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Gene Regulation and Targeted Therapy in Gastric Cancer Peritoneal Metastasis: Radiological Findings from Dual Energy CT and PET/CT
Published on: January 22, 2018
DNA methyltransferases and gastric cancer: insight into targeted therapy
Sadegh Fattahi1,2, Monireh Golpour3, Fatemeh Amjadi-Moheb4
1Cellular & Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, 4717647745, Babol, Iran.
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.
Insights
Gastric cancer, a leading cause of cancer mortality, involves epigenetic changes from DNA methyltransferases (DNMTs). This review explores DNMTs in gastric cancer and their inhibition for treating drug-resistant tumors.
Area of Science:
- Oncology
- Epigenetics
- Molecular Biology
Background:
- Gastric cancer is a significant global health concern and a leading cause of cancer-related deaths worldwide.
- Epigenetic alterations, particularly DNA methylation mediated by DNA methyltransferases (DNMTs), are recognized hallmarks in gastric cancer development.
- The reversible nature of epigenetic modifications presents therapeutic opportunities.
Purpose of the Study:
- To review the key factors and mechanisms influencing DNA methyltransferase (DNMT) levels in gastric cancer.
- To discuss the role of these modifications in gastric cancer progression.
- To explore the potential of DNMT inhibitors in overcoming multidrug resistance in gastric cancer treatment.
Main Methods:
- Literature review focusing on epigenetic alterations in gastric cancer.
- Analysis of factors influencing DNA methyltransferase (DNMT) levels, including genetic modifications, single nucleotide polymorphisms (SNPs), and infections.
- Examination of the therapeutic strategies involving DNMT inhibitors.
Main Results:
- Genetic factors, SNPs, and infections can modify DNA methyltransferase (DNMT) levels in gastric cancer.
- These modifications play a role in the progression of gastric cancer.
- DNMT inhibitors show promise in enhancing chemotherapy efficacy, especially in multidrug-resistant gastric cancer.
Conclusions:
- Understanding the triggers of DNMT modification is crucial for gastric cancer research.
- Targeting DNMTs offers a potential strategy to overcome treatment resistance in gastric cancer.
- Further research into DNMT inhibition could lead to improved therapeutic outcomes for gastric cancer patients.
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