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Artykuł

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Tytuł

Gene expression profiling of acute myeloid leukemia samples from adult AML-M1 and M2 patients through boutique microarrays, real-time PCR and droplet digital PCR

Autorzy

[ 1 ] Instytut Chemii Bioorganicznej Polskiej Akademii Nauk, Polska Akademia Nauk | [ P ] pracownik

Dyscyplina naukowa (Ustawa 2.0)

[7.5] Nauki biologiczne

Rok publikacji

2018

Opublikowano w

International Journal of Oncology

Rocznik: 2018 | Tom: 52 | Numer: 3

Typ artykułu

artykuł naukowy

Język publikacji

angielski

Streszczenie

EN Acute myeloid leukemia (AML) is the most common and severe form of acute leukemia diagnosed in adults. Owing to its heterogeneity, AML is divided into classes associated with different treatment outcomes and specific gene expression profiles. Based on previous studies on AML, in this study, we designed and generated an AML-array containing 900 oligonucleotide probes complementary to human genes implicated in hematopoietic cell differentiation and maturation, proliferation, apoptosis and leukemic transformation. The AML-array was used to hybridize 118 samples from 33 patients with AML of the M1 and M2 subtypes of the French-American-British (FAB) classification and 15 healthy volunteers (HV). Rigorous analysis of the microarray data revealed that 83 genes were differentially expressed between the patients with AML and the HV, including genes not yet discussed in the context of AML pathogenesis. The most overexpressed genes in AML were STMN1, KITLG, CDK6, MCM5, KRAS, CEBPA, MYC, ANGPT1, SRGN, RPLP0, ENO1 and SET, whereas the most underexpressed genes were IFITM1, LTB, FCN1, BIRC3, LYZ, ADD3, S100A9, FCER1G, PTRPE, CD74 and TMSB4X. The overexpression of the CPA3 gene was specific for AML with mutated NPM1 and FLT3. Although the microarray-based method was insufficient to differentiate between any other AML subgroups, quantitative PCR approaches enabled us to identify 3 genes (ANXA3, S100A9 and WT1) whose expression can be used to discriminate between the 2 studied AML FAB subtypes. The expression levels of the ANXA3 and S100A9 genes were increased, whereas those of WT1 were decreased in the AML-M2 compared to the AML-M1 group. We also examined the association between the STMN1, CAT and ABL1 genes, and the FLT3 and NPM1 mutation status. FLT3(+)/NPM1(-) AML was associated with the highest expression of STMN1, and ABL1 was upregulated in FLT3(+) AML and CAT in FLT3(-) AML, irrespectively of the NPM1 mutation status. Moreover, our results indicated that CAT and WT1 gene expression levels correlated with the response to therapy. CAT expression was highest in patients who remained longer under complete remission, whereas WT1 expression increased with treatment resistance. On the whole, this study demonstrates that the AML-array can potentially serve as a first-line screening tool, and may be helpful for the diagnosis of AML, whereas the differentiation between AML subgroups can be more successfully performed with PCR-based analysis of a few marker genes.

Strony (od-do)

656 - 678

DOI

10.3892/ijo.2017.4233

URL

https://www.spandidos-publications.com/ijo/52/3/656

Typ licencji

CC BY-ND (uznanie autorstwa - bez utworów zależnych)

Wersja tekstu w otwartym dostępie

ostateczna wersja opublikowana

Data udostępnienia

12.2017

Czas udostępnienia publikacji w sposób otwarty

przed opublikowaniem

Punktacja Ministerstwa / czasopismo

25

Punktacja Ministerstwa / czasopismo w ewaluacji 2017-2021

25