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Chronic myeloproliferative neoplasms

Reduced CXCR4-expression on CD34-positive blood cells predicts outcomes of persons with primary myelofibrosis

Abstract

The expression of the CXCR4 chemokine receptor on CD34-positive blood cells is reduced in persons with primary myelofibrosis (PMF). We analyzed the relevance of cytofluorimetric assessment of the percentage of CD34-positive blood cells that had a positive CXCR4 surface expression (CD34/CXCR4-se) in a large cohort of subjects with myeloproliferative neoplasms. Mean CD34/CXCR4-se was lower in subjects with PMF compared with those with essential thrombocythemia (ET) or polycythemia vera (PV). A cutoff value of 39% was associated with a diagnosis of pre-fibrotic PMF vs. ET with a positive predictive value of 97%. In PMF male sex, older age, and MPL mutation were independent correlates of reduced CD34/CXCR4-se and associated with a briefer interval to development of severe anemia, large splenomegaly, thrombocytopenia, leukopenia, elevated CD34-positive blood cells, blast transformation and death. We constructed a prognostic model including age >65 years, hemoglobin < 100 g/L, CD34-positive blood cells > 50 × 106/L, and CD34/CXCR4-se <39% at diagnosis. The model identified three risk cohorts with greater accuracy compared with the International Prognostic Scoring System. In conclusion, CD34/CXCR4-se is a highly sensitive marker of disease activity and a new potential diagnostic and prognostic biomarker in PMF.

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Fig. 1: Comparative expression of blood CD34/CXCR4-se (mean ± 1.96 standard error) in the subtypes of MPNs and normals.
Fig. 2: Comparative expression of CD34/CXCR-se (mean ± 1.96 standard error) of subjects with primary myelofibrosis stratified according to the driver mutations genotypes.
Fig. 3: Overall survival curves.

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References

  1. Rampal R, Al-Shahrour F, Abdel-Wahab O, Patel JP, Brunel J-P, Mermel CH, et al. Integrated genomic analysis illustrates the central role of JAK-STAT pathway activation in myeloproliferative neoplasm pathogenesis. Blood. 2014;123:e123–e133.

    Article  Google Scholar 

  2. Grinfeld J, Nangalia J, Baxter EJ, Wedge DC, Angelopoulos N, Cantrill R, et al. Classification and Personalized Prognosis in Myeloproliferative Neoplasms. N. Engl J Med. 2018;379:1416–30.

    Article  CAS  Google Scholar 

  3. Rao TN, Hansen N, Hilfiker J, Rai S, Majewska J-M, Lekovic D, et al. JAK2-mutant hematopoietic cells display metabolic alterations that can be targeted to treat myeloproliferative neoplasms. Blood. 2019;134:1832–46.

    Article  CAS  Google Scholar 

  4. Travelli C, Consonni FM, Sangaletti S, Storto M, Morlacchi S, Grolla AA, et al. Nicotinamide phosphoribosyltransferase acts as a metabolic gate for mobilization of myeloid-derived suppressor cells. Cancer Res. 2019;79:1938–51.

    Article  CAS  Google Scholar 

  5. Rosti V, Campanelli R, Massa M, Viarengo G, Villani L, Poletto V, et al. Increased plasma nicotinamide phosphoribosyltransferase is associated with a hyperproliferative phenotype and restrains disease progression in MPN-associated myelofibrosis. Am J Hematol. 2016;91:709–13.

    Article  CAS  Google Scholar 

  6. Rosti V, Massa M, Vannucchi AM, Bergamaschi G, Campanelli R, Pecci A, et al. The expression of CXCR4 is down-regulated on the CD34+ cells of patients with myelofibrosis with myeloid metaplasia. Blood Cells Mol Dis. 2007;38:280–6.

    Article  CAS  Google Scholar 

  7. Guglielmelli P, Zini R, Bogani C, Salati S, Pancrazzi A, Bianchi E, et al. Molecular profiling of CD34+ cells in idiopathic myelofibrosis identifies a set of disease-associated genes and reveals the clinical significance of Wilms’ tumor gene 1 (WT1). Stem Cells. 2007;25:165–73.

    Article  CAS  Google Scholar 

  8. Migliaccio AR, Martelli F, Verrucci M, Migliaccio G, Vannucchi AM, Ni H, et al. Altered SDF-+1/CXCR4 axis in patients with primary myelofibrosis and in the Gata1 low mouse model of the disease. Exp Hematol. 2008;36:158–71.

    Article  CAS  Google Scholar 

  9. Bogani C, Ponziani V, Guglielmelli P, Desterke C, Rosti V, Bosi A, et al. Hypermethylation of CXCR4 promoter in CD34+ cells from patients with primary myelofibrosis. Stem Cells. 2008;26:1920–30.

    Article  CAS  Google Scholar 

  10. Livun A, Newberry KJ, Manshouri T, Kusec R, Verstovsek S. Genes involved in maintaining the bone marrow stroma are dysregulated in patients with myelofibrosis: lenalidomide treatment up-regulates SOCS3. Anticancer Res. 2015;35:5219–23.

    CAS  PubMed  PubMed Central  Google Scholar 

  11. Barosi G, Viarengo G, Pecci A, Rosti V, Piaggio G, Marchetti M, et al. Diagnostic and clinical relevance of the number of circulating CD34(+) cells in myelofibrosis with myeloid metaplasia. Blood. 2001;98:3249–55.

    Article  CAS  Google Scholar 

  12. Cervantes F, Dupriez B, Pereira A, Passamonti F, Reilly JT, Morra E, et al. New prognostic scoring system for primary myelofibrosis based on a study of the International Working Group for Myelofibrosis Research and Treatment. Blood. 2009;113:2895–901.

    Article  CAS  Google Scholar 

  13. Swerdlow-SH, Campo E, Harris NL, et al. (Eds): WHO classification of tumours of haematopoietic and lymphoid tissues (Revised 4th edition). IARC: Lyon; 2017.

  14. Mesa RA, Green A, Barosi G, Verstovsek S, Vardiman J, Gale RP. MPN-associated myelofibrosis (MPN-MF). Leuk Res. 2011;35:12–13.

    Article  CAS  Google Scholar 

  15. Salim JP, Goette NP, Lev PR, Chazarreta CD, Heller PG, Alvarez C, et al. Dysregulation of stromal derived factor 1/CXCR4 axis in the megakaryocytic lineage in essential thrombocythemia. Br J Haematol. 2009;144:69–77.

    Article  CAS  Google Scholar 

  16. Barosi G, Massa M, Campanelli R, Fois G, Catarsi P, Viarengo G, et al. Primary myelofibrosis: Older age and high JAK2V617F allele burden are associated with elevated plasma high-sensitivity C-reactive protein levels and a phenotype of progressive disease. Leuk Res. 2017;60:18–23.

    Article  CAS  Google Scholar 

  17. Barosi G, Campanelli R, Catarsi P, De Amici M, Abbà C, Viarengo G, et al. Plasma sIL-2Rα levels are associated with disease progression in myelofibrosis with JAK2V617F but not CALR mutation. Leuk Res. 2020;90. https://doi.org/10.1016/j.leukres.2020.106319.

  18. McPherson S, Greenfield G, Andersen C, Grinfeldc J, Hasselbalch HC, Nangalia Y, et al. Methylation age as a correlate for allele burden, disease status, and clinical response in myeloproliferative neoplasm patients treated with vorinostat. Exp Hematol. 2019;79:26–34.

    Article  CAS  Google Scholar 

  19. Whetton AD, Azmi NC, Pearson S, Jaworska E, Zhang L, Blance R, et al. MPL W515L expression induces TGFβ secretion and leads to an increase in chemokinesis via phosphorylation of THOC5. Oncotarget. 2016;7:10739–55.

    Article  Google Scholar 

  20. Sakr H, Clark Schneider K, Murugesan G, Bodo J, Hsi ED, Cook JR. pSTAT3/pSTAT5 signaling patterns in molecularly defined subsets of myeloproliferative neoplasms. Appl Immunohistochem Mol Morphol. 2018;26:147–52.

    Article  CAS  Google Scholar 

  21. Chaligné R, James C, Tonetti C, Besancenot R, Le Coue JC, Fava F, et al. Evidence for MPL W515L/K mutations in hematopoietic stem cells in primitive myelofibrosis. Blood. 2007;110:3735–43.

    Article  Google Scholar 

  22. Guglielmelli P, Pancrazzi A, Bergamaschi G, Rosti V, Villani L, Antonioli E, et al. Anaemia characterises patients with myelofibrosis harbouring Mpl mutation. Br J Haematol. 2007;137:244–7.

    Article  CAS  Google Scholar 

  23. Vannucchi AM, Antonioli E, Guglielmelli P, Pancrazzi A, Guerini V, Barosi G, et al. Characteristics and clinical correlates of MPL 515W>L/K mutation in essential thrombocythemia. Blood. 2008;112:844–7.

    Article  CAS  Google Scholar 

  24. Ma Q, Jones D, Borghesani PR, Segal RA, Nagasawa T, Kishimoto T, et al. Impaired B-lymphopoiesis, myelopoiesis, and derailed cerebellar neuron migration in CXCR4- and SDF-1-deficient mice. Proc Natl Acad Sci USA. 1998;95:9448–53.

    Article  CAS  Google Scholar 

  25. Zhang Y, Dépond M, He L, Foudi A, Kwarteng EO, Lauret E, et al. CXCR4/CXCL12 axis counteracts hematopoietic stem cell exhaustion through selective protection against oxidative stress. Sci Rep. 2016;6:37827.

    Article  CAS  Google Scholar 

  26. Panieri E, Santoro MM. ROS homeostasis and metabolism: a dangerous liason in cancer cells. Cell Death Dis. 2016;7:e2253.

    Article  CAS  Google Scholar 

  27. Bakhoum SF, Cantley LC. The multifaceted role of chromosomal instability in cancer and its microenvironment. Cell. 2018;174:1347–60.

    Article  CAS  Google Scholar 

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GB, VR, RC, and MM designed the study, collected data from patients in Pavia, analyzed the results, and wrote the manuscript. LV and PC helped with the JAK2V617F, CALR and MPL mutation detection. CA and AC helped in analyzing the results. UM helped with the revision of bone marrow histology. RPG critically revised for important intellectual content, helped with manuscript writing and data interpretation.

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Correspondence to Giovanni Barosi.

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Barosi, G., Rosti, V., Catarsi, P. et al. Reduced CXCR4-expression on CD34-positive blood cells predicts outcomes of persons with primary myelofibrosis. Leukemia 35, 468–475 (2021). https://doi.org/10.1038/s41375-020-0926-6

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