Leukaemic stem cell (LSC) persistence remains a major obstacle to curing chronic myeloid leukaemia (CML). The bone morphogenic protein (BMP) pathway is deregulated in CML, with altered expression and response to the BMP ligands shown to impact on LSC expansion and behaviour. In this study, we determined whether alterations in the BMP pathway gene signature had any predictive value for therapeutic response by profiling 60 CML samples at diagnosis from the UK SPIRIT2 trial and correlating the data to treatment response using the 18-month follow-up data. There was significant deregulation of several genes involved in the BMP pathway with ACV1C, INHBA, SMAD7, SNAIL1 and SMURF2 showing differential expression in relation to response. Therapeutic targeting of CML cells using BMP receptor inhibitors, in combination with tyrosine kinase inhibitor (TKI), indicate a synergistic mode of action. Furthermore, dual treatment resulted in altered cell cycle gene transcription and irreversible cell cycle arrest, along with increased apoptosis compared to single agents. Targeting CML CD34+ cells with BMP receptor inhibitors resulted in fewer cell divisions, reduced numbers of CD34+ cells and colony formation when compared to normal donor CD34+ cells, both in the presence and absence of BMP4. In an induced pluripotent stem cell (iPSC) model generated from CD34+ hematopoietic cells, we demonstrate altered cell cycle profiles and dynamics of ALK expression in CML-iPSCs in the presence and absence of BMP4 stimulation, when compared to normal iPSC. Moreover, dual targeting with TKI and BMP inhibitor prevented the self-renewal of CML-iPSC and increased meso-endodermal differentiation. These findings indicate that transformed stem cells may be more reliant on BMP signalling than normal stem cells. These changes offer a therapeutic window in CML, with intervention using BMP inhibitors in combination with TKI having the potential to target LSC self-renewal and improve long-term outcome for patients.
Chronic myeloid leukaemia (CML) treatment involves targeting BCR-ABL to prevent its tyrosine kinase activity. TKIs effectively target progenitor cells, however leukaemic stem cell (LSC) are more quiescent and less sensitive to treatment1,2,3,4,5. Studies of CML patients on imatinib mesylate (IM) treatment for >4 years indicate BCR-ABL+ cells are retained in the primitive CD34+ CD38− population, even when a deep molecular response is achieved, thus CML LSC are not eradicated6,7. Recent clinical trials ‘The Stop Imatinib 1 (STIM1) and the STOP 2G-TKI Study’ are very encouraging with 38% and 43% of patients, respectively, sustaining long-term molecular responses when TKI was discontinued8,9. For many patients, TKI treatment alone is insufficient to cure CML, even when a sustained deep molecular response has been achieved, highlighting different pathophysiology for some patients.
Interest has therefore focused on developing new treatments to use in combination with TKI, thereby improving the number of patients who can discontinue treatment in the future without relapse. A feasible therapy approach would involve combining TKI with compounds to target alternative survival mechanisms, such as self-renewal pathways involved in HSC maintenance in the bone marrow (BM) niche and deregulated in CML10,11,12,13. These embryonic morphogenic pathways have a key role in hematopoiesis, with evidence suggesting LSCs hijack them to their advantage, making the BM microenvironment more suitable for their survival and proliferation14.
The TGFβ superfamily, including the bone morphogenic proteins (BMP) are important for sustaining BM homoeostasis. Transcriptome studies of CML LSCs and progenitors indicate that the TGFβ and BMP ligands are downregulated in chronic phase (CP)-CML, suggesting an extrinsic mechanism for TGFβ involvement in this disease15. Intriguingly, the BMP type I receptors, especially BMBR1B are overexpressed in CML LSCs, whereas SMAD1, BMP2 and BMP4 are downregulated16. Supporting our published microarray data17, which confirms that the BMP pathway and downstream signalling molecules are significantly deregulated in CP, accelerated phase (AP) and blast crisis (BC) CML in both primitive LSCs and progenitor subpopulations. These findings suggest CML LSCs may change their reliance/response to the BMP/TGFβ superfamily, especially as the disease progresses from CP to AP/BC17. This is supported by a study showing significantly higher levels of BMP2 and BMP4 ligands are present in CML patients’ BM, compared to normal donors. Moreover, CP-CML early progenitors express higher levels of type I receptors, making them more responsive to the increased levels of soluble BMP2 and BMP4 in the leukaemia BM niche, resulting in expansion. CML LSCs, when cultured in the presence of BMP2 or BMP4, maintained their primitive phenotype with enhanced long-term colony-forming potential16. LSCs from TKI-resistant patients also express higher levels of BMPR1B, BMP4 and TWIST1 with treatment preferentially selecting survival of BMPR1BHi cells within the immature population. Mesenchymal stem cells (MSC) from these patients also displayed higher levels of BMP4 secretion18. These data indicate that alterations in the BMP pathway may suppress differentiation and potentiate the survival of a permanent autonomous pool of LSCs in CP-CML.
In this study, we evaluate the BMP pathway and downstream targets in 60 CP-CML patients at diagnosis. These findings were correlated to treatment response to identify a subset of genes differentially expressed between good/intermediate/poor responders to treatment. We demonstrate targeting the BMP receptors (ALKs) in combination with IM is synergistic, resulting in irreversible cell cycle arrest and increased apoptosis of CML cells. Furthermore, CML CD34+ cells display greater sensitivity to BMP pathway inhibition than normal CD34+ cells, undergoing fewer cell divisions, with reduced CD34+ cells numbers and colony formation occurring following treatment. Furthermore, CML-iPSCs express higher levels of ALKs than normal iPSCs and are more sensitive to ALK inhibition, resulting in a reduced capacity to self-renew. Overall, our findings indicate a potential therapeutic window whereby dual treatment with TKI and ALK inhibitors could selectively target CML stem cells.
The BMP/SMAD pathway is deregulated in CP-CML
To characterise the BMP pathway, we analysed 60 CP-CML samples from the UK-based SPIRIT2 trial. A significant number of BMP-related genes were differentially expressed (Fig. 1a) in CML. Relative to normal controls, BMP2, TGFβ1, AVCR1 (ALK2), BMPR1A (ALK3), SMAD1 and SMAD2 showed opposite expression patterns when comparing the more primitive CML CD34+ population to the more mature MNCs. However, ACVR1B (ALK4), BMPR1B (ALK6), ACVRIC (ALK7), ACVR2A, SMAD5 SMAD6, RUNX1 and RUNX2 showed the same expression pattern in both populations. Using the 18-month follow-up data, patients were stratified into optimal, warning and treatment failure categories (termed “good/intermediate/poor TKI responders”) according to the European LeukemiaNet 2013 TKI response criteria19. We tracked gene expression patterns to clinical response, to identify a gene signature for TKI-responders vs non-responders (Fig. 1b and Table 1). In CD34+ samples, three genes ACVR1C, INHBA, SMAD7, and in MNC samples, four genes SMAD1, INHBA, SMURF2 and SNAIL1 showed significant differential expression in the good/intermediate/poor TKI responders. Interestingly, INHBA was the only gene upregulated in both the CD34+ and MNC intermediate/poor responders, this correlates with our previous data, indicating that INHBA is significantly upregulated in BC-CML LSC when compared to CP, and AP LSC, and normal HSC17 (GEO:GSE47927).
ALK inhibitors act synergistically with IM
Next we inhibited BMP signalling using two ALK inhibitors, LDN and DOR20,21. IC50 values determined from XTT assays and trypan blue exclusion experiments were used to set up combination drug analyses with IM in K562 cells. Synergy calculations performed using CalcuSyn. Both LDN and DOR act synergistically with IM (Fig. 2a), with combination treatment more effective at eradicating leukaemic cells than single agents. Specificity of action was confirmed by immunoblotting (Fig. 2b) with dual inhibition significantly reducing phosphorylation of BCR-ABL, CrKL and STAT5. DOR and LDN both inhibited the BMP pathway with reduced pSMAD1/5/8 (R-SMADs) observed ±BMP4 (Fig. 2b, c); IM had no effect. Treatment of CD34+ CP-CML cells with LDN or DOR ±IM resulted in downregulation of BMP-related genes, especially the SMAD and SMURF family of genes. Interestingly Activin A and it’s receptor BMPR1A (ALK3) were upregulated following inhibition especially following IM/DOR treatment, this was accompanied by upregulation of SMAD7 an Activin A inducible gene, which is a potent antagonist of TGFβ1 signalling (Fig. 2d).
The impact of targeting the BMP pathway on the cell cycle
BCR-ABL is a potent driver of cell cycle, with IM causing G1 cell cycle arrest in CML. To ascertain the status of key genes involved in G1-S progression, we profiled the SPIRIT2 samples. Fig 3a clearly demonstrates important drivers of G1-S phase transition such as CyclinE and CDK2 are upregulated in CP-CML. Interestingly, CML MNC express significantly higher levels of cell cycle genes than normal donors, indicative of the more immature/proliferative nature of the BCR-ABL-transformed cells. Using pathway analysis software, we mapped the links between BMP signalling and cell cycle in CML using gene profiling data (Figure S1).
BMP signalling upregulates the inhibitor of differentiation/DNA binding (ID) family of early response genes22. BCR-ABL also induces ID1 with high levels observed in CML22,23. ID expression is necessary for re-entry of quiescent cells into the cell cycle and G1-S progression24. Next, we ascertained whether treatment of CD34+ cells with IM alone and in combination with BMP inhibitors affected ID1 expression. As shown, IM reduced the expression of ID1 compared to NDC with expression further reduced in the combination approach (Fig. 3b). Cell cycle progression analysis showed DOR was more effective than LDN at perturbing progression in K562 cells (Fig. 3c). Treatment with IM or DOR arrested CML cells in G0-G1 phase, accompanied by a reduction in S/G2M (Fig. 3c–i). This increased with dual inhibition (Fig. 3c–ii). Assessment of cell cycle after dual IM/DOR treatment for 24 h followed by wash-out, indicates cell cycle arrest is irreversible (Fig. 3d–i). Gene profiling shows IM reduces the expression of CDK genes at 24 h with DOR having minimal effect at this time point (Fig. 3d–ii). Following treatment and wash-out, IM reduced the expression of CCNA1, CCNA2, CDC25A, CDC25B, E2F3 and E2F6 with dual inhibition (IM and DOR) further reducing expression (Fig. 3d–ii). Cell cycle analysis of CML CD34+ cells, revealed they were more sensitive to all treatment arms than normal CD34+, with a significant increase in cells in sub-G0 following dual treatment with LDN + IM, DOR alone and DOR + IM (Fig. 3e–ii). Similar results were obtained in the presence of BMP4 stimulation (Fig. S2A), with no changes when CD34+ were co-cultured on the stromal cell line HS5 (Figure S2B). Comparison of all the cell cycle data (Fig. S2C & D) indicates co-culture has a protective effect on CD34+ cell cycle arrest, preventing them from entering Sub-G0 following ALK inhibition. Important cell cycle genes also changed (Fig. 3f), with downregulation of CDC25A, CDC25B and CDC25C. CDKN1B, CDK6, ATM and TP53 enhanced when IM and ALK inhibitors were combined.
Dual inhibition results in increased apoptosis
To measure apoptosis, Annexin V/7AAD assays were performed in K562 (Fig. 4a), normal and CP-CML CD34+ cells (Fig. 4b). Inhibition of BCR-ABL and ALKs shifted CML cells into apoptosis. Results were more profound in IM + ALK inhibitor combination arms, with significantly higher levels of apoptosis observed in the CML CD34+ (Fig. 4b–ii, S3E) when compared to normal CD34+ cells (Fig. 4b–i, S3E). Similar results were observed in the presence of BMP4 stimulation (Fig. 4b–iii, iv & S3B). Co-culture on HS5 protected CD34+ cells from undergoing apoptosis in response to treatment (Fig. S3C–E). Higher levels of apoptosis occurred at 72 h in the NDC for normal and CML CD34+ cells co-cultured on HS5 (Fig. S3C–E), this is due to the increased proliferation observed, with on average a twofold expansion of cell numbers when compared to culture on plastic ±BMP4 at 72 h.
ALK inhibition reduces CML CD34+ cell division and numbers
To determine what effects BMP pathway inhibition had on cell division and overall CD34+ cell numbers, CD34+ cells were labelled with CellTrace™ Violet (CTV) and an APC-conjugated anti-CD34 antibody. Following 72 h drug treatment, proliferation and CD34-positivity were assessed by flow cytometry. Figure 5a & S4B clearly demonstrate that both normal and CML CD34+ cells are sensitive to DOR treatment, undergoing less cell divisions than NDC. CML CD34+ cells displayed enhanced sensitivity, responded to all treatment arms with more cells accumulating in CTVmax and early divisions than observed for normal CD34+, with the most dramatic effects observed within the DOR, IM + LDN and IM + DOR treatment arms (Fig. 5a–ii and S4B). Similar results were observed in the presence of BMP4 stimulation (Fig. 5b and S4C). Although BMP4 stimulation did not alter the capacity to divide, untreated CML cells underwent a 20.5% ± 12.6% (n = 3) expansion in CD34+ numbers following BMP4 stimulation, with no change observed in normal CD34+ numbers (Figure S4E–iii), confirming CML cells are more responsive to BMPs16. Co-culture on HS5 rendered the drugs less effective, however CML cells still accumulated in CTVmax and division 1 following DOR, IM + LDN and IM + DOR treatment, indicating the BMP inhibitors were still eliciting an effect albeit to a reduced capacity (Figure S4A & D). Figure 5c and S4E clearly demonstrate that IM, LDN and DOR lead to a reduction in CML CD34+ cells, with the biggest reduction observed following DOR, IM + LDN and IM + DOR treatment. To determine what effects inhibition had on CML cell expansion and differentiation along the different hematopoietic lineages, CFC assays were performed. In CML, CFCs were significantly decreased in all treatment arms with less colonies observed following combination treatment (Fig. 5d–ii, iii) with no significant effects on normal CD34+ (Fig. 5d–i). These findings indicate viable CML cells surviving 72 h of dual treatment are unable to proliferate and differentiate to the same capacity compared with IM alone, indicating BMP inhibitors may act synergistically with IM to target CML cells through irreversible cell cycle arrest and apoptosis.
CML-iPSC are reliant on the BMP pathway for their self-renewal
To investigate whether CML stem cells are more dependent on the BMP pathway than their normal counterparts, we utilised iPSC models. We generated iPSCs from CD34+ selected cells from normal donors and CP-CML patients (Fig. 6a). All six lines demonstrate typical characteristics of pluripotent stem cells; compact morphology, strong alkaline phosphatase (APh) activity, high expression of key pluripotency transcription factors and pluripotent cell surface markers. FISH analysis confirmed the presence of the Philadelphia chromosome in the three CML-iPSCs lines (Fig. 6a, b). Similar to CML CD34+ cells, gene profiling indicate components of the BMP pathway were differentially expressed in CML-iPSCs compared to normal iPSCs, with BMP2 strongly downregulated and SMURF1 strongly upregulated (Fig. 6c). To check the ability of normal and CML-iPSCs to respond to BMP ligands, we analysed AVCR1 (ALK2), BMPR1A (ALK3) and BMPR1B (ALK6) expression ±BMP4 stimulation by FACS. CML-iPSCs expressed significantly higher levels of AVCR1 (ALK2) and BMPR1A (ALK3) receptors than normal iPSCs, with high levels of BMPR1B (ALK6) expressed by both (Fig. 6d–i). Treatment with IM, BMP inhibitors or in combination, ±BMP4 stimulation, resulted in a significant reduction in AVCR1 (ALK2) expression (Fig. 6d–ii), with no changes in BMPR1A (ALK3) and BMPR1B (ALK6) (data not shown) in CML-iPSCs. Treatment had no effect on normal iPSCs (data not shown). Cell cycle analysis revealed altered profiles in CML-iPSCs compared to normal iPSCs with fewer cells in the sub-G0 stage and more in G0-G1 ±BMP4 stimulation (Fig. 6e). BMP signalling is important for controlling cell cycle, we therefore assessed the effects of single and dual treatments on cell cycle, ±BMP4 stimulation in our iPSC model of CML. Following 72 h treatment, no significant changes in the cell cycle profile occurred regardless of drug treatment or BMP4 stimulation (Figure S5A). To assess signalling pathways affected by BCR-ABL, we monitored the phosphorylation of pCrkL by immunoblotting following 4 h of treatment ±BMP4 stimulation in normal and CML-iPSCs (Fig. 6f–i). As expected, normal iPSCs have very low levels of CrkL with no change in phosphorylation observed following drug treatments or BMP4 stimulation. Whereas CML-iPSCs had high levels of pCrkL, which was significantly reduced following IM and DOR treatment. Densitometry analysis indicated IM + DOR had a synergistic effect on reducing pCrkL levels (Fig. 6f–ii).
A fundamental property of iPSCs is their ability to self-renew. Live APh staining was used to monitor pluripotent state in CML- and normal iPSCs treated with single and dual therapies for 72 h (Fig. 7a). APh stain intensity (green) was compared to total stain (orange); NDC sample was used as a comparator in each set. CML-iPSCs differentiated more than normal iPSCs when treated with IM and ALK inhibitors. This effect was more evident when colonies were treated with IM alone or in combination with DOR (Fig. 7b) especially following longer drug treatments (Figure S5B–i, ii) with dual inhibition more effective at reducing the pluripotency of CML-iPSCs. Single and dual inhibition also caused reduction in the expression of important pluripotency genes in CML colonies only, with all the genes assessed reduced by dual inhibition (Fig. 7c). Analysis of key differentiation genes indicate cells are primed to undergo meso-endodermal differentiation with ACTC1, MESP1 and PODXL all being upregulated following dual inhibition of CML-iPSCs (Fig. 7d). Overall these results indicate that CML-iPSC depend more on BMP signalling to sustain their stem cell properties than normal iPSC.
In CML, minimal residual disease persists in many patients on TKIs, with a high level of relapse occurring if TKI is withdrawn8,9. Therefore, additional kinase-independent mechanisms involved in LSC persistence need to be identified and targeted if treatment-free remission is to be achieved. Recent evidence indicates that some of the important regulatory networks involved in establishing primitive and definitive hematopoiesis during development are reactivated in leukaemias, giving rise to a LSC population with altered self-renewal and differentiation properties25. One pathway warranting further investigation is BMP signalling. BMPs are fundamentally important for osteoblast differentiation26,27, self-renewal and maintenance of HSCs, and expansion and differentiation of progenitor cells into mature hematopoietic cells28,29,30,31. Previously, we and others highlighted that the BMP pathway was deregulated in CML15,17. Furthermore, an earlier study demonstrated higher than normal levels of BMP ligands in the BM of CML patients and enhanced expression of BMPR1B receptor by CP-CML CD34+, with BMP2 or BMP4 stimulation, maintaining their primitive phenotype16. Data from the same group demonstrated that high BMPR1B and TWIST1 expression is linked to treatment resistance and disease progression32, with treatment resulting in upregulation of TWIST1 and selecting for survival of BMPR1BHi cells18. Furthermore, the LSC and MSC populations from these patients expressed higher levels of BMP4. In LTC-IC assays performed on BMPR1BHi and BMPR1BLo LSC, more LTC-IC were present in the presence of BMP2/4 and following IM and IM/IFNα treatment in the BMPR1BHi LSC, indicating the BMP signalling pathway has an important role in LSC maintenance and CML disease persistence18.
Components of the BMP pathway were significantly deregulated in both CD34+ cells and MNCs from CP-CML SPIRIT2 samples. In CD34+ cells, BMP2 was downregulated, whereas type 1 receptors AVCR1 (ALK2), BMPR1B (ALK6), TGFβΡ1 and several of the SMAD genes were upregulated. In contrast, BMP2 transcript was upregulated in MNC along with BMPR1A (ALK3), BMPR1B (ALK6) and SMADs. These findings support previous findings showing BMP2 is produced by the mature CML polymorphonuclear cells, and CML CD34+ cells are likely to have potentiated signalling in response to ligand16. TGFβ signalling is linked to poor TKI response in CML, with enrichment of the pathway observed at the single-cell level in poorly responding BCR-ABL− and BCR-ABL+ CML cells33. TGFβ signals through Foxo3A to confer apoptosis resistance in CML LSC34. Also TGFα is a potential biomarker for predicting patient response to TKI, with high levels in patient serum at diagnosis correlating to a failure to obtain a major molecular response35.
Correlating our expression data to TKI response, three genes (ACVR1C, INHBA and SMAD7) in the CD34+ samples, and four genes (SMAD1, INHBA, SMURF2 and SNAIL1) in the MNC samples, showed significant differential expression between the good/intermediate/poor responders. INHBA was more highly expressed in the poor response group, and is highly expressed in BC-CML17. Treatment of K562 with IM and the BMP pathway inhibitors also resulted in upregulation of Activin A and its receptor along with SMAD7 an Activin A inducible gene, which is a potent TGFβ1 antagonist. Interestingly, high levels of INHBA, correlates inversely with survival in solid tumours36,37 and is linked to immunosuppression38. In multiple myeloma, high levels of Activin A correlates with disease progression due to its role in BM niche remodelling through osteolysis39. Activin A via non-canonical SMAD2 signalling can also activate β-catenin leading to upregulation of the TCF/LEF transcriptional regulators38, a pathway well described in CML progression and TKI resistance40. These findings indicate an important role for BMP/TGFβ superfamily in the pathogenesis of CML and a potential switch from BMP to Activin A signalling in treatment resistance and progressive disease.
Cell cycle deregulation is well documented in CML41,42,43, with BMP signalling important for G1-S progression44. Targeting the BMP pathway in combination with TKI in CML resulted in cell cycle arrest, apoptosis and altered target gene expression. Moreover, cell division analysis revealed that DOR prevents CML CD34+ from dividing and reduces the total number of CD34+ cells, with similar results observed in the IM + DOR treatment arm. Total CFC counts also illustrate that the combination treatment had a more potent effect on long-term CML cell survival and colony formation than single-agent treatment. Analysis of normal CD34+ cells revealed significantly less sensitivity to the BMP pathway inhibition, indicating a potential therapeutic window to target this pathway in CML. Importantly, given the high BMP4 concentrations in the BM, inhibition of the pathway still occurred following BMP4 stimulation using both BMP pathway inhibitors.
We generated iPSCs as a stem cell model, the rationale for this approach was that pluripotent stem cells rely on the BMP pathway for self-renewal45,46,47 and the BMP pathway is important throughout HSC ontogeny, with recent evidence indicating that the first definitive HSC which arise during development are BMP-primed48. This enables HSCs to sustain their myeloid–lymphoid differentiation potential as they migrate and expand within different anatomical sites during development. However, by the time the HSCs populate the BM, the majority are no longer BMP activated, which could potentially reflect cell autologous changes or the influence of the different extrinsic signals within the BM microenvironment48. Reactivation of the pathway in CML could therefore have important influences on stem cell behaviour, especially cell fate decisions. Cell cycle regulation is tightly linked to pluripotency and stem cell fate. Here we demonstrate that higher numbers of CML-iPSCs are in G0-G1 compared to normal iPSCs, regardless of BMP4 stimulation. This is important as this property in LSCs promotes their quiescence even in the presence of TKI therapies. Targeting the iPSC lines had no effect on cell cycle progression in the presence or absence of BMP4 stimulation. However, our results indicate CML-iPSCs are sensitive to IM treatment, reflected through their increased differentiation when treated, highlighting a role for BCR-ABL in the stemness properties of CML-iPSCs. Our protein data correlates with previous studies, demonstrating phosphorylation of STAT5 and CrKL is significantly decreased after IM treatment49. Here we demonstrate that IM and DOR combination treatment synergistically reduces the phosphorylation of BCR-ABL and CrkL in CML-iPSCs.
CML progenitors express higher levels of BMPRIs on their surface16. Our iPSC data indicate CML-iPSCs also have significantly higher levels of ALK2 and ALK3 when compared to normal iPSCs, which is sustained in the presence of BMP4 stimulation. Inhibition of the BMP pathway alone and in combination with BCR-ABL significantly decreases the expression level of AVCR1 (ALK2) in CML-iPSCs. More importantly, we demonstrate that CML-iPSCs show a greater level of sensitivity to the dual treatments, which result in loss of pluripotency and increased differentiation when compared to normal iPSCs. This was confirmed by the upregulation of key genes involved in meso-endodermal differentiation and the downregulation of important pluripotency genes including NANOG. These findings highlight how deregulated BMP signalling in CML could lead to an altered balance between self-renewal and differentiation.
BMP/SMAD signalling regulates early response genes through BMP-responsive elements (BRE) in their promoters, including ID1, important for development, cell cycle G1 progression and tumorigenesis45,50. ID1 is upregulated in CML22,51,52 and promotes proliferation and migration50. ID1 expression is also enhanced through BCR-ABL-mediated STAT5 activation51. The ID1 promoter has a SRC-responsive element upstream of the translational start site, with SRC co-operating with SMAD to induce its expression53. Given that BCR-ABL interacts and activates SRC kinases, ID1 upregulation through BCR-ABL dependent and independent mechanisms is likely to have a key role in CML pathophysiology. Our data clearly demonstrate that IM reduces transcriptional levels of ID1 with further reductions in the presence of LDN and DOR in both CML CD34+ and CML-iPSCs. This has important implications as ID1 is known to mediate its effects by downregulating p53 and PTEN transcription, resulting in enhanced AKT phosphorylation and AKT-mediated canonical Wnt signalling22. ID1 can also enhance G1-S cell cycle progression and augments Hh and Wnt signalling through suppression of CULLIN3, an ubiquitin ligase, which targets CyclinE, GLI2 and DVL2 for degradation54. The BMP and Wnt pathways converge to regulate the CDX family of homeobox transcription factors, master regulators of HOX gene expression55,56. Given that deregulation of the Hh13,57 and Wnt57 pathways and the Hox axis57,58 have key roles in CML, it is tempting to speculate that ID1 could be an important orchestrator in this process (Fig. 7e).
Inhibiting type 1 BMP receptors with small-molecule inhibitors, in combination with TKIs, is a promising approach to deplete primitive CML stem/progenitor cells, especially given the emerging role of BMP pathway signalling in treatment resistance and disease relapse16,19. We demonstrate that combination treatment caused irreversible cell cycle arrest, increased apoptosis, reduced cell division and survival of CD34+ cells in CML compared to normal cells, with CML-iPSCs displaying less self-renewing potential and enhanced differentiation following therapy. Targeting pathways CML cells depend on for self-renewal especially BMP pathway is an attractive approach (Supplemental Table 1)59,60,61,62,63,64. Our results indicate a potential therapeutic window in CML, with intervention using BMP inhibitors in combination with TKI warranting further investigation to prevent LSCs self-renewal and improve treatment for patients in the future.
Materials and methods
Normal donors and CML samples were taken at diagnosis following informed consent in accordance with the Declaration of Helsinki, and approval of the Greater Glasgow and Clyde National Health Service. Samples were enriched for CD34+ cells using the CliniMACS (Miltenyi Biotec) immunomagnetic beads system. Cells were cryopreserved in 10% DMSO (Sigma-Aldrich) and 5% human albumin solution (Baxter Healthcare). SPIRIT2, a multicentre phase III randomised trial (NCT01460693; clinicaltrials.gov), in which CML patients were randomised into two groups, to compare the TKIs, IM (400 mg daily) vs Dasatinib (100 mg Daily). Sixty samples of cells were obtained from the biobank in Glasgow (30 CD34+ purified from peripheral blood, 30 MNC samples, 11 of which were matched, i.e. both CD34+ and MNC available from the same patients). Following thawing, RNA was extracted using RNAEasy Micro kits (Qiagen) or Picopure RNA isolation Kit (Thermo Fisher) to create an RNA bank of samples. Reverse transcription using Superscript III (Thermo Fisher) was then carried out to create cDNA library from all of the samples. Normal BM CD34+ cells were bought from Stem Cell Technologies and normal CD34+ from peripheral blood were obtained from the Glasgow Biobank. Six normal CD34+ and four normal MNC samples were used as comparators.
iPSC generation, maintenance and characterisation
CytoTune®-iPS Sendai Reprogramming Kit (Life Technologies) was used for iPSC generation from normal CD34+ (Stem Cell Technologies) and treatment naive CP-CML CD34+ cells as per manufacturer’s instructions (Thermo Fisher). In brief, reprogramming was performed as follows: CD34+ cells were cultured in StemSpan (Stem Cell Technologies) media supplemented with 10% Myelocult (Stem Cell Technologies, BC, Canada), interleukin (IL)-3 (10 ng/mL), IL-6, granulocyte-colony stimulating factor (G-CSF), stem cell factor (SCF), Fms-like tyrosine kinase-3 ligand (FLT3L), (all at 100 ng/mL) (PeproTech) and 1% Penicillin/Streptomycin (Invitrogen, Paisley, UK) for 2 days prior to viral transduction. hOCT3/4, hSOX2, hKlf4, hC-MYC vectors were used at multiplicity of infection (MOI) = 6. iPSCs, once generated, were cultured in TeSR-E8 medium (Stem Cell Technologies) on matrigel (Corning)-coated Nunclon petri dishes (Fisher Scientific) in feeder-free conditions. IPSCs were passaged using EZ-Passage tool and DMEM/F12 Dulbecco’s Modified Eagle Medium (Life Technologies) twice a week. Alkaline phosphatase (APh) staining was used to assess pluripotency (Sigma-Aldrich). Live APh staining was performed using IncuCyte ZOOM Live Cell Imaging System and software (Essen Bioscience). The expression level of key pluripotency markers OCT4, SOX2, SSEA4, and/or TRA-1-60 was detected using PSC 4-Marker Immunocytochemistry Kit (Life Technologies) according to manufacturer’s instructions.
Cell line and primary samples cell culture
K562 cells (DSMZ) were grown in RPMI 1640 (Sigma-Aldrich) with 10% foetal calf serum, 1 mM glutamine and 1% penicillin–streptomycin (Invitrogen). HS5 cells were grown in DMEM (Gibco) with 10% fetal calf serum, 1 mM glutamine and 1% penicillin–streptomycin (Invitrogen). 24 h prior to co-culture, HS5 were seeded on collagen coated 12-well plates at a cell density of 1.2 × 105 cells per well.
CD34+-enriched normal and CML cells were thawed and cultured overnight in serum free media (SFM) (Life Technologies) supplemented with; IL-3 (20 ng/mL), IL-6 (20 ng/mL), G-CSF (20 ng/mL), SCF and FLT3L (100 ng/mL) (PeproTech). Prior to treatment with inhibitors, culture media for CD34+ enriched cells was changed to more physiological growth factor concentrations; IL-3 (0.2 ng/mL), IL-6 (0.2 ng/mL), G-CSF (0.2 ng/mL), SCF and FLT3L (1 ng/mL).
Overall, 100 mM stock solution of IM (Stratech) was prepared in water and stored at 4 °C; BMP pathway inhibitors LDN-193189 (LDN) (Cellagen technology) and Dorsomorphin (DOR) (Abcam) were prepared using DMSO and 10 mM stocks stored at −20 °C. Inhibitors were diluted in complete media as required. LDN interrupts the BMP pathway through inhibiting AVCR1 (ALK2) and BMPR1A (ALK3), receptor phosphorylation, whereas DOR inhibits AVCR1 (ALK2), BMPR1A (ALK3), BMPR1B (ALK6), thereby preventing phosphorylation of SMADs 1, 5 and 8, and transcription of downstream genes.
Trypan blue exclusion cell counts and XTT bioreduction assay
Samples were diluted in Trypan Blue dye (Sigma-Aldrich) of an acid azo exclusion medium by preparing a 1:1 dilution of the cell suspension using a 0.4% Trypan Blue solution. Half maximal inhibitory concentration (IC50) of each of the BMP pathway inhibitors and IM in K562 cell line was established using XTT sodium 3′-[1-[(phenylamino)-carbonyl]-3,4-Tetrazzolium]-bis(4-methoxy-6-nitro) benzene sulphonic acid hydrate cell proliferation assay (Sigma-Aldrich) according to manufacturer’s instructions. The half maximal inhibitory concentration (IC50) of each of the BMP pathway inhibitors and IM were calculated using Prism software (GraphPad Software).
Synergy studies using CalcuSyn
Synergy studies of either LDN or DOR in combination with IM was performed using CalcuSyn (Biosoft). The median-effect graph which is a plot of x = log (Dose of drug) vs y = log (Fa) by the dose/the fraction unaffected and dose–effect curve together with the combination index (CI) ranges for these inhibitors was used to determine synergism in targeting CML cells. CalcySyn performs multiple drug dose–effect calculations using the median-effect methods described by T-C Chou and P. Talalay65. The resulting combination index (CI) theorem of Chou-Talalay was used to provide a quantitative definition for additive effect (CI = 1), synergism (CI < 1), and antagonism (CI > 1) in drug combinations.
For cell division analysis, CD34+ cells were stained with the proliferation dye CellTrace™ Violet (Thermo Fisher) and labelled with anti-CD34 (BD Biosciences), as recommended by manufactures protocol. For establishing a maximum point of fluorescence staining, cells were cultured in the presence of Colcemid (100 ng/mL, Invitrogen Life Technologies) to determine non-dividing cells after labelling (CTV max). All primary CD34+ cells were treated with IM, LDN, DOR or combinations in the presence and absence of BMP4 and cultured as described above in physiological growth factors or on the HS5 stromal cells. Annexin V/7AAD (BD Biosciences) staining was used to assess apoptosis by flow cytometry using 1 × 105 cells per condition. Propidium iodide (PI) staining buffer (BD Bioscience, Oxford, UK) was used to assess cell cycle progression as per manufacturer’s protocol. To test for re-entry into cell cycle, cells were treated with inhibitor concentrations as indicated for 24 h; cells were then washed x5 with PBS prior to culture in complete media for a further 24, 48 and 72 h and PI staining performed. BMP pathway type I receptors and ALKs 2, 3 and 6 (R&D systems) were detected by intracellular flow cytometry according to the manufacturer’s instructions. A list of antibodies used is provided in Table S2.
Fluorescence in situ hybridisation (FISH)
Detection of BCR-ABL fusion in CD34+ 38− CML cells by FISH was performed as previously reported2.
Protein analysis and quantitative real-time polymerase chain reaction
Whole cell lysates were prepared and SDS-PAGE western blotting was performed as described previously2 using PathScan Multiplex Western Cocktail primary antibody, pCRKL (Cell Signalling Technology), SHPTP2 (Santa Cruz Biotechnology), Anti-Phosphotyrosine Antibody, clone 4G10 and phospho-SMAD1/5/8 (Millipore). Immunofluorescent staining was performed on Poly-l-lysine slides, cells were fixed with 4% formaldehyde for 10 min and permeabilised with 0.5% Triton-X100 in PBS for 15 min. Following incubation with 5× blocking solution for 2 h, proteins were detected using anti-SMAD4 (Millipore) and phospho-SMAD1/5/8 primary antibodies overnight at 4 °C. Following detection using the corresponding conjugated secondary antibody, slides were then visualised under Zeiss epifluorescence microscope and images analysed using AxioVision Rel.4.8 microscopy software. A list of antibodies used is provided in Table S3. Quantitative real-time polymerase chain reaction (qRT-PCR) was undertaken using the Fluidigm BioMark HD System and TaqMan (Applied Biosystems) gene expression assays, as per manufacturer’s instructions. Eight low/medium copy number reference genes were used in the analysis. A list of primers used is provided in Table S4 with reference genes shaded in grey.
Assessment of hematopoietic progenitors
Colony-forming cell (CFC) assays were performed as described by Holyoake et al.1 Overall, 4 × 103/mL cells from each treatment arm were re-suspended in 300 µL SFM and inoculated in 3 mL Methocult H4034 (Stem Cell Technologies). This was then split into two 35 mM dishes and incubated in a humidified incubator. CFCs were counted on day 11.
Average responses from at least three independent experiments are shown (mean ± SEM). Statistical analysis was performed using GraphPad Prism 6 (GraphPad Software Inc.), using Anova, Welch’s test, Student’s paired t-test for matched samples, and Mann–Whitney U test for unpaired samples.
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This study was funded by PhD studentships from the NC3R’s (P. Toofan), Medical Research Scotland (C. Busch) and a project grant from the charity Animal Free Research UK (H. Morrison). This study was supported by the Glasgow Experimental Cancer Medicine Centre, which is funded by Cancer Research UK and the Chief Scientist’s Office, Scotland. We thank all CML patients, UK hematology departments and the SPIRIT2 Trials Management Group for access to CML samples and acknowledge A. Hair for sample processing. Cell-sorting facilities were funded by the Kay Kendall Leukaemia Fund (KKL501) and the Howat Foundation.
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The authors declare that they have no conflict of interest.
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Toofan, P., Busch, C., Morrison, H. et al. Chronic myeloid leukaemia cells require the bone morphogenic protein pathway for cell cycle progression and self-renewal. Cell Death Dis 9, 927 (2018). https://doi.org/10.1038/s41419-018-0905-2
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