Bachelor's degree in Medicine from the Federal University of Ceara (1999), with residency in Internal Medicine and Hematology/Hemotherapy at the University Hospital of Ribeirao Preto Medical School-USP (2000-2003), Ph.D in Internal Medicine/Hematology at Ribeirão Preto Medical School - USP (FMRP-USP) obtained in 2008, and Post-Doctoral fellowship at Prof. Daniel G. Tenen laboratory at Harvard Medical School (2011-2013). Assistant Professor of the Hematology, Hemotherapy, and Cell Therapy Division of the Department of Medical Imaging, Hematology, and Clinical Oncology, at FMRP-USP, with a progression to Associate Professor position in March 9th, 2023. Researcher and coordinator of the Graduate Program in Clinical Oncology, Stem Cells and Cell Therapy and vice-coordinator of the Master's Professional Program in Hemotherapy and Biotechnology at FMRP-USP. Experience in Internal Medicine with a focus on Hematology/Oncology, with emphasis on the following topics: etiopathogenesis, prognosis and treatment of myeloid neoplasms; phenotypic, molecular, and functional characterization of normal and neoplastic hematopoietic stem cells; and applications of molecular biology and flow cytometry for the study of hematopoietic neoplasms. (Source: Lattes Curriculum)
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Natural Killer (NK) cells, the major subset among Innate Lymphoid Cells (ILCs), can affect frequency and self-renewal of normal hematopoietic stem cells (Figueiredo-Pontes et al, Stem Cell Reports, 2021). On the other hand, NK maturation dysfunction may contribute to leukemogenesis in myeloproliferative neoplasms (Bianco & Arantes et al, submitted Frontiers in Oncology, 2021) and Acute My…
Considering that hematopoietic stem cells (HSC) directly respond to cytokines like IFNg, TNFa, TGFb, GM-CSF, MIP1, IL-10 and others, we hypothesized that Natural Killer (NK)-mediated cytokine production could regulate HSC function (subproject 1) and that its deregulation may favor malignant transformation (subproject 2). To address the role of NK function in normal hematopoiesis, we will …
Advances in immunotherapy have already been achieved with checkpoint inhibitors to enhance T cell responses such as inhibition of PD-1/PDL-1 in solid tumors and lymphoproliferative diseases, with promising results, and more scarce data from clinical trials in myeloid leukemias, as well as with Genetic Engineering of T lymphocytes (CAR-T cell therapy). However, for myeloid diseases, this t…
Acute Myeloid Leukemia (AML) is a hematopoietic neoplasm of the myeloid lineage, characterized by the proliferation of myeloid blasts in the bone marrow, in the peripheral blood and/or in other tissues. The treatment of patients with AML depends on the definition of the disease subtype and on the prognostic risk stratification. The analysis of genetic and molecular abnormalities present a…
Myeloproliferative Neoplasms (MPN) originate from molecular abnormalities at the hematopoietic stem cell (HSC) level, but alterations of the bone marrow niche may also contribute to the functional regulation of the neoplastic stem cells and of the normal residual HSCs and, thus, collaborate to the pathophysiology of the disease. Therefore, considering that these diseases are not only depe…
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Knowledge of the mechanisms underlying the normal development of blood cells will lead to new understanding of the pathogenesis of acute leukemias. Previous studies have demonstrated the role of the transcription factor abnormalities in acute myeloid leukemia (AML) in humans although this knowledge needs to be better translated into prognostic and therapeutic information. The major hypoth…
| 1 / 1 | Ongoing research grants |
| 1 / 1 | Completed research grants |
| 1 / 1 | Ongoing scholarships in Brazil |
| 6 / 4 | Completed scholarships in Brazil |
| 1 / 1 | Completed scholarships abroad |
| 10 / 8 | All research grants and scholarships |
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CV Lattes
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