Article (Scientific journals)
Aspects biologiques de la voie JAK/STAT dans les néoplasmes myéloprolifératifs classiques négatifs pour BCR-ABL.
Mosca, Matthieu; VERTENOEIL, Gaëlle; Toppaldoddi, Katte Rao et al.
2016In Bulletin du Cancer, 103 (6 Suppl 1), p. 16-28
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Keywords :
Calreticulin/genetics; Fusion Proteins, bcr-abl; Humans; Interferon-alpha/therapeutic use; Janus Kinase 2/antagonists & inhibitors/genetics; Mutation; Myeloproliferative Disorders/drug therapy/genetics; Receptors, Thrombopoietin/genetics; STAT Transcription Factors/genetics; Signal Transduction; Calreticulin; Calréticuline; Epigenetic mutations; JAK2V617F; MPL; Mutations; Myeloproliferative; Néoplasmes; d'épigénétique; myéloprolifératifs; neoplasms
Abstract :
[en] BIOLOGICAL ASPECTS OF JAK/STAT SIGNALING IN BCR-ABL-NEGATIVE MYELOPROLIFERATIVE NEOPLASMS: Myeloproliferative disorders more recently named Myeloproliferative neoplasms (MPN) display several clinical entities: chronic myeloid leukemia (CML), the classical MPN including polycythemia vera (PV), essential thrombocythemia (ET), primary myelofibrosis (PMF) and atypical and unclassifiable NMP. The term MPN is mostly used for classical BCR-ABL-negative (myeloproliferative disorder) (ET, PV, PMF). These are clonal diseases resulting from the transformation of an hematopoietic stem cell and leading to an abnormal production of myeloid cells. The genetic defects responsible for the myeloproliferative abnormalities are called « driver » mutations and all result in deregulation of the cytokine receptor / JAK2 / STAT axis. Among them, JAK2, the thrombopoietin receptor (MPL) and calreticulin (CALR) mutations are found in around 90% of the cases. These driver MPN mutations can be associated with other driver mutations also found in other hematological malignancies, especially in PMFs. These are chronic diseases with major risks being thrombosis, hemorrhage and cytopenias for PMF and the long-term progression to myelofibrosis and the transformation to leukemia. Most recent therapeutic have focused on targeting the JAK2 signaling pathway directly by inhibitors of JAK2 or indirectly. Interferon a allows in some cases hematologic and molecular remission patients.
Disciplines :
Hematology
Author, co-author :
Mosca, Matthieu 
VERTENOEIL, Gaëlle  ;  Centre Hospitalier Universitaire de Liège - CHU > Département de médecine interne > Service d'hématologie clinique
Toppaldoddi, Katte Rao
Plo, Isabelle
Vainchenker, William
 These authors have contributed equally to this work.
Language :
French
Title :
Aspects biologiques de la voie JAK/STAT dans les néoplasmes myéloprolifératifs classiques négatifs pour BCR-ABL.
Alternative titles :
[en] Not Available
Publication date :
2016
Journal title :
Bulletin du Cancer
ISSN :
0007-4551
eISSN :
1769-6917
Publisher :
Elsevier, Netherlands
Volume :
103
Issue :
6 Suppl 1
Pages :
S16-28
Peer reviewed :
Peer Reviewed verified by ORBi
Commentary :
© 2016 Société Française du Cancer. Publié par Elsevier Masson SAS.
Available on ORBi :
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