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Related Concept Videos

Phase II Reactions: Methylation Reactions01:17

Phase II Reactions: Methylation Reactions

Methylation is a phase II biotransformation process involving the attachment of a methyl group to a substrate. Enzymes known as methyltransferases orchestrate this reaction.
The mechanism of methylation unfolds in two stages. The first stage sees a methyltransferase enzyme facilitating the transfer of a methyl group from S-adenosylmethionine (SAM) to the substrate, forming S-adenosylhomocysteine (SAH). The second stage involves further metabolism of SAH into homocysteine, which can be recycled...
Antiprotozoal Agents01:21

Antiprotozoal Agents

Leishmaniasis is a widespread parasitic disease caused by several Leishmania species. It affects millions of people each year and remains a major public health problem in endemic regions. First-line treatment relies on pentavalent antimonials, including meglumine antimoniate and sodium stibogluconate. Even so, how these drugs work has not been fully clear, especially their interaction with parasite-specific biochemical pathways. One key target is trypanothione reductase (TR), an enzyme that...
Drugs that Destabilize Microtubules01:10

Drugs that Destabilize Microtubules

Microtubules are dynamic structures and can be regulated by microtubule targeting agents (MTAs). Microtubule destabilizing drugs are a class of MTAs that destabilize and prevent microtubules' polymerization. Both natural and synthetic chemicals can be found under this class of drugs. Vincristine and vinblastine, two vinca alkaloids, and colchicine were among the first to be discovered. These drugs can affect cells in various ways, either by inducing a change in cell morphology, preventing...
Chemotherapy-Induced Nausea and Vomiting: Dopamine Receptor Antagonists01:29

Chemotherapy-Induced Nausea and Vomiting: Dopamine Receptor Antagonists

Dopamine receptor antagonists, also known as antipsychotic agents, are critical in managing chemotherapy-induced vomiting. These antiemetic agents block dopamine receptors in the chemoreceptor trigger zone (CTZ), inhibiting signal transmission to the vomiting center. Antipsychotic agents encompass phenothiazines (PTZ), butyrophenones, benzamides, and thienobenzodiazepines (Zyprexa), which are utilized for their antiemetic and sedative properties.
Phenothiazines, such as prochlorperazine...
Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents01:29

Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents

Crohn's disease is an inflammatory bowel disorder marked by chronic inflammation of the GI tract. Various treatment strategies for Crohn's disease are employed, such as immunomodulatory agents, glucocorticoids, and biologics or anti-TNF therapy. Azathioprine (Imuran), a commonly used immunomodulatory drug for Crohn's disease, is converted in the body to mercaptopurine, which inhibits purine biosynthesis and cell proliferation. Both are utilized in severe cases of Inflammatory Bowel Disease...
Anthelminthic Agents01:15

Anthelminthic Agents

Anthelmintic drugs differ significantly from antiparasitic therapies targeting protozoa, primarily due to differences in parasite biology. Whereas most protozoal treatments act on proliferating cells, anthelmintics are typically directed against mature, nonproliferative helminths. The therapeutic approach considers the helminth's reliance on neuromuscular coordination, glucose metabolism, and microtubular integrity for survival, reproduction, and localization within the host. Most anthelmintics...

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Minimal residual disease eradication with epigenetic therapy in core binding factor acute myeloid leukemia.

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Validation of the 2016 revisions to the WHO classification in lower-risk myelodysplastic syndrome.

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Natural history of chronic myelomonocytic leukemia treated with hypomethylating agents.

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Related Experiment Video

Updated: Jun 29, 2026

Continuous Fluorescence-Based Endonuclease-Coupled DNA Methylation Assay to Screen for DNA Methyltransferase Inhibitors
06:07

Continuous Fluorescence-Based Endonuclease-Coupled DNA Methylation Assay to Screen for DNA Methyltransferase Inhibitors

Published on: August 5, 2022

Demethylating agents in myeloid malignancies.

Guillermo Garcia-Manero1

  • 1Department of Leukemia, University of Texas, MD Anderson Cancer Center, Houston, Texas 77030, USA. ggarciam@mdanderson.org

Current Opinion in Oncology
|October 9, 2008
PubMed
Summary

Demethylating agents like 5-azacitidine improve survival in myelodysplastic syndromes (MDS). Combination epigenetic therapies show promise for further advancing MDS treatment.

Area of Science:

  • Oncology
  • Epigenetics
  • Hematology

Background:

  • Myelodysplastic syndromes (MDS) are often associated with aberrant DNA methylation and gene silencing.
  • Approved demethylating agents, 5-azacitidine and decitabine, induce DNA hypomethylation.
  • These agents are thought to work by reexpressing epigenetically silenced genes.

Purpose of the Study:

  • To provide an updated summary of clinical experience with demethylating agents in MDS.
  • To review the efficacy and impact of current and emerging epigenetic therapies for MDS.

Main Methods:

  • Review of clinical trial data and published literature on 5-azacitidine and decitabine in MDS.
  • Analysis of recent phase III study results and ongoing randomized trials.

Related Experiment Videos

Last Updated: Jun 29, 2026

Continuous Fluorescence-Based Endonuclease-Coupled DNA Methylation Assay to Screen for DNA Methyltransferase Inhibitors
06:07

Continuous Fluorescence-Based Endonuclease-Coupled DNA Methylation Assay to Screen for DNA Methyltransferase Inhibitors

Published on: August 5, 2022

Main Results:

  • 5-Azacitidine has demonstrated a significant improvement in overall survival for higher-risk MDS patients.
  • Combination epigenetic therapies (hypomethylating agent + histone deacetylase inhibitor) show significant activity in MDS/acute myelogenous leukemia.
  • Decitabine survival study results are pending; randomized studies are evaluating combination superiority.

Conclusions:

  • Demethylating agents are the standard of care for higher-risk MDS, improving its natural history.
  • Further research into novel combination therapies holds potential for significant advances in MDS patient care.