• 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

16例人横纹肌肉瘤的染色体分析

Chromosomal analysis of sixteen human rhabdomyosarcomas.

作者信息

Wang-Wuu S, Soukup S, Ballard E, Gotwals B, Lampkin B

机构信息

Department of Human Genetics, Children's Hospital Medical Center, Cincinnati, Ohio 45229.

出版信息

Cancer Res. 1988 Feb 15;48(4):983-7.

PMID:3338090
Abstract

Chromosomal analysis of 16 rhabdomyosarcomas was done from four primary tumors and from 12 tumors after nude mouse passage. Seven tumors were alveolar; four of these had t(2;13)(q37;q14) and in two tumors it was the only structural abnormality. The other three alveolar tumors were near tetraploid with marker chromosomes and double minutes. In the nine embryonal tumors studied, one had a normal karyotype, and eight were abnormal. Although the eight tumors had no common structural abnormality, trisomy 2 was present in all.

摘要

对16例横纹肌肉瘤进行了染色体分析,其中4例取自原发性肿瘤,12例取自裸鼠传代后的肿瘤。7例为肺泡型;其中4例有t(2;13)(q37;q14),在2例肿瘤中这是唯一的结构异常。其他3例肺泡型肿瘤接近四倍体,有标记染色体和双微体。在研究的9例胚胎型肿瘤中,1例核型正常,8例异常。虽然这8例肿瘤没有共同的结构异常,但均存在2号染色体三体。

相似文献

1
Chromosomal analysis of sixteen human rhabdomyosarcomas.16例人横纹肌肉瘤的染色体分析
Cancer Res. 1988 Feb 15;48(4):983-7.
2
A specific chromosomal abnormality in rhabdomyosarcoma.横纹肌肉瘤中的一种特定染色体异常。
Cytogenet Cell Genet. 1987;45(3-4):148-55. doi: 10.1159/000132446.
3
Chromosome findings in human neuroblastomas xenografted in nude mice.裸鼠异种移植人神经母细胞瘤中的染色体发现
Jpn J Cancer Res. 1985 May;76(5):359-64.
4
Nonrandom chromosomal changes in transitional cell carcinoma of the bladder.膀胱移行细胞癌中的非随机染色体变化。
Cancer Res. 1984 Mar;44(3):1257-64.
5
Preservation of morphological, functional, and karyotypic traits during long-term culture and in vivo passage of two human skin squamous cell carcinomas.两个人类皮肤鳞状细胞癌在长期培养及体内传代过程中形态学、功能和核型特征的保存
Cancer Res. 1983 Dec;43(12 Pt 1):5995-6011.
6
Cytogenetic study of a spindle-cell rhabdomyosarcoma of the parotid gland.
Cancer Genet Cytogenet. 1999 Mar;109(2):150-3. doi: 10.1016/s0165-4608(98)00163-0.
7
Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma.着丝粒断裂是口腔鳞状细胞癌细胞遗传学异常的主要原因。
Genes Chromosomes Cancer. 1996 Jan;15(1):1-9. doi: 10.1002/(SICI)1098-2264(199601)15:1<1::AID-GCC1>3.0.CO;2-8.
8
Characterization of cell lines derived from xenografts of childhood rhabdomyosarcoma.源自儿童横纹肌肉瘤异种移植瘤的细胞系的特征分析
Cancer Res. 1987 Aug 15;47(16):4501-7.
9
Human embryonal cell carcinoma in nude mice.
Cancer Res. 1983 Nov;43(11):5526-32.
10
Chromosomal analysis of human prostatic adenocarcinoma cell lines.人前列腺腺癌细胞系的染色体分析
Cancer Res. 1980 Mar;40(3):524-34.

引用本文的文献

1
Downregulation of the paired box gene 3 inhibits the progression of skin cutaneous melanoma by inhibiting c-MET tyrosine kinase : PAX3 downregulation inhibits melanoma progression.配对盒基因 3 的下调通过抑制 c-MET 酪氨酸激酶抑制皮肤黑色素瘤的进展:PAX3 的下调抑制黑色素瘤的进展。
Mol Biol Rep. 2022 Oct;49(10):9137-9145. doi: 10.1007/s11033-022-07706-5. Epub 2022 Sep 4.
2
Evolving classification of rhabdomyosarcoma.横纹肌肉瘤的分类演变。
Histopathology. 2022 Jan;80(1):98-108. doi: 10.1111/his.14449.
3
The expression and function of PAX3 in development and disease.
PAX3 在发育和疾病中的表达和功能。
Gene. 2018 Aug 5;666:145-157. doi: 10.1016/j.gene.2018.04.087. Epub 2018 May 4.
4
Classification of rhabdomyosarcoma and its molecular basis.横纹肌肉瘤的分类及其分子基础。
Adv Anat Pathol. 2013 Nov;20(6):387-97. doi: 10.1097/PAP.0b013e3182a92d0d.
5
Structural and functional studies of FKHR-PAX3, a reciprocal fusion gene of the t(2;13) chromosomal translocation in alveolar rhabdomyosarcoma.结构与功能研究的 FKHR-PAX3,一个相互融合基因的 t(2;13) 染色体易位在肺泡横纹肌肉瘤。
PLoS One. 2013 Jun 14;8(6):e68065. doi: 10.1371/journal.pone.0068065. Print 2013.
6
Childhood rhabdomyosarcoma: recent advances and prospective views.儿童横纹肌肉瘤:最新进展和前瞻性观点。
J Dent Res. 2012 Apr;91(4):341-50. doi: 10.1177/0022034511421490. Epub 2011 Sep 13.
7
Nephroblastoma overexpressed (NOV/CCN3) gene: a paired-domain-specific PAX3-FKHR transcription target that promotes survival and motility in alveolar rhabdomyosarcoma cells.肾母细胞瘤过表达(NOV/CCN3)基因:PAX3-FKHR 转录靶标中的配对结构域特异性基因,可促进肺泡横纹肌肉瘤细胞的存活和迁移。
Oncogene. 2011 Aug 11;30(32):3549-62. doi: 10.1038/onc.2011.69. Epub 2011 Mar 21.
8
Comparative analysis of paired- and homeodomain-specific roles in PAX3-FKHR oncogenesis.PAX3-FKHR肿瘤发生中配对结构域和同源结构域特异性作用的比较分析。
Int J Clin Exp Pathol. 2009;2(4):370-83. Epub 2008 Dec 1.
9
Amplification and Over-Expression of the MDM2 Gene in Human Soft Tissue Tumours.人软组织肿瘤中MDM2基因的扩增与过表达
Sarcoma. 1997;1(1):17-22. doi: 10.1080/13577149778434.
10
Identification of a new class of PAX3-FKHR target promoters: a role of the Pax3 paired box DNA binding domain.一类新的PAX3-FKHR靶基因启动子的鉴定:Pax3配对结构域DNA结合域的作用
Oncogene. 2007 Mar 8;26(11):1595-605. doi: 10.1038/sj.onc.1209958. Epub 2006 Sep 11.