Prognostic significance of the PANK family expression in acute myeloid leukemia

被引:16
|
作者
Liu, Yan [1 ,2 ,3 ,4 ,5 ,6 ]
Cheng, Zhiheng [7 ]
Li, Qihui [3 ,4 ]
Pang, Yifan [8 ]
Cui, Longzhen [2 ]
Qian, Tingting [1 ,5 ]
Quan, Liang [1 ,5 ]
Dai, Yifeng [9 ]
Jiao, Yang [10 ,11 ]
Zhang, Zhihui [12 ]
Ye, Xu [1 ]
Shi, Jinlong [13 ]
Fu, Lin [1 ,5 ,6 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 2, Dept Hematol, Guangzhou 510260, Guangdong, Peoples R China
[2] Henan Univ, Huaihe Hosp, Translat Med Ctr, Kaifeng 475000, Peoples R China
[3] Peking Univ, Hosp 3, Dept Hematol, Beijing 100191, Peoples R China
[4] Peking Univ, Hosp 3, Lymphoma Res Ctr, Beijing 100191, Peoples R China
[5] Guangzhou Med Univ, Affiliated Hosp 2, Translat Med Ctr, Guangzhou 510260, Guangdong, Peoples R China
[6] Henan Univ, Dept Hematol, Huaihe Hosp, Kaifeng 475000, Peoples R China
[7] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol & Med Biol, Groningen, Netherlands
[8] William Beaumont Hosp, Dept Med, Royal Oak, MI 48073 USA
[9] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol & Med Biol, Div Med Biol,Immunoendocrinol, Groningen, Netherlands
[10] Zhejiang Univ, Life Sci Inst, Hangzhou 310058, Zhejiang, Peoples R China
[11] Zhejiang Univ, Innovat Ctr Cell Signaling Network, Hangzhou 310058, Zhejiang, Peoples R China
[12] Peking Univ, Dept Stomatol, Hosp 3, Beijing 100191, Peoples R China
[13] Chinese Peoples Liberat Army Gen Hosp, Dept Med Big Data, Beijing 100853, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Acute myeloid leukemia (AML); heterogeneity; pantothenate kinase (PANK); prognosis; MONOSOMAL KARYOTYPE; COMPLEX KARYOTYPE; TP53; GENE; MUTATIONS; CLASSIFICATION; EVOLUTION; NUMBER; IMPACT; LEVEL; NPM1;
D O I
10.21037/atm.2019.05.28
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Acute myeloid leukemia (AML) is a highly heterogenous hematological malignancy and its prognostication depends on the genetic mutation and expression profile of each patient. Pantothenate kinase (PANK) is a regulatory enzyme that controls coenzyme A (CoA) biosynthesis. It has four isoforms encoded by PANK1-4, respectively. Whether the expression of the PANK family has prognostic significance in AML remains unclear. Methods: We screened The Cancer Genome Atlas database for AML patients with complete PANK1-4 expression data. Eighty-four AML patients met the criteria and were included in this study. Clinical characteristics at diagnosis, including peripheral blood (PB) white blood cell counts (WBC), blast percentages in PB and bone marrow (BM), French-American-British (FAB) subtypes and the frequencies of common genetic mutations were described. Survival was estimated using the Kaplan-Meier method and the log-rank test. Multivariate Cox proportional hazard models were constructed for event-free survival (EFS) and overall survival (OS), using a limited backward elimination procedure. Results: Patients with high PANK2 expression had significantly longer event-free survival (EFS) and overall survival (OS) than patients with low PANK2 expression (P=0.007, P=0.016, respectively), whereas patients with high PANK4 expression had shorter EFS and OS than patients with low PANK4 expression (P=0.022, P=0.015, respectively). Multivariate analysis confirmed that high PANK4 expression was an independent risk factor for EFS and OS (both P<0.05). Conclusions: Our study suggested that high PANK2 expression might have favorable effects on AML, while high PANK4 expression was indicative of poor prognosis.
引用
收藏
页数:9
相关论文
共 50 条
  • [1] Prognostic significance of PAK family kinases in acute myeloid leukemia
    Quan, Liang
    Cheng, Zhiheng
    Dai, Yifeng
    Jiao, Yang
    Shi, Jinlong
    Fu, Lin
    CANCER GENE THERAPY, 2020, 27 (1-2) : 30 - 37
  • [2] Prognostic significance of PAK family kinases in acute myeloid leukemia
    Liang Quan
    Zhiheng Cheng
    Yifeng Dai
    Yang Jiao
    Jinlong Shi
    Lin Fu
    Cancer Gene Therapy, 2020, 27 : 30 - 37
  • [3] Prognostic significance of myeloperoxidase expression in childhood acute myeloid leukemia
    Roberson, Jessica R.
    Onciu, Mihaela
    Pounds, Stanley
    Rubnitz, Jeffrey E.
    Pui, Ching-Hon
    Razzouk, Bassem I.
    PEDIATRIC BLOOD & CANCER, 2008, 50 (03) : 542 - 548
  • [4] Prognostic significance of Spinster homolog gene family in acute myeloid leukemia
    Huang, Wenhui
    Qian, Tingting
    Cheng, Zhiheng
    Zeng, Tiansheng
    Si, Chaozeng
    Liu, Chaojun
    Deng, Cong
    Ye, Xu
    Liu, Yan
    Cui, Longzhen
    Fu, Lin
    JOURNAL OF CANCER, 2020, 11 (15): : 4581 - 4588
  • [5] Prognostic value of HMGN family expression in acute myeloid leukemia
    Cui, Wei
    Liu, Yuna
    Tan, Yanan
    Peng, Xingyue
    Cui, Longzhen
    Cheng, Zhiheng
    Dai, Yifeng
    Fu, Lin
    Zeng, Tiansheng
    Liu, Yan
    FUTURE ONCOLOGY, 2021, 17 (05) : 541 - 548
  • [6] Prognostic significance of natural killer ligand expression in acute myeloid leukemia
    Koldej, Rachel
    Ripley, Jane
    Chan, Christopher
    Smyth, Mark
    Neeson, Paul
    Ritchie, David
    Perera, Travis
    CANCER IMMUNOLOGY RESEARCH, 2016, 4 (01)
  • [7] Prognostic significance of BAALC expression in cytogenetically normal acute myeloid leukemia
    Chopra, Anita
    Verma, Deepak
    Kumar, Rajive
    Singh, Jay
    Ali, Shadab
    Bakhshi, Sameer
    Sharma, Atul
    Palanichamy, Jayanth Kumar
    Sharawat, Surender Kumar
    BRITISH JOURNAL OF HAEMATOLOGY, 2021, 193 : 78 - 79
  • [8] Prognostic significance of CXCR4 expression in acute myeloid leukemia
    Du, Wen
    Lu, Cong
    Zhu, Xinyun
    Hu, Dong
    Chen, Xiangjun
    Li, Juan
    Liu, Wei
    Zhu, Jiang
    He, Yanli
    Yao, Junxia
    CANCER MEDICINE, 2019, 8 (15): : 6595 - 6603
  • [9] Prognostic significance of cathepsin L expression in pediatric acute myeloid leukemia
    Pandey, Garima
    Bakhshi, Sameer
    Thakur, Bhaskar
    Jain, Prerna
    Chauhan, Shyam S.
    LEUKEMIA & LYMPHOMA, 2018, 59 (09) : 2175 - 2187
  • [10] Expression and prognostic significance of survivin in de novo acute myeloid leukemia (AML).
    Adida, C
    Recher, C
    Raffoux, E
    Daniel, MT
    Taksin, AL
    Rousselot, P
    Sigaux, F
    Degos, L
    Altieri, DC
    Dombret, H
    BLOOD, 2000, 96 (11) : 698A - 698A