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子宫平滑肌瘤中的7q22缺失:细胞遗传学综述

Deletion 7q22 in uterine leiomyoma. A cytogenetic review.

作者信息

Ozisik Y Y, Meloni A M, Surti U, Sandberg A A

机构信息

Cancer Center of Southwest Biomedical Research Institute, Scottsdale, Arizona 85251.

出版信息

Cancer Genet Cytogenet. 1993 Nov;71(1):1-6. doi: 10.1016/0165-4608(93)90195-r.

Abstract

The cytogenetic patterns of uterine leiomyomas have been extensively investigated, and cases characterized by specific clonal changes have been documented in detail. In these tumors one of the cytogenetic changes frequently observed has been a del(7), particularly del(7)(q22), usually as a sole anomaly. This is confirmed by our experience and by reports in the literature. The fact that del(7) is one of the most common abnormalities in leiomyoma raises the question of its role in tumor development. The main purpose of this review is to analyze the above aspect and to interpret its possible meaning. Our findings on cytogenetic abnormalities of chromosome 7 in leiomyoma, together with those reported in the literature, are reviewed and discussed. A listing of the genes located at 7q22 is also presented.

摘要

子宫平滑肌瘤的细胞遗传学模式已得到广泛研究,具有特定克隆性改变特征的病例也已被详细记录。在这些肿瘤中,经常观察到的细胞遗传学改变之一是7号染色体缺失,特别是del(7)(q22),通常作为唯一的异常情况。我们的经验以及文献报道均证实了这一点。7号染色体缺失是平滑肌瘤中最常见的异常之一,这一事实引发了其在肿瘤发生发展中作用的问题。本综述的主要目的是分析上述方面并解读其可能的意义。我们对平滑肌瘤中7号染色体细胞遗传学异常的研究结果,连同文献报道的结果,进行了回顾和讨论。同时还列出了位于7q22的基因。

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