• 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

单个个体中多发性卵巢畸胎瘤的多种起源

Diverse origins of multiple ovarian teratomas in a single individual.

作者信息

Carritt B, Parrington J M, Welch H M, Povey S

出版信息

Proc Natl Acad Sci U S A. 1982 Dec;79(23):7400-4. doi: 10.1073/pnas.79.23.7400.

DOI:10.1073/pnas.79.23.7400
PMID:6961419
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC347347/
Abstract

Centromere heteromorphisms and enzyme markers were examined in cells cultured from seven benign ovarian teratomas arising in a single patient. Three of the teratomas were homozygous for all eight enzyme and centromere markers found to be heterozygous in the host. The other four tumors were heterozygous at the centromeres of chromosomes 1, 16, 17, and 18, as in the patient, but were homozygous for at least one of the enzyme markers. The linkage phases of the heterozygous enzyme markers phosphogluconate dehydrogenase and phosphoglucomutase 1 and the chromosome 1 centromere heteromorphism were established for the patient and for three of the heterozygous teratomas by analysis of Chinese hamster-human somatic cell hybrids. The linkage phase of these markers in homozygous and heterozygous tumors was in every case different from that in the host. The finding of heterozygous centromeres in ovarian teratomas excludes suppression of meiosis II as a mechanism for their origin, and we suggest rather that they arise by failure of meiosis I. The linkage phases in the fully homozygous tumors are most readily derived from that in the patient, we suggest, by endoreduplication of a haploid gamete. The varied origin of ovarian teratomas has important implications for the suitability of such material for centromere-based gene mapping.

摘要

对一名患者身上出现的7个良性卵巢畸胎瘤培养的细胞进行了着丝粒多态性和酶标记物检测。其中3个畸胎瘤对于在宿主中发现为杂合子的所有8种酶和着丝粒标记物均为纯合子。另外4个肿瘤在1号、16号、17号和18号染色体的着丝粒处为杂合子,如同患者一样,但对于至少一种酶标记物为纯合子。通过对中国仓鼠 - 人类体细胞杂种的分析,确定了患者以及3个杂合性畸胎瘤中杂合性酶标记物6 - 磷酸葡萄糖酸脱氢酶和磷酸葡萄糖变位酶1与1号染色体着丝粒多态性的连锁相。在纯合子和杂合子肿瘤中这些标记物的连锁相在每种情况下都与宿主中的不同。卵巢畸胎瘤中存在杂合性着丝粒排除了减数分裂II抑制作为其起源机制的可能性,我们认为它们而是由减数分裂I失败产生的。我们认为,完全纯合子肿瘤中的连锁相最容易从患者的连锁相通过单倍体配子的核内复制得到。卵巢畸胎瘤的多样起源对于此类材料用于基于着丝粒的基因定位的适用性具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/845c/347347/35999feac7f1/pnas00462-0328-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/845c/347347/0bff4447f9f7/pnas00462-0327-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/845c/347347/08730bb77e1f/pnas00462-0328-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/845c/347347/65d85f8ca5c2/pnas00462-0328-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/845c/347347/35999feac7f1/pnas00462-0328-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/845c/347347/0bff4447f9f7/pnas00462-0327-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/845c/347347/08730bb77e1f/pnas00462-0328-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/845c/347347/65d85f8ca5c2/pnas00462-0328-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/845c/347347/35999feac7f1/pnas00462-0328-c.jpg

相似文献

1
Diverse origins of multiple ovarian teratomas in a single individual.单个个体中多发性卵巢畸胎瘤的多种起源
Proc Natl Acad Sci U S A. 1982 Dec;79(23):7400-4. doi: 10.1073/pnas.79.23.7400.
2
The origin of ovarian teratomas.卵巢畸胎瘤的起源。
J Med Genet. 1984 Feb;21(1):4-12. doi: 10.1136/jmg.21.1.4.
3
Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of origin.人类卵巢畸胎瘤的遗传学与生物学。I. 细胞遗传学分析及起源机制。
Am J Hum Genet. 1990 Oct;47(4):635-43.
4
Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers.
Am J Hum Genet. 1990 Oct;47(4):644-55.
5
Estimating distances from the centromere by means of benign ovarian teratomas in man.借助人类良性卵巢畸胎瘤估算着丝粒的距离。
Ann Hum Genet. 1976 Nov;40(2):191-6. doi: 10.1111/j.1469-1809.1976.tb00179.x.
6
Origin of immature teratoma of the ovary.卵巢未成熟畸胎瘤的起源。
Am J Obstet Gynecol. 1985 Aug 1;152(7 Pt 1):896-900. doi: 10.1016/s0002-9378(85)80088-0.
7
Gene loss in human teratomas.人类畸胎瘤中的基因缺失。
Proc Natl Acad Sci U S A. 1969 Jul;63(3):699-704. doi: 10.1073/pnas.63.3.699.
8
Parthenogenic origin of benign ovarian teratomas.良性卵巢畸胎瘤的孤雌生殖起源
N Engl J Med. 1975 Jan 9;292(2):63-6. doi: 10.1056/NEJM197501092920202.
9
Genetics and biology of human ovarian teratomas. III. Cytogenetics and origins of malignant ovarian germ cell tumors.人类卵巢畸胎瘤的遗传学与生物学。III. 恶性卵巢生殖细胞肿瘤的细胞遗传学与起源
Cancer Genet Cytogenet. 1992 Aug;62(1):58-65. doi: 10.1016/0165-4608(92)90040-f.
10
Benign ovarian teratomas. An analysis of their cellular origin.良性卵巢畸胎瘤。对其细胞起源的分析。
Cancer Genet Cytogenet. 1990 May;46(1):115-23. doi: 10.1016/0165-4608(90)90017-5.

引用本文的文献

1
Mature Cystic Teratoma: An Integrated Review.成熟囊性畸胎瘤:综合评价。
Int J Mol Sci. 2023 Mar 24;24(7):6141. doi: 10.3390/ijms24076141.
2
Evidence of metachronous development of ovarian teratomas: a case report of bilateral mature cystic teratomas of the ovaries and systematic literature review.卵巢畸胎瘤异时性发生的证据:双侧卵巢成熟性囊性畸胎瘤病例报告及系统文献综述
J Ovarian Res. 2017 Mar 14;10(1):17. doi: 10.1186/s13048-017-0313-8.
3
Role of the inositol polyphosphate-4-phosphatase type II Inpp4b in the generation of ovarian teratomas.

本文引用的文献

1
CHROMOSOME NUMBER AND MORPHOLOGY OF BENIGN OVARIAN CYSTIC TERATOMAS.良性卵巢囊性畸胎瘤的染色体数目与形态
N Engl J Med. 1964 Dec 10;271:1241-4. doi: 10.1056/NEJM196412102712405.
2
Chiasma derived genetic maps and recombination fractions: chromosome 1.交叉衍生的遗传图谱和重组率:第1号染色体
Ann Hum Genet. 1982 May;46(2):167-75. doi: 10.1111/j.1469-1809.1982.tb00707.x.
3
Gene order and localization of enzyme loci on the short arm of chromosome 1.1号染色体短臂上的基因顺序及酶基因座定位
肌醇多磷酸-4-磷酸酶 II 型 Inpp4b 在卵巢畸胎瘤发生中的作用。
Dev Biol. 2013 Jan 1;373(1):118-29. doi: 10.1016/j.ydbio.2012.10.011. Epub 2012 Oct 16.
4
Cyclin B-cdk activity stimulates meiotic rereplication in budding yeast.细胞周期蛋白B-细胞周期蛋白依赖性激酶活性刺激芽殖酵母中的减数分裂再复制。
Genetics. 2004 Aug;167(4):1621-8. doi: 10.1534/genetics.104.029223.
5
Microdissection-based analysis of mature ovarian teratoma.基于显微切割的成熟卵巢畸胎瘤分析。
Am J Pathol. 1999 Apr;154(4):987-91. doi: 10.1016/S0002-9440(10)65350-3.
6
gld-1, a tumor suppressor gene required for oocyte development in Caenorhabditis elegans.gld-1,一种秀丽隐杆线虫卵母细胞发育所需的肿瘤抑制基因。
Genetics. 1995 Feb;139(2):579-606. doi: 10.1093/genetics/139.2.579.
7
The origin of ovarian teratomas.卵巢畸胎瘤的起源。
J Med Genet. 1984 Feb;21(1):4-12. doi: 10.1136/jmg.21.1.4.
8
Genes for the 'H' subunit of human ferritin are present on a number of human chromosomes.人类铁蛋白“H”亚基的基因存在于多条人类染色体上。
Hum Genet. 1985;71(2):108-12. doi: 10.1007/BF00283363.
9
Chromosome 1 in relation to human disease.与人类疾病相关的1号染色体。
J Med Genet. 1986 Apr;23(2):107-15. doi: 10.1136/jmg.23.2.107.
10
Loss of heterozygosity in hypotriploid cell cultures from testicular tumours.睾丸肿瘤的亚三倍体细胞培养物中的杂合性缺失
Hum Genet. 1987 Nov;77(3):269-76. doi: 10.1007/BF00284484.
Ann Hum Genet. 1982 Oct;46(4):329-35. doi: 10.1111/j.1469-1809.1982.tb01583.x.
4
Further evidence for post-meiotic origin of teratomas in the human female.人类女性畸胎瘤减数分裂后起源的进一步证据。
Ann Hum Genet. 1970 Jul;34(1):21-30. doi: 10.1111/j.1469-1809.1970.tb00216.x.
5
Gene loss in human teratomas.人类畸胎瘤中的基因缺失。
Proc Natl Acad Sci U S A. 1969 Jul;63(3):699-704. doi: 10.1073/pnas.63.3.699.
6
Chiasma distribution at diakinesis in the normal human male.正常男性减数分裂终变期的交叉分布
Hereditas. 1974;76(1):55-78. doi: 10.1111/j.1601-5223.1974.tb01177.x.
7
A simple technique for demonstrating centromeric heterochromatin.一种用于显示着丝粒异染色质的简单技术。
Exp Cell Res. 1972 Nov;75(1):304-6. doi: 10.1016/0014-4827(72)90558-7.
8
Estimating distances from the centromere by means of benign ovarian teratomas in man.借助人类良性卵巢畸胎瘤估算着丝粒的距离。
Ann Hum Genet. 1976 Nov;40(2):191-6. doi: 10.1111/j.1469-1809.1976.tb00179.x.
9
Ovarian teratomas: cytologic data.卵巢畸胎瘤:细胞学数据。
Cytogenet Cell Genet. 1976;16(1-5):391-5. doi: 10.1159/000130640.
10
Somatic cell genetic evidence for the presence of a gene for citrullinemia on human chromosome 9.人类9号染色体上存在瓜氨酸血症基因的体细胞遗传学证据。
Cytogenet Cell Genet. 1977;19(1):44-8. doi: 10.1159/000130793.