Gene mutational pattern and expression level in 560 acute myeloid leukemia patients and their clinical relevance

Background Cytogenetic aberrations and gene mutations have long been regarded as independent prognostic markers in AML, both of which can lead to misexpression of some key genes related to hematopoiesis. It is believed that the expression level of the key genes is associated with the treatment outcome of AML. Methods In this study, we analyzed the clinical features and molecular aberrations of 560 newly diagnosed non-M3 AML patients, including mutational status of CEBPA, NPM1, FLT3, C-KIT, NRAS, WT1, DNMT3A, MLL-PTD and IDH1/2, as well as expression levels of MECOM, ERG, GATA2, WT1, BAALC, MEIS1 and SPI1. Results Certain gene expression levels were associated with the cytogenetic aberration of the disease, especially for MECOM, MEIS1 and BAALC. FLT3, C-KIT and NRAS mutations contained conversed expression profile regarding MEIS1, WT1, GATA2 and BAALC expression, respectively. FLT3, DNMT3A, NPM1 and biallelic CEBPA represented the mutations associated with the prognosis of AML in our group. Higher MECOM and MEIS1 gene expression levels showed a significant impact on complete remission (CR) rate, disease free survival (DFS) and overall survival (OS) both in univariate and multivariate analysis, respectively; and an additive effect could be observed. By systematically integrating gene mutational status results and gene expression profile, we could establish a more refined system to precisely subdivide AML patients into distinct prognostic groups. Conclusions Gene expression abnormalities contained important biological and clinical informations, and could be integrated into current AML stratification system. Electronic supplementary material The online version of this article (doi:10.1186/s12967-017-1279-4) contains supplementary material, which is available to authorized users.


Background
Acute myeloid leukemia (AML) is a group of hematological malignancies, arising from stem cells, whose leukemogenesis and clinical behavior was deeply affected by the underlying cytogenetic and molecular abnormalities [1][2][3]. Classic cytogenetic aberrations such as chromosomal translocations to form oncogenic fusion genes via rearrangement of coding sequences of the involved partner genes, such as t(15;17), t(8;21), t(16;16)/inv (16), have long been considered as diagnostic markers of each subgroup of AML, and even served in the surveillance of minimal residual disease (MRD), and more importantly, designing tailored treatment for the disease [4][5][6][7][8]. For more refined stratification, or redefinition of AML, molecular analysis of gene mutation with potential clinical relevance has been more widely used in recent years [9,10]. Traditionally, it was suggested that genetic abnormalities in leukemia could be roughly grouped into two classes according to their roles in pathogenesis: Class I, mutations involving signal transduction pathways and giving rise to proliferative advantages to leukemia clones, exemplified as C-KIT, FLT3 and NRAS; and Class II, mutations affecting transcription factors (TF) or co-factors and causing impaired differentiation such as point mutation of CEBPA, AML1 and gene fusion of AML1-ETO [11]. In our previous work, a Class III mutation associated with epigenetic modifier was proposed, such as DNMT3A, IDH1, IDH2, and TET2, which shared a common feature of aggressive diseases, old age and poor prognosis [12]. With the development of second generation sequencing technology, a greater number of new gene mutations were identified in AML; which provides opportunities to more comprehensively understand and overview the gene events in the disease from a panoramic angle. Through whole genome and exome sequencing in 200 AML patients, Ley et al. suggested 9 categories of gene mutations in AML: NPM1, activated signaling, myeloid TFs, TF fusions, DNA methylation, chromatin modifier, tumor suppressors, cohesin complex, and spliceosome. However, their function and potential clinical translation in guiding treatment and judging prognosis should be further confirmed in future clinical trials [13].
Until now, the roles of a sizable portion of gene mutations are addressed and integrated in clinical practice. For instance, FLT3 and CEBPA mutations being the most common gene mutations in Western and Chinese populations respectively; represent poor and favorable indicators in AML (biallelic for CEBPA) [11,12,[14][15][16]. Gene mutations associated with epigenetic modification are also considered as poor factors, such as MLL, DNMT3A, TET2, and ASXL1 mutations [12,17,18], while mutant NPM1 is regarded as a favorable one [12,19,20]. In addition, numerous clinical studies have proven the role of tumor suppressor genes such as TP53 and WT1 in cytogenetic normal AML (CN-AML) [21][22][23][24] and C-KIT in core binding factor AML (CBF-AML) [25]. Metallothionein III (MT3) may also act as a tumor suppressor gene of which the promoter hypermethylation can inactivate the gene and downregulate its expression level in pediatric AML [26]. Similar to cytogenetic abnormalities, gene mutation events are now involved in the classification or nomenclature in AML. In a recent large series of 1540 patients, clinical relevance of gene mutations was analyzed, and a new genomic classification of acute myeloid leukemia was proposed, which includes the categories of mutated chromatin, RNA-splicing genes, TP53 mutations, biallelic CEBPA mutations, MLL fusion gene, GATA2, MECOM, IDH2, and t(6;9)(p23;q34)/DEK-NUP214, with each of the subtypes presenting distinct clinical behaviors [27].
How these gene mutations are involved in the leukemogenesis needs further investigation. It is believed that normal hematopoiesis and cellular differentiation is highly dependent on the transcriptional regulation systems. The expression of lineage-determining transcription factor is in strict time order. Gene alterations, including fusions and mutations, could lead to the abnormal expression of key genes, and these kinds of misexpression disrupt the TF-dependent genetic network. In recent years, the expression level of several genes became research interest, exemplified as MECOM (also termed EVI1 and PRDM3), BAALC, ERG and WT1. A remote GATA2 hematopoietic enhancer alteration in inv(3) (q21;q26) by activating EVI1 expression was reported [28]. It is believed that the expression level of these genes is negatively associated with the treatment outcome of AML [29][30][31][32][33]; however, the results are controversial between western and eastern countries especially for BAALC and ERG [34,35]. The role of some new gene markers, such as MEIS1, which is up-regulated by MLL abnormalities, still needs to be addressed in AML [36,37].
Hence, we performed this study to systemically investigate the role of a series of gene expression in AML, including previously known ones and newly established ones. Moreover, we intent to integrate these new markers into current established gene mutation profile to provide a more precise stratification of AML.

Patients
The newly diagnosed non-M3 patients were selected from Shanghai Institute of Hematology (SIH). Patients with leukemia either transformed from myelodysplasia syndrome (MDS) or secondary to other malignancies were excluded from this study. Cytogenetic analysis was performed centrally in SIH in every patient. The bone marrow (BM) samples of de novo AML patients were studied mostly by R-and/or G-banding analysis, and were confirmed in most cases with relevant molecular markers [38].
This study was approved by the ethic board of Ruijin hospital. All patients had given informed consent for both treatment and cryopreservation of BM and peripheral blood (PB) according to the Declaration of Helsinki.

Treatment protocols
Younger AML patients (age ≤ 60) received standard first line treatment of DA like regimen, which consisted of daunorubicin 45-60 mg/m 2 , D1-3; and Ara-C 100 mg/m 2 , D1-7. In the consolidation therapy, they were treated with high-dose cytarabine based chemotherapy for 4 cycles. For old patients (age > 60, n = 86), the treatment was mainly decided by the physician: fit patients underwent a regimen similar to younger patients, but with a reduced consolidation cycles of high dose Ara-C to 2 cycles; unfit patients, underwent either low dose treatment, demethylation treatment or palliative care [39].

Molecular genetic analysis
Gene mutations/fusions were detected as previously reported [12]. The WT1 [40] and ABL1 control gene [41] RQ-PCR assays were performed as described before. The MECOM, ERG, GATA2, BAALC, MEIS1 and SPI1 expression levels were quantified by using the TaqMan Gene Expression Assay assays, according to the manufacturer's instructions (Assay ID: Hs00602795_m1, Hs01554629_m1, Hs00231119_m1, Hs00227249_m1, Hs01017441_m1, Hs02786711_m1, respectively). These seven genes' transcripts were normalized to ABL1 by using the respective plasmid standards to generate normalized copy numbers. Reactions were performed using ABI ViiA ™ 7 (Life technologies, USA). Each sample was analyzed in duplicate. Data were reported using a common threshold of 0.1. Positive and negative controls were included in all assays.

Statistical analyses
Fisher's exact P test was used to compare the gene expression levels in different subgroups, as well as the difference of CR rates. One way Anova test was used to compare the clinical features such as age and WBC count in different groups. OS was measured from the date of disease diagnosis to death (failure) or alive at last follow-up (censored). DFS was defined as the duration from the documentation of CR to treatment failure such as relapse, refractory disease, death, or alive in CR at last follow-up (censored). Kaplan-Meier analysis was used to calculate the distribution of OS and DFS. Hazard ratio analysis was performed to compare the difference of survivals. Binary logistic regression and COX model was used for the multivariate analysis of associations between mutational status and the achievement of CR and OS and DFS, respectively. A limited backward selection procedure was used to exclude redundant variates. All above statistical procedures were performed with the SPSS statistical software package, version 16.0. We cut the expression level of WT1, BAALC and ERG into high and low group by their median values in patients according to the previous reports [30,32]. For the continuance of analysis, the cut-off levels of MECOM, MEIS1, GATA2 and SPI1 were also chosen at their median values. Survival analysis showed that median value as cut-off value could separate patients with different prognosis in MECOM, MEISI and SPI1 expression group (OS: P < 0.001, P < 0.001 and P = 0.010, respectively), while using cut-off value at quartile 1 (Q1) or Q3 would lose the power to separate the patients (Additional file 2: Figure S2).

Patient characteristics and gene expression level
560 patients were entered into this study including 474 young patients (age ≤ 60 years old) and 86 elderly patients (age > 60 years old). The patients were classified into 3 groups: Group 1, Core Binding Factor AML (CBF-AML), which includes 89 patients, Group 2, Cytogenetic intermediate risk AML, which includes 401 patients with normal karyotype (CN-AML, 320 patients) or cytogenetic aberration without prognostic significance, and Group 3, Cytogenetic high risk patients (55 patients) group. Among group 2, young patients with normal karyotype (265 patients) or insignificant cytogenetic aberration accounted for 84% (336 patients), while elderly patients accounted for 16% (65 patients) including 55 CN-AML patients. Cytogenetic results were failed or unavailable in 15 patients. The distribution of the patients in FAB classification and cytogenetic abnormalities of enrolled patients was listed in Additional file 3: Table S1.
Age was strongly associated with several gene expression levels. The patients with higher MEISI expression had the higher median age (P = 0.026). Similarly, in old patients (age > 60), more patients harbored higher MEIS1 and SPI1 expression levels (66.3% vs. 33.7%, P = 0.001; 60.5% vs. 39.5%, P = 0.035, respectively). Female patients tended to have higher expression of MECOM, MEIS1 and WT1 (P = 0.038, P = 0.010 and P = 0.032, respectively). The high SPI1 expression group manifested the feature of high WBC count at disease presenting (P = 0.003). The detailed clinical features were shown in Table 1.
The potential relationship of mutual co-existence and co-exclusion was observed between gene mutation group and investigated gene expression level. FLT3 mutations were associated with high MEIS1 (P < 0.001), WT1 (P < 0.001), and GATA2 (P = 0.004) and lower BAALC (P = 0.007) expressions, respectively; while C-KIT was associated with lower MEIS1 (P < 0.001), WT1 (P < 0.001) and GATA2 (P = 0.008) and higher BAALC (P < 0.001) expressions, respectively. At the same time, another class I mutation, NRAS was not associated with any gene expression level. The mutual exclusion of Class II mutations was also reflected in gene expression level. CEBPA was associated with lower MECOM (P < 0.001), MEISI (P < 0.001), SPI1 (P < 0.001), and WT1 (P < 0.001) expressions, respectively. NPM1 was related with lower ERG (P < 0.001) and BAALC (P < 0.001), but higher MEIS1 (P < 0.001), WT1 (P < 0.001) and GATA2 (P = 0.001) expression levels, respectively. Other potential mutual relationship with gene expression level was also observed in epigenetic modifier gene mutations, such as DNMT3A and IDH1/2, respectively. The detailed data were shown in Fig. 1 and Additional file 5: Table  S3. Similarly, the relationship of gene mutational status and gene expression level in intermediate risk AML was shown in Additional file 6: Table S4.

Response to induction therapy
Firstly, we validated the prognostic value of known gene mutations in cytogenetic intermediate risk patients of our group and also in a separate group of young patients who received uniformed treatment. In univariate analysis, it was shown that FLT3 (P = 0.036) and biallelic CEBPA (P = 0.009) mutations were associated with lower and higher CR rate, respectively. In different gene expression groups, higher MECOM, MEIS1 and SPI1 expression was associated with a lower CR rate (58.0% vs. 74.4%, P = 0.001, 61.2% vs. 75.8%, P = 0.002, and 62.3% vs. 72.5%, P = 0.030, respectively), while other factors were not associated with the induction outcome of the cytogenetic intermediate risk patients (Table 3). A complete list of covariates that entered multivariate model was indicated in Table 4. Multivariate analysis indicated that age and cytogenetic risk remained independent prognostic factors for CR induction outcome, while molecular profile added more informative value in predicting the treating results, exemplified as NPM1mut/DNMT3A-wt (OR = 3.389, 95% CI 1.519-7.562; P = 0.003) and high MECOM and MEIS1 expression (OR = 0.576, 95% CI 0.377-0.880; P = 0.011, and OR = 0.389, 95% CI 0.251-0.603, P < 0.001, respectively), respectively. A multivariate analysis was also performed in cytogenetic intermediate risk group AML patients. The results were similar in terms of gene expression level (Additional file 7: Table S5). And similar results of both univariate analysis and multivariate analysis could be observed in younger patients as well (Additional file 8: Table S6, Additional file 9: Table S7, Additional file 10: Table S8).

Survival analysis
Survival stratification was performed in the intermediate cytogenetic group, which consisted major part of AML (nearly 70%). In our group, the median OS and DFS were observed at 17 ± 2.3 and 27.5 ± 4.2 months (24 ± 3.1 and 30 ± 5.0 months for young patients), respectively (among which, the median OS and DFS of CN-AML were 19 ± 2.9 and 30 ± 4.8 months (26 ± 4.8 and 34 ± 6.9 months for young patients), respectively).
Similarly, according to gene expression level, in univariate analysis, high MECOM (HR = 1.875, P < 0.001 for OS; and HR = 1.558, P = 0.017 for DFS), high MEIS1 (HR = 1.836, P < 0.001 for OS; and HR = 1.550, P = 0.016 for DFS) and high SPI1 (HR = 1.402, P = 0.008 for OS; and HR = 1.448, P = 0.039 for DFS) were associated with the survival. The two parameters, MECOM and MEIS1, even had an additive effect, high MECOM and high MEIS1 group showed worst prognosis, low MECOM and low MEIS1 group presented most favorable treatment outcome, while either high MECOM or MEIS1 group was in the middle (Fig. 2i, j). WT1 could be served in further discriminating the patients with both low MECOM and MEIS1 group, the high WT1 expression was associated with poor OS (HR = 2.655, P = 0.002) and DFS (HR = 2.889, P = 0.002).
According to above analysis and inter-relationship of gene expression level, we further stratified cytoge-  (Fig. 3).
In multivariate analysis, in whole group of AML patients, age and cytogenetic risk remained independent  Table S5). For young patients, all the above survival analysis were performed and demonstrated with the similar results (Additional file 9: Table S7, Additional file 10: Table S8; Additional file 12: Figure S4, Additional file 13: Figure S5, Additional file 14: Figure S6).

Discussion
Cytogenetic analysis serves as a traditional tool to discriminate the prognosis of the AML [10,[43][44][45][46]. However, the shortcomings such as lack of sensitivity, labor and time cost limits the further application of this technique. Genetic mutations that escape cytogenetic detection have increasingly been discovered and these mutations may serve as potential markers to extend the prognostic parameters in AML. Numerous systemic investigations involving a series of genes have been performed in AML using first or second generation of sequencing techniques, and prognostic value has been analyzed, especially for the most common ones, such as NPM1, CEBPA, FLT3 etc. [11,13,47]. New generation sequencing broadens our eyes to view more deeply about these gene mutations, not only the clinical behavior and prognosis, but also the disease nature. More classes of gene mutations were named, and even used in defining the special subgroup of AML [27]. A significant progress could be observed that the diagnosis of the disease strides from a simple morphological 7 FAB subtypes to a much complicated system involving cytogenetic aberrations, gene mutations, and even gene expression levels. Nowadays, examination of gene mutations was almost routinely performed all over the world in AML field, and integrated into the daily practice in treating AML.
However, in addition to gene mutations, some gene expression levels, which are caused by the regulation of a certain gene, or even several genes, are also involved in leukemogenesis. Among them, MECOM expression was the most widely reported. It was firstly reported to be associated with a specific translocation with extreme poor prognosis, inv(3)(q21q26.2), which has lower incidence in AML [48,49]. Then, it was also identified to have a high expression level in AML with other cytogenetic abnormalities and even CN-AML, exemplified as in MLL-AF9 pediatric AML, which was associated with poor prognosis [31]; as well as in M4/5, or MLL rearrangement in another Japanese series with 130 pediatric AML patients [35]. In addition to MECOM, several groups use WT1 expression level to monitor the minimal residual diseases (MRD) in BM and PB in AML, whose increasing strongly indicates poor prognosis and relapse [40]. When compared with universal recognition, MECOM and WT1 over-expression are poor indicators, while clinical value of BAALC and ERG are controversial. Some genes of myeloid transcriptional factors are also drawn of attraction, such as GATA2 and SPI1; especially for MEIS1, which is proved to be regulated by MLL mutation in previous reports [36]. Although great efforts have been made in recent decades, systemic examination of gene expression level and their cytogenetic and gene mutation background in AML is still lack. We performed this study to examine the cytogenetic abnormalities, gene mutational profile in 560 AML patients, and more importantly, a series of gene expression levels, such as MECOM, WT1, ERG, BAALC, and 3 new ones with potential value, GATA2, SPI1 and MEIS1, to try to address this question.
Firstly, we identified that certain gene expression levels were associated with the cytogenetic aberrations of the disease. In this study, MECOM expression was identified to be low in CN-AML group, but high in 11q23 aberration group. MEIS1 expression was low in t(8;21) group, but high in the group with poor cytogenetic makers. High BAALC expression was associated with CBF-AML, but less distributed in CN-and 11q23 AML. Moreover, gene mutational status was also associated with the gene clinical behaviors of the diseases. Such kind of mutual relationship with gene expression level was also observed in epigenetic modifier gene mutations.
In treatment outcome analysis, univariate analysis showed that FLT3 and higher MECOM, MEIS1 and SPI1 expressions were associated with a lower CR rate (P = 0.036, 0.001, 0.002 and 0.030 respectively), while CEBPA (P = 0.009) mutations were associated with a higher CR rate. Higher MECOM and MEIS1 expressions remained significant in multivariate analysis, while NPM1-mut/DNMT3A-wt appeared to be an independent factor (P = 0.003). In survival, biallelic CEBPA mutations and NPM1-mut/DNMT3A-wt were associated with favorable OS (P < 0.001 and P = 0.010, respectively) and DFS (P = 0.002 and P = 0.044, respectively), respective, while FLT3-ITD/TKD (P < 0.001 and P < 0.001, respectively) and DNMT3A (P = 0.014 and P = 0.023, respectively) were associated with poor prognosis. As for gene expression profile, high MECOM (P < 0.001 for OS; and P = 0.017 for DFS, respectively) and high MEIS1 (P < 0.001 for OS; and P = 0.016 for DFS, respectively) levels were associated with the survival. An additive effect could be observed when we combined the two gene expression levels together, high MECOM and high MEIS1 group showed worst prognosis, low MECOM and low MEIS1 group presented most favorable treatment outcome. Furthermore, WT1 could help to separate the low risk group of low MECOM and MEIS1 group into a more refined subgroup, the high WT1/low MECOM and MEIS1 expression was associated with relative poor OS (HR = 2.655, P = 0.002) and DFS (HR = 2.889, P = 0.002).
Finally, we have established a new system to stratify the AML integrating cytogenetic risk, gene mutational status and gene expression profile. Through examination of traditional cytogenetic markers, gene mutations, exemplified as DNMT3A, MLL, NPM1, CEBPA, FLT3 mutations etc., and more importantly gene expression profile, especially for MECOM, MEIS1 and WT1, one could discriminate the AML patients with different clinical behaviors.

Conclusions
Gene expression aberrations are associated with the cytogenetic abnormalities and gene mutations in AML, as well as the clinical behavior of the patients. Of note, their value in predicting the prognosis of AML was demonstrated in this study.