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005 | 20191018062648.0 | ||
008 | 130622s2012 xxx||||| |||| 00| 0 eng d | ||
040 | _cH120 | ||
041 | _aeng | ||
100 |
_9388 _aLahuerta Palacios, Juan José _eHematología y Hemoterapia |
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245 | 0 | 0 |
_aGenomic analysis of high-risk smoldering multiple myeloma. _h[artículo] |
260 |
_bHaematologica, _c2012 |
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300 | _a97(9):1439-43. | ||
500 | _aFormato Vancouver: López-Corral L, Mateos MV, Corchete LA, Sarasquete ME, de la Rubia J, de Arriba F, et al. Genomic analysis of high-risk smoldering multiple myeloma. Haematologica. 2012 Sep;97(9):1439-43. | ||
501 | _aPMID: 22331267 | ||
504 | _aContiene 24 referencias | ||
520 | _aSmoldering myeloma is an asymptomatic plasma cell dyscrasia with a heterogeneous propensity to progress to active myeloma. In order to investigate the biology of smoldering myeloma patients with high risk of progression, we analyzed the genomic characteristics by FISH, SNP-arrays and gene expression profile of a group of patients with high-risk smoldering myeloma included in a multicenter randomized trial. Chromosomal abnormalities detected by FISH and SNP-arrays at diagnosis were not associated to risk of progression to symptomatic myeloma. However, the overexpression of four SNORD genes (SNORD25, SNORD27, SNORD30 and SNORD31) was correlated with shorter time to progression (P<0.03). When plasma cells from high-risk smoldering patients who progressed to symptomatic myeloma were sequentially analyzed, newly acquired lesions together with an increase in the proportion of plasma cells carrying a given abnormality were observed. These findings suggest that gene expression profiling is a valuable technique to identify smoldering myeloma patients with high risk of progression. | ||
710 |
_9297 _aServicio de Hematología y Hemoterapia |
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856 |
_uhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3436247/ _yAcceso libre |
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942 |
_n0 _2ddc _cART |
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999 |
_c5053 _d5053 |