Low expression predicts adverse prognosis in cytogenetically normal acute myeloid leukemia

Dysregulation of NKD1 has been identified in several solid tumors. However, the status of NKD1 expression and its clinical implication in acute myeloid leukemia remain largely elusive. NKD1 transcript level in bone marrow mononuclear cells was detected by real-time quantitative polymerase chain reac...

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Main Authors: Jing-dong Zhou, Dong-ming Yao, Li Han, Gao-fei Xiao, Hong Guo, Ting-juan Zhang, Xi-xi Li, Qian Yuan, Lei Yang, Jiang Lin, Jun Qian
Format: Article
Language:English
Published: IOS Press 2017-04-01
Series:Tumor Biology
Online Access:https://doi.org/10.1177/1010428317699123
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spelling doaj-932c6647b4b7433ea8a27db11898a3692021-05-02T18:36:51ZengIOS PressTumor Biology1423-03802017-04-013910.1177/1010428317699123Low expression predicts adverse prognosis in cytogenetically normal acute myeloid leukemiaJing-dong Zhou0Dong-ming Yao1Li Han2Gao-fei Xiao3Hong Guo4Ting-juan Zhang5Xi-xi Li6Qian Yuan7Lei Yang8Jiang Lin9Jun Qian10Department of Hematology, Affiliated People’s Hospital of Jiangsu University, Zhenjiang, People’s Republic of ChinaLaboratory Center, Affiliated People’s Hospital of Jiangsu University, Zhenjiang, People’s Republic of ChinaMedical Laboratory, Second People’s Hospital of Huai’an, Huai’an, People’s Republic of ChinaLaboratory Center, Affiliated People’s Hospital of Jiangsu University, Zhenjiang, People’s Republic of ChinaLaboratory Center, Affiliated People’s Hospital of Jiangsu University, Zhenjiang, People’s Republic of ChinaDepartment of Hematology, Affiliated People’s Hospital of Jiangsu University, Zhenjiang, People’s Republic of ChinaDepartment of Hematology, Affiliated People’s Hospital of Jiangsu University, Zhenjiang, People’s Republic of ChinaLaboratory Center, Affiliated People’s Hospital of Jiangsu University, Zhenjiang, People’s Republic of ChinaDepartment of Hematology, Affiliated People’s Hospital of Jiangsu University, Zhenjiang, People’s Republic of ChinaLaboratory Center, Affiliated People’s Hospital of Jiangsu University, Zhenjiang, People’s Republic of ChinaDepartment of Hematology, Affiliated People’s Hospital of Jiangsu University, Zhenjiang, People’s Republic of ChinaDysregulation of NKD1 has been identified in several solid tumors. However, the status of NKD1 expression and its clinical implication in acute myeloid leukemia remain largely elusive. NKD1 transcript level in bone marrow mononuclear cells was detected by real-time quantitative polymerase chain reaction in 126 de novo acute myeloid leukemia patients and 30 controls. Clinical significance of NKD1 expression was obtained by the comparison between the patients with low and high NKD1 expression. NKD1 messenger RNA level was significantly decreased in acute myeloid leukemia patients compared with controls ( p  = 0.019). There were no significant differences between patients with low and high NKD1 expression in sex, age, peripheral blood cells, bone marrow blasts, French–American–British/World Health Organization subtypes, and karyotypes/karyotypic classifications ( p  > 0.05). Although no significant difference was observed in complete remission rate between NKD1 low and NKD1 high patients ( p  > 0.05), Kaplan–Meier analysis revealed that NKD1 low patients showed shorter overall survival time than NKD1 high patients in whole-cohort acute myeloid leukemia, non-M3 acute myeloid leukemia, and cytogenetically normal acute myeloid leukemia ( p  = 0.014, 0.063, and 0.020). Multivariate analyses disclosed the low NKD1 expression was an independent risk factor in cytogenetically normal acute myeloid leukemia patients (hazard ratio = 0.397, p  = 0.017). Moreover, the prognostic value of NKD1 expression was confirmed by gene expression profile data in cytogenetically normal acute myeloid leukemia patients ( p  = 0.028 and 0.011). NKD1 showed significantly increased level after induction chemotherapy achieved complete remission in follow-up paired acute myeloid leukemia patients ( p  < 0.001). These findings indicated that reduced NKD1 expression is associated with unfavorable clinical outcome in cytogenetically normal acute myeloid leukemia.https://doi.org/10.1177/1010428317699123
collection DOAJ
language English
format Article
sources DOAJ
author Jing-dong Zhou
Dong-ming Yao
Li Han
Gao-fei Xiao
Hong Guo
Ting-juan Zhang
Xi-xi Li
Qian Yuan
Lei Yang
Jiang Lin
Jun Qian
spellingShingle Jing-dong Zhou
Dong-ming Yao
Li Han
Gao-fei Xiao
Hong Guo
Ting-juan Zhang
Xi-xi Li
Qian Yuan
Lei Yang
Jiang Lin
Jun Qian
Low expression predicts adverse prognosis in cytogenetically normal acute myeloid leukemia
Tumor Biology
author_facet Jing-dong Zhou
Dong-ming Yao
Li Han
Gao-fei Xiao
Hong Guo
Ting-juan Zhang
Xi-xi Li
Qian Yuan
Lei Yang
Jiang Lin
Jun Qian
author_sort Jing-dong Zhou
title Low expression predicts adverse prognosis in cytogenetically normal acute myeloid leukemia
title_short Low expression predicts adverse prognosis in cytogenetically normal acute myeloid leukemia
title_full Low expression predicts adverse prognosis in cytogenetically normal acute myeloid leukemia
title_fullStr Low expression predicts adverse prognosis in cytogenetically normal acute myeloid leukemia
title_full_unstemmed Low expression predicts adverse prognosis in cytogenetically normal acute myeloid leukemia
title_sort low expression predicts adverse prognosis in cytogenetically normal acute myeloid leukemia
publisher IOS Press
series Tumor Biology
issn 1423-0380
publishDate 2017-04-01
description Dysregulation of NKD1 has been identified in several solid tumors. However, the status of NKD1 expression and its clinical implication in acute myeloid leukemia remain largely elusive. NKD1 transcript level in bone marrow mononuclear cells was detected by real-time quantitative polymerase chain reaction in 126 de novo acute myeloid leukemia patients and 30 controls. Clinical significance of NKD1 expression was obtained by the comparison between the patients with low and high NKD1 expression. NKD1 messenger RNA level was significantly decreased in acute myeloid leukemia patients compared with controls ( p  = 0.019). There were no significant differences between patients with low and high NKD1 expression in sex, age, peripheral blood cells, bone marrow blasts, French–American–British/World Health Organization subtypes, and karyotypes/karyotypic classifications ( p  > 0.05). Although no significant difference was observed in complete remission rate between NKD1 low and NKD1 high patients ( p  > 0.05), Kaplan–Meier analysis revealed that NKD1 low patients showed shorter overall survival time than NKD1 high patients in whole-cohort acute myeloid leukemia, non-M3 acute myeloid leukemia, and cytogenetically normal acute myeloid leukemia ( p  = 0.014, 0.063, and 0.020). Multivariate analyses disclosed the low NKD1 expression was an independent risk factor in cytogenetically normal acute myeloid leukemia patients (hazard ratio = 0.397, p  = 0.017). Moreover, the prognostic value of NKD1 expression was confirmed by gene expression profile data in cytogenetically normal acute myeloid leukemia patients ( p  = 0.028 and 0.011). NKD1 showed significantly increased level after induction chemotherapy achieved complete remission in follow-up paired acute myeloid leukemia patients ( p  < 0.001). These findings indicated that reduced NKD1 expression is associated with unfavorable clinical outcome in cytogenetically normal acute myeloid leukemia.
url https://doi.org/10.1177/1010428317699123
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