Additional trisomies amongst patients with chronic lymphocytic leukemia carrying trisomy 12: the accompanying chromosome makes a difference
Jazyk angličtina Země Itálie Médium print-electronic
Typ dokumentu dopisy, práce podpořená grantem
Grantová podpora
C34999/A18087
Cancer Research UK - United Kingdom
PubMed
27102498
PubMed Central
PMC5004477
DOI
10.3324/haematol.2015.140202
PII: haematol.2015.140202
Knihovny.cz E-zdroje
- Klíčová slova
- RBC, bio-engineered, cord blood, metabolic profile, native,
- MeSH
- chronická lymfatická leukemie genetika metabolismus mortalita terapie MeSH
- jednonukleotidový polymorfismus * MeSH
- lidé MeSH
- lidské chromozomy, pár 12 genetika MeSH
- trizomie genetika MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- dopisy MeSH
- práce podpořená grantem MeSH
AP HP Pitie Salpetriere Hospital Department of Hematology and UPMC Univ Paris 06 UMRS 1138 France
Cancer Sciences Faculty of Medicine University of Southampton UK
Consorcio Hospital General Universitario de Valencia Spain
Department of Haematology Royal Bournemouth Hospital UK
Fundación Pública Galega de Medicina Xenómica Santiago de Compostela Spain
Hematology Department and HCT Unit G Papanicolaou Hospital Thessaloniki Greece
Hospital Universitari Vall d'Hebron Barcelona Spain
Hospital Universitario Central de Asturias Oviedo Spain
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Dohner 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
Ibbotson R, Athanasiadou A, Sutton LA, et al. Coexistence of trisomies of chromosomes 12 and 19 in chronic lymphocytic leukemia occurs exclusively in the rare IgG-positive variant. Leukemia. 2012; 26(1):170–172. PubMed
Schwaenen C, Nessling M, Wessendorf S, et al. Automated array-based genomic profiling in chronic lymphocytic leukemia: development of a clinical tool and discovery of recurrent genomic alterations. Proc Natl Acad Sci USA. 2004;101(4):1039–1044. PubMed PMC
Sellmann L, Gesk S, Walter C, et al. Trisomy 19 is associated with trisomy 12 and mutated IGHV genes in B-chronic lymphocytic leukaemia. Br J Haematol. 2007;138(2):217–220. PubMed
Gunnarsson R, Mansouri L, Isaksson A, et al. Array-based genomic screening at diagnosis and during follow-up in chronic lymphocytic leukemia. Haematologica. 2011;96(8):1161–1169. PubMed PMC
Del Giudice I, Rossi D, Chiaretti S, et al. NOTCH1 mutations in +12 chronic lymphocytic leukemia (CLL) confer an unfavorable prognosis, induce a distinctive transcriptional profiling and refine the intermediate prognosis of +12 CLL. Haematologica. 2012;97(3):437–441. PubMed PMC
Baliakas P, Hadzidimitriou A, Sutton LA, et al. Recurrent mutations refine prognosis in chronic lymphocytic leukemia. Leukemia. 2015; 29(2):329–336. PubMed
Vardi A, Agathangelidis A, Sutton LA, et al. IgG-switched CLL has a distinct immunogenetic signature from the common MD variant: ontogenetic implications. Clin Cancer Res. 2014;20(2):323–330. PubMed
Belessi C, Stamatopoulos K, Hadzidimitriou A, et al. Analysis of expressed and non-expressed IGK locus rearrangements in chronic lymphocytic leukemia. Mol Med. 2005;11(1–12):52–58. PubMed PMC
Hadzidimitriou A, Darzentas N, Murray F, et al. Evidence for the significant role of immunoglobulin light chains in antigen recognition and selection in chronic lymphocytic leukemia. Blood. 2009; 113(2):403–411. PubMed
Xu W, Wang YH, Fan L, et al. Prognostic significance of serum immunoglobulin paraprotein in patients with chronic lymphocytic leukemia. Leuk Res. 2011;35(8):1060–1065. PubMed
Dearden C. Disease-specific complications of chronic lymphocytic leukemia. Hematology Am Soc Hematol Educ Program. 2008;450–456. PubMed
Molica S. Second neoplasms in chronic lymphocytic leukemia: incidence and pathogenesis with emphasis on the role of different therapies. Leuk Lymphoma. 2005;46(1):49–54. 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
Villamor N, Conde L, Martinez-Trillos A, et al. NOTCH1 mutations identify a genetic subgroup of chronic lymphocytic leukemia patients with high risk of transformation and poor outcome. Leukemia. 2013;27(5):1100–1106. PubMed