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人类非恶性肿瘤中频繁的克隆性染色体变化。

Frequent clonal chromosomal changes in human non-malignant tumors.

作者信息

Teyssier J R, Ferre D

机构信息

Histology-Embryology-Cytogenetics Laboratory, Faculty of Medicine, INSERM U314, University of Reims, France.

出版信息

Int J Cancer. 1989 Nov 15;44(5):828-32. doi: 10.1002/ijc.2910440514.

Abstract

A cytogenetic analysis has been performed on 109 non-malignant human solid tumors of various histological types after short-term culture. These tumors were derived from epithelial, mesenchymal, embryonal and neurogenic tissues. The chromosome count was in the diploid range in virtually all specimens. Clonal chromosomal changes were found in 37% of tumors: 20% had numerical deviations, 12% structural rearrangements, and 5% both karyotypic alterations. Chromosome 7 was most frequently involved in 25% of abnormal specimens. Our results suggest that chromosomal changes contribute to non-malignant tumorigenesis and that their analysis may provide information about the genetic events which shift benign tumor cells to malignant behavior.

摘要

对109例经短期培养的不同组织学类型的非恶性人类实体瘤进行了细胞遗传学分析。这些肿瘤来源于上皮组织、间充质组织、胚胎组织和神经组织。几乎所有标本的染色体计数都在二倍体范围内。在37%的肿瘤中发现了克隆性染色体变化:20%有数量偏差,12%有结构重排,5%既有核型改变。7号染色体在25%的异常标本中最常受累。我们的结果表明,染色体变化有助于非恶性肿瘤的发生,对其分析可能提供有关将良性肿瘤细胞转变为恶性行为的遗传事件的信息。

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