• 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

转化型 Ph 阴性骨髓增殖性肿瘤中的染色体异常与转化亚型相关,且独立于 JAK2 和 TET2 突变。

Chromosomal abnormalities in transformed Ph-negative myeloproliferative neoplasms are associated to the transformation subtype and independent of JAK2 and the TET2 mutations.

机构信息

Hématologie biologique, Hôpital Pitié-Salpêtrière, APHP, Paris, France.

出版信息

Genes Chromosomes Cancer. 2010 Oct;49(10):919-27. doi: 10.1002/gcc.20802.

DOI:10.1002/gcc.20802
PMID:20629097
Abstract

Evolution to myelofibrosis (MF), acute myeloid leukemia or myelodysplastic syndrome (AML/MDS) may occur over time in myeloproliferative neoplasms (MPN) patients most likely due to the acquisition of additional mutations. The Groupe Francophone de cytogenetique hematologique (GFCH) has collected and reviewed 82 patients with transformation of MPN (66 AML/MDS and 16 MF). JAK2V617F and TET2 mutations were searched for in 40 and 32 patients, respectively. Significantly more -7/del(7q) (P = 0.004) and -5/del(5q) (P = 0.03) were found in AML/MDS with a higher incidence of dup1q (P = 0.01) in MF. Some specific chromosomal abnormalities occurred together, for example -5/del(5q) and -17/del(17p) (P = 0.0007). In multivariate analysis, two factors were independently associated with an inferior overall survival (OS); AML/MDS transformation (P < 0.0001) and -5/del(5q) abnormality (P = 0.02). Although both giving rise to loss of 7q, der(1;7) differed from other 7q deletions in terms of distribution (lower frequency of AML/MDS, P = 0.02), association with chromosomal abnormalities (absence of -5/del(5q), P = 0.003; increased del(20q), P = 0.05), and longer OS (P = 0.0007). We detected 24/40 (60%) JAK2V617F and 8/25 (32%) TET2 mutations in samples following transformation, ranging from wild-type to mutated forms of both genes. The mutated and wild-type forms of the genes were not found to be associated with a specific chromosomal abnormality. There was no evidence that JAK2 or TET2 mutations were associated with the type of MPN transformation, whereas the type of cytogenetic abnormalities were strongly linked, perhaps indicating that they play a specific role in the transformation process.

摘要

在骨髓增生性肿瘤(MPN)患者中,随着时间的推移,骨髓纤维化(MF)、急性髓系白血病或骨髓增生异常综合征(AML/MDS)可能会发生演变,这很可能是由于获得了额外的突变。法语血液细胞遗传学组(GFCH)收集并回顾了 82 例 MPN 转化患者(66 例 AML/MDS 和 16 例 MF)。分别在 40 例和 32 例患者中检测 JAK2V617F 和 TET2 突变。在 AML/MDS 中,-7/del(7q)(P=0.004)和 -5/del(5q)(P=0.03)显著更多,而 MF 中 dup1q 的发生率更高(P=0.01)。一些特定的染色体异常同时发生,例如 -5/del(5q) 和 -17/del(17p)(P=0.0007)。多变量分析显示,有两个因素与较差的总生存期(OS)独立相关;AML/MDS 转化(P<0.0001)和 -5/del(5q) 异常(P=0.02)。尽管都导致 7q 的缺失,但 der(1;7)与其他 7q 缺失在分布上不同(AML/MDS 的频率较低,P=0.02),与染色体异常相关(不存在 -5/del(5q),P=0.003;del(20q) 增加,P=0.05),OS 更长(P=0.0007)。我们在转化后的样本中检测到 24/40(60%)JAK2V617F 和 8/25(32%)TET2 突变,范围从两个基因的野生型到突变型。基因的突变和野生型形式与特定的染色体异常无关。没有证据表明 JAK2 或 TET2 突变与 MPN 转化类型有关,而细胞遗传学异常类型与转化过程密切相关,可能表明它们在转化过程中发挥了特定的作用。

相似文献

1
Chromosomal abnormalities in transformed Ph-negative myeloproliferative neoplasms are associated to the transformation subtype and independent of JAK2 and the TET2 mutations.转化型 Ph 阴性骨髓增殖性肿瘤中的染色体异常与转化亚型相关,且独立于 JAK2 和 TET2 突变。
Genes Chromosomes Cancer. 2010 Oct;49(10):919-27. doi: 10.1002/gcc.20802.
2
Distribution of cytogenetic abnormalities in myelodysplastic syndromes, Philadelphia negative myeloproliferative neoplasms, and the overlap MDS/MPN category.骨髓增生异常综合征、费城染色体阴性的骨髓增殖性肿瘤以及重叠的骨髓增生异常综合征/骨髓增殖性肿瘤类别中细胞遗传学异常的分布情况。
Ann Hematol. 2009 Dec;88(12):1207-13. doi: 10.1007/s00277-009-0745-3. Epub 2009 May 5.
3
Genomic aberrations of myeloproliferative and myelodysplastic/myeloproliferative neoplasms in chronic phase and during disease progression.慢性期以及疾病进展过程中骨髓增殖性肿瘤和骨髓增生异常/骨髓增殖性肿瘤的基因组畸变。
Int J Lab Hematol. 2015 Apr;37(2):181-9. doi: 10.1111/ijlh.12257. Epub 2014 May 21.
4
Genetic analysis of transforming events that convert chronic myeloproliferative neoplasms to leukemias.转化事件的遗传分析,这些事件将慢性骨髓增殖性肿瘤转化为白血病。
Cancer Res. 2010 Jan 15;70(2):447-52. doi: 10.1158/0008-5472.CAN-09-3783. Epub 2010 Jan 12.
5
Isolated del(5q) in myeloid malignancies: clinicopathologic and molecular features in 143 consecutive patients.孤立性 del(5q)在髓系恶性肿瘤中的临床病理和分子特征:143 例连续患者的分析。
Am J Hematol. 2011 May;86(5):393-8. doi: 10.1002/ajh.21984.
6
Myeloid malignancies with isolated 7q deletion can be further characterized by their accompanying molecular mutations.孤立 7q 缺失的髓系恶性肿瘤可通过其伴随的分子突变进一步进行特征描述。
Genes Chromosomes Cancer. 2019 Oct;58(10):698-704. doi: 10.1002/gcc.22761. Epub 2019 May 1.
7
The 5q deletion size in myeloid malignancies is correlated to additional chromosomal aberrations and to TP53 mutations.骨髓恶性肿瘤中5号染色体长臂缺失的大小与其他染色体畸变及TP53基因突变相关。
Genes Chromosomes Cancer. 2016 Oct;55(10):777-85. doi: 10.1002/gcc.22377. Epub 2016 Jul 4.
8
Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms.与骨髓增生异常/骨髓增殖性肿瘤相关的4q24杂合性缺失和TET2突变
Blood. 2009 Jun 18;113(25):6403-10. doi: 10.1182/blood-2009-02-205690. Epub 2009 Apr 16.
9
Next-generation sequencing of the TET2 gene in 355 MDS and CMML patients reveals low-abundance mutant clones with early origins, but indicates no definite prognostic value.对 355 例 MDS 和 CMML 患者的 TET2 基因进行下一代测序显示,具有早期起源的低丰度突变克隆,但无明确的预后价值。
Blood. 2010 Nov 11;116(19):3923-32. doi: 10.1182/blood-2010-03-274704. Epub 2010 Aug 6.
10
Cytogenetics in the management of myelodysplastic neoplasms (myelodysplastic syndromes, MDS): Guidelines from the groupe francophone de cytogénétique hématologique (GFCH).骨髓增生异常肿瘤(骨髓增生异常综合征,MDS)的细胞遗传学管理:法国血液细胞遗传学组(GFCH)的指南。
Curr Res Transl Med. 2023 Oct-Dec;71(4):103409. doi: 10.1016/j.retram.2023.103409. Epub 2023 Sep 17.

引用本文的文献

1
Oncogenic and tumor suppressor genes expression in myeloproliferative neoplasms: The hidden side of a complex pathology.癌基因和抑癌基因在骨髓增殖性肿瘤中的表达:复杂病理的另一面。
J Clin Lab Anal. 2022 Apr;36(4):e24289. doi: 10.1002/jcla.24289. Epub 2022 Feb 17.
2
Myelodysplasia-Related Features of Acute Myeloid Leukemia Evolving From Philadelphia-Negative Myeloproliferative Neoplasms.源自费城染色体阴性骨髓增殖性肿瘤的急性髓系白血病的骨髓发育异常相关特征
Ann Lab Med. 2016 Jul;36(4):377-9. doi: 10.3343/alm.2016.36.4.377.
3
CD133 marks a stem cell population that drives human primary myelofibrosis.
CD133标记了一群驱动人类原发性骨髓纤维化的干细胞。
Haematologica. 2015 Jun;100(6):768-79. doi: 10.3324/haematol.2014.118463. Epub 2015 Feb 27.
4
Nucleic acid aptamer-guided cancer therapeutics and diagnostics: the next generation of cancer medicine.核酸适配体引导的癌症治疗与诊断:新一代癌症医学
Theranostics. 2015 Jan 1;5(1):23-42. doi: 10.7150/thno.10202. eCollection 2015.
5
Kinetics of del(7q) driven leukemogenesis in a patient with JAK2 V617F and TET2 mutated chronic myeloproliferative neoplasm.一名伴有JAK2 V617F和TET2突变的慢性骨髓增殖性肿瘤患者中,del(7q)驱动白血病发生的动力学研究
Leuk Res Rep. 2013 Jul 4;2(2):51-3. doi: 10.1016/j.lrr.2013.06.001. eCollection 2013.
6
TET2 mutations in Ph-negative myeloproliferative neoplasms: identification of three novel mutations and relationship with clinical and laboratory findings.TET2 突变在 Ph 阴性骨髓增殖性肿瘤中的研究:三种新突变的鉴定及其与临床和实验室发现的关系。
Biomed Res Int. 2013;2013:929840. doi: 10.1155/2013/929840. Epub 2013 May 25.
7
Mutations with epigenetic effects in myeloproliferative neoplasms and recent progress in treatment: Proceedings from the 5th International Post-ASH Symposium.骨髓增殖性肿瘤中的表观遗传学效应突变和近期治疗进展:第 5 届国际后 ASH 研讨会会议录。
Blood Cancer J. 2011 Mar 4;1(3):e7. doi: 10.1038/bcj.2011.4.
8
Role of TET2 mutations in myeloproliferative neoplasms.TET2 突变在骨髓增殖性肿瘤中的作用。
Curr Hematol Malig Rep. 2012 Mar;7(1):57-64. doi: 10.1007/s11899-011-0108-8.