Thesis Abstract

Abstract
Cancer is a complex disease characterized by uncontrolled cell growth and proliferation, leading to tumor formation and metastasis. Epigenetic alterations, such as DNA methylation, histone modifications, and non-coding RNA regulation, have emerged as critical players in cancer development and progression. This thesis aims to explore the role of epigenetics in cancer, focusing on how these molecular modifications influence gene expression patterns and cellular behavior. Chapter one provides an introduction to the topic, presenting the background of the study, the problem statement, objectives, limitations, scope, significance, structure of the thesis, and definitions of key terms. The second chapter is dedicated to a comprehensive literature review, analyzing ten key studies that have explored the relationship between epigenetics and cancer. Chapter three details the research methodology employed in this study, including the experimental design, sample collection, data analysis techniques, and statistical methods used to investigate the epigenetic changes in cancer cells. Key contents of this chapter include the selection of cell lines, DNA extraction and bisulfite conversion, chromatin immunoprecipitation assays, and bioinformatics analysis of epigenetic data. In chapter four, the findings of the study are discussed in detail, focusing on the epigenetic modifications identified in cancer cells and their functional implications. The role of DNA methylation in gene silencing, histone modifications in chromatin remodeling, and non-coding RNAs in post-transcriptional regulation are examined to understand how these epigenetic changes contribute to cancer progression. The final chapter summarizes the key findings of the study and provides a conclusion on the role of epigenetics in cancer development and progression. The implications of the results for cancer diagnosis, prognosis, and treatment are discussed, along with recommendations for future research directions in the field of cancer epigenetics. Overall, this thesis contributes to our understanding of how epigenetic alterations drive cancer pathogenesis and offers insights into potential therapeutic strategies targeting epigenetic regulators in cancer treatment.

Thesis Overview