000 02263na a2200373 4500
999 _c4229
_d4229
003 PC4229
005 20210625062801.0
008 130622s2013 xxx||||| |||| 00| 0 eng d
040 _cH12O
041 _aeng
100 _aArenas Cortés, Alicia
_92362
_eInstituto de Investigación i+12
100 _aAyala Díaz, Rosa María
_91206
_eHematología y Hemoterapia
100 _aBarrio García, Santiago
_91467
_eHematología y Hemoterapia
100 _aGallardo, Miguel
_92437
_eHematología y Hemoterapia
100 _aGarcia Martin, Rosa Maria
_92438
_eAnatomía Patológica
100 _aGilsanz Rodríguez, Florinda
_91015
_eHematología y Hemoterapia
100 _aJiménez Ubieto, Ana Isabel
_922
_eHematología y Hemoterapia
100 _aMartínez López, Joaquín
_9389
_eHematología y Hemoterapia
100 _aToldos González, Oscar
_91946
_eAnatomía Patológica
245 0 0 _aProteomic analysis reveals heat shock protein 70 has a key role in polycythemia Vera.
_h[artículo]
260 _bMolecular cancer,
_c2013
300 _a12:142.
500 _aFormato Vancouver: Gallardo M, Barrio S, Fernández M, Paradela A, Arenas A, Toldos O et al. Proteomic analysis reveals heat shock protein 70 has a key role in polycythemia Vera. Mol Cancer. 2013 Nov 19;12:142.
501 _aPMID: 24252366
504 _aContiene 35 referencias
520 _aJAK-STAT signaling through the JAK2V617F mutation is central to the pathogenesis of myeloproliferative neoplasms (MPN). However, other events could precede the JAK2 mutation. The aim of this study is to analyze the phenotypic divergence between polycytemia vera (PV) and essential thrombocytemia (ET) to find novel therapeutics targets by a proteomic and functional approach to identify alternative routes to JAK2 activation. Through 2D-DIGE and mass spectrometry of granulocyte protein from 20 MPN samples, showed differential expression of HSP70 in PV and ET besides other 60 proteins. Immunohistochemistry of 46 MPN bone marrow samples confirmed HSP70 expression. The median of positive granulocytes was 80% in PV (SD 35%) vs. 23% in ET (SD 34.25%). In an ex vivo model KNK437 was used as an inhibition model assay of HSP70, showed dose-dependent inhibition of cell growth and burst formation unit erythroid (BFU-E) in PV and ET, increased apoptosis in the erythroid lineage, and decreased pJAK2 signaling, as well as a specific siRNA for HSP70. These data suggest a key role for HSP70 in proliferation and survival of the erythroid lineage in PV, and may represent a potential therapeutic target in MPN, especially in PV.
710 _9330
_aServicio de Anatomía Patológica
710 _9297
_aServicio de Hematología y Hemoterapia
710 _9625
_aInstituto de Investigación imas12
856 _uhttp://pc-h12o-es.m-hdoct.a17.csinet.es/pdf/pc/4/pc4229.pdf
_ySolicitar documento
942 _n0
_2ddc
_cART