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Genetic characterization of B-cell prolymphocytic leukemia: a prognostic model involving MYC and TP53.
Chapiro, Elise; Pramil, Elodie; Diop, M'boyba; Roos-Weil, Damien; Dillard, Clémentine; Gabillaud, Clémentine; Maloum, Karim; Settegrana, Catherine; Baseggio, Lucile; Lesesve, Jean-François; Yon, Mélanie; Jondreville, Ludovic; Lesty, Claude; Davi, Frédéric; Le Garff-Tavernier, Magali; Droin, Nathalie; Dessen, Philippe; Algrin, Caroline; Leblond, Véronique; Gabarre, Jean; Bouzy, Simon; Eclache, Virginie; Gaillard, Baptiste; Callet-Bauchu, Evelyne; Muller, Marc; Lefebvre, Christine; Nadal, Nathalie; Ittel, Antoine; Struski, Stéphanie; Collonge-Rame, Marie-Agnès; Quilichini, Benoit; Fert-Ferrer, Sandra; Auger, Nathalie; Radford-Weiss, Isabelle; Wagner, Lena; Scheinost, Sebastian; Zenz, Thorsten; Susin, Santos A; Bernard, Olivier A; Nguyen-Khac, Florence.
Afiliação
  • Chapiro E; Cell Death and Drug Resistance in Lymphoproliferative Disorders Team, Centre de Recherche des Cordeliers, INSERM UMRS 1138, Paris, France.
  • Pramil E; Sorbonne Université, Paris, France.
  • Diop M; Service d'Hématologie Biologique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Roos-Weil D; Cell Death and Drug Resistance in Lymphoproliferative Disorders Team, Centre de Recherche des Cordeliers, INSERM UMRS 1138, Paris, France.
  • Dillard C; Sorbonne Université, Paris, France.
  • Gabillaud C; AMMICa, INSERM US23/Centre National de la Recherche UMS3655, Gustave Roussy, Villejuif, France.
  • Maloum K; Cell Death and Drug Resistance in Lymphoproliferative Disorders Team, Centre de Recherche des Cordeliers, INSERM UMRS 1138, Paris, France.
  • Settegrana C; Sorbonne Université, Paris, France.
  • Baseggio L; Service d'Hématologie Clinique, Hôpital Pitié-Salpêtrière, AP-HP, Paris, France.
  • Lesesve JF; Cell Death and Drug Resistance in Lymphoproliferative Disorders Team, Centre de Recherche des Cordeliers, INSERM UMRS 1138, Paris, France.
  • Yon M; Sorbonne Université, Paris, France.
  • Jondreville L; Service d'Hématologie Biologique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Lesty C; Service d'Hématologie Biologique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Davi F; Service d'Hématologie Biologique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Le Garff-Tavernier M; Service d'Hématologie Biologique, hospices Civils de Lyon, Lyon, France.
  • Droin N; Service d'Hématologie Biologique, Centre Hospitalier Régionaux et Universitaire Nancy, and INSERM U1256 NGERE, Université de Lorraine, Nancy, France.
  • Dessen P; Cell Death and Drug Resistance in Lymphoproliferative Disorders Team, Centre de Recherche des Cordeliers, INSERM UMRS 1138, Paris, France.
  • Algrin C; Sorbonne Université, Paris, France.
  • Leblond V; Cell Death and Drug Resistance in Lymphoproliferative Disorders Team, Centre de Recherche des Cordeliers, INSERM UMRS 1138, Paris, France.
  • Gabarre J; Sorbonne Université, Paris, France.
  • Bouzy S; Sorbonne Université, Paris, France.
  • Eclache V; Cell Death and Drug Resistance in Lymphoproliferative Disorders Team, Centre de Recherche des Cordeliers, INSERM UMRS 1138, Paris, France.
  • Gaillard B; Sorbonne Université, Paris, France.
  • Callet-Bauchu E; Service d'Hématologie Biologique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Muller M; Cell Death and Drug Resistance in Lymphoproliferative Disorders Team, Centre de Recherche des Cordeliers, INSERM UMRS 1138, Paris, France.
  • Lefebvre C; Service d'Hématologie Biologique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Nadal N; AMMICa, INSERM US23/Centre National de la Recherche UMS3655, Gustave Roussy, Villejuif, France.
  • Ittel A; AMMICa, INSERM US23/Centre National de la Recherche UMS3655, Gustave Roussy, Villejuif, France.
  • Struski S; Service d'Oncologie, Groupe Hospitalier Mutualiste de Grenoble, Grenoble, France.
  • Collonge-Rame MA; Sorbonne Université, Paris, France.
  • Quilichini B; Service d'Hématologie Clinique, Hôpital Pitié-Salpêtrière, AP-HP, Paris, France.
  • Fert-Ferrer S; Service d'Hématologie Clinique, Hôpital Pitié-Salpêtrière, AP-HP, Paris, France.
  • Auger N; Service d'Hématologie Biologique, Hôpital Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Radford-Weiss I; Laboratoire d'Hématologie, Hôpital Avicenne, AP-HP, Bobigny, France.
  • Wagner L; Laboratoire d'Hématologie, Hôpital Robert Debré, Reims, France.
  • Scheinost S; Service d'Hématologie Biologique, hospices Civils de Lyon, Lyon, France.
  • Zenz T; Laboratoire de Génétique, Centre Hospitalier Universitaire (CHU) Nancy, Nancy, France.
  • Susin SA; Laboratoire de Cytogénétique Onco-hématologique, CHU Grenoble, Grenoble, France.
  • Bernard OA; Service de génétique chromosomique et moléculaire, CHU Dijon, Dijon, France.
  • Nguyen-Khac F; Cytogénétique, Institut Universitaire du Cancer de Toulouse, Toulouse, France.
Blood ; 134(21): 1821-1831, 2019 11 21.
Article em En | MEDLINE | ID: mdl-31527074
B-cell prolymphocytic leukemia (B-PLL) is a rare hematological disorder whose underlying oncogenic mechanisms are poorly understood. Our cytogenetic and molecular assessments of 34 patients with B-PLL revealed several disease-specific features and potential therapeutic targets. The karyotype was complex (≥3 abnormalities) in 73% of the patients and highly complex (≥5 abnormalities) in 45%. The most frequent chromosomal aberrations were translocations involving MYC [t(MYC)] (62%), deletion (del)17p (38%), trisomy (tri)18 (30%), del13q (29%), tri3 (24%), tri12 (24%), and del8p (23%). Twenty-six (76%) of the 34 patients exhibited an MYC aberration, resulting from mutually exclusive translocations or gains. Whole-exome sequencing revealed frequent mutations in TP53, MYD88, BCOR, MYC, SF3B1, SETD2, CHD2, CXCR4, and BCLAF1. The majority of B-PLL used the IGHV3 or IGHV4 subgroups (89%) and displayed significantly mutated IGHV genes (79%). We identified 3 distinct cytogenetic risk groups: low risk (no MYC aberration), intermediate risk (MYC aberration but no del17p), and high risk (MYC aberration and del17p) (P = .0006). In vitro drug response profiling revealed that the combination of a B-cell receptor or BCL2 inhibitor with OTX015 (a bromodomain and extra-terminal motif inhibitor targeting MYC) was associated with significantly lower viability of B-PLL cells harboring a t(MYC). We concluded that cytogenetic analysis is a useful diagnostic and prognostic tool in B-PLL. Targeting MYC may be a useful treatment option in this disease.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína Supressora de Tumor p53 / Proteínas Proto-Oncogênicas c-myc / Leucemia Prolinfocítica Tipo Células B Tipo de estudo: Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína Supressora de Tumor p53 / Proteínas Proto-Oncogênicas c-myc / Leucemia Prolinfocítica Tipo Células B Tipo de estudo: Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Ano de publicação: 2019 Tipo de documento: Article