What if cell culture media do not mimic in vivo redox settings?
Abstract
Here, I address the topic of suitability for redox research of common settings in cell cultures. This is done through the prism of in vitro anticancer effects of vitamin C. Cell culture media show lower concentrations of iron and a higher level of oxygen compared to interstitial fluid. Such a setup promotes ascorbate-mediated production and accumulation of hydrogen peroxide, which efficiently kills a variety of cancer cell lines. However, the anticancer effects are annihilated if the iron level is corrected to mimic in vivo concentrations. It appears that the potential benefits of application of vitamin C in cancer treatment have been significantly overestimated. This might be true for other pro-oxidative agents as well, such as some (poly)phenols. We urgently need to establish medium formula and culture maintenance settings that are optimal for redox research.
Keywords:
Iron / Cell culture / Cancer / AscorbateSource:
Redox Report, 2016, 21, 3, 127-129Publisher:
- Taylor & Francis Ltd, Abingdon
Funding / projects:
DOI: 10.1179/1351000215Y.0000000036
ISSN: 1351-0002
PubMed: 26221760
WoS: 000376438900005
Scopus: 2-s2.0-84978636787
Collections
Institution/Community
Institut za multidisciplinarna istraživanjaTY - JOUR AU - Spasojević, Ivan PY - 2016 UR - http://rimsi.imsi.bg.ac.rs/handle/123456789/998 AB - Here, I address the topic of suitability for redox research of common settings in cell cultures. This is done through the prism of in vitro anticancer effects of vitamin C. Cell culture media show lower concentrations of iron and a higher level of oxygen compared to interstitial fluid. Such a setup promotes ascorbate-mediated production and accumulation of hydrogen peroxide, which efficiently kills a variety of cancer cell lines. However, the anticancer effects are annihilated if the iron level is corrected to mimic in vivo concentrations. It appears that the potential benefits of application of vitamin C in cancer treatment have been significantly overestimated. This might be true for other pro-oxidative agents as well, such as some (poly)phenols. We urgently need to establish medium formula and culture maintenance settings that are optimal for redox research. PB - Taylor & Francis Ltd, Abingdon T2 - Redox Report T1 - What if cell culture media do not mimic in vivo redox settings? EP - 129 IS - 3 SP - 127 VL - 21 DO - 10.1179/1351000215Y.0000000036 ER -
@article{ author = "Spasojević, Ivan", year = "2016", abstract = "Here, I address the topic of suitability for redox research of common settings in cell cultures. This is done through the prism of in vitro anticancer effects of vitamin C. Cell culture media show lower concentrations of iron and a higher level of oxygen compared to interstitial fluid. Such a setup promotes ascorbate-mediated production and accumulation of hydrogen peroxide, which efficiently kills a variety of cancer cell lines. However, the anticancer effects are annihilated if the iron level is corrected to mimic in vivo concentrations. It appears that the potential benefits of application of vitamin C in cancer treatment have been significantly overestimated. This might be true for other pro-oxidative agents as well, such as some (poly)phenols. We urgently need to establish medium formula and culture maintenance settings that are optimal for redox research.", publisher = "Taylor & Francis Ltd, Abingdon", journal = "Redox Report", title = "What if cell culture media do not mimic in vivo redox settings?", pages = "129-127", number = "3", volume = "21", doi = "10.1179/1351000215Y.0000000036" }
Spasojević, I.. (2016). What if cell culture media do not mimic in vivo redox settings?. in Redox Report Taylor & Francis Ltd, Abingdon., 21(3), 127-129. https://doi.org/10.1179/1351000215Y.0000000036
Spasojević I. What if cell culture media do not mimic in vivo redox settings?. in Redox Report. 2016;21(3):127-129. doi:10.1179/1351000215Y.0000000036 .
Spasojević, Ivan, "What if cell culture media do not mimic in vivo redox settings?" in Redox Report, 21, no. 3 (2016):127-129, https://doi.org/10.1179/1351000215Y.0000000036 . .