Literature DB >> 25530566

Low expressions of ARS2 and CASP8AP2 predict relapse and poor prognosis in pediatric acute lymphoblastic leukemia patients treated on China CCLG-ALL 2008 protocol.

Lei Cui1, Chao Gao2, Rui-Dong Zhang2, Ying Jiao2, Wei-Jing Li2, Xiao-Xi Zhao2, Shu-Guang Liu2, Zhi-Xia Yue2, Hu-Yong Zheng2, Guo-Ren Deng3, Min-Yuan Wu2, Zhi-Gang Li4, Hong-Ti Jia5.   

Abstract

ARS2 protein is important to early development and cell proliferation, in which ARS2-CASP8AP2 interaction is implicated. However, the predictive significance of ARS2 in childhood acute lymphoblastic leukemia (ALL) is unknown. Here we evaluate the predictive values of ARS2 expression and combined ARS2 and CASP8AP2 expression in relapse. We showed that ARS2 expression in ALL bone marrow samples at initial diagnosis was markedly lower than that in complete remission (CR). Likewise, the levels of ARS2 expression in the patients suffering from relapse were significantly lower than that of patients in continuous CR. Furthermore, low expression of ARS2 was closely correlated to poor treatment response including poor prednisone response and high minimal residual disease (MRD), and the patients with high MRD (≥10(-4)) and low ARS2 were more subject to relapse. The multivariate analyses for relapse free survival and event free survival revealed that ARS2 expression remained an independent prognostic factor after adjusting other risk factors. In addition, combined assessment of ARS2 and CASP8AP2 expression was more accurate to predict relapse, based on which an algorithm composed of ARS2 and CASP8AP2 expression, prednisone response and MRD (day 78) was proposed. Together, ARS2 and CASP8AP2 expressions can precisely predict high-risk of relapse and ALL prognosis.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  ARS2; Acute lymphoblastic leukemia; CASP8AP2; Minimal residual disease; Prognosis; Relapse

Mesh:

Substances:

Year:  2014        PMID: 25530566     DOI: 10.1016/j.leukres.2014.10.008

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


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