2013
DOI: 10.1049/iet-syb.2011.0045
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Developing an in silico model of the modulation of base excision repair using methoxyamine for more targeted cancer therapeutics

Abstract: Base Excision Repair (BER) is a major DNA repair pathway involved in the processing of exogenous nonbulky base damages from certain classes of cancer chemotherapy drugs as well as ionizing radiation. Methoxyamine (MX) is a small molecule chemical inhibitor of BER that is shown to enhance chemotherapy and/or ionizing radiation cytotoxicity in human cancers. In this paper, we have analysed the inhibitory effect of MX on the base excision repair pathway kinetics using a computational model of the repair pathway. … Show more

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Cited by 4 publications
(2 citation statements)
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“…MX is highly specific and rapidly binds to abasic sites on DNA. The MX-AP-site ligation is strong and stable [67]. Therefore, the phenotype of melanin production blockage is prolonged (10 days), and it is observed even in response to a short time of drug exposure.…”
Section: Discussionmentioning
confidence: 99%
“…MX is highly specific and rapidly binds to abasic sites on DNA. The MX-AP-site ligation is strong and stable [67]. Therefore, the phenotype of melanin production blockage is prolonged (10 days), and it is observed even in response to a short time of drug exposure.…”
Section: Discussionmentioning
confidence: 99%
“…There are several recent studies on drug sensitivity and anti‐cancer drug response prediction [15, 16]. In [17], random forest (RF) regression technique was used for obtaining a single drug or a group of drugs for certain cancer.…”
Section: Introductionmentioning
confidence: 99%