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Functional and genetic aberrations of in vitro-cultured marrow-derived mesenchymal stromal cells of patients with classical Philadelphia-negative myeloproliferative neoplasms

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References

  1. Keating A . Mesenchymal stromal cells. Curr Opin Hematol 2006; 13: 419–425.

    Article  Google Scholar 

  2. Lopez-Villar O, Garcia JL, Sanchez-Guijo FM, Robledo C, Vilaron EM, Hernandez-Campo P et al. Both expanded and uncultured mesenchymal stem cells from MDS patients are genomically abnormal, showing a specific genetic profile for the 5q- syndrome. Leukemia 2009; 23: 664–672.

    Article  CAS  Google Scholar 

  3. Blau O, Baldus CD, Hofmann WK, Thiel G, Nolte F, Burmeister T et al. Mesenchymal stroma cells of myelodysplastic syndrome and acute myeloid leukemia patients have distinct genetic abnormalities compared with leukemic blasts. Blood 2011; 118: 5583–5592.

    Article  CAS  Google Scholar 

  4. Geyh S, Oz S, Cadeddu RP, Fröbel J, Bruckner B, Kungden A et al. Insufficient stromal support in MDS results from molecular and functional deficits of mesenchymal stromal cells. Leukemia 2013; 27: 1841–1851.

    Article  CAS  Google Scholar 

  5. Raaijmakers MH, Mukherjee S, Guo S, Zhang S, Kobayashi T, Schoonmaker JA et al. Bone progenitor dysfunction induces myelodysplasia and secondary leukemia. Nature 2010; 464: 852–857.

    Article  CAS  Google Scholar 

  6. Pieri L, Guglielmelli P, Bogani C, Bosi A, Vannucchi AM . Mesenchymal stem cells from JAK2V617F mutant patients with primary myelofibrosis do not harbor JAK2 mutant allele. Leuk Res 2008; 32: 516–517.

    Article  CAS  Google Scholar 

  7. Sakaguchi Y, Sekiya I, Yagishita K, Ichinose S, Shinomiya K, Muneta T . Suspended cells from trabecular bone by collagenase digestion become virtually identical to mesenchymal stem cells obtained from marrow aspirates. Blood 2004; 104: 2728–2735.

    Article  CAS  Google Scholar 

  8. Bernardo ME, Zaffaroni N, Novara F, Cometa AM, Avanzini MA, Moretta A et al. Human bone marrow-derived mesenchymal stem cells do not undergo transformation after long-term in vitro culture and do not exhibit telomere maintenance mechanisms. Cancer Res 2007; 67: 9142–9149.

    Article  CAS  Google Scholar 

  9. Lecourt S, Vanneaux V, Leblanc T, Leroux G, Ternaux B, Benbunan M et al. Bone marrow microenvironment in Fanconi anemia: a prospective functional study in a cohort of fanconi anemia patients. Stem Cell Dev 2010; 19: 203–208.

    Article  CAS  Google Scholar 

  10. Tonon L, Bergamaschi G, Dellavecchia C, Rosti V, Lucotti C, Malabarba L et al. Unbalanced X-chromosome inactivation in haematopoietic cells from normal women. Br J Haematol 1998; 102: 996–1003.

    Article  CAS  Google Scholar 

  11. Greenbaum A, Hsu YM, Day RB, Schuettpelz LG, Christopher MJ, Borgerding JN et al. CXCL12 in early mesenchymal progenitors is required for hematopoietic stem-cell maintenance. Nature 2013; 495: 227–230.

    Article  CAS  Google Scholar 

  12. Flores-Figueroa E, Varma S, Montgomery K, Greenberg PL, Gratzinger D . Distinctive contact between CD34+ hematopoietic progenitors and CXCL12+ CD271+ mesenchymal stromal cells in benign and myelodysplastic bone marrow. Lab Invest 2012; 92: 1330–1341.

    Article  CAS  Google Scholar 

  13. Ben David U, Mayshar Y, Benvenisty N . Large scale analysis reveals acquisition of lineage-specific chromosomal aberrations in human. Cell Stem Cell 2011; 9: 97–102.

    Article  CAS  Google Scholar 

  14. Lose F, Duffy DL, Kay GF, Kedda MA, Spurdle AB . Skewed X chromosome inactivation and breast and ovarian cancer status: evidence for X-linked modifiers of BRCA1. J Natl Cancer Inst 2008; 100: 1519–1529.

    Article  CAS  Google Scholar 

  15. Swierczek SI, Piterkova L, Jelinek J, Agarwal N, Hammoud S, Wilson A et al. Methylation of AR locus does not always reflect X chromosome inactivation state. Blood 2012; 119: e100–e109, . Erratum in: Blood 2012; 120: 4447. Cairns, Bradley [corrected to Cairns, Bradley R].

    Article  CAS  Google Scholar 

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Avanzini, M., Bernardo, M., Novara, F. et al. Functional and genetic aberrations of in vitro-cultured marrow-derived mesenchymal stromal cells of patients with classical Philadelphia-negative myeloproliferative neoplasms. Leukemia 28, 1742–1745 (2014). https://doi.org/10.1038/leu.2014.97

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