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Epigenetic regulation of TGF-β and vice versa in cancers - A review on recent developments
1Biological and Life Sciences, School of Arts and Sciences, Ahmedabad University, Navrangpura, Ahmedabad 380009, Gujarat, India.
Abstract:
This review explores the complex relationship between epigenetic mechanisms and Transforming Growth Factor-beta (TGF-β) signalling pathways in the field of cancer research. The study provides an overview of the latest advancements in understanding the crucial functions of epigenetic alterations, such as DNA methylation, histone modifications, and chromatin remodeling, in significantly impacting the TGF-β signalling pathway. The dynamic epigenetic modifications are essential in determining the behaviour of cancer cells, impacting the interactions with the tumor microenvironment, and affecting the overall process of carcinogenesis. Significant attention is given to Breast cancer, Lung cancer, Liver cancer, Prostate cancer, and Pancreatic cancer. Research has revealed intricate regulatory networks in these cancers, involving long non-coding RNAs (lncRNAs), microRNAs (miRNAs), and histone post-translational modifications. These networks are closely connected to TGF-β signalling. Both findings highlight the significant interaction between epigenetic regulation and TGF-β signalling in cancer. They provide valuable insights that can guide the development of new treatment approaches to target both pathways and prevent cancer growth and metastasis.
Insights
Epigenetic alterations critically influence cancer cell behavior by modifying Transforming Growth Factor-beta (TGF-β) signaling. Understanding these epigenetic mechanisms offers new therapeutic strategies for various cancers.
Area of Science:
- Oncology
- Epigenetics
- Molecular Biology
Background:
- Epigenetic mechanisms, including DNA methylation and histone modifications, play a vital role in regulating gene expression.
- Transforming Growth Factor-beta (TGF-β) signaling is a key pathway implicated in cell growth, differentiation, and cancer progression.
- Dysregulation of TGF-β signaling is frequently observed in various cancers, contributing to tumorigenesis and metastasis.
Purpose of the Study:
- To review the intricate relationship between epigenetic modifications and TGF-β signaling in cancer research.
- To highlight the impact of epigenetic alterations on TGF-β pathway activity and cancer cell behavior.
- To explore potential therapeutic strategies targeting both epigenetic regulation and TGF-β signaling.
Main Methods:
- Literature review of recent advancements in cancer epigenetics and TGF-β signaling.
- Analysis of studies focusing on DNA methylation, histone modifications, and chromatin remodeling.
- Examination of regulatory networks involving non-coding RNAs (lncRNAs, miRNAs) in cancer.
Main Results:
- Epigenetic alterations significantly impact TGF-β signaling pathways in cancer.
- Specific epigenetic modifications are linked to altered TGF-β activity in breast, lung, liver, prostate, and pancreatic cancers.
- Complex regulatory networks involving lncRNAs and miRNAs are interconnected with TGF-β signaling in these cancers.
Conclusions:
- Epigenetic regulation and TGF-β signaling are deeply intertwined in the development and progression of cancer.
- Targeting both epigenetic mechanisms and TGF-β pathways holds promise for novel cancer therapies.
- Further research into these interactions can lead to improved strategies for cancer prevention and treatment.
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