Expression of COBLL1 encoding novel ROR1 binding partner is robust predictor of survival in chronic lymphocytic leukemia
Jazyk angličtina Země Itálie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
29122990
PubMed Central
PMC5792276
DOI
10.3324/haematol.2017.178699
PII: haematol.2017.178699
Knihovny.cz E-zdroje
- MeSH
- analýza přežití MeSH
- chronická lymfatická leukemie klasifikace diagnóza genetika mortalita MeSH
- lidé MeSH
- mutace MeSH
- pohyb buněk MeSH
- polarita buněk MeSH
- prognóza MeSH
- signální dráha Wnt MeSH
- sirotčí receptory podobné receptoru tyrosinkinasy metabolismus MeSH
- těžké řetězce imunoglobulinů genetika MeSH
- transkripční faktory metabolismus MeSH
- variabilní oblast imunoglobulinu genetika MeSH
- vazba proteinů MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- COBLL1 protein, human MeSH Prohlížeč
- ROR1 protein, human MeSH Prohlížeč
- sirotčí receptory podobné receptoru tyrosinkinasy MeSH
- těžké řetězce imunoglobulinů MeSH
- transkripční faktory MeSH
- variabilní oblast imunoglobulinu MeSH
Chronic lymphocytic leukemia is a disease with up-regulated expression of the transmembrane tyrosine-protein kinase ROR1, a member of the Wnt/planar cell polarity pathway. In this study, we identified COBLL1 as a novel interaction partner of ROR1. COBLL1 shows clear bimodal expression with high levels in chronic lymphocytic leukemia patients with mutated IGHV and approximately 30% of chronic lymphocytic leukemia patients with unmutated IGHV. In the remaining 70% of chronic lymphocytic leukemia patients with unmutated IGHV, COBLL1 expression is low. Importantly, chronic lymphocytic leukemia patients with unmutated IGHV and high COBLL1 have an unfavorable disease course with short overall survival and time to second treatment. COBLL1 serves as an independent molecular marker for overall survival in chronic lymphocytic leukemia patients with unmutated IGHV. In addition, chronic lymphocytic leukemia patients with unmutated IGHV and high COBLL1 show impaired motility and chemotaxis towards CCL19 and CXCL12 as well as enhanced B-cell receptor signaling pathway activation demonstrated by increased PLCγ2 and SYK phosphorylation after IgM stimulation. COBLL1 expression also changes during B-cell maturation in non-malignant secondary lymphoid tissue with a higher expression in germinal center B cells than naïve and memory B cells. Our data thus suggest COBLL1 involvement not only in chronic lymphocytic leukemia but also in B-cell development. In summary, we show that expression of COBLL1, encoding novel ROR1-binding partner, defines chronic lymphocytic leukemia subgroups with a distinct response to microenvironmental stimuli, and independently predicts survival of chronic lymphocytic leukemia with unmutated IGHV.
Central European Institute of Technology Masaryk University Brno Czech Republic
Generi Biotech s r o Hradec Králové Brno Czech Republic
Institute of Biostatistics and Analyses Masaryk University Brno Czech Republic
Institute of Experimental Biology Faculty of Science Masaryk University Brno Czech Republic
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Klein U, Tu Y, Stolovitzky GA, et al. Gene expression profiling of B cell chronic lymphocytic leukemia reveals a homogeneous phenotype related to memory B cells. J Exp Med. 2001;194(11):1625–1638. PubMed PMC
Rosenwald A, Alizadeh AA, Widhopf G, et al. Relation of gene expression phenotype to immunoglobulin mutation genotype in B cell chronic lymphocytic leukemia. J Exp Med. 2001;194(11):1639–1647. PubMed PMC
Masiakowski P, Carroll RD. A novel family of cell surface receptors with tyrosine kinase-like domain. J Biol Chem. 1992; 267(36):26181–26190. PubMed
Fukuda T, Chen L, Endo T, et al. Antisera induced by infusions of autologous Ad-CD154-leukemia B cells identify ROR1 as an oncofetal antigen and receptor for Wnt5a. Proc Natl Acad Sci USA. 2008; 105(8):3047–3052. PubMed PMC
Baskar S, Kwong KY, Hofer T, et al. Unique cell surface expression of receptor tyrosine kinase ROR1 in human B-cell chronic lymphocytic leukemia. Clin Cancer Res. 2008; 14(2):396–404. PubMed
Kotašková J, Pavlová Š, Greif I, et al. ROR1-based immunomagnetic protocol allows efficient separation of CLL and healthy B cells. Br J Haematol. 2016;175(2):339–342. PubMed
Daneshmanesh A, Hojjat-Farsangi M, Khan A, et al. Monoclonal antibodies against ROR1 induce apoptosis of chronic lymphocytic leukemia (CLL) cells. Leukemia. 2012; 26(6):1348–1355. PubMed
Berger C, Sommermeyer D, Hudecek M, et al. Safety of targeting ROR1 in primates with chimeric antigen receptor-modified T cells. Cancer Immunol Res. 2015;3(2):206–216. PubMed PMC
Hudecek M, Schmitt TM, Baskar S, et al. The B-cell tumor associated antigen ROR1 can be targeted with T cells modified to express a ROR1-specific chimeric antigen receptor. Blood. 2010;116(22):4532–4541. PubMed PMC
Kaucká M, Krejčí P, Plevová K, et al. Post-translational modifications regulate signalling by Ror1. Acta Physiol. 2011; 203(3):351–362. PubMed
Janovska P, Poppova L, Plevova K, et al. Autocrine signaling by Wnt-5a deregulates chemotaxis of leukemic cells and predicts clinical outcome in chronic lymphocytic leukemia. Clin Cancer Res. 2016; 22(2):459–469. PubMed PMC
Khan AS, Hojjat-Farsangi M, Daneshmanesh AH, et al. Dishevelled proteins are significantly upregulated in chronic lymphocytic leukaemia. Tumor Biol. 2016; z37(9):11947–11957. PubMed
Kaucká M, Plevová K, Pavlová Š, et al. The planar cell polarity pathway drives pathogenesis of chronic lymphocytic leukemia by the regulation of B-lymphocyte migration. Cancer Res. 2013;73(5):1491–1501. PubMed
Yu J, Chen L, Cui B, et al. Wnt5a induces ROR1/ROR2 heterooligomerization to enhance leukemia chemotaxis and proliferation. J Clin Invest. 2016;126(2):585–598. PubMed PMC
Plevova K, Francova HS, Burckova K, et al. Multiple productive immunoglobulin heavy chain gene rearrangements in chronic lymphocytic leukemia are mostly derived from independent clones. Haematologica. 2014;99(2):329–338. PubMed PMC
Baliakas P, Hadzidimitriou A, Sutton LA, et al. Clinical effect of stereotyped B-cell receptor immunoglobulins in chronic lymphocytic leukaemia: A retrospective multicentre study. Lancet Haematol. 2014; 1(2):e74–e84. PubMed
Baliakas P, Hadzidimitriou A, Sutton L, et al. Recurrent mutations refine prognosis in chronic lymphocytic leukemia. Leukemia. 2015;29(2):329–336. PubMed
Baliakas P, Iskas M, Gardiner A, et al. Chromosomal translocations and karyotype complexity in chronic lymphocytic leukemia: A systematic reappraisal of classic cytogenetic data. Am J Hematol. 2014; 89(3):249–255. PubMed
Malcikova J, Smardova J, Rocnova L, et al. Monoallelic and biallelic inactivation of TP53 gene in chronic lymphocytic leukemia: Selection, impact on survival, and response to DNA damage. Blood. 2009; 114(26):5307–5314. PubMed
Pospisilova S, Gonzalez D, Malcikova J, et al. ERIC recommendations on TP53 mutation analysis in chronic lymphocytic leukemia. Leukemia. 2012;26(7):1458–1461. PubMed
Cajanek L, Ganji RS, Henriques-Oliveira C, et al. Tiam1 regulates the Wnt/Dvl/Rac1 signaling pathway and the differentiation of midbrain dopaminergic neurons. Mol Cell Biol. 2013;33(1):59–70. PubMed PMC
de Groot REA, Ganji RS, Bernatik O, et al. Huwe1-mediated ubiquitylation of dishevelled defines a negative feedback loop in the Wnt signaling pathway. Sci Signal. 2014;7(317):ra26. PubMed
Arquint C, Sonnen KF, Stierhof Y-D, Nigg EA. Cell-cycle-regulated expression of STIL controls centriole number in human cells. J Cell Sci. 2012;125(Pt 5):1342–1352. PubMed
Cervenka I, Valnohova J, Bernatik O, et al. Dishevelled is a NEK2 kinase substrate controlling dynamics of centrosomal linker proteins. Proc Natl Acad Sci USA. 2016; 113(33):9304–9309. PubMed PMC
Bryja V, Schulte G, Arenas E. Wnt-3a utilizes a novel low dose and rapid pathway that does not require casein kinase 1-mediated phosphorylation of Dvl to activate β-catenin. Cell Signal. 2007;19(3):610–616. PubMed
Palomba ML, Piersanti K, Ziegler CGK, et al. Multidimensional single-cell analysis of BCR signaling reveals proximal activation defect as a hallmark of chronic lymphocytic leukemia B cells. PLoS One. 2014; 9(1):e79987. PubMed PMC
R Development Core Team R. R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing; 2011;p409 (R Foundation for Statistical Computing; vol.1). Available from: http://www.r-project.org.
Zhao S, Guo Y, Shyr Y. KEGGprofile: An annotation and visualization package for multi-types and multi-groups expression data in KEGG pathway. R package version 1.14.0.
Krzywinski MI, Schein JE, Birol I, et al. Circos: An information aesthetic for comparative genomics. Genome Res. 2009; 19(9):1639–1645. PubMed PMC
Ramsay AJ, Martínez-Trillos A, Jares P, Rodríguez D, Kwarciak A, Quesada V. Next-generation sequencing reveals the secrets of the chronic lymphocytic leukemia genome. Clin Transl Oncol. 2013; 15(1):3–8. PubMed
Kotaskova J, Tichy B, Trbusek M, et al. High expression of lymphocyte-activation gene 3 (LAG3) in chronic lymphocytic leukemia cells is associated with unmutated immunoglobulin variable heavy chain region (IGHV) gene and reduced treatment-free survival. J Mol Diagn. 2010;12(3):328–334. PubMed PMC
Zamò A, Ott G, Katzenberger T, et al. Establishment of MAVER-1 cell line, a model for leukemic and aggressie mantle cell lymphoma. Haematologica. 2006; 91(1):40–47. PubMed
Paganoni S, Ferreira A. Neurite extension in central neurons: a novel role for the receptor tyrosine kinases Ror1 and Ror2. J Cell Sci. 2005;118(Pt 2):433–446. PubMed PMC
Cui B, Ghia EM, Chen L, et al. High-level ROR1 associates with accelerated disease-progression in chronic lymphocytic leukemia. Blood. 2016;128(25):2931–2940. PubMed PMC
Döhner H, Stilgenbauer S, Benner A, et al. Genomic Aberrations and Survival in Chronic Lymphocytic Leukemia. N Engl J Med. 2000;343(26):1910–1916. PubMed
Hamblin TJ, Davis ZA, Oscier DG. Determination of how many immunoglobulin variable region heavy chain mutations are allowable in unmutated chronic lymphocytic leukaemia - Long-term follow up of patients with different percentages of mutations. Br J Haematol. 2008;140(3):320–323. PubMed
ten Hacken E, Burger JA. Microenvironment interactions and B-cell receptor signaling in Chronic Lymphocytic Leukemia: Implications for disease pathogenesis and treatment. Biochim Biophys Acta. 2016;1863(3):401–413. PubMed PMC
Burger JA. Chemokines and chemokine receptors in chronic lymphocytic leukemia (CLL): From understanding the basics towards therapeutic targeting. Semin Cancer Biol. 2010;20(6):424–430. PubMed
Carroll EA, Gerrelli D, Gasca S, et al. Cordon-bleu is a conserved gene involved in neural tube formation. Dev Biol. 2003; 262(1):16–31. PubMed
Gordon GJ, Jensen RV, Hsiao LL, et al. Using gene expression ratios to predict outcome among patients with mesothelioma. J Natl Cancer Inst. 2003;95(8):598–605. PubMed
Han SH, Kim SH, Kim HJ, et al. Cobll1 is linked to drug resistance and blastic transformation in chronic myeloid leukemia. Leukemia. 2017;31(7):1532–1539. PubMed
Benita Y, Cao Z, Giallourakis C, Li C, Gardet A, Xavier RJ. Gene enrichment profiles reveal T-cell development, differentiation, and lineage-specific transcription factors including ZBTB25 as a novel NF-AT repressor. Blood. 2010;115(26):5376–5384. PubMed PMC
Morabito F, Cutrona G, Gentile M, et al. Prognostic relevance of in vitro response to cell stimulation via surface IgD in binet stage a CLL. Br J Haematol. 2010; 149(1):160–163. PubMed
Lanham S, Hamblin T, Oscier D, Ibbotson R, Stevenson F, Packham G. Differential signaling via surface IgM is associated with VH gene mutational status and CD38 expression in chronic lymphocytic leukemia. Blood. 2003;101(3):1087–1093. PubMed
Irish JM, Czerwinski DK, Nolan GP, Levy R. Kinetics of B Cell Receptor Signaling in Human B Cell Subsets Mapped by Phosphospecific Flow Cytometry. J Immunol. 2006;177(3):1581–1589. PubMed
Irish JM, Czerwinski DK, Nolan GP, Levy R. Altered B-cell receptor signaling kinetics distinguish human follicular lymphoma B cells from tumor-infiltrating nonmalignant B cells. Blood. 2006;108(9):3135–3142. PubMed PMC
Thompson PA, O’Brien SM, Wierda WG, et al. Complex karyotype is a stronger predictor than del(17p) for an inferior outcome in relapsed or refractory chronic lymphocytic leukemia patients treated with ibrutinib-based regimens. Cancer. 2015; 121(20):3612–3621. PubMed PMC
Abruzzo LV, Barron LL, Anderson K, et al. Identification and validation of biomarkers of IgV(H) mutation status in chronic lymphocytic leukemia using microfluidics quantitative real-time polymerase chain reaction technology. J Mol Diagn. 2007; 9(4):546–555. PubMed PMC
Plesingerova H, Librova Z, Plevova K, et al. COBLL1, LPL and ZAP70 expression defines prognostic subgroups of chronic lymphocytic leukemia patients with high accuracy and correlates with IGHV mutational status. Leuk Lymphoma. 2017; 58(1):70–79. PubMed
Morabito F, Mosca L, Cutrona G, et al. Clinical monoclonal B lymphocytosis versus rai 0 chronic lymphocytic leukemia: A comparison of cellular, cytogenetic, molecular, and clinical features. Clin Cancer Res. 2013;19(21):5890–5900. PubMed
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