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.
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页数:9
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