Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3718
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dc.contributor.authorMir, Rafeeqen_US
dc.contributor.authorPradhan, Saurabh J.en_US
dc.contributor.authorGALANDE, SANJEEVen_US
dc.date.accessioned2019-07-23T11:12:47Z
dc.date.available2019-07-23T11:12:47Z
dc.date.issued2012-01en_US
dc.identifier.citationCurrent Drug Targets, 13(13), 1603-1615.en_US
dc.identifier.issn1389-4501en_US
dc.identifier.issn1873-5592en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3718-
dc.identifier.urihttps://doi.org/10.2174/138945012803530008en_US
dc.description.abstractCancer progression and metastasis involve series of alterations in the expression of multitude of genes. The structure and organization of chromatin play an important role in spatial arrangement of genes inside the nucleus thereby allowing different machineries to activate or silence the transcription of genes governed by various epigenetic events. Epigenetic modifications and dynamic changes in chromatin organization by organizer proteins have recently been shown to play an instrumental role in regulating cancer-promoting genes. Special AT-rich binding protein (SATB1) is a unique type of global regulator that integrates higher-order chromatin organization with regulation of gene expression. Aberrant expression of SATB1 has been shown to promote breast, hepatocellular, prostate and various other cancers. In this review we highlight upon the role of SATB1in chromatin organization and as global regulator of gene expression during cancer development. The expression of SATB1 progressively increases with the progression of cancers and it dynamically reprograms the expression of genes that are involved in epithelial-mesenchymal transition. SATB1 directly regulates the expression of ERRB2, MMP2, ABL1, E-cadherin and hence acts as key regulator in cancer development. Understanding the molecular mechanisms of regulation of SATB1 expression would therefore be extremely essential towards designing strategies to control it. Recent studies have provided important insights into regulation of SATB1 by FOXP3 and microRNAs. In this review we evaluate the potential of SATB1 as molecular target for cancer therapy.en_US
dc.language.isoenen_US
dc.publisherBentham Science Publishersen_US
dc.subjectChromatin Organizeren_US
dc.subjectSATB1en_US
dc.subjectNovel Molecular Targeten_US
dc.subjectCancer Therapyen_US
dc.subjectERRB2en_US
dc.subjectFOXP3en_US
dc.subjectmicroRNAsen_US
dc.subject2012en_US
dc.titleChromatin Organizer SATB1 As a Novel Molecular Target for Cancer Therapyen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitleCurrent Drug Targetsen_US
dc.publication.originofpublisherForeignen_US
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