Dysregulation of miR-125b predicts poor response to therapy in pediatric acute lymphoblastic leukemia
dc.Affiliation | October University for modern sciences and Arts (MSA) | |
dc.contributor.author | El-Khazragy N. | |
dc.contributor.author | Elshimy A.A. | |
dc.contributor.author | Hassan S.S. | |
dc.contributor.author | Matbouly S. | |
dc.contributor.author | Safwat G. | |
dc.contributor.author | Zannoun M. | |
dc.contributor.author | Riad R.A. | |
dc.contributor.other | Department of Clinical Pathology and Hematology | |
dc.contributor.other | Faculty of Medicine | |
dc.contributor.other | Ain Shams Medical Research Institute (MASRI) | |
dc.contributor.other | Ain Shams University | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt; Former Department of Biomedical Research | |
dc.contributor.other | Armed Forces College of Medicine (AFCM) | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt; Department of Medical Microbiology and Immunology | |
dc.contributor.other | Faculty of Medicine | |
dc.contributor.other | Cairo University | |
dc.contributor.other | New Giza University | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt; Department of Clinical Pathology | |
dc.contributor.other | National Cancer Institute | |
dc.contributor.other | Cairo University | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt; Department of Pediatrics | |
dc.contributor.other | Faculty of Medicine | |
dc.contributor.other | Ain Shams University | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt; Department of Cancer Biology | |
dc.contributor.other | Faculty of Biotechnology | |
dc.contributor.other | October University for Modern Sciences and Art (MSA) University | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt; Department of Pediatrics | |
dc.contributor.other | Faculty of Medicine | |
dc.contributor.other | Al Azhar University | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt; Department of Biotechnology and Molecular Biology | |
dc.contributor.other | Global Research Lab | |
dc.contributor.other | Cairo | |
dc.contributor.other | Egypt | |
dc.date.accessioned | 2020-01-09T20:40:38Z | |
dc.date.available | 2020-01-09T20:40:38Z | |
dc.date.issued | 2019 | |
dc.description | Scopus | |
dc.description | MSA Google Scholar | |
dc.description.abstract | Background: Acute lymphoblastic leukemia (ALL) is the most well-known sort of leukemia in children. In spite of favorable survival rates, some patients relapse and achieve a poor outcome. Methods: We analyzed miR-125b and Bcl-2 expressions in pediatric patients with ALL and evaluated their clinical utility as molecular markers for the prediction of disease outcomes. Results: Downregulation of miR-125b and increased Bcl-2 expression levels in pediatric patients with ALL were associated with poor prognosis at diagnosis. At day 28 of induction, miR-125b was significantly increased, whereas Bcl-2 was downregulated. Loss of miR-125b during diagnosis and its elevation after therapy are strongly correlated with short leukemia-free survival and worse survival. Moreover, the combination of miR-125b with Bcl-2 markers can clearly enhance the prediction of the disease outcome. Finally, a univariate analysis highlighted the independent prognostic value of miR-125 in a pediatric patient with ALL. Conclusions: miR-125b and Bcl-2 together are potent predictors for the prognosis and, therefore, can be used as therapeutic targets in childhood ALL. � 2018 Wiley Periodicals, Inc. | en_US |
dc.identifier.doi | https://doi.org/10.1002/jcb.28017 | |
dc.identifier.doi | PubMedID | |
dc.identifier.issn | 7302312 | |
dc.identifier.other | https://doi.org/10.1002/jcb.28017 | |
dc.identifier.other | PubMedID | |
dc.identifier.uri | https://t.ly/2ddvR | |
dc.language.iso | English | en_US |
dc.publisher | Wiley-Liss Inc. | en_US |
dc.relation.ispartofseries | Journal of Cellular Biochemistry | |
dc.relation.ispartofseries | 120 | |
dc.subject | October University for Modern Sciences and Arts | |
dc.subject | جامعة أكتوبر للعلوم الحديثة والآداب | |
dc.subject | University of Modern Sciences and Arts | |
dc.subject | MSA University | |
dc.subject | Bcl-2 | en_US |
dc.subject | childhood acute lymphoblastic leukemia (ALL) | en_US |
dc.subject | miR-125b | en_US |
dc.subject | prognostic factors | en_US |
dc.subject | antileukemic agent | en_US |
dc.subject | microRNA 125b | en_US |
dc.subject | protein bcl 2 | en_US |
dc.subject | acute lymphoblastic leukemia | en_US |
dc.subject | Article | en_US |
dc.subject | cancer chemotherapy | en_US |
dc.subject | cancer prognosis | en_US |
dc.subject | cancer specific survival | en_US |
dc.subject | child | en_US |
dc.subject | childhood leukemia | en_US |
dc.subject | clinical outcome | en_US |
dc.subject | controlled study | en_US |
dc.subject | down regulation | en_US |
dc.subject | female | en_US |
dc.subject | gene expression | en_US |
dc.subject | human | en_US |
dc.subject | major clinical study | en_US |
dc.subject | male | en_US |
dc.subject | predictive value | en_US |
dc.subject | priority journal | en_US |
dc.subject | treatment response | en_US |
dc.title | Dysregulation of miR-125b predicts poor response to therapy in pediatric acute lymphoblastic leukemia | en_US |
dc.type | Article | en_US |
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