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1号染色体异常:小儿实体瘤的一个常见特征。

Chromosome 1 abnormalities: a common feature of pediatric solid tumors.

作者信息

Douglass E C, Green A A, Hayes F A, Etcubanas E, Horowitz M, Wilimas J A

出版信息

J Natl Cancer Inst. 1985 Jul;75(1):51-4.

PMID:2989603
Abstract

Abnormalities of chromosome 1 were found in 32 of 46 pediatric solid tumors including Ewing's sarcoma, Wilms' tumor, rhabdomyosarcoma, primitive neuroectodermal tumor, and hepatoblastoma. Trisomy of 1q was the most common abnormality, and breakpoints were most frequent in the region 1cen to 1p22. Abnormalities of chromosome 1 are not specific to any type of tumor. However, their frequent occurrence indicates that they may endow a clonal advantage in the development of cancer.

摘要

在46例儿童实体瘤(包括尤因肉瘤、肾母细胞瘤、横纹肌肉瘤、原始神经外胚层肿瘤和肝母细胞瘤)中,有32例发现了1号染色体异常。1q三体是最常见的异常,断点最常出现在1cen至1p22区域。1号染色体异常并非特定于任何一种肿瘤类型。然而,它们的频繁出现表明,它们可能在癌症发展过程中赋予克隆优势。

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