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胰岛素样生长因子1受体表达与慢性淋巴细胞白血病中的NOTCH1突变、12号染色体三体及侵袭性临床病程相关。

Insulin growth factor 1 receptor expression is associated with NOTCH1 mutation, trisomy 12 and aggressive clinical course in chronic lymphocytic leukaemia.

作者信息

Maura Francesco, Mosca Laura, Fabris Sonia, Cutrona Giovanna, Matis Serena, Lionetti Marta, Agnelli Luca, Barbieri Marzia, D'Anca Marianna, Manzoni Martina, Colombo Monica, Massucco Carlotta, Reverberi Daniele, Gentile Massimo, Recchia Anna Grazia, Bossio Sabrina, Ilariucci Fiorella, Musolino Caterina, Di Raimondo Francesco, Cortelezzi Agostino, Morabito Fortunato, Ferrarini Manlio, Neri Antonino

机构信息

Department of Clinical Sciences and Community Health, University of Milano and Hematology 1 CTMO, Foundation IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milano, Italy.

SS Molecular Diagnostics, IRCCS S. Martino-IST, Genova, Italy.

出版信息

PLoS One. 2015 Mar 18;10(3):e0118801. doi: 10.1371/journal.pone.0118801. eCollection 2015.

Abstract

IGF1R is emerging as an important gene in the pathogenesis of many solid and haematological cancers and its over-expression has been reported as frequently associated with aggressive disease and chemotherapy resistance. In this study we performed an investigation of the role of IGF1R expression in a large and representative prospective series of 217 chronic lymphocytic leukaemia (CLL) patients enrolled in the multicentre O-CLL1 protocol (clinicaltrial.gov #NCT00917540). High IGF1R gene expression was significantly associated with IGHV unmutated (IGHV-UM) status (p<0.0001), high CD38 expression (p<0.0001), trisomy 12 (p<0.0001), and del(11)(q23) (p=0.014). Interestingly, higher IGF1R expression (p=0.002) characterized patients with NOTCH1 mutation (c.7541_7542delCT), identified in 15.5% of cases of our series by next generation sequencing and ARMS-PCR. Furthermore, IGF1R expression has been proven as an independent prognostic factor associated with time to first treatment in our CLL prospective cohort. These data suggest that IGF1R may play an important role in CLL biology, in particular in aggressive CLL clones characterized by IGHV-UM, trisomy 12 and NOTCH1 mutation.

摘要

胰岛素样生长因子1受体(IGF1R)正逐渐成为许多实体癌和血液系统癌症发病机制中的一个重要基因,据报道其过表达常与侵袭性疾病和化疗耐药相关。在本研究中,我们对217例慢性淋巴细胞白血病(CLL)患者进行了一项调查,这些患者来自多中心O-CLL1方案(clinicaltrial.gov #NCT00917540),具有代表性且为前瞻性队列。IGF1R基因高表达与IGHV未突变(IGHV-UM)状态(p<0.0001)、高CD38表达(p<0.0001)、12号染色体三体(p<0.0001)和del(11)(q23)(p=0.014)显著相关。有趣的是,较高的IGF1R表达(p=0.002)是NOTCH1突变(c.7541_7542delCT)患者的特征,在我们队列的15.5%病例中通过下一代测序和ARMS-PCR检测到该突变。此外,在我们的CLL前瞻性队列中,IGF1R表达已被证明是与首次治疗时间相关的独立预后因素。这些数据表明,IGF1R可能在CLL生物学中发挥重要作用,特别是在以IGHV-UM、12号染色体三体和NOTCH1突变为特征的侵袭性CLL克隆中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cc3/4365018/66b0bd463daf/pone.0118801.g001.jpg

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