• 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

套细胞淋巴瘤细胞系中的基因组失衡和核型变异模式

Genomic imbalances and patterns of karyotypic variability in mantle-cell lymphoma cell lines.

作者信息

Camps Jordi, Salaverria Itziar, Garcia Maria J, Prat Esther, Beà Sílvia, Pole Jessica C, Hernández Lluis, Del Rey Javier, Cigudosa Juan Cruz, Bernués Marta, Caldas Carlos, Colomer Dolors, Miró Rosa, Campo Elías

机构信息

Departament de Biologia Cellular, Fisiologia i Immunologia and Institut de Biotecnologia i de Biomedicina, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain.

出版信息

Leuk Res. 2006 Aug;30(8):923-34. doi: 10.1016/j.leukres.2005.11.013. Epub 2006 Jan 31.

DOI:10.1016/j.leukres.2005.11.013
PMID:16448697
Abstract

Mantle-cell lymphoma (MCL) is genetically characterized by 11q13 chromosomal translocations involving the CCND1 gene. We have characterized five MCL cell lines, JVM-2, GRANTA-519, REC-1, JEKO-1, and NCEB-1, combining metaphase and array comparative genomic hybridization, multicolor-FISH, and molecular analysis. Our results revealed common gained regions at 2p14, 9q31.2-qter, 11q13.1-q21, 13q14-q21.2, 13q34-qter and 18q21.1-q22.1, and losses at 1p21.2-p31.1, 2p11.2, 8p21.2-pter, 9p21.3-pter, 11q23.3-qter, 17p11.2-pter, and 17q21.2-q22.2. All cell lines except JVM-2, displayed moderate or high numerical chromosome instability. In addition, an ongoing level of chromosome rearrangements was observed in REC-1. Surprisingly, NCEB-1 carried several stable mouse chromosomes and showed expression of both human and murine bcl-2 protein. Our findings indicate that these cell lines represent three patterns of chromosome evolution in MCL and may be useful to understand the pathogenesis of this neoplasm.

摘要

套细胞淋巴瘤(MCL)的遗传学特征是涉及CCND1基因的11q13染色体易位。我们结合中期和阵列比较基因组杂交、多色荧光原位杂交及分子分析,对5种MCL细胞系JVM-2、GRANTA-519、REC-1、JEKO-1和NCEB-1进行了特征分析。我们的结果揭示了在2p14、9q31.2 - qter、11q13.1 - q21、13q14 - q21.2、13q34 - qter和18q21.1 - q22.1存在常见的获得区域,以及在1p21.2 - p31.1、2p11.2、8p21.2 - pter、9p21.3 - pter、11q23.3 - qter、17p11.2 - pter和17q21.2 - q22.2存在缺失区域。除JVM-2外,所有细胞系均表现出中度或高度的染色体数目不稳定性。此外,在REC-1中观察到持续的染色体重排水平。令人惊讶的是,NCEB-1携带了几条稳定的小鼠染色体,并同时表达人源和鼠源bcl-2蛋白。我们的研究结果表明,这些细胞系代表了MCL中染色体进化的三种模式,可能有助于理解这种肿瘤的发病机制。

相似文献

1
Genomic imbalances and patterns of karyotypic variability in mantle-cell lymphoma cell lines.套细胞淋巴瘤细胞系中的基因组失衡和核型变异模式
Leuk Res. 2006 Aug;30(8):923-34. doi: 10.1016/j.leukres.2005.11.013. Epub 2006 Jan 31.
2
Comprehensive whole genome array CGH profiling of mantle cell lymphoma model genomes.套细胞淋巴瘤模型基因组的全基因组阵列比较基因组杂交综合分析。
Hum Mol Genet. 2004 Sep 1;13(17):1827-37. doi: 10.1093/hmg/ddh195. Epub 2004 Jun 30.
3
Multiple recurrent chromosomal breakpoints in mantle cell lymphoma revealed by a combination of molecular cytogenetic techniques.联合分子细胞遗传学技术揭示套细胞淋巴瘤中的多个复发性染色体断点
Genes Chromosomes Cancer. 2008 Dec;47(12):1086-97. doi: 10.1002/gcc.20609.
4
Molecular cytogenetic study of a mantle cell lymphoma with a complex translocation involving the CCND1 (11q13) region.一例伴有涉及CCND1(11q13)区域复杂易位的套细胞淋巴瘤的分子细胞遗传学研究
Cancer Genet Cytogenet. 2004 Oct 1;154(1):67-71. doi: 10.1016/j.cancergencyto.2004.02.002.
5
Molecular cytogenetic characterization of the mantle cell lymphoma cell line GRANTA-519.
Cancer Genet Cytogenet. 2004 Sep;153(2):144-50. doi: 10.1016/j.cancergencyto.2004.01.006.
6
Mantle cell lymphoma-derived cell lines: unique research tools.
Leuk Res. 2006 Aug;30(8):911-3. doi: 10.1016/j.leukres.2006.02.015. Epub 2006 Mar 23.
7
Detailed assessment of copy number alterations revealing homozygous deletions in 1p and 13q in mantle cell lymphoma.套细胞淋巴瘤中1p和13q纯合缺失的拷贝数改变的详细评估。
Leuk Res. 2007 Sep;31(9):1219-30. doi: 10.1016/j.leukres.2006.10.022. Epub 2006 Dec 11.
8
Combined spectral karyotyping, comparative genomic hybridization, and in vitro apoptyping of a panel of Burkitt's lymphoma-derived B cell lines reveals an unexpected complexity of chromosomal aberrations and a recurrence of specific abnormalities in chemoresistant cell lines.对一组伯基特淋巴瘤来源的B细胞系进行联合光谱核型分析、比较基因组杂交和体外凋亡分析,揭示了染色体畸变的意外复杂性以及化疗耐药细胞系中特定异常的复发情况。
Int J Oncol. 2006 Mar;28(3):605-17.
9
Genomic aberrations in mantle cell lymphoma detected by interphase fluorescence in situ hybridization. Incidence and clinicopathological correlations.通过间期荧光原位杂交检测套细胞淋巴瘤中的基因组畸变。发生率及临床病理相关性。
Haematologica. 2008 May;93(5):680-7. doi: 10.3324/haematol.12330. Epub 2008 Mar 26.
10
Molecular cytogenetic characterization of pancreas cancer cell lines reveals high complexity chromosomal alterations.胰腺癌细胞系的分子细胞遗传学特征揭示了高度复杂的染色体改变。
Cytogenet Genome Res. 2007;118(2-4):148-56. doi: 10.1159/000108295.

引用本文的文献

1
Expanded profiling of WD repeat domain 5 inhibitors reveals actionable strategies for the treatment of hematologic malignancies.WD 重复结构域 5 抑制剂的扩展分析揭示了治疗血液系统恶性肿瘤的可行策略。
Proc Natl Acad Sci U S A. 2024 Aug 27;121(35):e2408889121. doi: 10.1073/pnas.2408889121. Epub 2024 Aug 21.
2
Resistance to PRMT5-targeted therapy in mantle cell lymphoma.套细胞淋巴瘤中对 PRMT5 靶向治疗的耐药性。
Blood Adv. 2024 Jan 9;8(1):150-163. doi: 10.1182/bloodadvances.2023010554.
3
G Protein-Coupled Estrogen Receptor Agonist G-1 Inhibits Mantle Cell Lymphoma Growth in Preclinical Models.
G蛋白偶联雌激素受体激动剂G-1在临床前模型中抑制套细胞淋巴瘤生长。
Front Oncol. 2021 Jun 15;11:668617. doi: 10.3389/fonc.2021.668617. eCollection 2021.
4
Potent efficacy of MCL-1 inhibitor-based therapies in preclinical models of mantle cell lymphoma.基于 MCL-1 抑制剂的疗法在套细胞淋巴瘤的临床前模型中具有强大的疗效。
Oncogene. 2020 Feb;39(9):2009-2023. doi: 10.1038/s41388-019-1122-x. Epub 2019 Nov 26.
5
Molecular signatures for CCN1, p21 and p27 in progressive mantle cell lymphoma.进行性套细胞淋巴瘤中CCN1、p21和p27的分子特征
J Cell Commun Signal. 2019 Sep;13(3):421-434. doi: 10.1007/s12079-018-0494-y. Epub 2018 Nov 21.
6
Phosphatidylinositol 3-kinase δ blockade increases genomic instability in B cells.磷脂酰肌醇3激酶δ阻断增加B细胞中的基因组不稳定性。
Nature. 2017 Feb 23;542(7642):489-493. doi: 10.1038/nature21406. Epub 2017 Feb 15.
7
Chk1 inhibition significantly potentiates activity of nucleoside analogs in TP53-mutated B-lymphoid cells.Chk1抑制作用显著增强核苷类似物在TP53突变的B淋巴细胞中的活性。
Oncotarget. 2016 Sep 20;7(38):62091-62106. doi: 10.18632/oncotarget.11388.
8
Detection of Enhancer-Associated Rearrangements Reveals Mechanisms of Oncogene Dysregulation in B-cell Lymphoma.增强子相关重排的检测揭示了B细胞淋巴瘤中癌基因失调的机制。
Cancer Discov. 2015 Oct;5(10):1058-71. doi: 10.1158/2159-8290.CD-15-0370. Epub 2015 Jul 30.
9
Prevalence and characterization of murine leukemia virus contamination in human cell lines.人类细胞系中鼠白血病病毒污染的发生率及特征
PLoS One. 2015 Apr 30;10(4):e0125622. doi: 10.1371/journal.pone.0125622. eCollection 2015.
10
Global phosphoproteomic profiling reveals distinct signatures in B-cell non-Hodgkin lymphomas.全球磷酸化蛋白质组学分析揭示了B细胞非霍奇金淋巴瘤的独特特征。
Am J Pathol. 2014 May;184(5):1331-42. doi: 10.1016/j.ajpath.2014.01.036. Epub 2014 Mar 22.