Litcius/Paper detail

Resistance to Hypomethylating Agents in Myelodysplastic Syndrome and Acute Myeloid Leukemia From Clinical Data and Molecular Mechanism

Guangjie Zhao, Qian Wang, S. Li, Xiaoqin Wang

2021Frontiers in Oncology25 citationsDOIOpen Access PDF

Abstract

The nucleoside analogs decitabine (5-AZA-dC) and azacitidine (5-AZA) have been developed as targeted therapies to reverse DNA methylation in different cancer types, and they significantly improve the survival of patients who are not suitable for traditional intensive chemotherapies or other treatment regimens. However, approximately 50% of patients have a response to hypomethylating agents (HMAs), and many patients have no response originally or in the process of treatment. Even though new combination regimens have been tested to overcome the resistance to 5-AZA-dC or 5-AZA, only a small proportion of patients benefited from these strategies, and the outcome was very poor. However, the mechanisms of the resistance remain unknown. Some studies only partially described management after failure and the mechanisms of resistance. Herein, we will review the clinical and molecular signatures of the HMA response, alternative treatment after failure, and the causes of resistance in hematological malignancies.

Topics & Concepts

DecitabineAzacitidineHypomethylating agentMedicineMyeloid leukemiaMyelodysplastic syndromesOncologyMechanism (biology)Internal medicineDNA methylationPharmacologyBone marrowBiologyGeneBiochemistryPhilosophyEpistemologyGene expressionAcute Myeloid Leukemia ResearchHistone Deacetylase Inhibitors ResearchEpigenetics and DNA Methylation