TY - JOUR
T1 - MYH10 protein expression in platelets as a biomarker of RUNX1 and FLI1 alterations
AU - Antony-Debré, Iléana
AU - Bluteau, Dominique
AU - Itzykson, Raphael
AU - Baccini, Veŕonique
AU - Renneville, Aline
AU - Boehlen, Françoise
AU - Morabito, Margot
AU - Droin, Nathalie
AU - Deswarte, Caroline
AU - Chang, Yunhua
AU - Leverger, Guy
AU - Solary, Eric
AU - Vainchenker, William
AU - Favier, Rémi
AU - Raslova, Hana
PY - 2012/9/27
Y1 - 2012/9/27
N2 - RUNX1 gene alterations are associated with acquired and inherited hematologic malignancies that include familial platelet disorder/acute myeloid leukemia, primary or secondary acute myeloid leukemia, and chronic myelomonocytic leukemia. Recently, we reported that RUNX1-mediated silencing of nonmuscle myosin heavy chain IIB (MYH10) was required for megakaryocyte ploidization and maturation. Here we demonstrate that runx1 deletion in mice induces the persistence of MYH10 in platelets, and a similar persistence was observed in platelets of patients with constitutional (familial platelet disorder/acute myeloid leukemia) or acquired (chronic myelomonocytic leukemia) RUNX1 mutations. MYH10 was also detected in platelets of patients with the Paris-Trousseau syndrome, a thrombocytopenia related to the deletion of the transcription factor FLI1 that forms a complex with RUNX1 to regulate megakaryopoiesis, whereas MYH10 persistence was not observed in other inherited forms of thrombocytopenia. We propose MYH10 detection as a new and simple tool to identify inherited platelet disorders and myeloid neoplasms with abnormalities in RUNX1 and its associated proteins.
AB - RUNX1 gene alterations are associated with acquired and inherited hematologic malignancies that include familial platelet disorder/acute myeloid leukemia, primary or secondary acute myeloid leukemia, and chronic myelomonocytic leukemia. Recently, we reported that RUNX1-mediated silencing of nonmuscle myosin heavy chain IIB (MYH10) was required for megakaryocyte ploidization and maturation. Here we demonstrate that runx1 deletion in mice induces the persistence of MYH10 in platelets, and a similar persistence was observed in platelets of patients with constitutional (familial platelet disorder/acute myeloid leukemia) or acquired (chronic myelomonocytic leukemia) RUNX1 mutations. MYH10 was also detected in platelets of patients with the Paris-Trousseau syndrome, a thrombocytopenia related to the deletion of the transcription factor FLI1 that forms a complex with RUNX1 to regulate megakaryopoiesis, whereas MYH10 persistence was not observed in other inherited forms of thrombocytopenia. We propose MYH10 detection as a new and simple tool to identify inherited platelet disorders and myeloid neoplasms with abnormalities in RUNX1 and its associated proteins.
UR - http://www.scopus.com/inward/record.url?scp=84866878349&partnerID=8YFLogxK
U2 - 10.1182/blood-2012-04-422352
DO - 10.1182/blood-2012-04-422352
M3 - Article
C2 - 22677128
AN - SCOPUS:84866878349
SN - 0006-4971
VL - 120
SP - 2719
EP - 2722
JO - Blood
JF - Blood
IS - 13
ER -