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dc.contributor.authorDeshmukh, A.
dc.contributor.authorBinju, M.
dc.contributor.authorArfuso, Frank
dc.contributor.authorNewsholme, Philip
dc.contributor.authorDharmarajan, Arunasalam
dc.identifier.citationDeshmukh, A. and Binju, M. and Arfuso, F. and Newsholme, P. and Dharmarajan, A. 2017. Role of epigenetic modulation in cancer stem cell fate. International Journal of Biochemistry and Cell Biology. 90: pp. 9-16.

© 2017 Elsevier Ltd A sub-population of the tumor micro-environment consists of cancer stem cells (CSCs), which are responsible for the initiation and recurrence of cancer. Recently, epigenetic processes such as DNA methylation, histone modification, and chromatin remodeling have been found to be involved in inducing epigenetic factors in CSCs. Most of these processes, such as DNA methylation, generally occur in the genome that is rich in Cytosine-Guanine repeat sequences, also known as CpG islands, which are distributed throughout the human genome. The Polycomb gene (PcG) complex is a chromatin modifier facilitating the maintenance of embryonic and adult stem cells. Recent evidence suggests that the PcG is also involved in maintaining CSC stemness. We have presented various aspects and examples of how epigenetic modulation may drive or promote tumorigenesis and metastasis by alteration of key transcriptomic programs and signaling pathways in CSCs.

dc.titleRole of epigenetic modulation in cancer stem cell fate
dc.typeJournal Article
dcterms.source.titleInternational Journal of Biochemistry and Cell Biology
curtin.departmentSchool of Biomedical Sciences
curtin.accessStatusFulltext not available

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