Clinical significance of up-regulated ID1 expression in Chinese de novo acute myeloid leukemia

被引:1
作者
Zhou, Jing-Dong [1 ]
Yang, Lei [1 ]
Zhu, Xiao-Wen [1 ]
Wen, Xiang-Mei [2 ]
Yang, Jing [1 ]
Guo, Hong [2 ]
Chen, Qin [2 ]
Yao, Dong-Ming [2 ]
Ma, Ji-Chun [2 ]
Lin, Jiang [2 ]
Qian, Jun [1 ]
机构
[1] Jiangsu Univ, Affiliated Peoples Hosp, Dept Hematol, Zhenjiang 212002, Peoples R China
[2] Jiangsu Univ, Affiliated Peoples Hosp, Lab Ctr, Zhenjiang 212002, Peoples R China
基金
中国国家自然科学基金;
关键词
ID1; expression; prognosis; acute myeloid leukemia; CYTOGENETIC ABNORMALITIES; LUNG ADENOCARCINOMA; PROGNOSTIC-FACTOR; ID-1; PROTEIN; CANCER; INHIBITOR; CELLS; DIFFERENTIATION-1; OVEREXPRESSION; CLASSIFICATION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To investigate the clinical significance of ID1 expression in Chinese de novo AML patients. Real-time quantitative PCR was carried out to detect the status of ID1 expression in 102 de novo AML patients and 28 controls. ID1 transcript level was significantly increased in AML compared to normal controls (P= 0.029). The age in the patients with high ID1 expression is significantly older than in those with low ID1 expression (P= 0.044). ID1 overexpression occurred with the highest frequency in the patients with poor karyotype (7/7, 100%), lower frequency in the patients with intermediate karyotype (28/60, 47%), and the lowest frequency in the patients with favorable karyotype (12/31, 39%). Both whole AML and non-M3 patients with high ID1 expression had significantly lower rate of complete remission than those with low ID1 expression (P= 0.007 and 0.038). ID1 high-expressed patients showed significantly shorter overall survival (OS) than ID1 low-expressed patients in both whole AML and non-M3 according to Kaplan-Meier analysis (P= 0.007 and 0.040). However, multivariate analysis indicated that ID1 overexpression was not an independent risk factor in both whole AML and non-M3 patients. However, the adverse impact of ID1 overexpression on outcome was revealed by both Kaplan-Meier analysis and multivariate analysis in the non-M3 patients less than 60 years old. Our study reveals that ID1 overexpression may be associated with higher risk karyotype classification and act as an independent risk factor in young non-M3 patients.
引用
收藏
页码:5336 / 5344
页数:9
相关论文
共 40 条
[1]  
[Anonymous], CANC BIOL THER
[2]   THE PROTEIN ID - A NEGATIVE REGULATOR OF HELIX-LOOP-HELIX DNA-BINDING PROTEINS [J].
BENEZRA, R ;
DAVIS, RL ;
LOCKSHON, D ;
TURNER, DL ;
WEINTRAUB, H .
CELL, 1990, 61 (01) :49-59
[3]   PROPOSED REVISED CRITERIA FOR THE CLASSIFICATION OF ACUTE MYELOID-LEUKEMIA - A REPORT OF THE FRENCH-AMERICAN-BRITISH COOPERATIVE GROUP [J].
BENNETT, JM ;
CATOVSKY, D ;
DANIEL, MT ;
FLANDRIN, G ;
GALTON, DAG ;
GRALNICK, HR ;
SULTAN, C .
ANNALS OF INTERNAL MEDICINE, 1985, 103 (04) :620-625
[4]   Pretreatment cytogenetic abnormalities are predictive of induction success, cumulative incidence of relapse, and overall survival in adult patients with de novo acute myeloid leukemia:: results from Cancer and Leukemia Group B (CALGB 8461) [J].
Byrd, JC ;
Mrózek, K ;
Dodge, RK ;
Carroll, AJ ;
Edwards, CG ;
Arthur, DC ;
Pettenati, MJ ;
Patil, SR ;
Rao, KW ;
Watson, MS ;
Koduru, PRK ;
Moore, JO ;
Stone, RM ;
Mayer, RJ ;
Feldman, EJ ;
Davey, FR ;
Schiffer, CA ;
Larson, RA ;
Bloomfield, CD .
BLOOD, 2002, 100 (13) :4325-4336
[5]   ID1 expression associates with other molecular markers and is not an independent prognostic factor in cytogenetically normal acute myeloid leukaemia [J].
Damm, Frederik ;
Wagner, Katharina ;
Goerlich, Kerstin ;
Morgan, Michael ;
Thol, Felicitas ;
Yun, Haiyang ;
Delwel, Ruud ;
Valk, Peter J. M. ;
Lowenberg, Bob ;
Heuser, Michael ;
Ganser, Arnold ;
Krauter, Juergen .
BRITISH JOURNAL OF HAEMATOLOGY, 2012, 158 (02) :208-215
[6]   Overexpression of Id-1 is associated with tumor angiogenesis and poor clinical outcome in oral squamous cell carcinoma [J].
Dong, Zuoqing ;
Liu, Shaohua ;
Zhou, Chengjun ;
Sumida, Tomoki ;
Hamakawa, Hiroyuki ;
Chen, Zhenggang ;
Liu, Pei ;
Wei, Fengcai .
ORAL ONCOLOGY, 2010, 46 (03) :154-157
[7]   Acute myeloid leukaemia [J].
Estey, Elihu ;
Doehner, Hartmut .
LANCET, 2006, 368 (9550) :1894-1907
[8]   MicroRNA 29b functions in acute myeloid leukemia [J].
Garzon, Ramiro ;
Heaphy, Catherine E. A. ;
Havelange, Violaine ;
Fabbri, Muller ;
Volinia, Stefano ;
Tsao, Twee ;
Zanesi, Nicola ;
Kornblau, Steven M. ;
Marcucci, Guido ;
Calin, George A. ;
Andreeff, Michael ;
Croce, Carlo M. .
BLOOD, 2009, 114 (26) :5331-5341
[9]   The clinical significance of cytogenetic abnormalities in acute myeloid leukaemia [J].
Grimwade, D .
BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY, 2001, 14 (03) :497-529
[10]   Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials [J].
Grimwade, David ;
Hills, Robert K. ;
Moorman, Anthony V. ;
Walker, Helen ;
Chatters, Stephen ;
Goldstone, Anthony H. ;
Wheatley, Keith ;
Harrison, Christine J. ;
Burnett, Alan K. .
BLOOD, 2010, 116 (03) :354-365