Epigenetic targeting in pancreatic cancer
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Updated: May 3, 2026

Author Spotlight: Reprogramming Cancer Cells to iPSCs to Study Disease Progression and Treatment Targets
Published on: February 2, 2024
Jasmijn G M van Kampen1, Monica A J Marijnissen-van Zanten2, Femke Simmer2
1Department of Pathology 824, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, The Netherlands; Department of Urology 267, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, The Netherlands.
Abstract:
The prognosis of pancreatic cancer patients is very poor, with a 5-year survival of less than 6%. Therefore, there is an urgent need for new therapeutic options in pancreatic cancer. In the past years it became evident that deregulation of epigenetic mechanisms plays an important role in pancreatic carcinogenesis. This review focuses on the exploitation of drugs that alter histone modifications, DNA methylation and microRNA expression as options for the treatment of pancreatic cancer.
Insights
Pancreatic cancer has a poor prognosis, necessitating novel treatments. This review explores epigenetic drugs targeting histone modifications, DNA methylation, and microRNA for pancreatic cancer therapy.
Area of Science:
- Oncology
- Epigenetics
- Molecular Biology
Background:
- Pancreatic cancer exhibits a dismal prognosis, with a 5-year survival rate below 6%, highlighting the critical need for innovative therapeutic strategies.
- Epigenetic alterations, including changes in DNA methylation, histone modifications, and microRNA expression, are increasingly recognized as significant drivers of pancreatic carcinogenesis.
Purpose of the Study:
- This review synthesizes current research on epigenetic mechanisms in pancreatic cancer.
- The primary focus is to evaluate the therapeutic potential of drugs targeting epigenetic modifications for pancreatic cancer treatment.
Main Methods:
- Literature review of studies investigating epigenetic alterations in pancreatic cancer.
- Analysis of preclinical and clinical data on epigenetic drugs, including those affecting histone modifications, DNA methylation, and microRNA.
Main Results:
- Epigenetic deregulation is a key factor in the development and progression of pancreatic cancer.
- Drugs targeting epigenetic mechanisms show promise as a new class of therapeutic agents for pancreatic cancer.
Conclusions:
- Targeting epigenetic modifications represents a promising avenue for developing novel treatments for pancreatic cancer.
- Further research and clinical trials are warranted to fully realize the potential of epigenetic therapies in improving patient outcomes for pancreatic cancer.
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