoblastoma, neuroblastoma, Wilms' tumor, and rhabdomyosarcoma loss of heterozygosity for specific chromosome loci has been suggested to be a critical step in cancer development. Oncogene abnormalities can also be useful as a molecular tumor factor to foresee the prognosis of the disease. The present article is a review on the role of the oncogenes and suppressor genes in pediatric solid tumors.

摘要

肿瘤细胞的分子和基因分析表明,细胞癌基因和抑癌基因参与了肿瘤转化。在儿童肿瘤中,如N - myc等癌基因在肿瘤进展中起重要作用。在视网膜母细胞瘤、神经母细胞瘤、肾母细胞瘤和横纹肌肉瘤中,特定染色体位点的杂合性缺失被认为是癌症发展的关键步骤。癌基因异常也可作为一种分子肿瘤因素来预测疾病的预后。本文是关于癌基因和抑癌基因在儿童实体瘤中作用的综述。

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