• 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

MLL-SEPT 融合基因相关和不相关的急性髓系白血病中 septin 基因家族的表达模式。

Expression pattern of the septin gene family in acute myeloid leukemias with and without MLL-SEPT fusion genes.

机构信息

Department of Genetics, Portuguese Oncology Institute, Porto, Portugal.

出版信息

Leuk Res. 2010 May;34(5):615-21. doi: 10.1016/j.leukres.2009.08.018. Epub 2009 Sep 12.

DOI:10.1016/j.leukres.2009.08.018
PMID:19748670
Abstract

Septins are proteins associated with crucial steps in cell division and cellular integrity. In humans, 14 septin genes have been identified, of which five (SEPT2, SEPT5, SEPT6, SEPT9, and SEPT11) are known to participate in reciprocal translocations with the MLL gene in myeloid neoplasias. We have recently shown a significant down-regulation of both SEPT2 and MLL in myeloid neoplasias with the MLL-SEPT2 fusion gene. In this study, we examined the expression pattern of the other 13 known septin genes in altogether 67 cases of myeloid neoplasia, including three patients with the MLL-SEPT2 fusion gene, four with MLL-SEPT6 fusion, and three patients with the MLL-SEPT9 fusion gene. When compared with normal controls, a statistically significant down-regulation was observed for the expression of both MLL (6.4-fold; p=0.008) and SEPT6 (1.7-fold; p=0.002) in MLL-SEPT6 leukemia. Significant down-regulation of MLL was also found in MLL-MLLT3 leukemias. In addition, there was a trend for SEPT9 down-regulation in MLL-SEPT9 leukemias (4.6-fold; p=0.077). Using hierarchical clustering analysis to compare acute myeloid leukemia genetic subgroups based on their similarity of septin expression changes, we found that MLL-SEPT2 and MLL-SEPT6 neoplasias cluster together apart from the remaining subgroups and that PML-RARA leukemia presents under-expression of most septin family genes.

摘要

Septins 是与细胞分裂和细胞完整性的关键步骤相关的蛋白质。在人类中,已经鉴定出 14 种 septin 基因,其中 5 种(SEPT2、SEPT5、SEPT6、SEPT9 和 SEPT11)已知参与髓系肿瘤中与 MLL 基因的相互易位。我们最近表明,在具有 MLL-SEPT2 融合基因的髓系肿瘤中,SEPT2 和 MLL 都显著下调。在这项研究中,我们在总共 67 例髓系肿瘤中检查了其他 13 种已知 septin 基因的表达模式,包括 3 例具有 MLL-SEPT2 融合基因的患者、4 例具有 MLL-SEPT6 融合基因的患者和 3 例具有 MLL-SEPT9 融合基因的患者。与正常对照相比,在 MLL-SEPT6 白血病中观察到 MLL(6.4 倍;p=0.008)和 SEPT6(1.7 倍;p=0.002)的表达明显下调。在 MLL-MLLT3 白血病中也发现 MLL 明显下调。此外,在 MLL-SEPT9 白血病中 SEPT9 下调趋势(4.6 倍;p=0.077)。使用层次聚类分析根据 septin 表达变化的相似性比较急性髓系白血病遗传亚组,我们发现 MLL-SEPT2 和 MLL-SEPT6 肿瘤与其余亚组一起聚类,而 PML-RARA 白血病表现出大多数 septin 家族基因的低表达。

相似文献

1
Expression pattern of the septin gene family in acute myeloid leukemias with and without MLL-SEPT fusion genes.MLL-SEPT 融合基因相关和不相关的急性髓系白血病中 septin 基因家族的表达模式。
Leuk Res. 2010 May;34(5):615-21. doi: 10.1016/j.leukres.2009.08.018. Epub 2009 Sep 12.
2
Molecular characterization of the MLL-SEPT6 fusion gene in acute myeloid leukemia: identification of novel fusion transcripts and cloning of genomic breakpoint junctions.急性髓系白血病中MLL-SEPT6融合基因的分子特征:新型融合转录本的鉴定及基因组断裂点连接的克隆
Haematologica. 2008 Jul;93(7):1076-80. doi: 10.3324/haematol.12594. Epub 2008 May 19.
3
MLL-SEPTIN gene fusions in hematological malignancies.MLL-SEPTIN 基因融合在血液系统恶性肿瘤中的作用。
Biol Chem. 2011 Aug;392(8-9):713-24. doi: 10.1515/BC.2011.072. Epub 2011 Jun 30.
4
Disruption of Sept6, a fusion partner gene of MLL, does not affect ontogeny, leukemogenesis induced by MLL-SEPT6, or phenotype induced by the loss of Sept4.MLL的融合伴侣基因Sept6的破坏不影响个体发育、MLL-SEPT6诱导的白血病发生或Sept4缺失诱导的表型。
Mol Cell Biol. 2005 Dec;25(24):10965-78. doi: 10.1128/MCB.25.24.10965-10978.2005.
5
MLL-SEPT6 fusion transcript with a novel sequence in an infant with acute myeloid leukemia.一名急性髓系白血病婴儿中具有新序列的MLL-SEPT6融合转录本
Cancer Genet Cytogenet. 2006 Jul 15;168(2):162-7. doi: 10.1016/j.cancergencyto.2006.02.020.
6
Genetic and clinical characterization of 45 acute leukemia patients with MLL gene rearrangements from a single institution.一家单中心 45 例急性白血病伴 MLL 基因重排患者的遗传学和临床特征。
Mol Oncol. 2012 Oct;6(5):553-64. doi: 10.1016/j.molonc.2012.06.004. Epub 2012 Jul 14.
7
Coexistence of alternative MLL-SEPT9 fusion transcripts in an acute myeloid leukemia with t(11;17)(q23;q25).在一例伴有t(11;17)(q23;q25)的急性髓系白血病中存在多种MLL-SEPT9融合转录本共存。
Cancer Genet Cytogenet. 2010 Feb;197(1):60-4. doi: 10.1016/j.cancergencyto.2009.10.010.
8
Both SEPT2 and MLL are down-regulated in MLL-SEPT2 therapy-related myeloid neoplasia.在MLL-SEPT2治疗相关的髓系肿瘤中,SEPT2和MLL均下调。
BMC Cancer. 2009 May 15;9:147. doi: 10.1186/1471-2407-9-147.
9
[Rearrangements of the mixed lineage leukemia gene in acute myeloid leukemia].[急性髓系白血病中混合谱系白血病基因的重排]
Zhonghua Yi Xue Za Zhi. 2006 Aug 29;86(32):2256-60.
10
Down-regulation of DLX3 expression in MLL-AF4 childhood lymphoblastic leukemias is mediated by promoter region hypermethylation.MLL-AF4型儿童淋巴细胞白血病中DLX3表达的下调是由启动子区域高甲基化介导的。
Oncol Rep. 2007 Aug;18(2):417-23.

引用本文的文献

1
Co-existence of :: fusion and variant in a pediatric case with acute myeloid leukemia: a case report and literature review.一名急性髓系白血病儿科病例中融合基因与变异共存:病例报告及文献综述
Front Oncol. 2023 Dec 13;13:1308786. doi: 10.3389/fonc.2023.1308786. eCollection 2023.
2
MLL-SEPT5 Fusion Transcript in Myelodysplastic Syndrome Patient With t(11;22)(q23;q11).伴有t(11;22)(q23;q11)的骨髓增生异常综合征患者中的MLL-SEPT5融合转录本
Front Med (Lausanne). 2021 Dec 22;8:783229. doi: 10.3389/fmed.2021.783229. eCollection 2021.
3
Congenital X-linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6.
先天性 X 连锁中性粒细胞减少伴骨髓增生异常和体细四倍体,源于 SEPT6 种系突变。
Am J Hematol. 2022 Jan 1;97(1):18-29. doi: 10.1002/ajh.26382. Epub 2021 Nov 3.
4
Transcriptional control of CBX5 by the RNA binding proteins RBMX and RBMXL1 maintains chromatin state in myeloid leukemia.RNA结合蛋白RBMX和RBMXL1对CBX5的转录调控维持了髓系白血病中的染色质状态。
Nat Cancer. 2021 Jul;2:741-757. doi: 10.1038/s43018-021-00220-w. Epub 2021 Jul 5.
5
Impact of spliceosome mutations on RNA splicing in myelodysplasia: dysregulated genes/pathways and clinical associations.剪接体突变对骨髓增生异常综合征中 RNA 剪接的影响:失调的基因/通路和临床关联。
Blood. 2018 Sep 20;132(12):1225-1240. doi: 10.1182/blood-2018-04-843771. Epub 2018 Jun 21.
6
Acute myeloid leukemia with translocation: A case report and review of the literature.伴有易位的急性髓系白血病:一例报告及文献复习
SAGE Open Med Case Rep. 2018 Jan 4;6:2050313X17750334. doi: 10.1177/2050313X17750334. eCollection 2018.
7
Mitochondria mediate septin cage assembly to promote autophagy of Shigella.线粒体介导septin笼组装以促进志贺氏菌的自噬。
EMBO Rep. 2016 Jul;17(7):1029-43. doi: 10.15252/embr.201541832. Epub 2016 Jun 3.
8
High SEPT9_i1 protein expression is associated with high-grade prostate cancers.SEPT9_i1蛋白高表达与高级别前列腺癌相关。
PLoS One. 2015 Apr 21;10(4):e0124251. doi: 10.1371/journal.pone.0124251. eCollection 2015.
9
Comparative expression analysis of Septin 14 in testes of infertile men with normal spermatogenesis and spermatogenic failure.正常精子发生和生精功能障碍的不育男性睾丸中Septin 14的比较表达分析。
Iran J Reprod Med. 2014 Mar;12(3):205-8.
10
Unraveling the equine lymphocyte proteome: differential septin 7 expression associates with immune cells in equine recurrent uveitis.解析马淋巴细胞蛋白质组:差异表达的septin 7与马复发性葡萄膜炎中的免疫细胞相关。
PLoS One. 2014 Mar 10;9(3):e91684. doi: 10.1371/journal.pone.0091684. eCollection 2014.