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病理学与分子生物学的交汇之处:人类神经母细胞瘤中的N-myc扩增作为癌基因改变临床应用的范例

Where pathology meets molecular biology: N-myc amplification in human neuroblastoma as a paradigm for the clinical use of an oncogene alteration.

作者信息

Schwab M

机构信息

German Cancer Research Center, Division of Cytogenetics, Heidelberg.

出版信息

Verh Dtsch Ges Pathol. 1994;78:26-33.

PMID:7533996
Abstract

Increase of the dosage of cellular oncogenes by DNA amplification is a frequent genetic alteration of cancer cells. The presence of amplified cellular oncogenes is usually signalled by conspicuous chromosomal abnormalities, "double minutes" (DMs) or "homogeneously staining chromosomal regions" (HSRs). Some human cancers carry a specific amplified oncogene at high incidence. In neuroblastomas the amplification of N-myc has been found associated with aggressively growing cancers and is an indicator for poor prognosis. N-myc amplification is of predictive value for identifying neuroblastoma patients that require specific therapeutic regimens and for identifying patients that do not benefit from chemotherapy.

摘要

通过DNA扩增增加细胞癌基因的剂量是癌细胞常见的基因改变。扩增的细胞癌基因的存在通常由明显的染色体异常、“双微体”(DMs)或“均匀染色染色体区域”(HSRs)来指示。一些人类癌症中特定的癌基因扩增发生率很高。在神经母细胞瘤中,已发现N - myc扩增与侵袭性生长的癌症相关,并且是预后不良的指标。N - myc扩增对于识别需要特定治疗方案的神经母细胞瘤患者以及识别对化疗无反应的患者具有预测价值。

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