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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/111768
Title: 
MicroRNA Signature Obtained From the Comparison of Aggressive With Indolent Non-Hodgkin Lymphomas: Potential Prognostic Value in Mantle-Cell Lymphoma
Author(s): 
Institution: 
  • Ontario Canc Inst
  • Univ Toronto
  • Princess Margaret Hosp
  • Mt Sinai Hosp
  • Sunnybrook Hlth Sci Ctr
  • Univ Hlth Network
  • Toronto Gen Hosp
  • Queens Univ
  • Univ Alberta
  • British Columbia Canc Agcy
  • Dana Farber Canc Inst
  • Harvard Univ
  • Universidade Estadual Paulista (UNESP)
  • Univ Perugia
ISSN: 
0732-183X
Sponsorship: 
  • Canadian Institute of Health Research
  • Frank Fletcher Memorial Fund
  • University of Toronto Fellowship
  • Wallace H. Coulter Foundation
  • Terry Fox Foundation
  • Biology of Cancer: Insights from Genomic Analysis of Lymphoid Neoplasms
  • Canada Foundation for Innovation
  • Irving and Mary Storfer Mantle Cell Lymphoma Research Fund
  • Princess Margaret Hospital Foundation
  • La Societe de Recherche sur le Cancer/Cancer Research Society
  • Galloway Fund
  • Ontario Ministry of Health and Long Term Care
  • Canada Research Chair Program
Sponsorship Process Number: 
  • Canadian Institute of Health ResearchSTP-53912
  • Terry Fox Foundation019001
  • Canada Foundation for Innovation12301
  • Canada Foundation for Innovation203383
Abstract: 
Purpose Mantle-cell lymphoma (MCL) has a variable natural history but is incurable with current therapies. MicroRNAs (miRs) are useful in prognostic assessment of cancer. We determined an miR signature defining aggressiveness in B-cell non-Hodgkin lymphomas (NHL) and assessed whether this signature aids in MCL prognosis.MethodsWe assessed miR expression in a training set of 43 NHL cases. The miR signature was validated in 44 additional cases and examined on a training set of 119 MCL cases from four institutions in Canada. miRs significantly associated with overall survival were examined in an independent cohort of 114 MCL cases to determine association with patient outcome. miR expression was combined with current clinical prognostic factors to develop an enhanced prognostic model in patients with MCL.ResultsFourteen miRs were differentially expressed between aggressive and indolent NHL; 11 of 14 were validated in an independent set of NHL (excluding MCL). miR-127-3p and miR-615-3p were significantly associated with overall survival in the MCL training set. Their expression was validated in an independent MCL patient set. In comparison with Ki-67, expression of these miRs was more significantly associated with overall survival among patients with MCL. miR-127-3p was combined with Ki-67 to create a new prognostic model for MCL. A similar model was created with miR-615-3p and Mantle Cell Lymphoma International Prognostic Index scores.ConclusionEleven miRs are differentially expressed between aggressive and indolent NHL. Two novel miRs were associated with overall survival in MCL and were combined with clinical prognostic models to generate novel prognostic data for patients with MCL. (C) 2013 by American Society of Clinical Oncology
Issue Date: 
10-Aug-2013
Citation: 
Journal Of Clinical Oncology. Alexandria: Amer Soc Clinical Oncology, v. 31, n. 23, p. 2903-+, 2013.
Time Duration: 
2903-+
Publisher: 
Amer Soc Clinical Oncology
Source: 
http://dx.doi.org/10.1200/JCO.2012.45.3050
URI: 
Access Rights: 
Acesso restrito
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/111768
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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