Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3718
Title: Chromatin Organizer SATB1 As a Novel Molecular Target for Cancer Therapy
Authors: Mir, Rafeeq
Pradhan, Saurabh J.
GALANDE, SANJEEV
Dept. of Biology
Keywords: Chromatin Organizer
SATB1
Novel Molecular Target
Cancer Therapy
ERRB2
FOXP3
microRNAs
2012
Issue Date: Jan-2012
Publisher: Bentham Science Publishers
Citation: Current Drug Targets, 13(13), 1603-1615.
Abstract: Cancer 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.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3718
https://doi.org/10.2174/138945012803530008
ISSN: 1389-4501
1873-5592
Appears in Collections:JOURNAL ARTICLES

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