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Novel gene signature reveals prognostic model in acute lymphoblastic leukemia
被引:4
作者:

Chen, Panpan
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Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China

Gao, Guanfei
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Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China

Xu, Yuanlin
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Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China

Jia, Peijun
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Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China

Li, Yan
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Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China

Li, Yating
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Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China

Cao, Jiaming
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机构:
Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China

Du, Jiangfeng
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机构:
Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China

Zhang, Shijie
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h-index: 0
机构:
Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China

Zhang, Jingxin
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h-index: 0
机构:
Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China
机构:
[1] Zhengzhou Univ, Sch Life Sci, Zhengzhou, Peoples R China
基金:
中国国家自然科学基金;
关键词:
acute lymphoblastic leukemia;
prognostic value;
risk model;
bioinformatics analysis;
database;
CHILDHOOD;
CLASSIFICATION;
REGRESSION;
SURVIVAL;
RELAPSE;
PREDICT;
IMPACT;
D O I:
10.3389/fcell.2022.1036312
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Acute lymphoblastic leukemia (ALL) is a type of hematological malignancy and has a poor prognosis. In our study, we aimed to construct a prognostic model of ALL by identifying important genes closely related to ALL prognosis. We obtained transcriptome data (RNA-seq) of ALL samples from the GDC TARGET database and identified differentially expressed genes (DEGs) using the "DESeq " package of R software. We used univariate and multivariate cox regression analyses to screen out the prognostic genes of ALL. In our results, the risk score can be used as an independent prognostic factor to predict the prognosis of ALL patients [hazard ratio (HR) = 2.782, 95% CI = 1.903-4.068, p < 0.001]. Risk score in clinical parameters has high diagnostic sensitivity and specificity for predicting overall survival of ALL patients, and the area under curve (AUC) is 0.864 in the receiver operating characteristic (ROC) analysis results. Our study evaluated a potential prognostic signature with six genes and constructed a risk model significantly related to the prognosis of ALL patients. The results of this study can help clinicians to adjust the treatment plan and distinguish patients with good and poor prognosis for targeted treatment.
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