• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

完全性葡萄胎滋养层细胞的细胞遗传学

Cytogenetics of trophoblasts from complete hydatidiform moles.

作者信息

Habibian R, Surti U

机构信息

Department of Pathology, University of Pittsburgh, PA.

出版信息

Cancer Genet Cytogenet. 1987 Dec;29(2):271-87. doi: 10.1016/0165-4608(87)90238-x.

DOI:10.1016/0165-4608(87)90238-x
PMID:3677047
Abstract

The risk of developing choriocarcinoma following a complete hydatidiform mole (CHM) is 2000-4000 times greater than the risk following a normal pregnancy. To understand more fully the increased susceptibility of the molar trophoblast to malignant transformation, we separated the trophoblastic cells from the stromal cells in 14 complete moles and cultured them for cytogenetic analysis. The numerical and structural abnormalities found were compared with those found in the trophoblasts from normal pregnancy and malignant choriocarcinoma cell lines. The percentage of polyploid cells was 2.8 times greater in molar trophoblasts than in normal trophoblasts. Although we found no consistent chromosomal abnormality in the molar trophoblasts, these cells were significantly more vulnerable to chromosomal breakage than the molar fibroblasts, normal trophoblasts, normal fibroblasts, and maternal decidual cells. Out of a total of 103 breakpoints observed in 338 cells, 42 coincided with known fragile sites, 18 with the location of protooncogenes, 27 with breakpoints reported in other neoplasia, and 18 with breakpoints found in four choriocarcinoma cell lines. The chromosomes in choriocarcinoma cell lines have hypotetraploid mode and many structural rearrangements. Our results suggest that the genetic instability found in the molar trophoblasts may be responsible for progressive karyotypic changes and greater susceptibility to malignant transformation.

摘要

完全性葡萄胎(CHM)后发生绒毛膜癌的风险比正常妊娠后发生绒毛膜癌的风险高2000 - 4000倍。为了更全面地了解葡萄胎滋养层细胞对恶性转化易感性增加的情况,我们从14例完全性葡萄胎中分离出滋养层细胞和基质细胞,并对其进行培养以进行细胞遗传学分析。将所发现的数量和结构异常与正常妊娠滋养层细胞及恶性绒毛膜癌细胞系中的异常情况进行比较。葡萄胎滋养层细胞中多倍体细胞的百分比比正常滋养层细胞高2.8倍。虽然我们在葡萄胎滋养层细胞中未发现一致的染色体异常,但这些细胞比葡萄胎成纤维细胞、正常滋养层细胞、正常成纤维细胞和母体蜕膜细胞更容易发生染色体断裂。在338个细胞中观察到的总共103个断点中,42个与已知的脆性位点重合,18个与原癌基因的位置重合,27个与其他肿瘤中报道的断点重合,18个与在四个绒毛膜癌细胞系中发现的断点重合。绒毛膜癌细胞系中的染色体呈亚四倍体模式且有许多结构重排。我们的结果表明,葡萄胎滋养层细胞中发现的遗传不稳定性可能是导致核型逐步变化以及对恶性转化易感性增加的原因。

相似文献

1
Cytogenetics of trophoblasts from complete hydatidiform moles.完全性葡萄胎滋养层细胞的细胞遗传学
Cancer Genet Cytogenet. 1987 Dec;29(2):271-87. doi: 10.1016/0165-4608(87)90238-x.
2
Sister chromatid exchange and chromosome breakage in complete hydatidiform moles.
Cancer Genet Cytogenet. 1992 Aug;62(1):53-7. doi: 10.1016/0165-4608(92)90039-b.
3
Chromosome and cellular origin of choriocarcinoma.绒毛膜癌的染色体及细胞起源
Cancer Res. 1981 Aug;41(8):3137-43.
4
Cytogenetic and clinicopathologic studies of partial moles.部分性葡萄胎的细胞遗传学和临床病理研究
Obstet Gynecol. 1986 Aug;68(2):259-62.
5
[Changes in gene expression profiles of hydatidiform mole and choriocarcinoma as compared with trophoblast hyperplasia].[与滋养层细胞增生相比,葡萄胎和绒毛膜癌基因表达谱的变化]
Zhonghua Zhong Liu Za Zhi. 2004 Dec;26(12):727-31.
6
Syndromes of hydatidiform moles. Partial vs. complete.葡萄胎综合征。部分性与完全性。
J Reprod Med. 1984 Nov;29(11):788-91.
7
Hydatidiform mole in a Danish material. Morphology and cytogenetics. A preliminary communication.
Acta Radiol Oncol. 1984;23(2-3):97-102. doi: 10.3109/02841868409135996.
8
Expression of HOX gene products in normal and abnormal trophoblastic tissue.HOX基因产物在正常和异常滋养层组织中的表达。
Gynecol Oncol. 2003 Sep;90(3):512-8. doi: 10.1016/s0090-8258(03)00357-3.
9
Malignant potential of homozygous and heterozygous complete moles.纯合子和杂合子完全性葡萄胎的恶性潜能。
Cancer Res. 1984 Mar;44(3):1226-30.
10
Hydatidiform mole: a chromosomal search for a recessive mutation.
Hum Reprod. 1986 Aug;1(5):337-40. doi: 10.1093/oxfordjournals.humrep.a136416.

引用本文的文献

1
Overcoming challenges associated with broad sharing of human genomic data.克服与人类基因组数据广泛共享相关的挑战。
Nat Genet. 2025 Feb;57(2):287-294. doi: 10.1038/s41588-024-02049-2. Epub 2025 Jan 22.