نمایش پرونده ساده آیتم

dc.contributor.authorYousefi, B
dc.contributor.authorShafiei-Irannejad, V
dc.contributor.authorAzimi, A
dc.contributor.authorSamadi, N
dc.contributor.authorZarghami, N
dc.date.accessioned2018-08-26T05:36:57Z
dc.date.available2018-08-26T05:36:57Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/39720
dc.description.abstractPeroxisome proliferator-activated receptor gamma (PPAR?) plays key roles in regulating cellular differentiation, proliferation and apoptosis pathways. As such, they are considered promising targets for anticancer drug development, especially for breast cancer, multiple myeloma and hematologic malignancies. Chronic myeloid leukemia (CML) is a myeloproliferative disorder arising from an oncogenic Bcr-Abl tyrosine kinase. Inhibitors of this oncogene by small molecules such as imatinib are effective only in 75% of the patient's population. One of the potential strategies to overcome this resistance is to devise combination therapy protocols with other therapeutic agents including PPAR ligands. Since PPAR ligands are potentially interesting in different hematologic malignancies, this article will review the potential of PPAR ligands for use in CML treatment.
dc.language.isoEnglish
dc.relation.ispartofCellular and molecular biology (Noisy-le-Grand, France)
dc.subjectDrug Resistance, Neoplasm
dc.subjectFusion Proteins, bcr-abl
dc.subjectHumans
dc.subjectLeukemia, Myelogenous, Chronic, BCR-ABL Positive
dc.subjectModels, Biological
dc.subjectPPAR gamma
dc.subjectProtein Kinase Inhibitors
dc.titlePPAR-gamma in overcoming kinase resistance in chronic myeloid leukemia.
dc.typearticle
dc.citation.volume62
dc.citation.issue8
dc.citation.spage52
dc.citation.epage5
dc.citation.indexPubmed


فایلهای درون آیتم

فایلهاسایزفرمتنمایش

هیچ فایل مرتبطی وجود ندارد

این آیتم در مجموعه های زیر مشاهده می شود

نمایش پرونده ساده آیتم