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Publicação:
Circulating microRNAs expression profile in newly diagnosed and imatinib treated chronic phase–chronic myeloid leukemia

dc.contributor.authorFerreira, Letícia Antunes Muniz [UNESP]
dc.contributor.authorCapannacci, Juliana
dc.contributor.authorHokama, Newton Key [UNESP]
dc.contributor.authorNogueira, Célia Regina [UNESP]
dc.contributor.authorCeccarelli, Michele
dc.contributor.authorCerulo, Luigi
dc.contributor.authorD’Angelo, Fulvio
dc.contributor.authorde Oliveira Montandon Hokama, Paula [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionHospital Dr. Amaral Carvalho
dc.contributor.institutionSannio University
dc.date.accessioned2018-12-11T17:22:43Z
dc.date.available2018-12-11T17:22:43Z
dc.date.issued2018-01-01
dc.description.abstractChronic myeloid leukemia (CML) is a stem cell derived malignant disorder result of translocation t(9;22)(q34;q11) called Philadelphia chromosome (Ph+). microRNAS (miRNAs) are involved in several biological processes, altering the progression of various pathologies, including CML. This study evaluated whether circulating miRNAs display differential expression profiles in peripheral blood of CML-Chronic Phase (CML-CP) patients newly diagnosed in comparison with CML-CP treated with imatinib. We obtained peripheral blood samples from CML-CP Ph+ patients divided among group 1 (untreated newly diagnosed) and group 2 (treated with imatinib). A pool of total leukocytes from healthy donors was considered as control group. Expression analyses were performed for 768 miRNAs by RT-qPCR array. Bioinformatic tools were used to identify significant pathways and interaction networks. We found 80 deregulated miRNAs between the groups and, according to bioinformatic analysis, they are involved in different pathways, including molecular mechanisms of cancer. The study allows better understanding of disease molecular behavior, and it is useful for possible monitoring CML treatment and prognostic biomarkers identification.en
dc.description.affiliationDepartment of Internal Medical São Paulo State University (UNESP-FMB)
dc.description.affiliationLaboratory of Molecular Biology Hospital Dr. Amaral Carvalho
dc.description.affiliationDepartment of Science and Technology Sannio University
dc.description.affiliationUnespDepartment of Internal Medical São Paulo State University (UNESP-FMB)
dc.identifierhttp://dx.doi.org/10.1080/10428194.2018.1499905
dc.identifier.citationLeukemia and Lymphoma.
dc.identifier.doi10.1080/10428194.2018.1499905
dc.identifier.issn1029-2403
dc.identifier.issn1042-8194
dc.identifier.lattes4132731111630799
dc.identifier.scopus2-s2.0-85053345241
dc.identifier.urihttp://hdl.handle.net/11449/176842
dc.language.isoeng
dc.relation.ispartofLeukemia and Lymphoma
dc.relation.ispartofsjr0,976
dc.relation.ispartofsjr0,976
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectBiomarkers
dc.subjectchronic phase
dc.subjectgene expression regulation
dc.subjectimatinib mesylate
dc.subjectleukemia
dc.subjectmicroRNAs
dc.subjectmyeloid
dc.subjectPhiladelphia chromosome
dc.titleCirculating microRNAs expression profile in newly diagnosed and imatinib treated chronic phase–chronic myeloid leukemiaen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.lattes4132731111630799
unesp.author.lattes7607038776901890[4]
unesp.author.orcid0000-0003-4840-8753[1]
unesp.author.orcid0000-0001-7089-1310[2]
unesp.author.orcid0000-0001-7555-7215[3]
unesp.author.orcid0000-0002-7354-9518[4]
unesp.author.orcid0000-0002-4702-6617[5]
unesp.author.orcid0000-0001-8342-3487[6]
unesp.author.orcid0000-0002-4940-4693[7]
unesp.author.orcid0000-0003-3474-4422[8]
unesp.author.orcid0000-0002-4014-0660[4]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentClínica Médica - FMBpt

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