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dc.contributor.authorHancer, Veysel Sabri
dc.contributor.authorDiz-Kucukkaya, Reyhan
dc.contributor.authorAktan, Melih
dc.date.accessioned2019-08-13T12:10:23Z
dc.date.accessioned2019-08-13T16:03:41Z
dc.date.available2019-08-13T12:10:23Z
dc.date.available2019-08-13T16:03:41Z
dc.date.issued2012
dc.identifier.issn1357-0560
dc.identifier.urihttps://dx.doi.org/10.1007/s12032-011-9821-3
dc.identifier.urihttp://hdl.handle.net/11446/3144
dc.descriptionWOS: 000303539000103en_US
dc.descriptionPubMed ID: 21264533en_US
dc.description.abstractRai and Binet staging systems that have been used as a standard method for evaluating the prognosis of chronic lymphocytic leukemia (CLL) have some restrictions in distinguishing the early stage CLL patients that will progress rapidly. To solve this shortcoming, prognostic parameters other than staging have become important in the recent years. Intracellular upregulation of Fc mu receptor (FCMR, FAIM3/TOSO) gene in the leukemic lymphocytes of the patients with CLL may be an important parameter in predicting the progression of the disease. In this study, FCMR mRNA expression levels were evaluated in 50 CLL patients and in 50 healthy controls. FCMR mRNA expression was found to be significantly higher in CLL patients than in healthy controls. We, then, evaluated FCMR mRNA levels according to the stages of CLL. Rai stage 0, I, II cases were compared with stage III and IV, and Binet A was compared with Binet B and C according to FCMR mRNA levels. In cases with higher risks, Rai stage III, IV and Binet stage B and C, FCMR mRNA levels were also significantly higher. In addition, overexpression of the FCMR seems to be promoting the chromosomal abnormalities. As a result, we found that the mRNA levels of FCMR in the CLL patients are 23-fold higher than that of the control group and this may suggest that it can be associated with the disease progression and survival. For this reason and because of the simplicity of analyzing with Q-PCR, it can be a useful clinical parameter, after its importance has been shown in larger and multi-variate studies.en_US
dc.language.isoengen_US
dc.publisherHUMANA PRESS INCen_US
dc.identifier.doi10.1007/s12032-011-9821-3en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectFCMRen_US
dc.subjectGene expressionen_US
dc.subjectCLLen_US
dc.titleOverexpression of Fc mu receptor (FCMR, TOSO) gene in chronic lymphocytic leukemia patientsen_US
dc.typearticleen_US
dc.relation.journalMEDICAL ONCOLOGYen_US
dc.departmentDBÜen_US
dc.identifier.issue2en_US
dc.identifier.volume29en_US
dc.identifier.startpage1068en_US
dc.identifier.endpage1072en_US
dc.contributor.authorID0000-0003-2994-1077en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Hancer, Veysel Sabri] Istanbul Bilim Univ, Dept Med Biol & Genet, TR-34394 Istanbul, Turkey -- [Diz-Kucukkaya, Reyhan] Istanbul Bilim Univ, Dept Internal Med, Div Hematol, TR-34394 Istanbul, Turkey -- [Aktan, Melih] Istanbul Univ, Dept Internal Med, Div Hematol, Istanbul, Turkeyen_US


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