BIRC6 (APOLLON) is down-regulated in acute myeloid leukemia and its knockdown attenuates neutrophil differentiation
© Schläfli et al.; licensee BioMed Central Ltd. 2012
Received: 4 August 2012
Accepted: 16 August 2012
Published: 4 September 2012
Inhibitors of apoptosis (IAPs) were intensively investigated in the context of cancer where they promote tumor growth and chemoresistence. Overexpression of the IAP BIRC6 is associated with unfavorable clinical features and negatively impacts relapse-free survival in childhood acute myeloid leukemia (AML). Currently, BIRC6 levels in adult primary AML have not been compared to the expression in normal myeloid cells. Thus, we compared for the first time BIRC6 levels in adult primary AML patient samples to normal myeloid cells and studied its regulation and function during neutrophil differentiation.
We found significantly lower BIRC6 levels in particular AML subtypes as compared to granulocytes from healthy donors. The lowest BIRC6 expression was found in CD34+ progenitor cells. Moreover, BIRC6 expression significantly increased during neutrophil differentiation of AML cell lines and knocking down BIRC6 in NB4 acute promyelocytic leukemia (APL) cells significantly impaired neutrophil differentiation, but not cell viability.
Together, we found an association of low BIRC6 levels with an immature myeloid phenotype and describe a function for BIRC6 in neutrophil differentiation of APL cells.
KeywordsBIRC6 Acute myeloid leukemia Acute promyelocytic leukemia ATRA Neutrophil differentiation
Inhibitor of apoptosis
Acute myeloid leukemia
Acute promyelocytic leukemia
All-trans retinoic acid
Bacalovirus IAP repeat
Acute lymphoblastic leukemia.
BIRC6 (a.k.a. APOLLON, BRUCE) is an exceptionally large protein of 528 kDa belonging to the family of inhibitor of apoptosis (IAP). BIRC6 contains one bacalovirus IAP repeat (BIR) domain that shows homology to the IAP Survivin. Furthermore, BIRC6 is the only IAP with an ubiquitin-conjugating domain further pointing to a particular function of this protein in the IAP family . Several groups reported that BIRC6 executes its function via inhibition of Smac and Caspase-9[2, 3]. Moreover, a study in breast cancer cells revealed that BIRC6 inhibits cell death by p53 destabilization and inactivation of caspase-3. The role of p53-dependent BIRC6 effector functions was confirmed by investigations of Ren et al. in mice and human lung cancer cells .
Due to their anti-apoptotic function it was hypothesized that overexpression of IAPs might contribute to tumorigenesis. Survivin, for example, one of the best studied IAPs is up regulated in most tumors and has been associated with their chemoresistence [6, 7]. Recently, Houdt et al.  observed BIRC6 overexpression in colon cancer stem cells when compared to more differentiated tumor cells. BIRC6 expression protected colon cancer stem cells from the cytotoxic effects of oxaliplatin and cisplatin. Furthermore, knocking-down BIRC6 led to growth inhibition in several cancer cell lines and xenografted mice and rendered the tumor cells more sensitive to 5-fluoruracil treatment in vivo and in vitro. The significance of IAPs in the pathology of hematological malignancies however remains poorly understood and controversial data regarding an effect on prognosis were published. Carter et al.  did not find any prognostic significance for Survivin or XIAP expression in adult AML samples, whereas BIRC6 overexpression is associated with unfavorable clinical features and negatively impacts on the 3-year relapse-free survival in childhood acute myeloid leukemia (AML) . Similar results were obtained by Ismail et al. in childhood AML and acute lymphoblastic leukemia (ALL) . Abe et al.  found lower expression of BIRC6 in bone marrow-derived cells of healthy donors compared to de novo AML samples.
To our knowledge, BIRC6 levels in primary AML have never been compared to the respective expression in normal myeloid cells. Thus, we aimed at comparing BIRC6 levels in a large cohort (n = 98) of adult AML patient samples and mature neutrophils from healthy donors. Since a hallmark of AML is a differentiation block of hematopoietic precursors at different developmental stages and since this block can be overcome by treating acute promylocytic leukemia (APL) patients with all-trans retinoic acid (ATRA) and low dose chemotherapy, we also analyzed the role of BIRC6 during neutrophil differentiation of AML cells.
Materials and methods
Primary patient samples
AML patient characteristics from the HOVON/SAKK cohort
No. of patients
Cell lines and culture conditions
The acute myeloid leukemia (AML) cell lines HL60, FAB M2, the ATRA-resistant subline HL60-R, NB4, FAB M3 (acute promyelocytic leukemia; APL), the ATRA-resistant subline NB4-R2 and HT93 were kept in RPIMI-1640 culture media (Sigma-Aldrich, Buchs, Schweiz) containing 10 % foetal bovine serum (FBS). In order to differentiate the AML cell lines towards granulocytes 1 μM all-trans retinoic acid (ATRA) was added to the cells that were seeded at a density of 0.2x106 cells/ml. Successful neutrophil differentiation was assessed by CD11b surface and by increased granulocyte colony-stimulating factor receptor (G-CSFR; CSF3R) mRNA expression.
Quantitative real-time RT-PCR (qPCR) and TaqMan Low Density Array (LDA)
For RNA extraction the miRCURY RNA Isolation Kit from Exiqon was used. RT-PCR has been described elsewhere . Quantitative measurement of BIRC6 and G-CSFR mRNA was performed using the TaqMan® Gene Expression assays Hs00212288_m1 and Hs00167918_m1, respectively (Applied Biosystems, Rotkreuz, Switzerland). LDA measurements as well as data analysis were done as described . HMBS primers and probes have been described previously . Measurements were carried out on an ABI PRISM 7500 Sequence Detection System (Applied Biosystems, Rotkreuz, Switzerland).
Generation of BIRC6 knock-down cell lines
NB4 cells were transduced with a lentiviral vector (pLKO.1) expressing a small hairpin (sh)RNA targeting the BIRC6 mRNA (NM_016252.x-2281s1c1, Sigma-Aldrich, Buchs, Schweiz). Lentivirus production has been described previously . As a non-targeting control we used the SHC002 lentiviral vector. Two days after transduction, NB4 cells were selected with 1.5ug/ml puromycin (Sigma-Aldrich, Buchs, Schweiz) for one week.
Cell viability assay
For Trypan blue exclusion assay cells were washed with PBS before diluting 1:10 in 0.4 % Trypan blue solution (Sigma-Aldrich, Buchs, Switzerland). For AnnexinV staining 1x105 cells were washed in 500 μl binding buffer (PBS with 0.33 g/L Ca2+) and resuspended in a final volume of 100 μl. 5 μl AnnexinV-PE were added (Immunotools, Germany) and the samples were incubated for 15 minutes at room temperature, before FACS analysis.
Differences between two groups were assessed using the non-parametric Mann–Whitney-U test. P-values <0.05 were considered to be statistically significant.
Repression of BIRC6 mRNA in AML patients with particular chromosomal aberrations
Significant BIRC6 inductions during ATRA-induced neutrophil differentiation
Overall, our findings clearly show an association of increased BIRC6 expression with neutrophil development of AML and CD34+ progenitor cells.
Knocking down BIRC6 attenuates neutrophil differentiation but not cell death and proliferation of APL cells
Since BIRC6 is involved in the inhibition of apoptosis, we were asking if the observed lack of neutrophil differentiation in NB4 BIRC6 knockdown cells is due to increased cell death in these cells. For this purpose we assessed cell death by Trypan blue exclusion and Annexin V flow cyotometry at day 4 and 6 of ATRA treatment. We did not find any significant differences in cell viability between NB4 control and BIRC6 knockdown cells during ATRA-induced neutrophil differentiation (Figure 3D and E). Furthermore, control transduced as well as BIRC6 knockdown NB4 cells showed no significant differences in total cell counts at day 4 and 6 of ATRA treatment (Figure 3F).
In summary, we showed that inhibiting BIRC6 significantly affects neutrophil differentiation of APL cells, but not cell viability.
In this report we publish for the first time that AML patient samples with the t(8;21), the t(15;17) or a complex karyotype express BIRC6 significantly lower than normal human granulocytes. Subtype-specific BIRC6 expression in AML is supported by earlier findings published by Ismail et al. . Low expression of the anti-apoptotic IAP BIRC6 in AML may seem controversial given the often high expression of IAPs in cancer. Our findings of high BIRC6 expression in granulocytes versus AML may reflect the cellular differentiation status of these cells rather than a cancer-associated deregulation. This hypothesis is confirmed by our observation that BIRC6 mRNA levels are clearly reduced in CD34+ myeloid precursor cells and increase during granulocyte differentiation. These data are in line with previous findings showing that BIRC6 is down-regulated in bone marrow-derived cells if compared to de novo AML samples . Furthermore, the expression of the BIRC6 related XIAP is induced upon monocyte differentiation and contributes to monocyte cell survival. In the same study, XIAP levels declined during neutrophil differentiation supporting the cell type specific regulation of IAPs in myeloid cells . Consistent with the monocyte specific expression of XIAP, a correlation of XIAP levels with monocytic markers in AML was found . In contrast to these finding in adult AML, in childhood de novo acute myeloid leukemia the levels of XIAP correlated with an immature FAB-subtype . This may suggest different XIAP functions in distinct leukemic entities.
In conclusion, we were able to link increased BIRC6 mRNA expression with neutrophil differentiation and inhibiting BIRC6 resulted in attenuated neutrophil differentiation but did not alter cell survival. In summary, we established a new role for BIRC6 in neutrophil differentiation of AML cells.
We gratefully acknowledge Dr. P.J.M. Valk and Dr. B. Löwenberg and the HOVON (Dutch-Belgian Hematology-Oncology) cooperative group for providing primary AML patient samples. Deborah Shan and Joy Chen are acknowledged for excellent technical support. This work was supported by grants from Cancer Research Switzerland KFS 02486-08-2009 (to MPT), the Bern University Research Foundation (to MPT), the Ursula-Hecht-Foundation for Leukemia Research (to MFF), the Bernese Foundation of Cancer Research (to MFF), the Marlies-Schwegler Foundation (to MFF), the Werner and Hedy Berger-Janser Foundation of Cancer Research (to MFF and MPT), and the Joyce Klein Stock Gift and NIH R01HL091219 (to BET).
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