2019
DOI: 10.1016/j.biomaterials.2019.04.004
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Carbon monoxide (CO)-Strengthened cooperative bioreductive anti-tumor therapy via mitochondrial exhaustion and hypoxia induction

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Cited by 65 publications
(47 citation statements)
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“…Moreover, tirapazamine (TPZ) is a hypoxia‐responsive activated anticancer drug. It is frequently used in many latest designs of hypoxia‐sensitive platform 126,131,144–146 . In the presence of hypoxia, TPZ undergoes the metabolism of an intracellular reductase to form a highly reactive radical species capable of provoking DNA breaks and chromosomal aberrations, leaving cell structural damage and death 147 .…”
Section: Endogenous‐triggered Smart Materialsmentioning
confidence: 99%
“…Moreover, tirapazamine (TPZ) is a hypoxia‐responsive activated anticancer drug. It is frequently used in many latest designs of hypoxia‐sensitive platform 126,131,144–146 . In the presence of hypoxia, TPZ undergoes the metabolism of an intracellular reductase to form a highly reactive radical species capable of provoking DNA breaks and chromosomal aberrations, leaving cell structural damage and death 147 .…”
Section: Endogenous‐triggered Smart Materialsmentioning
confidence: 99%
“…As an endogenous signaling molecule, CO has a variety of biomedical functions, such as regulating blood pressure, reducing inflammation, sensitizing the tumor cells to chemotherapy, and dysfunctionalizing mitochondrial aerobic breathing energy supply [ 134 ]. Based on these functionalities, the study of CO as a therapeutic agent has received widespread attention [ 136 , 137 ]. However, to avoid the toxicity of CO, it is essential to deliver CO specifically to the tumor sites and release the payload on demand.…”
Section: Carbon-containing Reactive Species For Cancer Therapymentioning
confidence: 99%
“…(d) Synthetic schematic of PPPPB-CO-TPZ NPs for antitumor therapy upon laser irradiation. Reprinted with permission [ 137 ]. Copyright 2019, Elsevier.…”
Section: Carbon-containing Reactive Species For Cancer Therapymentioning
confidence: 99%
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“…In this case, there are two basic requirements: i) the agent needs to be able to attenuate CP's nephrotoxicity; and ii) the agent must not reduce the efficacy of CP as a chemotherapeutic in treating cancer. With the known ability of CO to inhibit and/or sensitize cancer cells toward chemotherapy, 106,[214][215][216][217][218][219][220][221][222][223][224] including CP-resistant cancer cells, 225 CO delivered in any form represents an attractive agent for this purpose. Motterlini and co-workers reported in 2006 the first study of the protective effects of metal-based CO-RMs in drug-related kidney injury.…”
Section: Author Manuscriptmentioning
confidence: 99%