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Expression of Hippo pathway molecules in myeloproliferative neoplasms

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Author(s):
Maira da Costa Cacemiro
Total Authors: 1
Document type: Doctoral Thesis
Press: Ribeirão Preto.
Institution: Universidade de São Paulo (USP). Faculdade de Ciências Farmacêuticas de Ribeirão Preto (PCARP/BC)
Defense date:
Examining board members:
Fabíola Attié de Castro; Carlos Alberto Scrideli
Advisor: Fabíola Attié de Castro
Abstract

Myeloproliferative neoplasms (MPN) are hematological disorders characterized by increased proliferation of mature myeloids cells of one or more hematopoietic series: granulocytic, erythrocytic, megakaryocytic or mastocytic. Patients with MPN may present mutations such as JAK2V617F, MPL and CALR, which were essential descriptions for the beginning of pathophysiological elucidation of MPN. The NMP neoplastic cells show resistance to apoptosis and exacerbated cell proliferation. It is known that these entities are considered also oncoinflamatory and pre-leukaemic. Despite all this knowledge about the molecular and cellular mechanisms involved in the pathogenesis of MPN, there are no effective treatments that cure or alter the natural history of progression of these disorders to AML. For the above, a participatory potential of the Hippo signaling pathway members in the pathophysiology of the most frequent negative BCR-ABL1 MPN, the polycythemia vera (PV), essential thrombocythemia (ET) and primary myelofibrosis (PMF) were investigated. The Hippo signaling pathway has been described as tumor suppressor and is responsible for the regulation of proliferation, differentiation and cell death. The correlation analysis of the expression levels of the Hippo pathway genes with the plasma cytokine profile of patients with PV, ET and PMF, the association with the mutational status and the expression of the genes that regulate intrinsic cellular apoptosis were performed. The main findings in patients with PV were decreased expression of the tumor suppressor genes LATS2, MST1 and MST2 accompanied by the presence of high concentration of proinflammatory cytokines and phenotype of resistance to apoptosis. In ET, relevant data were the detection of decreased expression of the tumor suppressor genes LATS1, LATS2 MST1 and SAV1, and the observation of the relationship between high expression of the SAV1 and MOB1B genes and the mutation of the CALR. In PMF, stands out the reduction of the SAV1 and TAZ gene expression of the Hippo signaling pathway and the AURKB gene of the cell cycle. In conclusion, the data indicate that decreased expression of the tumor suppressor genes of the Hippo pathway contributes to the pathophysiology and neoplastic cell resistance phenotype to the apoptosis of MPN. (AU)

FAPESP's process: 14/04234-9 - Expression of molecules of HIPPO/LATS pathway in chronic neoplasms myeloproliferative
Grantee:Maira da Costa Cacemiro
Support Opportunities: Scholarships in Brazil - Doctorate