High expression of AK1 predicts inferior prognosis in acute myeloid leukemia patients undergoing chemotherapy

被引:6
作者
Qin, Tong [1 ]
Zhao, Hongmian [1 ]
Shao, Yunli [2 ]
Hu, Ning [1 ]
Shi, Jinlong [3 ,4 ,5 ]
Fu, Lin [1 ,6 ,7 ]
Zhang, Yijie [8 ]
机构
[1] Henan Univ, Dept Hematol, Huaihe Hosp, Kaifeng 475000, Peoples R China
[2] Henan Univ, Dept Hematol, Affiliated Hosp 1, Kaifeng 475000, Peoples R China
[3] Henan Univ, Translat Med Ctr, Huaihe Hosp, Kaifeng 475000, Peoples R China
[4] Chinese Peoples Liberat Army Gen Hosp, Dept Biomed Engn, Beijing 100853, Peoples R China
[5] Chinese Peoples Liberat Army Gen Hosp, Dept Med Big Data, Beijing 100853, Peoples R China
[6] Guangzhou Med Univ, Dept Hematol, Affiliated Hosp 2, Guangzhou 510260, Peoples R China
[7] Guangzhou Med Univ, Translat Med Ctr, Affiliated Hosp 2, Guangzhou 510260, Peoples R China
[8] Henan Univ, Dept Med, Huaihe Hosp, Kaifeng 475000, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
ADENYLATE KINASE-1; GENE; MUTATIONS; SURVIVAL; CANCER;
D O I
10.1042/BSR20200097
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The purpose of the present study was to investigate whether expression levels of adenylate kinase 1 (AK1) were associated with prognosis of acute myeloid leukemia (AML) in patients treated with chemotherapy or allogeneic hematopoietic stem cell transplantation (allo-HSCT). 85 AML patients with AK1 expression report who received chemotherapy-alone and 71 who underwent allo-HSCT from The Cancer Genome Atlas database were identified and grouped into either AK1high or AK1low based on their AK1 expression level relative to the median. Then, overall survival (OS) and event-free survival (EFS) were compared between patients with high vs. low AK1 expression. In the chemotherapy group, high AK1 expression was favorable for both EFS (P=0.016) and OS (P=0.014). In the allo-HSCT group, there was no association for AK1 expression levels and clinical outcomes. Further analyses suggested that in the high AK1 expression group, EFS and OS were longer in patients treated with allo-HSCT compared with those treated with chemotherapy (P=0.0011; P<0.0001, respectively), whereas no significant differences were observed in the low AK1 expression group. In summary, we reported AK1 as an independent unfavorable prognostic factor of AML patients undergoing chemotherapy, and its use could also facilitate clinical decision-making in selecting treatment for AML patients. Patients with high AK1 expression may be recommended for early allo-HSCT.
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页数:10
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共 21 条
  • [1] DNMT3A R882 Mutation with FLT3-ITD Positivity Is an Extremely Poor Prognostic Factor in Patients with Normal-Karyotype Acute Myeloid Leukemia after Allogeneic Hematopoietic Cell Transplantation
    Ahn, Jae-Sook
    Kim, Hyeoung-Joon
    Kim, Yeo-Kyeoung
    Lee, Seun-Shin
    Jung, Sung-Hoon
    Yang, Deok-Hwan
    Lee, Je-Jung
    Kim, Nan Young
    Choi, Seung Hyun
    Jung, Chul Won
    Jang, Jun-Ho
    Kim, Hee Je
    Moon, Joon Ho
    Sohn, Sang Kyun
    Won, Jong-Ho
    Kim, Sung-Hyun
    Kim, Dennis Dong Hwan
    [J]. BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2016, 22 (01) : 61 - 70
  • [2] 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)
    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
    [J]. BLOOD, 2002, 100 (13) : 4325 - 4336
  • [3] wt p53 dependent expression of a membrane-associated isoform of adenylate kinase
    Collavin, L
    Lazarevic, D
    Utrera, R
    Marzinotto, S
    Monte, M
    Schneider, C
    [J]. ONCOGENE, 1999, 18 (43) : 5879 - 5888
  • [4] The European LeukemiaNet AML Working Party consensus statement on allogeneic HSCT for patients with AML in remission: an integrated-risk adapted approach
    Cornelissen, Jan J.
    Gratwohl, Alois
    Schlenk, Richard F.
    Sierra, Jorge
    Bornhaeuser, Martin
    Juliusson, Gunnar
    Racil, Zdenek
    Rowe, Jacob M.
    Russell, Nigel
    Mohty, Mohamad
    Lowenberg, Bob
    Socie, Gerard
    Niederwieser, Dietger
    Ossenkoppele, Gert J.
    [J]. NATURE REVIEWS CLINICAL ONCOLOGY, 2012, 9 (10) : 579 - 590
  • [5] Acute Myeloid Leukemia
    Doehner, Hartmut
    Weisdorf, Daniel J.
    Bloomfield, Clara D.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (12) : 1136 - 1152
  • [6] Diagnosis and management of acute myeloid leukemia in adults: recommendations from an international expert panel, on behalf of the European LeukemiaNet
    Doehner, Hartmut
    Estey, Elihu H.
    Amadori, Sergio
    Appelbaum, Frederick R.
    Buechner, Thomas
    Burnett, Alan K.
    Dombret, Herve
    Fenaux, Pierre
    Grimwade, David
    Larson, Richard A.
    Lo-Coco, Francesco
    Naoe, Tomoki
    Niederwieser, Dietger
    Ossenkoppele, Gert J.
    Sanz, Miguel A.
    Sierra, Jorge
    Tallman, Martin S.
    Loewenberg, Bob
    Bloomfield, Clara D.
    [J]. BLOOD, 2010, 115 (03) : 453 - 474
  • [7] Defective metabolic signaling in adenylate kinase AK1 gene knock-out hearts compromises post-ischemic coronary reflow
    Dzeja, Petras P.
    Bast, Peter
    Pucar, Darko
    Wieringa, Be
    Terzic, Andre
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (43) : 31366 - 31372
  • [8] CME Information: Acute myeloid leukemia: 2014 update on risk-stratification and management
    Estey, Elihu H.
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 2014, 89 (11) : 1063 - 1081
  • [9] Genomics-Driven Oncology: Framework for an Emerging Paradigm
    Garraway, Levi A.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (15) : 1806 - 1814
  • [10] Adenylate Kinase: A Ubiquitous Enzyme Correlated with Medical Conditions
    Ionescu, Mihaela Ileana
    [J]. PROTEIN JOURNAL, 2019, 38 (02) : 120 - 133