DNA methyltransferases and gastric cancer: insight into targeted therapy

Author:

Fattahi Sadegh12,Golpour Monireh3,Amjadi-Moheb Fatemeh4,Sharifi-Pasandi Marzieh3,Khodadadi Parastesh4,Pilehchian-Langroudi Maryam4,Ashrafi Gholam Hossein5,Akhavan-Niaki Haleh4

Affiliation:

1. Cellular & Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, 4717647745, Babol, Iran

2. North Research Center, Pasteur Institute, Amol, 4615885399, Iran

3. Molecular & Cell Biology Research Center, Student Research Committee, Faculty of Medicine, Mazandaran University of Medical Science, Sari, 4817844718, Iran

4. Department of Genetics, Faculty of Medicine, Babol University of Medical Sciences, 4717647745, Babol, Iran

5. School of Life Science, Pharmacy & Chemistry, SEC Faculty, Cancer Theme, Kingston University London, Kingston upon Thames, London KT1 2EE, UK

Abstract

Gastric cancer is a major health problem worldwide occupying most frequent causes of cancer-related mortality. In addition to genetic modifications, epigenetic alterations catalyzed by DNA methyltransferases (DNMTs) are a well-characterized epigenetic hallmark in gastric cancer. The reversible nature of epigenetic alterations and central role of DNA methylation in diverse biological processes provides an opportunity for using DNMT inhibitors to enhance the efficacy of chemotherapeutics. In this review, we discussed key factors or mechanisms such as SNPs, infections and genetic modifications that trigger DNMTs level modification in gastric cancer, and their potential roles in cancer progression. Finally, we focused on how inhibitors of the DNMTs can most effectively be used for the treatment of gastric cancer with multidrug resistance.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Genetics

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