Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.biocel.2011.09.005
Title: TXNIP (VDUP-1, TBP-2): A major redox regulator commonly suppressed in cancer by epigenetic mechanisms
Authors: Zhou, J. 
Yu, Q.
Chng, W.-J.
Keywords: Acute myeloid leukemia
DNA methylation
DNMT inhibitor
DZNep
Epigenetics
HDAC inhibitor
Histone modification
MicroRNA
Oxidative stress
Polycomb-repressive complex 2 (PRC2)
Reactive oxygen species (ROS)
Solid tumor
TXNIP/VDUP-1/TBP-2
Issue Date: Dec-2011
Citation: Zhou, J., Yu, Q., Chng, W.-J. (2011-12). TXNIP (VDUP-1, TBP-2): A major redox regulator commonly suppressed in cancer by epigenetic mechanisms. International Journal of Biochemistry and Cell Biology 43 (12) : 1668-1673. ScholarBank@NUS Repository. https://doi.org/10.1016/j.biocel.2011.09.005
Abstract: TXNIP (also named as VDUP-1 or TBP-2) was originally isolated in HL60 cells treated with Vitamin D3. Subsequently, it has been identified as a major redox regulator and a Tumor Suppressor Gene (TSG) in various solid tumors and hematological malignancies. In the present review, we will first provide an overview of TXNIP gene and protein structures, followed by a summary of the studies that have demonstrated its frequent repression in human cancers and relevant clinical significance, as well as functional characterization in animal models. We will then highlight our current knowledge of TXNIP signaling and biological functions. Next, we will discuss the evidence that clearly have demonstrated that the epigenetic silencing of TXNIP in cancer through various molecular mechanisms. The therapeutic use of small molecular inhibitors to reactivate TXNIP expression for cancer treatment will also be discussed in this review. © 2011 Elsevier Ltd.
Source Title: International Journal of Biochemistry and Cell Biology
URI: http://scholarbank.nus.edu.sg/handle/10635/110795
ISSN: 13572725
DOI: 10.1016/j.biocel.2011.09.005
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