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dc.contributor.authorDavudian, S
dc.contributor.authorMansoori, B
dc.contributor.authorShajari, N
dc.contributor.authorMohammadi, A
dc.contributor.authorBaradaran, B
dc.date.accessioned2018-08-26T05:38:21Z
dc.date.available2018-08-26T05:38:21Z
dc.date.issued2016
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/40036
dc.description.abstractBACH1 (BTB and CNC homology 1, basic leucine zipper transcription factor 1) is a transcriptional factor and a member of cap 'n' collar (CNC) and basic region leucine zipper factor family. In contrast to other bZIP family members, BACH1 appeared as a comparatively specific transcription factor. It acts as transcription regulator and is recognized as a recently hypoxia regulator and functions as an inducible repressor for the HO-1 gene in many human cell types in response to stress oxidative. In regard to studies lately, although, BACH1 has been related to the regulation of oxidative stress and heme oxidation, it has never been linked to invasion and metastasis. Recent studies have showed that BACH1 is involved in bone metastasis of breast cancer by up-regulating vital metastatic genes like CXCR4 and MMP1. This newly discovered aspect of BACH1 gene provides new insight into cancer progression study and stands on its master regulator role in metastasis process, raising the possibility of considering it as a potential target for cancer therapy.
dc.language.isoEnglish
dc.relation.ispartofGene
dc.subjectAnimals
dc.subjectBasic-Leucine Zipper Transcription Factors
dc.subjectBone Neoplasms
dc.subjectBreast Neoplasms
dc.subjectCell Movement
dc.subjectFanconi Anemia Complementation Group Proteins
dc.subjectHeme Oxygenase-1
dc.subjectHumans
dc.subjectMolecular Targeted Therapy
dc.subjectNeoplasm Metastasis
dc.subjectOxidative Stress
dc.subjectProto-Oncogene Proteins c-maf
dc.titleBACH1, the master regulator gene: A novel candidate target for cancer therapy.
dc.typearticle
dc.citation.volume588
dc.citation.issue1
dc.citation.spage30
dc.citation.epage7
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1016/j.gene.2016.04.040


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