• 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

位于6号染色体6q27带的AF6基因定位于上皮性卵巢癌最小缺失区域的远端。

AF6 gene on chromosome band 6q27 maps distal to the minimal region of deletion in epithelial ovarian cancer.

作者信息

Saha V, Lillington D M, Shelling A N, Chaplin T, Yaspo M L, Ganesan T S, Young B D

机构信息

Department of Medical Oncology, St. Bartholomew's Hospital, London, United Kingdom.

出版信息

Genes Chromosomes Cancer. 1995 Nov;14(3):220-2. doi: 10.1002/gcc.2870140311.

DOI:10.1002/gcc.2870140311
PMID:8589040
Abstract

Chromosome 6 has been shown to contain at band q27 a minimal region of deletion associated with epithelial ovarian cancers and AF6, a gene disrupted in acute myeloid leukemia with t(6;11)(q27;q23). Using rapid amplification of cDNA ends by polymerase chain reaction, the breakpoint in AF6 was confirmed and a cDNA clone identified. This clone was used as a probe to screen a chromosome 6 cosmid library, and a single cosmid C-109F0645 was isolated. By fluorescence in situ hybridization, C-109F0465 was found to map distal to the critically deleted region associated with ovarian malignancies. AF6 is therefore distinct from and lies telomeric to this region.

摘要

已证明6号染色体在q27带含有与上皮性卵巢癌相关的最小缺失区域,以及AF6基因,该基因在伴有t(6;11)(q27;q23)的急性髓细胞白血病中发生破坏。通过聚合酶链反应快速扩增cDNA末端,确认了AF6中的断点并鉴定了一个cDNA克隆。该克隆用作探针筛选6号染色体黏粒文库,分离出单个黏粒C-109F0645。通过荧光原位杂交发现,C-109F0465定位于与卵巢恶性肿瘤相关的关键缺失区域的远端。因此,AF6与该区域不同且位于其端粒侧。

相似文献

1
AF6 gene on chromosome band 6q27 maps distal to the minimal region of deletion in epithelial ovarian cancer.位于6号染色体6q27带的AF6基因定位于上皮性卵巢癌最小缺失区域的远端。
Genes Chromosomes Cancer. 1995 Nov;14(3):220-2. doi: 10.1002/gcc.2870140311.
2
Molecular analysis of the rearranged genome and chimeric mRNAs caused by the t(6;11)(q27;q23) chromosome translocation involving MLL in an infant acute monocytic leukemia.对一名婴儿急性单核细胞白血病中由涉及MLL的t(6;11)(q27;q23)染色体易位导致的重排基因组和嵌合mRNA进行分子分析。
Genes Chromosomes Cancer. 2000 Apr;27(4):412-7.
3
Incidence and characterization of MLL gene (11q23) rearrangements in acute myeloid leukemia M1 and M5.急性髓系白血病M1和M5中MLL基因(11q23)重排的发生率及特征
Blood. 1996 Mar 15;87(6):2496-505.
4
Analysis of the t(6;11)(q27;q23) in leukemia shows a consistent breakpoint in AF6 in three patients and in the ML-2 cell line.白血病中t(6;11)(q27;q23)的分析显示,在三名患者及ML-2细胞系中,AF6存在一致的断点。
Genes Chromosomes Cancer. 1996 Apr;15(4):206-16. doi: 10.1002/(SICI)1098-2264(199604)15:4<206::AID-GCC2>3.0.CO;2-5.
5
Fusion of the MLL gene with two different genes, AF-6 and AF-5alpha, by a complex translocation involving chromosomes 5, 6, 8 and 11 in infant leukemia.在婴儿白血病中,MLL基因通过涉及5号、6号、8号和11号染色体的复杂易位与两个不同基因AF-6和AF-5α融合。
Oncogene. 1996 Nov 21;13(10):2121-30.
6
Identification of a MLL-MLLT4 fusion gene resulting from a t(6;11)(q27;q23) presenting as a del(11q) in a child with T-cell acute lymphoblastic leukemia.在一名患T细胞急性淋巴细胞白血病的儿童中鉴定出由t(6;11)(q27;q23)导致的MLL-MLLT4融合基因,该患儿表现为del(11q)。
Leuk Lymphoma. 2010 Aug;51(8):1570-3. doi: 10.3109/10428194.2010.494261.
7
A novel chromosomal inversion at 11q23 in infant acute myeloid leukemia fuses MLL to CALM, a gene that encodes a clathrin assembly protein.婴儿急性髓系白血病中11q23处的一种新型染色体倒位将MLL与CALM融合,CALM是一种编码网格蛋白组装蛋白的基因。
Genes Chromosomes Cancer. 2003 Jan;36(1):26-36. doi: 10.1002/gcc.10136.
8
Identification of complex genomic breakpoint junctions in the t(9;11) MLL-AF9 fusion gene in acute leukemia.急性白血病中t(9;11) MLL-AF9融合基因复杂基因组断点连接的鉴定
Genes Chromosomes Cancer. 1997 Oct;20(2):185-95.
9
Chimeric MLL products with a Ras binding cytoplasmic protein AF6 involved in t(6;11) (q27;q23) leukemia localize in the nucleus.涉及t(6;11)(q27;q23)白血病的带有Ras结合胞质蛋白AF6的嵌合MLL产物定位于细胞核。
Oncogene. 1997 Oct 2;15(14):1681-7. doi: 10.1038/sj.onc.1201332.
10
MLL-AF6 fusion resulting from a new three-way translocation t(6;11;7) in a patient with acute myeloid leukemia.一名急性髓系白血病患者因新的三向易位t(6;11;7)导致MLL-AF6融合。
Leukemia. 2001 Oct;15(10):1674-6. doi: 10.1038/sj.leu.2402213.

引用本文的文献

1
Loss of polarity protein AF6 promotes pancreatic cancer metastasis by inducing Snail expression.极性蛋白 AF6 通过诱导 Snail 表达促进胰腺癌转移。
Nat Commun. 2015 May 26;6:7184. doi: 10.1038/ncomms8184.
2
Loss of AF-6/afadin induces cell invasion, suppresses the formation of glandular structures and might be a predictive marker of resistance to chemotherapy in endometrial cancer.AF-6/afadin缺失会诱导细胞侵袭,抑制腺体结构形成,并且可能是子宫内膜癌化疗耐药的预测标志物。
BMC Cancer. 2015 Apr 12;15:275. doi: 10.1186/s12885-015-1286-x.
3
PHF10 is required for cell proliferation in normal and SV40-immortalized human fibroblast cells.
在正常和SV40永生化的人成纤维细胞中,细胞增殖需要PHF10。
Cytogenet Genome Res. 2009;126(3):227-42. doi: 10.1159/000251960. Epub 2010 Jan 6.
4
Afadin: A novel actin filament-binding protein with one PDZ domain localized at cadherin-based cell-to-cell adherens junction.肌动蛋白结合蛋白:一种新型肌动蛋白丝结合蛋白,具有一个PDZ结构域,定位于基于钙黏蛋白的细胞间黏附连接。
J Cell Biol. 1997 Oct 20;139(2):517-28. doi: 10.1083/jcb.139.2.517.