- Open Access
Epigenetic abnormalities in myeloproliferative neoplasms: a target for novel therapeutic strategies
© Springer-Verlag 2011
- Received: 5 May 2011
- Accepted: 29 June 2011
- Published: 9 July 2011
The myeloproliferative neoplasms (MPNs) are a group of clonal hematological malignancies characterized by a hypercellular bone marrow and a tendency to develop thrombotic complications and to evolve to myelofibrosis and acute leukemia. Unlike chronic myelogenous leukemia, where a single disease-initiating genetic event has been identified, a more complicated series of genetic mutations appear to be responsible for the BCR-ABL1-negative MPNs which include polycythemia vera, essential thrombocythemia, and primary myelofibrosis. Recent studies have revealed a number of epigenetic alterations that also likely contribute to disease pathogenesis and determine clinical outcome. Increasing evidence indicates that alterations in DNA methylation, histone modification, and microRNA expression patterns can collectively influence gene expression and potentially contribute to MPN pathogenesis. Examples include mutations in genes encoding proteins that modify chromatin structure (EZH2, ASXL1, IDH1/2, JAK2V617F, and IKZF1) as well as epigenetic modification of genes critical for cell proliferation and survival (suppressors of cytokine signaling, polycythemia rubra vera-1, CXC chemokine receptor 4, and histone deacetylase (HDAC)). These epigenetic lesions serve as novel targets for experimental therapeutic interventions. Clinical trials are currently underway evaluating HDAC inhibitors and DNA methyltransferase inhibitors for the treatment of patients with MPNs.
- Myeloproliferative neoplasm
- Histone deacetylase inhibitor
- DNA methyltransferase inhibitor
Myeloproliferative neoplasms (MPNs) represent a diverse set of hematologic malignancies that have received intense scientific investigation in recent years with a goal of developing novel disease modifying strategies. In 2008, the World Health Organization (WHO) revised the classification of hematologic malignancies to reflect new molecular insights into the pathogenesis of these disorders. Currently, the MPNs include chronic myelogenous leukemia (CML), polycythemia vera (PV), essential thrombocythemia (ET), primary myelofibrosis (PMF), systemic mastocytosis, chronic eosinophilic leukemia not otherwise specified, chronic neutrophilic leukemia and “MPN, unclassifiable”; CML, PMF, PV, and ET represent the four major clinical entities and will be the subject of this review (Tefferi et al. 2007b).
CML is distinct among the MPNs in that it is defined by a specific cytogenetic abnormality (Philadelphia chromosome) involving a balanced translocation between the long arms of chromosomes 9 and 22 [t(9;22)(q34;q11)]. The gene fusion product resulting from this translocation, BCR-ABL1, gives rise to a constitutively activated and unregulated cytoplasmic tyrosine kinase that causes uncontrolled proliferation and differentiation of hematopoietic cells (Deininger et al. 2000). The molecular understanding of this pathway led to development of imatinib mesylate (Gleevec)—an oral BCR-ABL1 inhibitor—which has revolutionized the treatment of this MPN. In the International Randomized Study of Interferon plus cytosine arabinoside and STI571, imatinib therapy was found to induce a complete cytogenetic remission in 76% of CML patients versus 15% of patients in the interferon arm leading to a 6-year overall survival of 88% (O’Brien et al. 2003; Hochhaus et al. 2009). In contrast to CML, pharmacologic interventions for the other common Philadelphia chromosome (Ph-) negative MPNs (PMF, ET, and PV) have not been shown to significantly alter disease progression and overall survival (Mascarenhas 2009).
In 2005, an activating point mutation (V617F) in the autoinhibitory region of the JAK2 tyrosine kinase was first documented in 96%, 50%, and 50% of patients with PV, ET, and MF, respectively. JAK2V617F has served as a target for the development of a number of tyrosine kinase inhibitors (Baxter et al. 2005; James et al. 2005; Kralovics et al. 2005; Levine et al. 2005). These novel agents have been tested in phases I, II, and III studies and as a class have been effective in palliating the constitutional symptoms and reducing symptomatic splenomegaly in the majority of patients (Pardanani et al. 2010a, b; Santos et al. 2010; Verstovsek et al. 2009, 2010; Hexner et al. 2009; Moliterno et al. 2009). However, these agents have to date not been shown to significantly improve cytopenias, restore normal bone marrow morphology, and induce cytogenetic remissions in MF patients. In fact, molecular responses, as demonstrated by significant reduction in the JAK2V617F allele burden, have not been achieved. Thus, newer therapies directed against epigenetic, immunological, and molecular alterations of these Ph-negative MPNs are necessary, and many are currently being evaluated in clinical trials. In this review, we discuss epigenetic alterations in the Ph-negative classic MPNs, specifically focusing on epigenetic therapies as they relate to the underlying pathophysiology of these blood cancers.
The MPNs are collectively characterized by a hyperproliferative bone marrow and excessive myeloid cell production. An increased risk for venous and arterial thrombosis and transformation to acute leukemia exist and pose a serious threat of morbidity and mortality to patients. Cachexia, fatigue, global weakness, progressive splenomegaly, and constitutional symptoms (fever, night sweats, and weight loss) can plague patients with the various MPNs and are particularly troublesome in MF. Although elevated peripheral blood counts typify ET and PV, MF is most often characterized by anemia and thrombocytopenia. Standardized diagnostic criteria, validated risk stratification schema, and response criteria to therapeutic intervention exist for these related disorders which have recently been created to facilitate the evaluation of potential new therapeutic modalities (Dupriez et al. 1996; Barosi et al. 2005; Tefferi et al. 2006, 2007b; Passamonti et al. 2008; Cervantes et al. 2009).
PV is defined by an increase in red cell mass in the absence of conditions that induce secondary erythropoiesis and specific diagnostic criteria exist to aid in confirming the diagnosis (Thiele and Kvasnicka 2009). The average age of onset is 60–65 years with an annual incidence ranging from 0.5 to 2.6 cases per 100,000 persons per year (Hoffman 2005). Patients with PV have been found to have a 1.6-fold higher mortality than control populations with the main causes of mortality and morbidity being arterial and venous thrombosis, hemorrhage, evolution to MF, and leukemic transformation (Hoffman 2005). PV is thought to arise from a multipotent hematopoietic progenitor cell or stem cell. Nearly 95% of patients express the JAK2V617F mutation (James et al. 2005; Verstovsek et al. 2006). Presently, treatment for low-risk individuals (<60 years of age and no history of thrombosis) is low-dose aspirin and phlebotomy to maintain the hematocrit below 45% for men and 42% for women. In higher-risk individuals, cytoreductive therapy such as hydroxyurea and interferon-alpha has been used with the goals to reduce the risk of thrombosis, normalize peripheral blood counts, decrease splenomegaly, and ameliorate hypercatabolic and constitutional symptoms (Scherber and Mesa 2011).
ET, the most common MPN in the USA, is defined by a platelet count greater than 450,000 × 109/L (changed from 600,000 × 109/L in 2008 WHO classification update) in the absence of any other MPN or reason for reactive thrombocytosis (Tefferi et al. 2007b). Patients with ET generally have a similar age-matched median survival for the first decade after diagnosis that can shorten thereafter usually secondary to thrombosis or hemorrhage (Wolanskyj et al. 2006). In approximately 50% of patients with ET, JAK2V617F is expressed and in comparison to PV, the allele burden is lower (James et al. 2005). Like PV, treatment consists of aspirin and cytoreductive agents such as hydroxyurea or anagrelide for patients at high risk for thrombosis. Approximately 10% of ET patients over the first decade can transform to a myelofibrotic phase (post-ET-related myelofibrosis) with clinical features essentially indistinguishable from primary myelofibrosis (Wolanskyj et al. 2006).
PMF is the least common of the classic Ph-negative MPNs and has the worst prognosis with a median survival of 3–5 years from the time of diagnosis (Rozman et al. 1991; Tefferi 2000). The annual incidence is 0.2–1.5 cases per 100,000 persons per year with predominance in males over 50 years of age. The JAK2V617F mutation is found in about half of patients with PMF (James et al. 2005). Myelofibrosis, arising from a background of polycythemia vera or essential thrombocythemia, is denoted post-PV/ET MF, and the treatment approach remains the same as PMF. Collectively these conditions are referred to simply as MF. Patients with MF can be risk stratified for risk of death from transformation to acute leukemia or catastrophic thrombosis and complications of portal hypertension by various risk stratification systems that are used mostly for research purposes in deciding appropriate treatment options (Passamonti et al. 2010; Dupriez et al. 1996; Dingli et al. 2006; Tefferi et al. 2007a; Cervantes et al. 2009; Tam et al. 2009). Therapeutic approaches for the treatment of MF include immunomodulatory agents such as thalidomide and lenalidomide in combination with prednisone, which have response rates of 20–40% (Mesa et al. 2003, 2010). Androgens have also been used to selectively manage the anemia associated with MF, with response rates close to 40% (Cervantes et al. 2005). A few prospective studies have used erythropoiesis-stimulating agents with conflicting results (Cervantes et al. 2006; Tsiara et al. 2007). Chemotherapeutic agents including hydroxyurea, melphalan, busulfan, and 2-chlorodeoxyadenosine have also been used to control the myeloproliferative aspects of the disease (Chang and Gross 1988; Tefferi et al. 1997; Petti et al. 2002). The only present approach capable of curing MF is allogeneic hematopoietic stem cell transplantation, which must be evaluated on a case-by-case basis and balanced against considerable transplant-related morbidity and mortality (Kroger et al. 2009; Rondelli et al. 2010).
In 2005, with the discovery of the JAK2V617F mutation, a substantial breakthrough in the understanding of the pathogenesis of Ph-negative MPNs led to the rapid development of new class of agents. Within a year, preclinical studies demonstrated that a G to T point mutation in exon 14 of the JAK2 tyrosine kinase gene (valine-to-phenylalanine at codon 617) was associated with the development of an MPN-like phenotype—erythrocytosis, leukocytosis, splenomegaly, and eventually changes resembling transformation to myelofibrosis (Bumm et al. 2006; Lacout et al. 2006; Wernig et al. 2006; Zaleskas et al. 2006). In vivo murine studies rapidly spawned the development of new oral small molecule inhibitors designed to inhibit the JAK2V617F-induced constitutively active signaling pathway. For the first time in decades, a renewed sense of optimism for producing effective disease modifying agents for the treatment of MPNs brought laboratory investigators and clinician scientists to the same table.
One agent, INCB018424 (Incyte), a potent and selective JAK1/JAK2 inhibitor, which demonstrated preclinical benefits in a JAK2V617F expressing MPN mouse model, recently completed a phase 1/2 clinical trial (Quintas-Cardama et al. 2010; Verstovsek et al. 2010). At the 15-mg twice-daily dosing, 17 of 33 MF patients with or without the JAK2V617F mutation (52%) had an objective clinical response (>50% decrease in splenomegaly) for 12 months and significant reduction in symptoms such as weight loss, fatigue, night sweats, and pruritus. Grade 3 or 4 adverse events occurred in less than 10% of patients and are mainly due to myelosuppression. This agent is being investigated in a randomized, double-blind, placebo-controlled phase III study to assess overall clinical efficacy in spleen reduction and improvement in MF-related disease symptoms as measured by an MF-specific quality-of-life tool, and the results of this trial are expected to be revealed in the latter part of 2011 (Scherber and Mesa 2011; Mesa et al. 2009a).
Other JAK2 inhibitors undergoing clinical evaluation include the non-specific multi-tyrosine kinase inhibitor CEP-701 (Cephalon), the selective JAK2 inhibitor SB1518 (SBIO), TG101348 (TargeGen), and CYT387 (YM BioSciences; Pardanani et al. 2010a, b; Verstovsek et al. 2009). Studies with newer agents directed against the constitutive tyrosine kinase activity induced by the JAK2V617F mutation are promising but still limited. While offering significant improvement in clinical symptoms, these agents do not appear to alter disease progression which has led to the continued interest in investigating alternative targeted therapies such as mammalian target of rapamycin inhibitors, immunomodulatory drugs, and anti-fibrosing agents which act to exploit additional aberrant pathways and proposed mechanisms of disease pathobiology (Scherber and Mesa 2011; Hoffman and Rondelli 2007).
Other gene mutations influencing the MPN phenotype have also been identified. Mutations in exon 12 of JAK2 have been described in a fraction of JAK2V617F-negative PV patients (Scott et al. 2007). Somatic activating mutations in the codon of MPL (the receptor for thrombopoietin) W515L/K occur in 10% of patients with PMF and 8% of JAK2V617F-negative ET, and in some patients, the MPL and JAK2V617F mutation can coexist (Pardanani et al. 2006; Beer et al. 2008; Vannucchi et al. 2008). These mutations are of low frequency and unlikely to serve as worthy drug targets.
Epigenetic alterations involved in the pathogenesis of Ph-negative MPNs
The biologic events leading to the initiation and progression of MPNs are likely not only caused by the acquisition of genetic mutations, such as the JAK2V617F mutation, but may also due to epigenetic changes that do not affect the primary sequence of DNA but rather alter gene expression by remodeling chromatin. Chromatin remodeling is accomplished primarily through two main mechanisms: (a) post-translational modification of histones, such as methylation, acetylation, phosphorylation, ADP-ribosylation glycosylation, and ubiquitination. Among all the types of histone modifications, methylation and acetylation at specific lysine residues are considered crucial histone marks affecting chromatin structure and gene expression (Kouzarides 2007). (b) DNA methylation with the addition of a methyl group to cytosine–phosphate–guanine (CpG) dinucleotide repeats within gene regulatory DNA sequences modulates the transcription of various genes (Metivier et al. 2008).
The attachment of a methyl group to the five-carbon position of cytosine base located 5′ to a guanosine base in the CpG dinucleotide islands of gene promoter sites influences the access of transcriptional machinery to DNA (Mani and Herceg 2010). This enzymatic process is regulated by DNA methyltransferases (DNMT). DNMT3A and DNMT3B are involved in de novo DNA methylation and DNMT1 in the maintenance of DNA methylation. The methylation status of a particular gene is an important determinant of gene expression, and both DNA hypomethylation and hypermethylation patterns have been implicated in the pathogenesis of many cancer types (Feinberg and Tycko 2004; Esteller 2007).
Other less well-characterized epigenetic modifications include post-transcriptional regulation of gene expression by a heterogeneous class of non-coding RNAs such as microRNAs (miRNAs) (Berdasco and Esteller 2010). MiRNAs bind to the 3′ untranslated region (3′UTR) of target mRNAs and either repress protein translation or cause mRNA degradation (Ambros 2004). MiRNAs (miR21, miR24, miR144, miR146a, miR150, miR155, miR221, miR222, miR223, miR451) play fundamental roles in the normal differentiation and activity of hematopoietic cells (Havelange and Garzon 2010). Data from both in vitro and in vivo studies indicate that miRNAs are important regulators of hematopoiesis and play a role in the pathogenesis of some acquired hematologic disorders, functioning either as tumor suppressors (miR-15/16) or as oncogenes (miR-17-92 cluster; Lawrie 2007). Microarray studies have defined miRNA signatures in hematopoietic cell lineages and related hematologic malignancies (Calin et al. 2004, 2005; Bruchova et al. 2007; Georgantas et al. 2007), and comparison of normal and patient samples has revealed aberrantly expressed miRNA that reflect a disease specific signature (Debernardi et al. 2007; Gramantieri et al. 2007; Meng et al. 2007; Venturini et al. 2007). Changes in miRNA expression can occur through different mechanisms including transcriptional deregulation, epigenetic alterations, gene mutations, DNA copy number abnormalities, and impaired miRNA processing (Deng et al. 2008). These disease specific-miRNA epigenetic signatures may provide a basis for new therapeutic interventions by specifically targeting miRNA expression.
MiRNA expression profiling of megakaryocytes in PMF but not ET has revealed that in the pre-fibrotic form of PMF, autonomous proliferation of the megakaryocytic lineage is associated with significant accumulation of miR-146b as compared to normal megakaryopoiesis (Hussein et al. 2009). These data reflect an active miRNA system in MPN megakaryocytes which appears to be one of the underlying defects associated with disease progression. Recently, Girardot et al. 2010 reported that in a fraction of MPN patient platelets, Mir 28 negatively regulates MPL expression. Mir 28 targets the 3′UTR region of MPL and inhibits its translation as well as other proteins potentially involved in megakaryocyte differentiation including E2F6, a transcription factor belonging to the E2F family and ERK2.
List of genes in which expression can be altered by epigenetic mechanisms in MPNs
ET, PV, PMF
Ihalainen et al. (1994)
V-abl Abelson murine leukemia viral oncogene homolog 1
ET, PV, PMF
Aviram et al. (2003)
Cyclin-dependent kinase inhibitor 2A
Cyclin-dependent kinase inhibitor 2b
Wang et al. (2002)
Secreted Frizzled-related protein 1
Bennemann et al. (2010); Pehlivan et al. (2009)
Secreted Frizzled-related protein 2
ET, PV, PMF
Bennemann et al. (2010)
Wnt inhibitory factor-1
ET, PV, PMF
Suzuki et al. (2007)
Suppressor of cytokine signaling 1
ET, PV, PMF, MF-BP
Suppressor of cytokine signaling 3
Polycythemia rubra vera protein 1
Jelinek et al. (2007)
C-X-C chemokine receptor type 4
Bogani et al. (2008)
Retinoic acid receptor beta 2
Mutations involving the ten to 11 translocation-2 (TET2) family gene located in the minimal loss of heterozygosity region at 4q24 have been identified in several myeloid malignancies (Delhommeau et al. 2009). The exact function of TET2 is not yet clear, but it appears to act as a tumor suppressor gene (Schaub et al. 2010; Delhommeau et al. 2009). Homozygosity for TET2 mutations as a result of uniparental disomy or deletion of the TET2 locus does not appear to confer a proliferative advantage to hematopoietic progenitor cell clones which would argue against a role as a tumor suppressor gene (Schaub et al. 2011). TET2 is a member of the α-ketoglutarate-dependent enzyme family that catalyzes the conversion of 5-methylcytosine of DNA to 5-hydroxymethylcytosine and induces subsequent DNA demethylation (Ito et al. 2010; Tahiliani et al. 2009). TET2 mutations have been reported in almost all coding regions including missense, nonsense, or frameshift mutations. Moreover, these mutations are not exclusively bi-allelic (both copies of TET2) and therefore considered TET2 loss of function mutations (Delhommeau et al. 2009). TET2 loss of function would be anticipated to result in DNA hypermethylation which has been recently reported in acute myeloid leukemia (AML) blast cells.
Overall, the frequency of TET2 mutations in Ph-negative MPNs has been reported to be 12–17% (Delhommeau et al. 2009; Tefferi et al. 2009b). A higher TET2 mutation frequency has been detected in older MPN patients (>60 years) and has been shown to be highly correlated with JAK2V617F allele burdening these patients (Tefferi et al. 2009b). In fact, studies support the role of TET2 in JAK2V617F-positive PV as not a disease-initiating event preceding the acquisition of the JAK2 mutation, but as a latter event that can confer a proliferative advantage to the JAK2V617F-bearing clone (Swierczek et al. 2010; Delhommeau et al. 2009). However, other studies utilizing colony-forming assays failed to demonstrate a consistent temporal relationship between the acquisition of the somatic mutations of TET2 and JAK2 (Schaub et al. 2010). TET2 mutations have largely not been uniformly shown to have prognostic significance; no influence was demonstrated on survival, rate of leukemic transformation, or thrombotic tendency in MPN patients (Hussein et al. 2010; Tefferi et al. 2009a, b). In contrast, TET2 mutations have been identified in blast phase MPN samples and not observed in the paired background MPN samples of both JAK2 wild-type and mutant MPNs obtained prior to blastic transformation (Abdel-Wahab et al. 2010a). This finding would suggest that the acquisition of TET2 mutations may be a possible step in MPN leukemic transformation.
ASXL1 is one of three mammalian homologs of the additional sex combs gene in Drosophila (69). The ASXL1 gene is located on chromosome 20q11 and encodes an enhancer of the trithorax group (trxG) and Polycomb group (PcG) proteins (ETP) chromatin modifier complex (Fisher et al. 2003). The PcG proteins (repressors) and trxG proteins (activators) serve to regulate gene expression of homeotic genes, such as Hox genes via histone methylation (Fisher et al. 2010a). PcG and trxG proteins function at the level of chromatin by forming multi-protein complexes: which are the three PRC1, Polycomb repressor complex 2 (PRC2), PhoRC and SET-1-like complex, BRM, and MLL supercomplex, respectively (Baskind et al. 2009). These complexes work together to establish and maintain methylation marks primarily on the tail of histones. Mammalian PcG and trx genes display hematopoietic lineage and differentiation stage-specific expression patterns and are required for normal hematopoiesis. Mammalian ASXL proteins are predicted to have dual activator/repressor functions depending on their cellular context. An ASXL1 knockout mouse model is characterized by a defect in frequency of differentiation of both myeloid and lymphoid cells, without an effect on hematopoietic stem cells and does not result in a myelodysplastic or leukemic phenotype (Fisher et al. 2010b). This would seem to indicate that ASXL1 mutations alone are not sufficient to induce malignant transformation.
ASXL1 mutations have been documented in myelodysplastic syndrome (MDS; 10%) and chronic myelomonocytic leukemia (40%) patients and most recently in 8% of MPN patients that were all negative for JAK2V617 (Carbuccia et al. 2009). The ASXL1 mutations were also found in the CD34+ cell population supporting the principle of a primitive hematopoietic stem as the origin of the MPN clone and further suggesting that acquisition of ASXL1 mutations can occur early in MPN pathogenesis. Although the ASXL1 mutations are associated with poor overall survival and increased risk for transformation to blast crisis in chronic myelomonocytic leukemia patients, it is not yet clear what influence it has on the behavior of Ph-negative MPNs.
Mutations involving the enhancer of zeste homolog 2 (EZH2) gene located on chromosome 7q36.1, which encodes the catalytic component of the histone methyltransferase PRC2 have also been described in MPN patients (Stegelmann et al. 2010). PRC2 is a multi-protein enzyme complex responsible for the trimethylation of lysine 27 on histone H3 (H3K27me3; Cao and Zhang 2004; Simon and Lange 2008). The PRC2 complex contains multiple subunits: EZH2, SUz12, EED, and YY1. PRC2 can also recruit other Polycomb complexes, DNMTs, and HDACs to the gene site resulting in chromatin compaction and additional repressive activity (Chase and Cross 2011).
Activating and inactivating mutations of EZH2 have been reported in human malignancies. The EZH2 Y641 mutation (within the SET domain) which is found in lymphoma cells results in a gain of function with increased levels of H3K27me3 (Morin et al. 2010). The mutations associated with myeloid malignancies are thought to result in loss of histone methyltransferase activity. Forty-nine EZH2 mutations have been found in 42 individuals out of 614 patients with myeloid disorders (Ernst et al. 2010). Thirteen percent of MF patients in this cohort harbored an EZH2 mutation. A total of ten EZH2 mutations were identified in exons involving deletions, insertions, and missense mutations in patients with PMF, post-PV/ET MF, and MPN-associated acute myeloid leukemia. Microarray and SNP analysis did not show association with copy number alterations or uniparental disomy. Additionally, no association was seen with JAK2V617F allele burden. Degree of splenomegaly and leukocytosis was clinical findings found to be statistically associated in MPN patients expressing EZH2 mutations. Upregulation of EZH2 gene expression has been documented in MPNs, most frequently in PMF patients suggesting a potential role of tumor suppressor gene silencing as a mechanism in disease progression (Skov et al. 2010a). Additionally, EZH2 and ASXL1 mutations were not found to be mutually exclusive events in MPNs. Retrospective analysis of the presence of EZH2 mutations in archived MPN bone marrow samples has not been shown to have prognostic significance in PMF patients (Abdel-Wahab et al. 2010b).
Three-deazaneplanocin A (DZNep) is a carbocyclic adenosine analog that inhibits s-adenosylhomocysteine hydrolase and results in the accumulation of s-adenosylhomocysteine, disrupting methylation of targets by EZH2 (Chase and Cross 2011). Although the effects of DZNep are global and not specific to EZH2, this drug has been tested as a single agent in solid tumor cell lines and in combination with a HDACi in primary AML cells (Fiskus et al. 2009). The combination of this agent with the pan-HDACi, LBH589 (Panobinostat, Novartis), was shown in vitro to selectively induce apoptosis in AML primary cells and not normal CD34+ cells. This effect was correlated with reduction in EZH2 protein level and induction in p16, p21, and p27 gene expression. Combined therapy in a NOD/SCID mouse model with HL-60 AML led to an improvement in survival when compared to each agent alone (Fiskus et al. 2009). This compound is currently being investigated in early phase clinical trials.
Expression of miR-101-1 and 101-2 which negatively regulate EZH2 has been shown to be decreased in MPNs and displayed an inverse relationship with EZH2 mRNA expression (Swierczek et al. 2011). This may provide an additional mechanism for EZH2 gene dysregulation and contribute to MPN disease progression and disease severity.
Isocitrate dehydrogenase 1 and 2, IDH1 and IDH2, located on chromosome 2q33.3 and 15q26.1, respectively, encode NADP+-dependent enzymes that catalyze oxidative decarboxylation of isocitrate to α-ketoglutarate (Tefferi et al. 2010). The IDH mutant has decreased affinity for isocitrate and instead converts α-ketoglutarate to hydroxyl-glutarate which has been implicated in malignant transformation (Dang et al. 2009). IDH gene mutations have been documented in solid tumors and de novo AML (Chou et al. 2010; Yan et al. 2009). A recent study in AML has revealed that the presence of IDH1/2 mutations result in production of 2-hydroxyglutarate and is associated with a specific global DNA hypermethylation signature (Figueroa et al. 2010). Both IDH1/2 mutations and TET2 mutations lead to similar hypermethylation signatures and patterns of impaired myeloid differentiation and increased expression of stem cell markers. Additionally, it has been shown that IDH1/2 mutations generate impaired enzymatic activity of α-ketoglutarate-dependent TET2 protein and result in increased stem cell/progenitor cell marker expression (Figueroa et al. 2010). Thus, the expression of IDH1/2 mutations can lead to a TET2-dependent epigenetic effect.
IDH1/2 mutational frequency in MPNs is approximately 0.8%, 1.9%, and 4.2% for ET, PV, and PMF, respectively (Tefferi et al. 2010). Thirty-eight IDH 1/2 mutations have been discovered in a large screening study of MPN patients and can coexist equally with mutations in JAK2, MPL, and TET2 (Tefferi et al. 2010). The types of IDH1/2 mutations seen in MPNs are distinctly different than the ones observed in brain tumors and overlapped with those documented in AML and include IDH1-R132, IDH2-R140, and IDH2-R172. Over 21% of patients with blast phase-related MPN carry an IDH1/2 mutation, and this was irrespective of JAK2V617F status (Green and Beer 2010; Pardanani et al. 2010c). This appears to indicate that IDH1/2 mutations can also influence the transformation of MPN to blast phase disease.
Interestingly, leukemic blasts and progenitor cells can possess both mutated IDH2 and JAK2V617F, and in other patients with MPN-transformed leukemia, the mutated IDH1/2 may be present in blasts with wild-type JAK2 and absent in the progenitor cells with JAK2V617F (Green and Beer 2010). These data raise the possibility of the presence of two subclones originating from a yet unidentified primary clone or two independent competing clones arising in the same individual. Further studies are needed to further clarify these findings and determine their possible significance.
Ikaros is a Kruppel-like zinc finger transcription factor that is integral to the development of normal hematopoiesis and is encoded by the Ikaros family zinc finger 1 (IKZF1) gene located at 7p.12 (Georgopoulos 2002; Westman et al. 2002). The exact mechanism by which this mutation influences chromatin remains unclear. IKZF1 influences maturation and differentiation of a variety of cell types at different stages of development including those of the hematopoietic system (Westman et al. 2002). IKZF1 interacts with the histone deacetylase repressor complexes NURD (HDAC1 and 2) and SIN3 which likely exerts a repressive influence on genes important in myelopoiesis.
IKZF1 mutations were first identified in cells from Ph-positive acute lymphocytic leukemia patients and are believed to play a role in leukemic transformation (Iacobucci et al. 2009). In a study of blast phase MPN patients, a recurrent loss of chromosomal region 7p.12 led investigators to the discovery of IKZF1 deletions in 21% of patients with blast phase MPN and only 0.2% of chronic phase MPN patients, providing a very compelling argument for a role of IKZF1 in leukemic transformation (Jager et al. 2010). IKZF1 mutants are associated with increased STAT5 expression and resultant activation of the JAK–STAT pathway (Jager et al. 2010). IKZF1 mutation appears to be a late event occurring after the acquisition of JAK2V617F, and its exact pathogenetic role in MPN leukemic transformation remains unclear (Jager et al. 2010).
Genome-wide methylation pattern studies on MPN patient samples demonstrate a distinct chromatin altered pattern in PMF when compared to PV/ET patient samples (Nischal et al. 2010). Both hyper- and hypomethylated loci were found in neutrophils of PMF patients. Hypomethylated promoter sites involved genes responsible for cytokine signaling and MAP kinases. The presence of JAK2V617F additionally was found to influence the degree of DNA hypomethylation and supports a proposed role for JAK/STAT pathway influence on the methylome and ultimately on gene transcription and disease phenotype (Nischal et al. 2010).
Recently, alternative pathways by which JAK2V617F might affect hematopoiesis have been identified, and Dawson and co-workers found that 35% of the JAK2 regulated genes did not contain a STAT5 binding site (Dawson et al. 2009). This group determined that JAK2 can be localized to not only the cytoplasm but also the nucleus where it phosphorylates histone H3 at tyrosine residue 41 (Y41). H3Y41 results in release of the transcriptional repression by heterochromatin protein 1α from chromatin. Furthermore, Liu and co-workers have shown that JAK2V617F phosphorylates and downregulates the activity of PRMT5, an arginine methyltransferase discussed below (Liu et al. 2011). This event leads to a gain of function that affects the gene expression pattern and the behavior of hematopoietic progenitor cells by downregulating histone arginine methylation.
The type II arginine methyltransferase PRMT5 catalyzes the symmetric dimethylation of arginine residues on histones H2a, H3, and H4 (Branscombe et al. 2001). PRMT5 is a target of JAK2-mediated phosphorylation and in JAK2V617F expressing cells leads to downregulation of PRMT5 activity and decreased global histone methylation. Forced PRMT5 gene over-expression in primary PV CD34+ cells results in a reduction in cell proliferation and differentiation and supports the role of downregulated PRMT5 activity via JAK2 mediated phosphorylation in the molecular pathogenesis of PV. This provides a very interesting pathogenetic view of JAK2-mediated chromatin modification as a downstream target of the activated tyrosine kinase pathway.
Suppressors of cytokine signaling (SOCS1, SOCS2, and SOCS3) are negative regulators of the JAK–STAT pathway and are both induced by and act in a negative feedback loop to downregulate JAK/STAT signaling (Greenhalgh and Hilton 2001). Epigenetic silencing of SOCS1/3 is an additional pathogenetic mechanism leading to cytokine signaling hypersensitivity. SOCS1 hypermethylation has been reported in a fraction of patients with Ph-negative MPNs and can be seen in both JAK2V617F-positive and JAK2 wild-type patients (Jost et al. 2007; Teofili et al. 2008). However, the methylation pattern that was observed in these studies was noted in SOCS1 exon 2 (also seen in normal control blood cells) but not the gene promoter site and thus the relevance of this observation to MPN pathogenesis is not evident. Hypermethylation of SOCS3 has been detected in PMF but not PV/ET patients. A trend for lower SOCS3 expression in JAK2V617F-negative PMF patients was noted in one study (Fernandez-Mercado et al. 2008). SOCS methylation status was not correlated with any identifiable clinical variables or outcome (Fourouclas et al. 2008). SOCS2 silencing by hypermethylation has also been shown in MPN-derived cell lines as well as primary MPN cells and can coexist in cells that carry the JAk2V617F mutation (Quentmeier et al. 2008).
Secreted Frizzled-related protein (SFRP) actively antagonizes the Wnt signaling pathway which is integral to the maintenance and proliferation of hematopoietic stem cells (Willert et al. 2003). Upregulation of the Wnt pathway and downregulation of SFRP has been shown in other hematologic malignancies. SFRP2 promoter hypermethylation was detected in 27%, 30%, and 26% of PV, ET, and PMF patient samples, respectively (Bennemann et al. 2010). Hypermethylation of SFRP-2 promoter site was not seen in any cases of CML.
Over-expression of polycythemia rubra vera-1 (PRV-1) mRNA, a GPI-linked protein expressed by neutrophils of patients with ET/PV, has been shown to be inversely related to the C30 promoter site methylation status (Jelinek et al. 2007). PRV-1 (CD177) is a hematopoietic cell surface receptor with yet unclear function normally expressed on neutrophils and can be upregulated in certain settings including, sepsis, pregnancy, and after granulocyte colony-stimulating factor administration. Although the mRNA transcript is over-expressed in all patients with PV, the protein product is not and is comparable to the level observed in normal control neutrophils (Klippel et al. 2002). The JAK2V617F allele burden was also inversely related to C30 methylation, and a trend toward significance was appreciated with an inverse relationship to JAK2V617F allele burden.
In MF, extramedullary hematopoiesis of CD34+ hematopoietic stem cells (HSC) in the spleen and other organs is responsible for many of the signs and symptoms attributed to this disease. This abnormal cell trafficking from the bone marrow niche is believed to be a result of reduced CD34+ cell expression of CXC chemokine receptor 4 (CXCR4), leading to constitutively mobilized peripheral blood HSC (Rosti et al. 2007). CXCR4 is a receptor for stromal-derived factor-1 (SDF-1; CXCL12) and induces normal HSC and progenitor cell chemotaxis to the marrow space. The CXCR4 receptor in PMF cells, compared to normal controls, is susceptible to epigenetic modification from hypermethylation of CpG islands within its promoter region (Bogani et al. 2008). Treatment with the demethylating agent 5-aza-2′-deoxycytidine (5-AzaD; DEC) in vitro increased membrane expression of CXCR4 and improved migration of CD34+ cells in the presence of SDF-1 (Shi et al. 2007). Moreover, sequential treatment of PMF CD34+ cells with 5-AzaD and trichostatin A (TSA), a HDAC inhibitor, increased preferential homing of PMF CD34+ cells to the bone marrow and not the spleen of NOD/SCID mice (Wang et al. 2009a, b). These agents also reduced the proportion of JAK2V617F-positive HPCs, homozygous HPCs, and cells that contained chromosomal abnormalities. Most recently, treatment with sequential 5-azacytidine (5-Aza)/TSA in a JAK2V617F+ PMF CD34+ cell transplant NOD/SCID mouse model led to dramatic reduction in number of these cells suggesting potential use of these agents in treating the mutated stem cell population in PMF (Wang et al. 2010).
The HDAC family consists of 18 genes, subdivided into four classes based on their homology to yeast ortholog. The HDACs can be divided into two families, first is the Zn2+-dependent HDAC family composed of class I (HDACs 1, 2, 3 and 8), class II a/b (HDACs 4, 5, 6, 7, 9, and 10), and class IV (HDAC 11), and the second is the NAD-dependent class III SIRT enzymes (Biancotto et al. 2010). Histone acetylation is regulated by the dynamic and antagonistic action of two classes of enzymes, HDACs and HATs. HATs execute the transfer of an acetyl group from acetyl Co-A to the ε-amino group of lysine residues, whereas HDACs catalyze the removal of acetyl groups. Acetylation of histones and non-histone proteins can alter DNA–protein binding, protein–protein interaction, and/or subcellular localization. Considerable evidence indicates that the acetylation status of histones and non-histone proteins play a key role in the regulation of cellular signaling and disease progression (Haberland et al. 2009; Spange et al. 2009). For instance, global gene expression profiling of MPN patient blood cells revealed HDAC gene deregulation (Skov et al. 2010b). HDAC 9 and 11 gene over-expression was documented in various MPN subtypes, and an increase in HDAC 6 gene expression was observed during MPN disease progression. These data support the possible role of HDAC enzyme inhibition as a treatment approach to MPNs.
List of genes in which altered expression can lead to epigenetic deregulation in MPNs
ET, PV, PMF, MF-BP
Additional sex combs like 1
ET, PMF, MF-BP
Carbuccia et al. (2009)
Enhancer of zeste homolog 2
MDS/MPN, PMF, MF-BP
Ernst et al. (2010)
Isocitrate dehydrogenase 1 and 2
ET, PV, PMF, MF-BP
Ikaros family zinc finger 1
Jager et al. (2010)
Janus-associated kinase 2
ET, PV, PMF, MF-BP
Protein arginine methyltransferase 5
Liu et al. (2011)
Chromatin-modifying agents under investigation for MPN therapy
Mechanism of action
Phase of study in MPN
Histone deacetylase inhibitors
Class I/II HDAC inhibition
HSP 90 inhibition
Class I/II HDAC inhibition
Suberoylanilide hydroxamic acid
Class I/II HDAC inhibition
DNA methyltransferase inhibitors
DNA methyltransferase I inhibition
DNA methyltransferase I inhibition
A phase II pilot study of ITF2357 at 50 mg orally twice daily for 24 weeks in patients with JAKV617F-positive PV, ET, and PMF showed three major responses among 16 MF patients treated (Rambaldi et al. 2010). This agent also improved pruritus and reduced splenomegaly in 75% of PV/ET and 38% of MF patients. A trend toward reduction in JAK2V617F allele burden was observed. No major grade III/IV adverse events were observed. LBH589 has been evaluated in two phase I/II studies. In the first study, the agent was used in both high-risk JAK2V617F-positive and JAK2V617F-negative PMF and post-ET/PV MF patients (Mascarenhas et al. 2009). This agent was associated with improvements in anemia in two patients and significant reduction in palpable splenomegaly. Thrombocytopenia was found to be the DLT and the recommended phase II dose was determined to be 25 mg given orally three times weekly. In the second study among 12 patients with PMF or post-ET/PV MF, four patients demonstrated reduction in spleen size greater than 50% (DeAngelo et al. 2010). One previously untreated JAK2V617F-positive patient demonstrated a partial response according to IWG response criteria. Three additional patients demonstrated clinical improvement lasting ≥8 weeks. Four patients had stable disease. Similar to the first study, the most common adverse event was thrombocytopenia. Phase II studies of LBH589 in this setting are currently underway and are anticipated to be reported next year. A single report exists of a patient with MF that achieved normalization of peripheral blood counts within 6 weeks of treatment with SAHA (Lee 2009).
LBH589 clinical activity has been correlated with biomarker response including reduction in downstream substrates of the JAK/STAT pathway (p-STAT3, p-STAT5, p-AKT, p-ERK1/2, and p-PIM protein levels), reduction in Bcl-Xl and MCL-1 as well as modest reduction in JAK2V617F allele burden in treated patients (DeAngelo et al. 2010). Additionally, Ac-α-tubulin and HSP70 levels were found to be elevated after treatment with LBH589 which supports the mechanism of both HDAC6 and HSP90 inhibition.
Thrombocytopenia is the major dose-limiting toxicity of HDACi treatment and can pose a serious clinical risk of bleeding in the treatment of patients with MF and low baseline platelet counts. Recently, in vitro studies on primary murine megakaryocytes and murine and human cell lines has revealed that the predictable clinical thrombocytopenia induced by LBH589 is not an effect on reduced platelet survival but instead a decrease in proplatelet formation (Bishton et al. 2011). Reductions in Rho-GTPase proteins Rac1, CDC42, and RhoA after exposure to LBH589 are correlated with an increase in phosphorylated myosin light chain 2 and postulated to reduce proplatelet production in megakaryocytes. Studies by Iancu-Rubin et al. (2010) show that LBH589-induced thrombocytopenia is also likely due to a reduction in proplatelet production mediated by hyperacetylation of tubulin which is an integral component of the microtubule cytoskeleton and necessary for proplatelet extension. This work highlights the importance of the impact of HDAC inhibition on non-histone protein function. The use of a thrombopoietin mimetic in combination with LBH589 to support the drug-induced toxicity of thrombocytopenia may offer an approach that will allow more effective clinical use in MPN patients that already have low platelet counts at baseline. Alternatively, LBH589 may prove to be very useful in the treatment of patients with ET, where reducing the platelet count would be advantageous.
Two DNMTi, 5-Aza (Vidaza) and DEC (Decitabine) have been used extensively, and with success, for the treatment of MDS (Silverman et al. 2002, 2006; Kantarjian et al. 2007); these agents now also have rational application for the treatment of MPNs and have been examined in a number of phase I and II clinical trials. In two phase II studies, 5-Aza was tested as a 7- and 5-day course every 4 weeks in patients with refractory/relapsing PMF or post-ET/PV MF (Quintas-Cardama et al. 2008; Mesa et al. 2009b). No significant clinical response was seen although global hypomethylation was observed. Myelosuppression was the major adverse event in these two studies. DEC, however, has shown potential for clinical response in PMF as well as MF-BP (Mascarenhas et al. 2010; Danilov et al. 2009). In a phase II multi-center study of 20 patients with PMF treated with low-dose DEC as a subcutaneous injection, a 37% response rate was seen and two patients with MF-BP obtained a complete and partial response by WHO criteria (Odenike et al. 2008). In those patients with clinical response, a 61% mean reduction in circulating peripheral blood CD34+ cells was noted. However, no change in CXCR4 expression was seen. As is seen with 5-Aza, myelosuppression was the most common toxicity. A small retrospective study of the combined use of DEC with gemtuzumab ozogamicin in patients with MF and MF-BP supports a potential combination therapeutic approach (Al-Ameri et al. 2010).
Future studies will be designed combining both HDACi and DNMTi given either concomitantly or in sequence in MPN patients. Both scientific rationale as discussed above and clinical experience in the treatment of MDS provides a strong rationale for this treatment approach in MPNs. Additionally, as it has become clear that unlike CML which has a defined pathogenetic mechanism that can be exploited effectively, the Ph-negative MPNs are indeed more complex in their pathogenesis. These hematologic malignancies will likely require a therapeutic strategy including combinations of drugs that will affect both epigenetic events and intracellular signaling pathways in an attempt to target the MPN HSC clone. Studies combining the use of both HDACi and DNMTi together and with JAK2 inhibitors are being designed and will almost certainly herald a new era of combination therapy that will hopefully result in clinical advances.
The Ph-negative MPNs are a group of myeloid malignancies that have enjoyed a tremendous amount of attention in recent years due to successive laboratory based discoveries in molecular pathology stemming from the discovery of the JAK2V617F mutation in 2005. There is growing evidence of multiple mutational events that likely contribute to MPN pathogenesis and influence disease phenotype. Many of these gene mutations alter the MPN epigenome, and multiple genes have been identified as targets of epigenetic deregulation in MPN cells. Supported by sound scientific rationale, chromatin-modifying agents have been tested in early phase studies with a hint of efficacy and will continue to be tested more rigorously alone and in combination. An MPN-specific epigenetic signature is evolving and will likely soon play a vital role in MPN classification, prognostication, and treatment of these diverse hematopoietic stem cell neoplasms.
The authors would like to acknowledge Dr. Mingjiang Xu and Dr James Bieker for their help in reviewing sections of this manuscript.
Conflict of interest
Dr. Ronald Hoffman receives research support from Novartis and Celegene. Drs. Mascarenhas, Roper, and Chaurasia have no relevant conflict of interest to report.
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