Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/51180
Campo DC Valoridioma
dc.contributor.authorGómez Casares, María Teresaen_US
dc.contributor.authorDe La Iglesia Íñigo, Silvia Narcisaen_US
dc.contributor.authorPerera, Mariaen_US
dc.contributor.authorLemes, Angelinaen_US
dc.contributor.authorCampo, Conradoen_US
dc.contributor.authorGonzalez San Miguel, Jose D.en_US
dc.contributor.authorBosch, Jose M.en_US
dc.contributor.authorSuarez, Alexiaen_US
dc.contributor.authorGuerra, Luisaen_US
dc.contributor.authorRodriguez-Perez, JCen_US
dc.contributor.authorMolero Labarta, María Teresaen_US
dc.contributor.otherRodriguez-Perez, J.C.-
dc.contributor.otherSan-Miguel, Jesus-
dc.date.accessioned2018-11-24T22:11:18Z-
dc.date.available2018-11-24T22:11:18Z-
dc.date.issued2002en_US
dc.identifier.issn1042-8194en_US
dc.identifier.urihttp://hdl.handle.net/10553/51180-
dc.description.abstractIt has been demonstrated that some myeloid blasts express renin, but normal bone marrow (BM) does not display this expression. The aim of the present work was to analyze the renin expression in different hematological malignancies and different myeloid cell lines. We investigated the expression of renin by RT-PCR in BM from patients with hematological malignancies (106 patients), in nine normal BM from healthy donors and in leukemic cell lines (K562, KU812, MEG-01, U-937 and HL60), as well in K562 cell line subjected to differentiation treatments. We have observed renin expression in cells from acute myeloid leukemia (AML), chronic myelogenous leukemia (CML) and acute lymphoblastic leukemia (ALL) cases. The highest frequency was observed in AML-non acute promyelocytic leukemia(APL) cases (47.2% of the cases). The disappearance of this expression was associated with the status of complete remission of AML. Renin is expressed in some myeloid human leukemia cell lines such as K562, KU812 and MEG-01. However, when K562 cells were treated with inducers of growth inhibition and/or differentiation, the expression did not disappear, indicating that renin expression is associated with a blastic phenotype rather than with cell proliferation. The obtained findings suggest that the renin expression could have a role on the disease development and could be used as an aberrant marker of leukemia.en_US
dc.languageengen_US
dc.relation.ispartofLeukemia and Lymphomaen_US
dc.sourceLeukemia & Lymphoma[ISSN 1042-8194],v. 43 (12), p. 2377-2381en_US
dc.subject32 Ciencias médicasen_US
dc.subject3205 Medicina internaen_US
dc.subject.otherReninen_US
dc.subject.otherLeukemiaen_US
dc.subject.otherK562en_US
dc.subject.otherDifferentiationen_US
dc.subject.otherAceen_US
dc.titleRenin expression in hematological malignancies and its role in the regulation of hematopoiesisen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1080/1042819021000040080en_US
dc.identifier.scopus0036891604-
dc.identifier.isi000178910400019-
dcterms.isPartOfLeukemia & Lymphoma-
dcterms.sourceLeukemia & Lymphoma[ISSN 1042-8194],v. 43 (12), p. 2377-2381-
dc.contributor.authorscopusid6602513846-
dc.contributor.authorscopusid6507415496-
dc.contributor.authorscopusid7005775092-
dc.contributor.authorscopusid6603001986-
dc.contributor.authorscopusid7006774620-
dc.contributor.authorscopusid6603074735-
dc.contributor.authorscopusid7402325631-
dc.contributor.authorscopusid57197197067-
dc.contributor.authorscopusid7103192549-
dc.contributor.authorscopusid7005446255-
dc.contributor.authorscopusid56294842200-
dc.description.lastpage2381en_US
dc.identifier.issue12-
dc.description.firstpage2377en_US
dc.relation.volume43en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.identifier.wosWOS:000178910400019-
dc.contributor.daisngid796368-
dc.contributor.daisngid784722-
dc.contributor.daisngid160376-
dc.contributor.daisngid666760-
dc.contributor.daisngid260927-
dc.contributor.daisngid149774-
dc.contributor.daisngid2959850-
dc.contributor.daisngid3523358-
dc.contributor.daisngid59713-
dc.contributor.daisngid245684-
dc.contributor.daisngid611105-
dc.identifier.investigatorRIDC-1247-2010-
dc.identifier.investigatorRIDV-8977-2018-
dc.description.numberofpages5en_US
dc.utils.revisionen_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr1,335-
dc.description.jcrqQ3-
dc.description.scieSCIE-
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.deptGIR Biopoética, Semiótica Cognitiva y Neuroestética-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.deptGIR IUIBS: Patología y Tecnología médica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0003-0505-5126-
crisitem.author.orcid0000-0003-1399-836X-
crisitem.author.orcid0000-0003-0023-1063-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameGómez Casares, María Teresa-
crisitem.author.fullNameDe La Iglesia Íñigo, Silvia Narcisa-
crisitem.author.fullNameBosch Benítez, José Miguel-
crisitem.author.fullNameRodríguez Pérez,José Carlos-
crisitem.author.fullNameMolero Labarta, María Teresa-
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