Differences in cisplatin distribution in sensitive and resistant ovarian cancer cells: a TEM/NanoSIMS study.
Ronald F S LeeTina RiedelStéphane EscrigCatherine MaclachlanGraham W KnottCurt A DaveyKai JohnssonAnders MeibomPaul J DysonPublished in: Metallomics : integrated biometal science (2018)
Cisplatin is a widely used anti-cancer drug, but its effect is often limited by acquired resistance to the compound during treatment. Here, we use a combination of transmission electron microscopy (TEM) and nanoscale-secondary ion mass spectrometry (NanoSIMS) to reveal differences between cisplatin uptake in human ovarian cancers cells, which are known to be susceptible to acquired resistance to cisplatin. Both cisplatin sensitive and resistant cell lines were studied, revealing markedly less cisplatin in the resistant cell line. In cisplatin sensitive cells, Pt was seen to distribute diffusely in the cells with hotspots in the nucleolus, mitochondria, and autophagosomes. Inductively coupled plasma mass spectrometry (ICP-MS) was used to validate the NanoSIMS results.
Keyphrases
- mass spectrometry
- induced apoptosis
- cell cycle arrest
- multiple sclerosis
- liquid chromatography
- endothelial cells
- cell death
- gene expression
- oxidative stress
- capillary electrophoresis
- high resolution
- emergency department
- endoplasmic reticulum stress
- ms ms
- signaling pathway
- genome wide
- single cell
- young adults
- gas chromatography
- pluripotent stem cells
- solid state