Identification of immune and stromal cell infiltration-related gene signature for prognosis prediction in acute lymphoblastic leukemia

被引:0
|
作者
Yu, Wen-Liang [1 ,2 ,3 ]
Hua, Zi-Chun [1 ,2 ,3 ,4 ]
机构
[1] China Pharmaceut Univ, Sch Biopharm, Nanjing 211198, Peoples R China
[2] Nanjing Univ, Changzhou High Tech Res Inst, Changzhou 213164, Peoples R China
[3] Jiangsu TargetPharma Labs Inc, Changzhou 213164, Peoples R China
[4] Nanjing Univ, Sch Life Sci, Nanjing 210023, Peoples R China
来源
AGING-US | 2022年 / 14卷 / 18期
基金
中国国家自然科学基金;
关键词
acute lymphoblastic leukemia; immune cell infiltration; overall survival; bone marrow microenvironment; bioinformatics; SURVIVAL; HETEROGENEITY; EXPRESSION; REVEALS;
D O I
暂无
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 common and life-threatening hematologic malignancy, its occurrence and progression are closely related to immune/stromal cell infiltration in the bone marrow (BM) microenvironment. However, no studies have described an immune/stromal cell infiltration-related gene (ISCIRG)-based prognostic signature for ALL. A total of 444 patients involving 437 bulk and 7 single-cell RNA-seq datasets were included in this study. Eligible datasets were searched and reviewed from the database of TCGA, TARGET project and GEO. Then an integrated bioinformatics analysis was performed to select optimal prognosis-related genes from ISCIRGs, construct a nomogram model for predicting prognosis, and assess the predictive power. After LASSO and multivariate Cox regression analyses, a seven ISCIRGs-based signature was proved to be able to significantly stratify patients into high-and low-risk groups in terms of OS. The seven genes were confirmed that directly related to the composition and status of immune/stromal cells in BM microenvironment by analyzing bulk and single-cell RNA-seq datasets. The calibration plot showed that the predicted results of the nomogram were consistent with the actual observation results of training/validation cohort. This study offers a reference for future research regarding the role of ISCIRGs in ALL and the clinical care of patients.
引用
收藏
页码:7470 / 7504
页数:35
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