http://www.cnr.it/ontology/cnr/individuo/prodotto/ID27501
PI-PLCbeta-1 and activated Akt levels are linked to azacitidine responsiveness in high-risk myelodysplastic syndromes. (Articolo in rivista)
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- PI-PLCbeta-1 and activated Akt levels are linked to azacitidine responsiveness in high-risk myelodysplastic syndromes. (Articolo in rivista) (literal)
- Anno
- 2008-01-01T00:00:00+01:00 (literal)
- Alternative label
Follo MY, Finelli C, Bosi C, Martinelli G, Mongiorgi S, Baccarani M, Manzoli L, Blalock WL, Martelli AM, Cocco L. (2008)
PI-PLCbeta-1 and activated Akt levels are linked to azacitidine responsiveness in high-risk myelodysplastic syndromes.
in Leukemia
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- Follo MY, Finelli C, Bosi C, Martinelli G, Mongiorgi S, Baccarani M, Manzoli L, Blalock WL, Martelli AM, Cocco L. (literal)
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- Cellular Signalling Laboratory, Department of Anatomical Sciences, University of Bologna, Bologna, Italy; Institute of Hematology and Medical Oncology L. e A. Sera`gnoli, University of Bologna, Bologna, Italy; Hematology Unit, Ospedale Civile di Piacenza; Piacenza, Italy; Istituto per i Trapianti dOrgano e lImmunocitologia del C.N.R., Sezione di Bologna c/o I.O.R., Bologna, Italy.
(literal)
- Titolo
- PI-PLCbeta-1 and activated Akt levels are linked to azacitidine responsiveness in high-risk myelodysplastic syndromes. (literal)
- Abstract
- Nuclear lipid metabolism has widely been implicated in cell growth,
differentiation and neoplastic transformation. Phosphoinositide-
phospholipase C (PI-PLC) b-1 is a key enzyme in nuclear signal
transduction, and it is involved in many cellular processes, such as
proliferation and differentiation.1 The involvement of PI-PLCb-1 in
hematopoietic differentiation prompted us to investigate the role of this
signaling molecule in hematological malignancies, focusing particularly on
patients affected by myelodysplastic syndromes (MDS) at higher risk of
evolution into acute myeloid leukemia (AML). By using fluorescence in situ
hybridization (FISH) analysis, our group demonstrated, in a small number of
high-risk MDS patients,2 that subjects bearing a mono-allelic cryptic
deletion of the PIPLCb- 1 gene had a worse clinical outcome, as compared
with patients having both alleles. In a subsequent study, it has also been
shown that the expression profile of both PI-PLCb-1a and PI-PLCb-1b mRNAs,
which are the two alternative splicing isoforms of PI-PLCb-1, is altered in
high-risk MDS, as compared to healthy donors.3 Interestingly, MDS cells
always expressed higher levels of PI-PLCb-1b mRNA as compared to PI-PLCb-1a
mRNA; this difference may reflect a specific role of PI-PLCb-1 in MDS,
given that the PI-PLCb-1a splicing isoform demonstrates both nuclear and
cytoplasmatic localization, while PI-PLCb-1b splicing isoform is localized
only in the nucleus. Furthermore, our recent studies demonstrated that not
only is Akt specifically phosphorylated in high-risk MDS patients, but also
mTOR and its downstream targets are activated,4 affecting cell survival and
proliferation of MDS cells. (literal)
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