Abstract

The prognosis of cytogenetically normal acute myeloid leukemia (CN-AML) varies greatly among patients. Achievement of complete remission (CR) after chemotherapy is indispensable for a better prognosis. To develop a gene signature predicting overall survival (OS) in CN-AML, we performed data mining procedure based on whole genome expression data of both blood cancer cell lines and AML patients from open access database. A gene expression signature including 42 probes was derived. These probes were significantly associated with both cytarabine half maximal inhibitory concentration values in blood cancer cell lines and OS in CN-AML patients. By using cox regression analysis and linear regression analysis, a chemo-sensitive score calculated algorithm based on mRNA expression levels of the 42 probes was established. The scores were associated with OS in both the training sample (p=5.13 × 10−4, HR=2.040, 95% CI: 1.364-3.051) and the validation sample (p=0.002, HR=2.528, 95% CI: 1.393-4.591) of the GSE12417 dataset from Gene Expression Omnibus. In The Cancer Genome Atlas (TCGA) CN-AML patients, higher scores were found to be associated with both worse OS (p=0.013, HR=2.442, 95% CI: 1.205-4.950) and DFS (p=0.015, HR=2.376, 95% CI: 1.181-4.779). Results of gene ontology (GO) analysis showed that all the significant GO Terms were correlated with cellular component of mitochondrion. In summary, a novel gene set that could predict prognosis of CN-AML was identified presently, which provided a new way to identify genes impacting AML chemo-sensitivity and prognosis.

Highlights

  • Acute myeloid leukemia (AML), characterized by the rapid growth of abnormal white blood cells interfering with the production of normal blood cells, is the most common type of acute leukemia affecting adults

  • Our results indicated that chemo-sensitivity score might be used for predicting prognosis of AML patients after cytarabine based chemotherapy

  • Evidence has shown that AML patients who achieved complete remission (CR) had longer overall survival (OS) than non-CR patients [18,19,20], and chemo-resistance is the main reason for treatment failure in AML [25,26,27]

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Summary

Introduction

Acute myeloid leukemia (AML), characterized by the rapid growth of abnormal white blood cells interfering with the production of normal blood cells, is the most common type of acute leukemia affecting adults. Outcomes of AML vary greatly among patients after chemotherapy. Clinical studies have shown that the five-year survival rate of AML varies from 18% to 82%, and relapse rate varies from 33% to 80% [1,2,3,4]. It is well known that chromosomal abnormalities are major prognostic factors in AML. AML patients can be divided into favorable, intermediate and unfavorable cytogenetics risk groups which show different survival profiles [5]. The detailed mechanism of the prognosis variation in normal karyotype www.impactjournals.com/oncotarget

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