Citations 152

Antigen-mediated regulation in monoclonal gammopathies and myeloma

JCI Insight | April 18, 2018 | Volume: 3 | Issue: 8 | Pages: No page available

10.1172/jci.insight.98259 | PMID 29669929

A role for antigen-driven stimulation has been proposed in the pathogenesis of monoclonal gammopathy of undetermined significance (MGUS) and multiple myeloma (MM) based largely on the binding properties of monoclonal Ig. However, insights into antigen binding to clonal B cell receptors and in vivo responsiveness of the malignant clone to antigen-mediated stimulation are needed to understand the role of antigenic stimulation in tumor growth. Lysolipid-reactive clonal Ig were detected in Gaucher disease (GD) and some sporadic gammopathies. Here, we show that recombinant Ig (rIg) cloned from sort-purified single tumor cells from lipid-reactive sporadic and GD-associated gammopathy specifically bound lysolipids. Liposome sedimentation and binding assays confirmed specific interaction of lipid-reactive monoclonal Ig with lysolipids. The clonal nature of lysolipid-binding Ig was validated by protein sequencing. Gene expression profiling and cytogenetic analyses from 2 patient cohorts showed enrichment of nonhyperdiploid tumors in lipid-reactive patients. In vivo antigen-mediated stimulation led to an increase in clonal Ig and plasma cells (PCs) in GD gammopathy and also reactivated previously suppressed antigenically related nonclonal PCs. These data support a model wherein antigenic stimulation mediates an initial polyclonal phase, followed by evolution of monoclonal tumors enriched in nonhyperdiploid genomes, responsive to underlying antigen. Targeting underlying antigens may therefore prevent clinical MM.
The p97 Inhibitor CB-5083 Is a Unique Disrupter of Protein Homeostasis in Models of Multiple Myeloma

Molecular Cancer Therapeutics | September 6, 2017 | Volume: 16 | Issue: 11 | Pages: 2375-2386

10.1158/1535-7163.mct-17-0233 | PMID 28878026

Abstract Inhibition of the AAA ATPase, p97, was recently shown to be a novel method for targeting the ubiquitin proteasome system, and CB-5083, a first-in-class inhibitor of p97, has demonstrated broad antitumor activity in a range of both hematologic and solid tumor models. Here, we show that CB-5083 has robust activity against multiple myeloma cell lines and a number of in vivo multiple myeloma models. Treatment with CB-5083 is associated with accumulation of ubiquitinated proteins, induction of the unfolded protein response, and apoptosis. CB-5083 decreases viability in multiple myeloma cell lines and patient-derived multiple myeloma cells, including those with background proteasome inhibitor (PI) resistance. CB-5083 has a unique mechanism of action that combines well with PIs, which is likely owing to the p97-dependent retro-translocation of the transcription factor, Nrf1, which transcribes proteasome subunit genes following exposure to a PI. In vivo studies using clinically relevant multiple myeloma models demonstrate that single-agent CB-5083 inhibits tumor growth and combines well with multiple myeloma standard-of-care agents. Our preclinical data demonstrate the efficacy of CB-5083 in several multiple myeloma disease models and provide the rationale for clinical evaluation as monotherapy and in combination in multiple myeloma. Mol Cancer Ther; 16(11); 2375–86. ©2017 AACR.
Multiple myeloma cells’ capacity to decompose H2O2 determines lenalidomide sensitivity

Blood | December 28, 2016 | Volume: 129 | Issue: 8 | Pages: 991-1007

10.1182/blood-2016-09-738872 | PMID 28028022

Key Points IMiDs inhibit TrxR-mediated intracellular decomposition of H2O2 and caused oxidative stress in MM cells. MM cells with lower antioxidative capacity were more vulnerable to lenalidomide-induced H2O2 accumulation and its associated cytotoxicity.
Phase II trial of nab‐paclitaxel in patients with relapsed or refractory multiple myeloma

American Journal of Hematology | September 1, 2016 | Volume: 91 | Issue: 12 | Pages: No page available

10.1002/ajh.24548 | PMID 27581088

Abstract 541: Successful oncolytic virotherapy in a bortezomib resistant syngeneic mouse model of multiple myeloma: Implications for translational significance

Cancer Research | July 26, 2016 | Volume: 76 | Issue: 14_Supplement | Pages: 541-541

10.1158/1538-7445.am2016-541

Abstract Introduction: Multiple myeloma (MM) is a malignancy of plasma cells that is still considered incurable due to the 90% relapse rate in patients. Despite the advent of new agents the majority of MM patients relapse secondary to therapy resistance. The potential of reovirus (RV) as a novel therapeutic agent for MM under in vitro, in vivo and ex vivo conditions has been demonstrated by us and a phase I clinical trial of MM with RV therapy has shown indications of efficacy. Recently we have shown that RV could synergize with several standard of care MM drugs such as bortezomib (BTZ), carfilzomib (CFZ) and dexamethasone and importantly, enhance its therapeutic potential in therapy resistant human MM cell lines in vitro. Utilizing the syngeneic Vk*MYC BTZ resistant transplantable MM mouse model, we demonstrate that mice harbouring BTZ insensitive MM tumors significantly respond to RV treatment. Our data indicate that this RV treatment sensitivity is manifested via, direct oncolysis in conjunction with immune modulatory effects. Methods: Vk*MYC myeloma cells (Vk12598) were injected via tail vein (IV) into 3 groups of C57BL/6 wt recipient mice. Seven days post tumor injection, mice were treated with PBS (vehicle) or live (LV) or dead reovirus (DV) (5×10⁁8 PFU) administered IV every 6 days in a total of 5 doses. Serum gamma globulins (M-spike) were assessed weekly by serum protein electrophoresis. Mice were sacrificed on day 35 post tumour injection and their spleens and bone marrow (BM) were harvested. Splenic and BM cells were stained for CD45+/CD45R-/CD138+ (MM tumors), CD4+/CD8+ (T cells), CD3+/NKG2D+ (NKT cells), CD11b+Ly6C+ (monocytic myeloid derived suppressor cells (Mo-MDSC) and CD11b+Ly6G+ (polymorphonuclear (PMN) - MDSCs) and analyzed by flow cytometry. Results: Mice treated with RV demonstrated highly significant (P<0.001) reductions in their M-spikes at 4 and 5 weeks post treatment. RV treatment led to a significant NKT cell accumulation in splenic and BM of RV treated mice in comparison to vehicle treated mice suggestive of immune activation due to RV. Further, RV treatment led to a significant increase in BM Mo-MDSC number but not PMN-MDSC numbers. Interestingly, significant down regulation of splenic PMN-MDSCs was seen with RV treatment. Conclusions: Our results indicate reovirotherapy is successful in a validated syngeneic BTZ resistant MM model. These results have important implications for future clinical trials. Currently we are conducting further experiments to assess the immune modulatory (such as T - memory and T - regulatory cells) contributions of RV in this model. Citation Format: Chandini M. Thirukkumaran, Zhong Qiao Shi, Joanne Luider, Karen Kopciuk, Marta Chesi, Leif Bergsagel, Yuan Dong, Chunfen Zhang, Ahmed Mostafa, Kathy Gratton, Satbir Thakur, Don Morris. Successful oncolytic virotherapy in a bortezomib resistant syngeneic mouse model of multiple myeloma: Implications for translational significance. [abstract]. In: Proceedings of the 107th Annual Meeting of the American Association for Cancer Research; 2016 Apr 16-20; New Orleans, LA. Philadelphia (PA): AACR; Cancer Res 2016;76(14 Suppl):Abstract nr 541.
Abstract B155: Anti-CD137 mAb therapy of multiple myeloma

Cancer Immunology Research | May 20, 2016 | Volume: 4 | Issue: 1_Supplement | Pages: B155-B155

10.1158/2326-6074.cricimteatiaacr15-b155

Abstract Multiple myeloma is a blood cancer that arises in the bone marrow from malignant plasma cells. Although treatments have dramatically improved during the last decade, multiple myeloma remains an incurable disease responsible for more than 10 000 deaths per year in the United States. CD137 is a costimulatory molecule expressed on activated T cells and NK cells. We recently established that agonist monoclonal antibodies (mAbs) against CD137 (clone 3H3) significantly reduce tumor burden and improve survival in a mouse model of multiple myeloma1. We found that anti-CD137 mAb therapeutic activity requires the presence of both CD8 T cells and NK cells but is independent of Fc receptors. Moreover, we observed increased numbers of T cells in the bone marrow of anti-CD137 mAb treated mice. CD8 T cells were increased while the percentage of Tregs was reduced. Thus, anti-CD137 mAbs protect mice against multiple myeloma by inducing potent NK cell and CD8 T cell responses. In the present study, we investigate further the therapeutic interest and the potential limitations of anti-CD137 mAbs. To this aim, we used multiple myeloma cell lines derived from Vk*MYC transgenic mice. Wild-type (WT) mice intravenously injected with Vk*MYC cells develop a disease very similar to human multiple myeloma. High percentages of malignant plasma cells are observed in the bone marrow and in the spleen 5 weeks after injection and disease progression can be followed by the level of serum gamma-globulin (M protein). We first observed that, although early anti-CD137 mAb treatment efficiently protected the mice against multiple myeloma, this treatment loses efficacy when given more than 3 weeks after Vk*MYC cell injection. Interestingly, CD4 cell depletion restores the efficacy of late anti-CD137 mAb treatment, indicating that Treg-mediated suppression may limit the therapeutic efficacy of anti-CD137 mAbs. In line with previous studies, we observed that NK cell numbers in the spleen are dramatically reduced 12 days after the initiation of anti-CD137 mAb treatment. NK cell numbers are also decreased in other organs including liver, lung and blood. Importantly, we found that NK cells are still poorly represented in the spleen 3 weeks after the last treatment with anti-CD137 mAbs. Finally, we observed that anti-CD137 mAb treatment induced T cell activation and increases T cell infiltration in the liver. Consistent with the cases of severe hepatitis observed in patients treated with anti-CD137 mAbs, we noted that some of anti-CD137 mAb treated mice that had survived multiple myeloma developed severe liver damage. Such liver damage could be observed more than 100 days after the last therapy with anti-CD137 mAbs. In conclusion, we report several side effects induced by anti-CD137 mAbs treatment that last long after the treatment has been interrupted. These results encourage being particularly careful when administrating this drug to patients. Our study demonstrates the utility of mouse models to investigate the anti-tumor benefits versus toxicity of immunotherapies. We are planning to use this approach to assess the therapeutic efficacy of anti-CD137 mAbs in combination with other treatments. We speculate that the prior reduction of tumor burden by chemotherapy or stem cell transplantation will allow better efficacy of anti-CD137 mAbs at lower doses. The use of mice injected with multiple myeloma cell lines will help determining which combination allows efficient anti-tumor responses at late multiple myeloma stages with limited toxicity. 1 Guillerey C*, De Andrade LF*, Vuckovic S, Miles K, Ngiow SF, Yong MCR, Teng MWL, Colonna M, Ritchie DS, Chesi M, Bergsagel PL, Hill GR, Smyth MJ*, Martinet L* Immunosurveillance and therapy of multiple myeloma is CD226-dependent; Journal of Clinical Investigation, May 1;125(5):2077-89. Citation Format: Camille Guillerey, Lucas Ferrari de Andrade, Slavica Vuckovic, David Ritchie, Marta Chesi, Leif Bergsagel, Geoffrey R. Hill, Ludovic Martinet, Mark J. Smyth. Anti-CD137 mAb therapy of multiple myeloma. [abstract]. In: Proceedings of the CRI-CIMT-EATI-AACR Inaugural International Cancer Immunotherapy Conference: Translating Science into Survival; September 16-19, 2015; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2016;4(1 Suppl):Abstract nr B155.
Chromogranin A Is Preferentially Cleaved into Proangiogenic Peptides in the Bone Marrow of Multiple Myeloma Patients

Cancer Research | February 11, 2016 | Volume: 76 | Issue: 7 | Pages: 1781-1791

10.1158/0008-5472.can-15-1637 | PMID 26869462

Abstract Angiogenesis has been postulated to be critical for the pathogenesis of multiple myeloma, a neoplastic disease characterized by abnormal proliferation of malignant plasma cells in the bone marrow (BM). Cleavage of the N- and C-terminal regions of circulating chromogranin A (CgA, CHGA), classically an antiangiogenic protein, can activate latent antiangiogenic and proangiogenic sites, respectively. In this study, we investigated the distribution of CgA-derived polypeptides in multiple myeloma patients and the subsequent implications for disease progression. We show that the ratio of pro/antiangiogenic forms of CgA is altered in multiple myeloma patients compared with healthy subjects and that this ratio is higher in BM plasma compared with peripheral plasma, suggesting enhanced local cleavage of the CgA C-terminal region. Enhanced cleavage correlated with increased VEGF and FGF2 BM plasma levels and BM microvascular density. Using the Vk*MYC mouse model of multiple myeloma, we further demonstrate that exogenously administered CgA was cleaved in favor of the proangiogenic form and was associated with increased microvessel density. Mechanistic studies revealed that multiple myeloma and proliferating endothelial cells can promote CgA C-terminal cleavage by activating the plasminogen activator/plasmin system. Moreover, cleaved and full-length forms could also counter balance the pro/antiangiogenic activity of each other in in vitro angiogenesis assays. These findings suggest that the CgA-angiogenic switch is activated in the BM of multiple myeloma patients and prompt further investigation of this CgA imbalance as a prognostic or therapeutic target. Cancer Res; 76(7); 1781–91. ©2016 AACR.
UCHL1is a biomarker of aggressive multiple myeloma required for disease progression

Oncotarget | October 27, 2015 | Volume: 6 | Issue: 38 | Pages: 40704-40718

10.18632/oncotarget.5727 | PMID 26513019

Abstract IA25: Targeting genetic heterogeneity in multiple myeloma through immune activation.

Clinical Cancer Research | August 21, 2015 | Volume: 21 | Issue: 17_Supplement | Pages: IA25-IA25

10.1158/1557-3265.hemmal14-ia25

Abstract Multiple myeloma (MM) cells are the malignant counterpart of post-germinal center (GC) long-lived PCs, characterized by strong BM dependence, somatic hypermutation (SHM) of immunoglobulin (Ig) genes, and isotype class switch recombination (CSR) resulting in absence of IgM expression in all but 1% of tumors. Virtually every case of MM is preceded by a pre-malignant PC tumor called monoclonal gammopathy of undetermined significance (MGUS) that, like MM, produces a typical M-spike by SPEP or free light chain in the urine. Translocations involving the immunoglobulin heavy chain (IgH) locus are present in at least half of MM cases and are thought to result from errors during the physiological process of CSR or SHM. These translocations result in dysregulated expression of an oncogene that is juxtaposed to the strong Ig enhancers. There are three recurrent primary IgH translocation groups in MM: CYCLIN D (11q13-CYCLIN D1; 12p13-CYCLIN D2; 6p25-CYCLIN D3) MAF (16q23-MAF; 20q12-MAFB; 8q24.3-MAFA; MMSET/(FGFR3)-4p16-(MMSET in all but also FGFR3 in 80% of these tumors. Multiple trisomies represent an alternative pathogenetic pathway. There is a consensus that chromosome content reflects at least two pathways of pathogenesis. Nearly half of MGUS and MM tumors are hyperdiploid (HRD), usually with extra copies of three or more specific chromosomes (3,5,7,9,11,15,19, 21). Strikingly, HRD tumors rarely (~10%) have a primary IgH translocation, whereas Non-hyperdiploid (NHRD) tumors usually (~70%) have an IgH translocation. Almost all cases of plasma cell neoplasm starting from the MGUS stage and independently on the chromosome content aberrantly express one or more of the CYCLIN D genes and it has been proposed that dysregulation of a CYCLIN D gene provides a unifying, early oncogenic event in MGUS and MM. Consistently, the dysregulation of CYCLIN D1 in mouse B cells is sufficient to induce a monoclonal gammopathy that does not progress to MM. Secondary oncogenic events drive MGUS and MM progression MYC dysregulation. There is increased expression of c-MYC in most newly diagnosed MM tumors compared to MGUS tumor. Recently, it was shown that sporadic activation of a MYC transgene (Vk*MYC) in GC B cells in an MGUS prone mouse strain led to the universal development of MM tumor. Hence, increased MYC expression may be responsible for progression from MGUS to MM. Complex translocations involving MYC appear to be secondary progression events that often do not involve Ig loci, but rather other super enhancers that are very active in plasma cells. They are rare or absent in MGUS, but recently identified in over 40% of untreated MM, and 90% of MM cell lines. Activating mutations of RAS and BRAF. The prevalence of activating NRAS or KRAS mutations is about 15-18% each in newly diagnosed and relapsed MM tumors, and recently, BRAF mutations were described in 4% of MM tumors. Expression of an activated of KRAS in mouse B cells is sufficient to induce a monoclonal gammopathy but it does not progress to MM. Not surprisingly, dysregulating pairs of CYCLIN D1, KRAS and/or MYC in mouse B cells accelerated the progression of MM. Activating mutations of NFkappaB pathway. Extrinsic ligands (APRIL and BAFF) produced by BM stromal cells provide critical survival signals to long-lived PCs by stimulating TACI, BCMA, and BAFF receptors to activate the NFKB pathways. Most MGUS and MM tumors highly express NFKB target genes, suggesting a continued role of extrinsic signaling in PC tumors and at least in part explaining the constant dependency of MM cells on the BM microenvironment. Activating mutations in positive regulators and inactivating mutations in negative regulators of the NFKB pathway have been identified in at least 20% of untreated MM tumors and ~50% of HMCLs, rendering the cells less dependent on ligand-mediated NFKB activation and most likely contributing to extra-medullary spread of the disease. Additional changes include monosomy 13 (DIS3, mir15/16, RB1), del17p (TP53), add1q (MCL1) and del1p (CDKN2C, FAM46C). While the role of these putative tumor suppressor/oncogene remain to be defined, we found that loss of one copy of miR15/16 cooperated with MYC to cause the progression of MM in mice, while loss of one copy of RB1 did not, implicating loss of miR15/16 as one driving force behind selection for monosomy 13 in human MM. High-risk MM is associated with intra-clonal tumor heterogeneity Recent evidence indicates that tumor heterogeneity is prevalent in MM, as in many other cancers, and that different subclones are present within the tumor population, characterized by distinct genetic mutations that contributed independently to the tumor progression. The degree of clonal heterogeneity is presumably related to the degree of genomic instability, and appears to correlate with the presence of high-risk genetics. Three patterns of relapse are seen following successful therapy. A third of the time the dominant clone at diagnosis predominates, unchanged, at relapse. A third of the time the diagnostic clone has acquired additional genetic changes at relapse. And a third of the time an ancestral clone to the one dominant at diagnosis emerges, lacking some of the genetic changes present in the diagnostic clone, and having acquired additional genetic changes. Activating the immune system to overcome tumor heterogeneity MM cells develop a malignant relationship with components of the innate immune system in the BM. Initially inflammatory macrophages support MM tumor development, but over time convert to an immunosuppressive M2 phenotype. This relationship can be disrupted by activating signaling downstream of TLR and TNFR receptors in macrophages through the use of IAP antagonists which target for destruction negative regulators of these pathways (cIAP1/2). In MM bearing mice with a mature (but not those with an immature) immune system this results in a complete response, with no evidence of a direct anti-tumor effect of IAP antagonists on the tumor cells at clinically relevant doses. This has led to a phase II clinical trial of IAP antagonists to activate the innate immune system in patients with MM. The treatment is associated with dramatic activation and mobilization of macrophages, with cytokine release and early evidence of anti-tumor effects. Conclusion Significant progress has been made is understanding the molecular pathogenesis and biology of MM. Oncogenic pathways can be activated through cell intrinsic or extrinsic mechanisms. Similar to other cancers, MM is characterized by multi-stage accumulation of genetic abnormalities deregulating different pathways. Much of this knowledge is already being utilized for diagnosis, prognosis and risk-stratification of patients. Importantly, from a clinical standpoint, this knowledge has led to development of novel therapeutic strategies, some of which are already in clinical use, and many others showing promise in pre-clinical and early clinical studies. Citation Format: Marta Chesi, P. Leif Bergsagel. Targeting genetic heterogeneity in multiple myeloma through immune activation. [abstract]. In: Proceedings of the AACR Special Conference on Hematologic Malignancies: Translating Discoveries to Novel Therapies; Sep 20-23, 2014; Philadelphia, PA. Philadelphia (PA): AACR; Clin Cancer Res 2015;21(17 Suppl):Abstract nr IA25.
Advances in the pathogenesis and diagnosis of multiple myeloma

International Journal of Laboratory Hematology | May 15, 2015 | Volume: 37 | Issue: S1 | Pages: 108-114

10.1111/ijlh.12360 | PMID 25976968

SummaryMultiple myeloma (MM) is a tumor of indolent, bone marrow (BM) localized, isotype‐switched plasma cells. Recently, the diagnostic criteria have been amended to include some patients who would previously have been diagnosed with ultra‐high‐risk smoldering MM and benefit from immediate treatment. Genetically it can be divided into tumors with different recurrent immunoglobulin heavy chain gene translocations (4p16, 11q13, 6p21, 16q23, 20q11) and tumors characterized by hyperdiploidy with multiple trisomies. Recent genomic studies have shown that almost half of untreated patients have a genetic rearrangements of the MYC locus that result in juxtaposition of ectopic super‐enhancers adjacent to MYC, as well as somatic mutations that activate the RAS/MAPK pathway (NRAS, KRAS, BRAF, FGFR3). Mutations that result in constitutive activation of the NFkB pathway and that inactivate TP53, CDKN2C, KDM6A, FAM46C, and DIS3 are also recurrent. A major insight from these studies has been the recognition of the high degree of subclonal heterogeneity in MM, which is more frequent in patients with high‐risk genetics. The subclones may alternate in dominance under alternating therapeutic pressure, a phenomenon known as ‘clonal tides’. The identification of marked subclonal heterogeneity argues in those patients for the use of therapeutic strategies to maximize response, and long‐term suppressive therapies to prevent tumor regrowth and development of additional subclones.