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积液中癌细胞的细胞遗传学研究。

Cytogenetic study of cancer cells in effusions.

作者信息

Musilová J, Michalová K

出版信息

Cancer Genet Cytogenet. 1986 Jan 15;19(3-4):271-9. doi: 10.1016/0165-4608(86)90056-7.

Abstract

A cytogenetic study of 71 malignant effusions caused by different histopathologic types of cancer was performed by a direct technique. Abnormal metaphases were present in 50 effusions (70.4%); a detailed analysis of banded karyotypes was possible in 20 of these. Trisomies and monosomies were present in 18 of 20 cases. The most common trisomies were +19, +3, +5, +8, +9, +10, +16 and +22; the most frequent monosomies were -X, -2, -5, -7, and -21. Clonal structural abnormalities were identified in 18 of 20 cases. In most instances, they were extensive, and some chromosomes were involved in a nonrandom fashion. Chromosomes #1, #13, and #6 were the most frequently involved in these rearrangements. A common marker chromosome, t(7;9)(p11;q12), was observed in two patients with cancer of the endometrium. Double minutes (DMs) were present in two patients, and there was a homogeneously stained region (HSR) in one.

摘要

采用直接技术对71例由不同组织病理学类型癌症引起的恶性积液进行了细胞遗传学研究。50例积液(70.4%)中存在异常中期分裂相;其中20例可对带型核型进行详细分析。20例中有18例存在三体和单体。最常见的三体是+19、+3、+5、+8、+9、+10、+16和+22;最常见的单体是-X、-2、-5、-7和-21。20例中有18例发现克隆性结构异常。在大多数情况下,这些异常较为广泛,一些染色体以非随机方式受累。1号、13号和6号染色体最常参与这些重排。在两名子宫内膜癌患者中观察到一条常见的标记染色体t(7;9)(p11;q12)。两名患者出现双微体(DMs),一名患者出现均匀染色区(HSR)。

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