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Review

Epigenetic Bases of Aberrant Glycosylation in Cancer

1
Department of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, 40126 Bologna, Italy
2
Department of Medicine and Surgery (DMC), University of Insubria, 21100 Varese, Italy
*
Authors to whom correspondence should be addressed.
Academic Editor: Nicoletta Sacchi
Int. J. Mol. Sci. 2017, 18(5), 998; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18050998
Received: 11 April 2017 / Revised: 27 April 2017 / Accepted: 2 May 2017 / Published: 6 May 2017
(This article belongs to the Special Issue Cancer Epigenetics)
In this review, the sugar portions of glycoproteins, glycolipids, and glycosaminoglycans constitute the glycome, and the genes involved in their biosynthesis, degradation, transport and recognition are referred to as “glycogenes”. The extreme complexity of the glycome requires the regulatory layer to be provided by the epigenetic mechanisms. Almost all types of cancers present glycosylation aberrations, giving rise to phenotypic changes and to the expression of tumor markers. In this review, we discuss how cancer-associated alterations of promoter methylation, histone methylation/acetylation, and miRNAs determine glycomic changes associated with the malignant phenotype. Usually, increased promoter methylation and miRNA expression induce glycogene silencing. However, treatment with demethylating agents sometimes results in silencing, rather than in a reactivation of glycogenes, suggesting the involvement of distant methylation-dependent regulatory elements. From a therapeutic perspective aimed at the normalization of the malignant glycome, it appears that miRNA targeting of cancer-deranged glycogenes can be a more specific and promising approach than the use of drugs, which broad target methylation/acetylation. A very specific type of glycosylation, the addition of GlcNAc to serine or threonine (O-GlcNAc), is not only regulated by epigenetic mechanisms, but is an epigenetic modifier of histones and transcription factors. Thus, glycosylation is both under the control of epigenetic mechanisms and is an integral part of the epigenetic code. View Full-Text
Keywords: glycome; glycosyltransferases; DNA methylation; miRNA targeting glycome; glycosyltransferases; DNA methylation; miRNA targeting
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MDPI and ACS Style

Dall’Olio, F.; Trinchera, M. Epigenetic Bases of Aberrant Glycosylation in Cancer. Int. J. Mol. Sci. 2017, 18, 998. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18050998

AMA Style

Dall’Olio F, Trinchera M. Epigenetic Bases of Aberrant Glycosylation in Cancer. International Journal of Molecular Sciences. 2017; 18(5):998. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18050998

Chicago/Turabian Style

Dall’Olio, Fabio, and Marco Trinchera. 2017. "Epigenetic Bases of Aberrant Glycosylation in Cancer" International Journal of Molecular Sciences 18, no. 5: 998. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18050998

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