Abstract: APTs as miRNA targets provide a novel molecular mechanism for how primary CLL cells escape from CD95-mediated apoptosis. Palmitoylation as a novel posttranslational modification in CLL might also impact on survival signaling, proliferation, and migration.

Abstract: FcμR is a more selective target for the CAR T-cell therapy of CLL compared with currently used targets, including CD19.

Abstract: Rationale: The BTK inhibitor ibrutinib has proved to be highly effective in both treatment naїve and refractory or relapsed CLL patients. In contrast to most other therapeutic options, where unmutated IGVH correlates with adverse prognosis, response to ibrutinib is independent of IGVH mutation status. This compulsorily raises the question why CLL cells with an unmutated IGVH are equally susceptible to BTK inhibition. One key aspect might be understanding the global (phospho)proteome of UM-CLL and M-CLL cells which has not been investigated so far. Methods: We performed a comprehensive proteomics and phosphopreoteomics analysis of 14 CLL samples with unmutated or mutated IgVH using quantitative mass spectrometry (MS). ITRAQ labelling and TiO2 enrichment/HILIC fractionation were utilized for this approach. Results: Altogether we identified 9184 phosphopeptides corresponding to 2854 proteins. We found the typical pS:pT:pY ratio, with 89% of all detected phosphopeptides containing a phosphorylated serine (pS), 10% a phosphorylated threonine (pT) and 1% a phosphorylated tyrosine (pY) in CLL samples. Strikingly, UM-CLL showed a higher basal phosphorylation level than M-CLL samples with significantly higher phosphorylation of 92 out of 102 identified proteins (P 〈 0.05) Interestingly, ibrutinib reverted this phosphorylation pattern predominantly in UM-CLL but not M-CLL samples and led to a shift of the ratio towards phosphotyrosine in UM-CLL (pS:pT:pY in %: 30:9:61) but not in M-CLL (pS:pT:pY: 78:7:15). Most of the indentified phosphopeptides clustered in pathways that regulate migration and motility and cell survival and death. Regarding the BCR pathway, we identified known and novel p-sites: Lyn (8 sites), PIK3AP1 (5), PLCG2 (5), Syk (4), BLK (4), PIK3R4 (2), LCK (2), BTK (1), PIK3C2B (1), PIK3C3 (1), PIK3CD (1). In this context a novel molecule, MARCKS attracted our attention. We identified three different p-sites (S101, T150 and S170) which were differentially phosphorylated in M-CLL and UM-CLL. Moreover, our proteome approach revealed distinct expression levels of 38 proteins out of 3466 isolated proteins between the two groups (1,5-fold changes; P 〈 0.01), among them MARCKS. Expression of MARCKS was significantly higher in M-CLL samples. MARCKS, a PKC substrate, was shown to play a critical role in invasiveness and metastasis of various cancer types, but its role in CLL is unclear. Since MARCKS has not been associated with CLL, we proved our findings from MS in a larger cohort of CLL patients both on protein level (n=36) and on transcription level (n=337). Strikingly, shorter PFS of CLL patients (n=337) undergoing chemoimmunotherapy correlates with low expression of MARCKS independently of the mutational status. We further investigated the cellular function of MARCKS in CLL cells utilizing CRISPR/Cas9 to generate KO cells. We were able to show that MARCKS regulates migration towards CXCL12 and that a loss of MARCKS leads to significantly increased migration. As MARCKS is upstream of AKT at the plasma membrane, we wondered if its expression might be relevant for AKT signalling. Importantly, we found that AKT phosphorylation (S473) was significantly upregulated in MARCKS KO cells indicating that MARCKS is involved in AKT regulation. Since MARCKS seems to be involved in tumor microenvironment (TME) interaction, we determined the influence of TME stimuli on MARCKS regulation. Interestingly, MARCKS was upregulated by CD40:CD40L interaction but phosphorylated upon BCR stimulation in both M-CLL and UM-CLL as assessed by immunoblot. Furthermore, we identified MARCKS to be targeted by ibrutinib, as phosphorylation at S170 was reduced upon ibrutinib treatment. Conclusion: For the first time we could show a comprehensive picture of the phosphoproteome and proteome of UM-CLL and M-CLL samples. Strikingly, the basal phosphorylation level was significantly higher in UM-CLL and was more susceptible to ibrutinib treatment. Our findings reveal a relevant association of MARCKS expression with CLL prognosis, supported by the functional evidence that MARCKS acts upstream as novel modulator of AKT signalling and controls migration towards CXCL12. These data indicate that MARCKS is a novel and relevant target of ibrutinib especially in the context of the TME. Disclosures Bahlo: Roche: Honoraria, Other: Travel Grants. Fischer:Roche: Other: Travel support. Wendtner:Roche: Consultancy, Honoraria, Other: travel support, Research Funding; Janssen: Consultancy, Honoraria, Other: travel support, Research Funding; Gilead: Consultancy, Honoraria, Research Funding; Genetech: Consultancy, Honoraria, Other: travel support, Research Funding; GlaxoSmithKline: Consultancy, Honoraria, Other: travel support, Research Funding; Abbvie: Consultancy, Honoraria, Other: travel support, Research Funding; Mundipharma: Consultancy, Honoraria, Research Funding; MorphoSys: Consultancy, Honoraria, Other: travel support, Research Funding; Pharmacyclics: Consultancy, Honoraria, Other: travel support, Research Funding; Gilead: Consultancy, Honoraria, Other: travel support, Research Funding. Stilgenbauer:Pharmcyclics: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; AbbVie: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Amgen: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Genzyme: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Mundipharma: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Genentech: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; GSK: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Sanofi: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Janssen: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Boehringer-Ingelheim: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Gilead: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Novartis: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Celgene: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Hoffmann La-Roche: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding. Hallek:Pharmacyclics: Honoraria, Research Funding; Celgene: Honoraria, Research Funding; Mundipharma: Honoraria, Research Funding; Janssen: Honoraria, Research Funding; Gilead: Honoraria, Research Funding; Abbvie: Honoraria, Research Funding; Roche: Honoraria, Research Funding.

Abstract: Background: The Fc receptor for IgM (FcmR/ TOSO) is significantly overexpressed on chronic lymphocytic leukemia (CLL) cells from peripheral blood, but becomes down-regulated in the tumor microenvironment by e.g. CD40:CD40L interaction. Since the functional role of FcmR on lymphomagenesis is still not understood, we developed a conditional knockout mouse with B cell-specific FcmR-depletion. These mice were crossbred with the Eµ-TCL1 murine model, which develops a CLL-like phenotype. Results: The depletion of FcmR/TOSO in TCL1 mice (Eµ-Tcl1tg/wt FcmRfl/fl CD19cre/wt; further on called TCT) revealed a significantly shorter overall survival (296 days; n=40) compared to the TOSO expressing control mice (Eµ-Tcl1tg/wt FcmRwt/wt CD19cre/wt; TC; 344 days; n=106; Log-rank p 〈 0.0001). In addition, these mice show a significantly higher blood leukocyte count and lower platelet and erythrocyte count. Leukocytes could be identified as CLL-characteristic leukemic CD19+/CD5+ B cells. Altogether TCT exhibited a faster progress of disease. Spleen immunohistochemistry revealed the transformation of most TCT (14/17 transformed) into an even more aggressive phenotype with increased splenomegaly and change in tissue and cell morphology compared to TC (9/9 not transformed). While characterizing these cells by flow cytometry, we identified a significantly higher expression of IgM on malignant B cells from TCT in comparison to TC mice. This finding indicates that the BCR itself might have a different contribution to lymphomagenesis in FcmR knock-out settings. Therefore, to validate the functional role of FcmR in the process of lymphomagenesis, we performed transcriptome profiling by RNA-Seq using splenic leukemic cells (CD19+ CD5+) from 36-week old TC (n=4) and TCT (n=4) mice. 2089 genes were found to be significantly modulated in the malignant cells of TCT mice, from which 1221 were downregulated and 868 showed an upregulation (significant change in mean expression; p 〈 0.05). To investigate the role of IgM on TCT mice, purified malignant B cells were incubated for two hours with F(ab')2 goat anti-mouse IgM. Strikingly, TCT mice showed 3941 genes (2054 downregulated, 1887 upregulated) with significant difference in expression compared to TC (p 〈 0.05). The gene expression profiles of the anti-IgM treated mice revealed a stronger regulation of BCR signalling in TCT mice, suggesting that FcmR represents an important factor in these processes. We examined the gene expression profiles, using Ingenuity Pathway Analysis Software. Analysis revealed that the most deregulated functions include interferon-signalling, recruitment of leukocytes, infection of cells and cellular movement. Conclusion: Here we present functional evidence that loss of FcmR results in increased IgM/BCR on the surface of non-switched leukemia. Moreover, malignant cells with loss of FcmR are more susceptible to BCR stimulation and show a signature of signalling pathways, which contribute to inflammation in B cell malignancies. Disclosures Fingerle-Rowson: MorphoSys: Employment. Pallasch:Gilead: Research Funding. Wendtner:Abbvie: Consultancy, Honoraria, Other: travel support, Research Funding; Mundipharma: Consultancy, Honoraria, Research Funding; Gilead: Consultancy, Honoraria, Research Funding; GlaxoSmithKline: Consultancy, Honoraria, Other: travel support, Research Funding; Gilead: Consultancy, Honoraria, Other: travel support, Research Funding; Genetech: Consultancy, Honoraria, Other: travel support, Research Funding; Janssen: Consultancy, Honoraria, Other: travel support, Research Funding; Pharmacyclics: Consultancy, Honoraria, Other: travel support, Research Funding; MorphoSys: Consultancy, Honoraria, Other: travel support, Research Funding; Roche: Consultancy, Honoraria, Other: travel support, Research Funding.