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Comprehensive Epigenetic Profiling with decitabine? 


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Decitabine, a demethylating drug, is crucial in cancer therapy due to its efficacy in treating various cancers, including acute myelogenous leukemia (AML). Studies highlight its role in altering DNA methylation patterns, impacting gene expression and treatment response. Decitabine's synergistic effects with other treatments, like TRAIL, have shown promise in enhancing anti-tumor responses in gastric cancer cells by upregulating death receptor 4 (DR4) through epigenetic modifications. Furthermore, single-cell transposable element methylation sequencing (scTEM-seq) provides a cost-effective method to assess global DNA methylation levels, aiding in understanding the heterogeneous regulation of DNA methylation. These findings underscore the importance of comprehensive epigenetic profiling with decitabine to optimize cancer treatment strategies and improve patient outcomes.

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Decitabine enhances TRAIL efficacy in gastric cancer by upregulating DR4 through epigenetic modifications, showcasing its potential as a sensitizing agent for novel treatment strategies.
Decitabine shows potent demethylation effects in diverse cancer cell lines, with a predictive DNA methylation signature for treatment response, especially in hematopoietic/lymphatic cancers, aiding in personalized therapy.
Single-cell transposable element methylation sequencing (scTEM-seq) with decitabine treatment reveals global DNA methylation heterogeneity and altered gene expression, enhancing understanding of epigenetic regulation in cancer.
A single nucleotide polymorphism chip-based method (MSNP) allows comprehensive genetic and epigenetic profiling, validated in decitabine therapy for leukemia and tumor/normal tissue comparisons, enhancing understanding of epigenetic changes.

Related Questions

What is the latest research on epigenetics?5 answersEpigenetics is a rapidly evolving field of research that focuses on heritable changes in gene expression without alterations in gene sequences. It encompasses various mechanisms such as DNA methylation, histone modification, and non-coding RNA regulation. Recent studies have shown the importance of epigenetics in the occurrence and development of diseases such as cervical cancer, endometriosis, and various other conditions. Epigenetic marks, including DNA methylation and histone modifications, play crucial roles in gene regulation and can be disrupted in diseases. Understanding the interactions and changes in epigenetic factors is essential for identifying disease mechanisms and developing therapeutic approaches. Research has also focused on the evolutionary patterns of epigenetic mechanisms across different taxa, the influence of epigenetics on animal plasticity and adaptation, and the role of epigenetic features in germline-restricted chromosomes. Overall, the latest research in epigenetics provides insights into disease development, evolutionary biology, and potential therapeutic strategies.
How does ATAC-seq work to measure epigenetic?5 answersATAC-seq is a method used to measure epigenetic regulation of gene expression by assessing chromatin accessibility. It involves the fragmentation of DNA using a transposase enzyme called Tn5, which cuts the genome and inserts sequencing adapters. This allows for the identification of DNA regulatory sites and the detection of changes in chromatin configuration. The technique has been optimized and improved in various studies, such as the development of combinatorial indexing ATAC sequencing (txci-ATAC-seq), the purification of hyperactive Tn5 transposase, and the use of an updated and optimized protocol called Omni-ATAC. Additionally, the normalization of ATAC-seq data is crucial for accurate downstream analysis, as GC-content effects can bias results. Overall, ATAC-seq provides a powerful tool for studying epigenetic regulation by examining chromatin accessibility at the genome-wide level.
What are some of the epigenetic multi-omic assays that are being used in oncoimmunology?5 answersEpigenetic multi-omic assays used in oncoimmunology include single-cell epigenomic assays such as DNA methylation sequencing and ATAC-seq, as well as single-nucleus methyl-3C sequencing (sn-m3C-seq). These assays allow for the analysis of gene regulatory landscapes and the identification of critical cis-regulatory sequences. Additionally, the integration of DNA methylation, mRNA, and microRNA profiling can provide insights into molecular changes associated with diseases like sarcoidosis, potentially serving as diagnostic/prognostic biomarkers and drug targets. Another approach is the combination of single-cell gene expression and chromatin accessibility profiles to infer gene regulatory networks, as demonstrated by scMEGA (Single-cell Multiomic Enhancer-based Gene Regulatory Network Inference). Furthermore, the integration of genomics, epigenomics, transcriptomics, and proteomics can provide a comprehensive view of the complex interplay between biomolecules in a single cell type, as shown in the analysis of human primary naive CD4+ T cells.
How do epigenetics lead to cancer?5 answersEpigenetic alterations contribute to the development of cancer by regulating gene expression programs that promote tumorigenesis. These alterations occur through mechanisms such as DNA methylation and histone modifications. Epigenetic changes can disrupt the normal functioning of genes, leading to uncontrolled cell division, invasion, and metastasis. In cancer, epigenetic modifications can occur in conjunction with genetic alterations, further driving the cancer phenotype. The reversible nature of epigenetic modifications has made them an attractive target for drug development, leading to the emergence of epigenetic therapies for cancer treatment. Epigenetic biomarkers and drugs have been utilized for diagnosis, monitoring, and treatment choice in the clinical setting. The integration of genetic and epigenetic mutations, along with environmental factors, influences cellular metabolism and proliferation rates, contributing to the onset and progression of cancer.
How can restriction enzymes be used to study epigenetics?3 answersRestriction enzymes can be used to study epigenetics by analyzing DNA methylation patterns and chromatin structure. DNA methylation is a key epigenetic modification involved in gene regulation and silencing. Restriction enzymes sensitive to DNA methylation, such as HpaII/MspI, can be used to identify methylated CpG sites in the genome. By comparing the digestion patterns of methylated and unmethylated DNA, researchers can determine the methylation status of specific regions. Additionally, frequently cutting restriction enzymes can be used to study telomeres, which are repetitive sequences at the ends of chromosomes. These enzymes can analyze telomere length and chromatin structure, independent of the presence of interstitial telomeric sequences (ITSs). Overall, restriction enzymes provide valuable tools for investigating epigenetic modifications and their impact on gene expression and genome stability.
What is Epigenomics ?4 answersEpigenomics is the study of molecular signatures associated with discrete regions within genomes, which play important roles in various nuclear processes. It involves profiling the epigenomic landscape associated with genes, repetitive regions, transposons, transcription, differential expression, cis-regulatory elements, and three-dimensional chromatin interactions. Epigenomic research has greatly improved our understanding of plant genomes and has the potential to analyze epigenetic modifications across the entire genome. Epigenetics, on the other hand, is the study of non-genotoxic, reversible, heritable mechanisms that influence gene expression without changing the DNA sequence. It involves the study of how signals from the environment can change gene expression through the creation of molecules and chemical bonds that can last a lifetime. Epigenetic changes can have consequences for the emotional life of individuals and for society.

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