| Literature DB >> 25130173 |
Jing Nie1, Lin Liu2, Xiang Li1, Weidong Han3.
Abstract
Epigenetic alterations are strongly associated with cancer development and drug resistance. The use of the DNA methylation inhibitor decitabine (Dacogen®) has been approved in the treatment of hematological malignancies, and its clinical effects on solid tumors have gained attention. Here, we present a review of the molecular regulation mechanisms, clinical experiences and biological evaluation for novel decitabine-based therapies in solid tumors. We also discuss the following questions: What is the best administration schedule of decitabine in solid tumors? Is there tumor type specificity for decitabine-based epigenetic therapy? What are the biological function and mechanism of decitabine in suppressing tumor development? Is there a correlation between DNA demethylation and clinical response? Importantly, low-dose decitabine and combined therapy show significant improvement in solid tumor treatment. However, the correlation studies are preliminary, and key biomarkers for prognosis need further investigation.Entities:
Keywords: Decitabine; Demethylating drug; Drug sensitivity; Tumor therapy
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Year: 2014 PMID: 25130173 DOI: 10.1016/j.canlet.2014.08.010
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679