Increased expression of miR-221 is associated with shorter overall survival in T-cell acute lymphoid leukemia
- Hamilton L Gimenes-Teixeira1,
- Antonio R Lucena-Araujo1,
- Guilherme A dos Santos1,
- Dalila L Zanette2,
- Priscila S Scheucher1,
- Luciana C Oliveira1,
- Leandro F Dalmazzo1,
- Wilson A Silva-Júnior2,
- Roberto P Falcão1 and
- Eduardo M Rego1, 3Email author
© Gimenes-Teixeira et al.; licensee BioMed Central Ltd. 2013
Received: 4 March 2013
Accepted: 4 April 2013
Published: 8 April 2013
CD56 expression has been associated with a poor prognosis in lymphoid neoplasms, including T-cell acute lymphoblastic leukemia (T-ALL). MicroRNAs (miRNAs) play an important role in lymphoid differentiation, and aberrant miRNA expression has been associated with treatment outcome in lymphoid malignancies. Here, we evaluated miRNA expression profiles in normal thymocytes, mature T-cells, and T-ALL samples with and without CD56 expression and correlated microRNA expression with treatment outcome.
The gene expression profile of 164 miRNAs were compared for T-ALL/CD56+ (n=12) and T-ALL/CD56- (n=36) patients by Real-Time Quantitative PCR. Based on this analysis, we decided to evaluate miR-221 and miR-374 expression in individual leukemic and normal samples.
miR-221 and miR-374 were expressed at significantly higher levels in T-ALL/CD56+ than in T-ALL/CD56- cells and in leukemic blasts compared with normal thymocytes and peripheral blood (PB) T-cells. Age at diagnosis (15 or less vs grater than 15 years; HR: 2.19, 95% CI: 0.98-4.85; P=0.05), miR-221 expression level (median value as cut off in leukemic samples; HR: 3.17, 95% CI: 1.45-6.92; P=0.004), and the expression of CD56 (CD56- vs CD56+; HR: 2.99, 95% CI: 1.37-6.51; P=0.006) were predictive factors for shorter overall survival; whereas, only CD56 expression (HR: 2.73, 95% CI: 1.03-7.18; P=0.041) was associated with a shorter disease-free survival rate.
miR-221 is highly expressed in T-ALL and its expression level may be associated with a poorer prognosis.
KeywordsT-cell acute lymphoid leukemia miRNA CD56 Treatment outcome
Neural-cell adhesion molecule (N-CAM; CD56) is a known marker of natural killer (NK) cells . The two best characterized forms of NK-cell malignancy are the aggressive NK-cell leukemia (ANKL) and the extra nodal NK-cell lymphoma, nasal type (ENKL) [2, 3]. However, CD56 is also expressed on a subset of normal T cells and occasionally on blasts in T-cell acute lymphoblastic leukemia (T-ALL) . The expression status of CD56 identified a subgroup of patients with T-ALL who did not respond well to therapy [4, 5]. From an ontogenetic point of view, NK cells arise from T/NK bi-potential common progenitors [6, 7]; therefore, NK-cells are functionally and phenotypically very similar to T-cells, particularly cytotoxic T-cells.
MicroRNAs (miRNAs) play an important role in lymphoid differentiation and in innate immune response [8–10], and aberrant miRNA expression has been associated with treatment outcome in hematological malignancies [11–13]. Wang et al. demonstrated that miR-378 and miR-30e are suppressors of NK cell cytotoxicity and their expression is regulated by IFNα . Furthermore, Chiaretti et al. recently described a large set of myeloid-related miRNAs overexpressed in a subset of adult T-ALL patients; interestingly, the “myeloid-like” cases presented with higher expression levels of miR-223 and poorer prognoses compared with T-ALL patients without overexpression of myeloid-related genes .
Some miRNAs may be relevant in T-ALL leukemogenesis. Mavrakis et al. identified five miRNAs (miR-19b, miR-20a, miR-26a, miR-92, and miR-223) in a human T-ALL library that were capable of promoting T-ALL development in a mouse model . Moreover, these miRNAs acted synergistically with tumor suppressor genes implicated in the pathogenesis of T-ALL . In the present study, we compared expression of 164 miRNAs in T-ALL blasts with and without CD56 expression and correlated these profiles with T-cell development and treatment outcome.
Results and discussion
We did not detect differences in miR-221 and miR-374 expression when comparing triple positive thymocytes (CD3+/CD4+/CD8+) and mature T-cells in PB of healthy subjects. Our results do not corroborate the study by Kirigin et al. , which analyzed miRNAs in different stages of T-cell differentiation in the murine thymus and bone marrow using next generation sequencing. The authors demonstrated that there was greater expression of miR-221 and miR-222 in early stages compared with mature thymocytes. However, the comparison between the two studies must be regarded with caution because Kirigin et al.  have used a more complex strategy of cell sorting, and analyzed T-cell subsets that do not completely overlap with those of our study. The double positive (DP) thymocytes in their study had the immunophenotype CD90+CD4+CD8+CD3low and were compared with CD4 single positive (SP) (CD90+CD4+CD8-CD24lowCD3high), and CD8SP (CD90+CD42CD8+CD24lowCD3high) subsets. In addition, the most significant difference in miR-221 expression demonstrated by Kirigin et al.  was between double negative four (DN4, CD90+CD4-CD8-CD3lowCD44-CD25-) thymocytes and CD4SP and CD8SP mature T-cells , and such analysis was not performed in the present study.
miR-221 is up-regulated in several human malignancies; whereas, there are few reports associating miR-374 with tumorigenesis. Nevertheless, the mechanisms leading to the higher expression of these miRNAs are unknown. Recently, Santhekadur et al.  demonstrated that RNA Induced Silencing Complex (RISC) proteins SND1 and AEG-1 induce miR-221 expression in a NFκB dependent way in liver cancer cells. An alternative explanation would be that extracellular stimuli may interfere with miRNAs expression. With this regard, Davis et al.  demonstrated that miR-221 is a mediator of Platelet Derived Growth Factor (PDGF) signaling through modulation of p27Kip1. Remarkably, high levels of PGDF signaling were described as a decisive factor for proliferation and survival in cytotoxic T and natural killer cell neoplasms .
The transcription factor BCL11B has been identified as a putative target of miR-221 and it has been previously demonstrated that BCL11B expression is required to repress natural killer cell–associated genes and essential for T lineage commitment [20–22]. Overexpression of BCL11B was reported in T-ALL  and in adult T-cell leukemia/lymphoma  and its silencing in Molt-4 cells was associated with increased expression of the antiapoptotic protein Bcl-2 . Previously reported miR-221 targets include the cell cycle regulators CDKN1B/p27Kip1 and CDKN1C/p57Kip2 [25–27]. Le Sage et al.  demonstrated that cancer cell lines require high expression of miR-221/222 to maintain low p27kip1 levels and continuous proliferation. Therefore, it is conceivable that miR-221 acts as an oncogene through inhibition of p27kip1 in T-ALL. Another known target of miR-221 is the receptor c-KIT. Fellicetti et al.  showed an inverse correlation between miR-221 and miR-222 expression and c-KIT protein levels during melanoma progression. In addition, c-KIT is rapidly up-regulated following NOTCH signaling in T-cell development, and the development of primitive cells into non T-cell fates (NK or myeloid) was found to be c-kit independent .
Clinical and immunophenotypic features of T-ALL patients at diagnosis according to expression of miR-221 and miR-374
22.8 (1 – 66)
17.4 (2 – 44)
23.6 (1 – 66)
16.8 (2 – 44)
Mediastinal mass (%)
CNS involvement (%)
Blasts BM1 (%)
77.3 (20 – 100)
90.5 (28 – 100)
77.6 (20 – 100)
90.7 (28 – 100)
Blasts PB1 (%)
63.4 (0 – 100)
78.5 (10 – 100)
61.5 (0 – 100)
86 (10 – 100)
10.4 (3.6 – 15.6)
10.4 (4.6 – 17.1)
10.1 (3.6 – 15.8)
10.8 (5.3 – 17.1)
WBC1 count × 109/l
104 (4.6 – 314)
202.3 (4.5 – 790)
118 (4.5 – 781)
196 (18 – 789)
Platelets1 × 109/l
149.4 (9 – 652)
48.8 (9 – 185)
140 (9 – 652)
55.8 (9 – 231)
Pre thymic (%)
Mature T (%)
Univariate and multivariate analyses for CR, OS, and DFS in 48 patients with T-ALL
miR-221 expression (low vs high)
WBC counts (≤ 30×109/L vs > 30×109/L)
Age at diagnosis (≤ 15 vs > 15)
CD56 expression (CD56- vs CD56+)
miR-221 expression (low vs high)
WBC counts (≤ 30x109/L vs > 30×109/L)
Age at Diagnosis (≤ 15 vs > 15)
CD56 expression (CD56- vs CD56+)
miR-221 expression (low vs high)
WBC counts (≤ 30×109/L vs > 30×109/L)
Age at diagnosis (≤ 15 vs > 15)
CD56 expression (CD56- vs CD56+)
We selected the T-ALL/CD56+ and CD56- subgroups based on previous studies by Dalmazzo et al.  and Fischer et al. , which suggest that CD56 identifies a subgroup of patients with distinct immunophenotypic and clinical features, such as higher resistance to therapy and older age. Nevertheless, after risk adapted treatment, the prognostic impact of CD56 expression was not significant in the study by Fisher et al.  in contrast to the results reported by Dalmazzo et al. . We must point out that 47/48 (98%) patients reported here were also included in the study of Dalmazzo et al. , although the follow-up data were updated.
Our results suggest that miR-221 may be a useful biomarker in T-ALL. Patients with T-ALL/CD56-with high expression of miR-221, as well as those with T-ALL/CD56+ presented shorter OS and, therefore may require a more careful monitoring of the response to treatment and/or may be considered candidates to more intensive therapy. However, our conclusions are limited by the sample size and need to be further investigated in a larger cohort.
Forty-eight bone marrow samples from T-ALL patients were analyzed. All cases were diagnosed in the Hematology Laboratory of the University Hospital of the Medical School of Ribeirão Preto, University of São Paulo from May 1997 to April 2008. The diagnosis of T-ALL was established based on the World Health Organization criteria . Patients were treated according to the HyperCVAD  (n = 6), Berlin-Frankfurt-Munich 90 (BFM-90)  (n = 16), or Brazilian Childhood Leukemia Treatment Group – Acute Lymphoid Leukemia 99 (GBTLI-ALL99)  (n = 20) protocols. Six patients were excluded from survival analyses; one patient died before the beginning of treatment and the others five had no clinical data available. This study was approved by the local Ethics Committee (process #7147/2005).
Purification of thymocytes and peripheral blood T-cells
Thymic samples were obtained as surgical tissue discards from five pediatric patients (aged 2 days to 5 years) undergoing cardiac surgery at the University Hospital of the Medical School of Ribeirão Preto. Thymocytes were isolated by cutting the thymic lobes into small pieces and forcing them through plastic mesh. Triple positive thymocytes (CD3+/CD4+/CD8+) were purified by immunomagnetic separation (Miltenyi Biotec) after labeling with anti-CD4 and anti-CD8 antibodies, and then passed through a lymphocyte separation column (Miltenyi Biotec, Germany) for the positive selection of labeled cells. After isolation, all samples were more than 95% pure.
Peripheral blood mononuclear cells (PBMCs) from five healthy donors were harvested by centrifugation on Ficoll-Hypaque (Sigma Aldrich, USA) density gradients, and PB T/CD3+ cells were isolated using magnetic-activated cell sorting (MACS; Miltenyi Biotec, Germany), according to the manufacturer’s protocol. The homogeneity of PB T/CD3+ cells was confirmed by flow cytometry, and the purity was greater than 85% in all samples.
Immunophenotyping of the blasts was performed by flow cytometry. The technique and the panel of fluorochrome-conjugated monoclonal antibodies were described previously . We also expanded the panel and analyzed the expression of TdT, CD34, cytoplasmic CD3 (cCD3), surface CD3 (sCD3), CD4, and CD8 in leukemic cells. The minimum threshold for a positive reaction to a given antibody was defined as 20% of blasts positive for the respective antigen.
RNA extraction and real-time quantitative PCR of miRNAs
Total RNA from leukemic samples and healthy donors was isolated using Trizol reagent (Invitrogen, Carlsbad, CA, USA). Complementary DNA (cDNA) was synthesized from 1 μg of total RNA using a High Capacity cDNA reverse transcription Kit (Applied BioSystems, Foster City, CA, USA), following the manufacturer’s instructions. The TaqMan® MicroRNA Assays Human Panel (Applied BioSystems, Foster City, CA, USA) was employed to assess the expression levels of 164 miRNAs in leukemic samples. Due to the limited amount of RNA, we pooled the samples according to the immunophenotype (T-ALL/CD56+ versus T-ALL/CD56-) and performed a preliminary analysis comparing the two groups. Comparisons with coefficients of variation greater than 5% were excluded. We defined a strength cut-off for differential expression as ≥ 4 and ≤ 0.25. The fold change was calculated using the comparative cycle threshold (Ct) method, in which the geometric mean of expression of RNUs 6B, 19, 38B and 66 was used for normalization.
Based on this preliminary analysis, we decided to evaluate expression of miR-221 and miR-374 in individual T-ALL, normal thymic, and PB samples. TaqMan-based Real Time Quantitative Polymerase Chain Reaction (RQ-PCR) assays were performed using specific RT-stem-looped primers and probes (Applied BioSystems, Foster City, CA, USA). All reactions were carried out in duplicate.
The median values of miR-221 and miR-374 expression in leukemic samples were used as references to classify T-ALL patients into high and low expression groups. Student’s t and Fisher’s exact tests were employed to compare differences between the groups. Overall survival (OS) was estimated by the Kaplan–Meier method. Differences among groups were compared by log-rank test. Multivariate regression analysis was performed for OS using the Cox proportional hazards model. All P-values were two sided. The level of significance was set at 5%. All the statistical tests were performed using the Statistical Package for the Social Sciences (SPSS) v.17.0 software (SPSS Inc, Chicago, IL, USA) and Stata Statistic/Data Analysis 9.1 (Stata Corporation, College Station, TX, USA).
This study was supported by Fundação de Amparo a Pesquisa do Estado de São Paulo (FAPESP: Grant #1998/14247-6) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq: #573754/2008-0). H.L. Gimenes-Teixeira and A.R. Lucena-Araujo received fellowships from CNPq and FAPESP (grants no. 150349/2011-4 and 07/55067-1, respectively).
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