• 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

滤泡性淋巴瘤中6q16.3缺失最小区域的描绘以及跨越6q16 - q21区域6兆碱基的细菌人工染色体重叠群的构建。

Delineation of a minimal region of deletion at 6q16.3 in follicular lymphoma and construction of a bacterial artificial chromosome contig spanning a 6-megabase region of 6q16-q21.

作者信息

Henderson Laura-Jane, Okamoto Ichiro, Lestou Valia S, Ludkovski Olga, Robichaud Marc, Chhanabhai Mukesh, Gascoyne Randy D, Klasa Richard J, Connors Joseph M, Marra Marco A, Horsman Douglas E, Lam Wan L

机构信息

British Columbia Cancer Agency, Vancouver, BC, Canada.

出版信息

Genes Chromosomes Cancer. 2004 May;40(1):60-5. doi: 10.1002/gcc.20013.

DOI:10.1002/gcc.20013
PMID:15034870
Abstract

Regional deletions of 6q are frequent karyotypic alterations in malignant lymphoma and are associated with an adverse clinical outcome. One such region of recurrent deletion is 6q16-q21; however, the specific genes affected have not been identified. Our objective in this study was to identify cases with deletion of 6q16-q21 in follicular lymphoma and to define a minimal region of deletion. A physical map of 6q16.2-q21 was constructed using map information from both sequence-based and bacterial artificial chromosome (BAC) fingerprint-based maps. Forty-three BAC clones spanning a 6-Mb region of 6q16.2-q21 were identified and obtained from the RP-11 library. Selected BACs were fluorescence-labeled and hybridized to a series of 34 follicular lymphomas with a regional 6q deletion detected by G banding. Twenty-four cases with deletion of the 6q16.3 region were detected. A minimal deletion of 2.3 Mb was defined. Our study has identified a limited region of deletion of 6q16.3 that may implicate four known genes in follicular lymphoma and possibly in other cancers. A BAC contig spanning a 6-Mb region has been anchored to the 6q16.2-q21 region. This map represents a useful resource for gene identification in this region, not only in lymphoma but also in other neoplasms with 6q alterations.

摘要

6q区域的缺失是恶性淋巴瘤中常见的核型改变,且与不良临床预后相关。一个反复出现缺失的区域是6q16 - q21;然而,受影响的具体基因尚未确定。我们在本研究中的目的是识别滤泡性淋巴瘤中6q16 - q21缺失的病例,并确定最小缺失区域。利用基于序列和基于细菌人工染色体(BAC)指纹图谱的图谱信息构建了6q16.2 - q21的物理图谱。从RP - 11文库中鉴定并获得了跨越6q16.2 - q21区域6 Mb的43个BAC克隆。选择的BAC进行荧光标记,并与一系列34例通过G显带检测到有6q区域缺失的滤泡性淋巴瘤进行杂交。检测到24例6q16.3区域缺失的病例。确定了2.3 Mb的最小缺失区域。我们的研究确定了6q16.3的一个有限缺失区域,该区域可能涉及滤泡性淋巴瘤以及可能其他癌症中的四个已知基因。一个跨越6 Mb区域的BAC重叠群已定位到6q16.2 - q21区域。该图谱不仅是淋巴瘤,也是其他有6q改变的肿瘤中该区域基因鉴定的有用资源。

相似文献

1
Delineation of a minimal region of deletion at 6q16.3 in follicular lymphoma and construction of a bacterial artificial chromosome contig spanning a 6-megabase region of 6q16-q21.滤泡性淋巴瘤中6q16.3缺失最小区域的描绘以及跨越6q16 - q21区域6兆碱基的细菌人工染色体重叠群的构建。
Genes Chromosomes Cancer. 2004 May;40(1):60-5. doi: 10.1002/gcc.20013.
2
Defining the region(s) of deletion at 6q16-q22 in human prostate cancer.确定人类前列腺癌6q16 - q22区域的缺失区域。
Genes Chromosomes Cancer. 2002 Jul;34(3):306-12. doi: 10.1002/gcc.10065.
3
Identification of candidate tumor-suppressor genes in 6q27 by combined deletion mapping and electronic expression profiling in lymphoid neoplasms.通过联合缺失定位和电子表达谱分析在淋巴瘤中鉴定6q27上的候选肿瘤抑制基因。
Genes Chromosomes Cancer. 2003 Aug;37(4):421-6. doi: 10.1002/gcc.10231.
4
Substantial reduction of the gastric carcinoma critical region at 6q16.3-q23.1.6q16.3 - q23.1处胃癌关键区域的显著缩小。
Genes Chromosomes Cancer. 1999 Sep;26(1):29-34.
5
Array comparative genomic hybridization reveals a very high frequency of deletions of the long arm of chromosome 6 in testicular lymphoma.阵列比较基因组杂交显示睾丸淋巴瘤中6号染色体长臂缺失的频率非常高。
Genes Chromosomes Cancer. 2006 Oct;45(10):976-81. doi: 10.1002/gcc.20361.
6
Deletion of 6q16-q21 in human lymphoid malignancies: a mapping and deletion analysis.人类淋巴恶性肿瘤中6q16 - q21的缺失:定位与缺失分析
Cancer Res. 2000 Jun 1;60(11):2775-9.
7
A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region.一个跨越11q23上SDHD基因的高分辨率整合图谱:一个1.1兆碱基的细菌人工染色体(BAC)重叠群、一个部分转录图谱以及肿瘤抑制区域中的15个新的重复多态性。
Eur J Hum Genet. 2001 Feb;9(2):121-9. doi: 10.1038/sj.ejhg.5200585.
8
Chromosome band 6q deletion pattern in malignant lymphomas.恶性淋巴瘤中6号染色体长臂缺失模式
Cancer Genet Cytogenet. 2006 Mar;165(2):106-13. doi: 10.1016/j.cancergencyto.2005.06.025.
9
Molecular cytogenetic analysis of follicular lymphoma (FL) provides detailed characterization of chromosomal instability associated with the t(14;18)(q32;q21) positive and negative subsets and histologic progression.滤泡性淋巴瘤(FL)的分子细胞遗传学分析提供了与t(14;18)(q32;q21)阳性和阴性亚群及组织学进展相关的染色体不稳定性的详细特征。
Cytogenet Genome Res. 2007;118(2-4):337-44. doi: 10.1159/000108318.
10
A BAC-based STS-content map spanning a 35-Mb region of human chromosome 1p35-p36.一个基于细菌人工染色体(BAC)的序列标签位点(STS)内容图谱,覆盖人类1号染色体1p35 - p36区域的35兆碱基。
Genomics. 2001 May 15;74(1):55-70. doi: 10.1006/geno.2001.6511.

引用本文的文献

1
Double-hit pancreatic B-lymphoblastic lymphoma with a variant translocation t(2;18)(p11;q21).伴有变异易位 t(2;18)(p11;q21)的双打击胰腺 B 细胞淋巴母细胞淋巴瘤。
Int J Hematol. 2019 Jul;110(1):107-114. doi: 10.1007/s12185-019-02646-6. Epub 2019 Apr 8.
2
Amplification of 2p as a genomic marker for transformation in lymphoma.2p扩增作为淋巴瘤转化的基因组标志物。
Genes Chromosomes Cancer. 2014 Sep;53(9):750-68. doi: 10.1002/gcc.22184. Epub 2014 May 15.
3
Mutations in linker histone genes HIST1H1 B, C, D, and E; OCT2 (POU2F2); IRF8; and ARID1A underlying the pathogenesis of follicular lymphoma.
连接组蛋白基因 HIST1H1B、C、D 和 E;OCT2(POU2F2);IRF8 和 ARID1A 的突变是滤泡性淋巴瘤发病机制的基础。
Blood. 2014 Mar 6;123(10):1487-98. doi: 10.1182/blood-2013-05-500264. Epub 2014 Jan 16.
4
Comprehensive copy number profiles of breast cancer cell model genomes.乳腺癌细胞模型基因组的综合拷贝数图谱。
Breast Cancer Res. 2006;8(1):R9. doi: 10.1186/bcr1370. Epub 2006 Jan 3.
5
Genomic and gene expression profiling of minute alterations of chromosome arm 1p in small-cell lung carcinoma cells.小细胞肺癌细胞中1号染色体臂微小改变的基因组和基因表达谱分析。
Br J Cancer. 2005 Apr 25;92(8):1553-60. doi: 10.1038/sj.bjc.6602452.