Anticancer efficacy of the hypoxia‐activated prodrug evofosfamide is enhanced in combination with proapoptotic receptor agonists against osteosarcoma
Vasilios Liapis; Aneta Zysk; Mark DeNichilo; Irene Zinonos; Shelley Hay; Vasilios Panagopoulos; Alexandra Jayne Shoubridge; Christopher Difelice · 2017 · Cancer Medicine
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
The study found no significant effect — useful as a negative control or null benchmark for your own design.
Abstract
Tumor hypoxia is a major cause of treatment failure for a variety of malignancies. However, hypoxia also leads to treatment opportunities as demonstrated by the development of compounds that target regions of hypoxia within tumors. Evofosfamide is a hypoxia-activated prodrug that is created by linking the hypoxia-seeking 2-nitroimidazole moiety to the cytotoxic bromo-isophosphoramide mustard (Br-IPM). When evofosfamide is delivered to hypoxic regions of tumors, the DNA cross-linking toxin, Br-IPM, is released leading to cell death. This study assessed the anticancer efficacy of evofosfamide in
Abstract by Vasilios Liapis; Aneta Zysk; Mark DeNichilo; Irene Zinonos; Shelley Hay; Vasilios Panagopoulos; Alexandra Jayne Shoubridge; Christopher Difelice, Cancer Medicine (2017) — licensed CC BY 4.0.
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Metadata source: OpenAlex · DOI 10.1002/cam4.1115
