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Differences in cisplatin distribution in sensitive and resistant ovarian cancer cells: A TEM/NanoSIMS study

  • Ronald F.S. Lee
  • , Tina Riedel
  • , Stéphane Escrig
  • , Catherine Maclachlan
  • , Graham W. Knott
  • , Curt A. Davey
  • , Kai Johnsson
  • , Anders Meibom
  • , Paul J. Dyson

Research output: Contribution to journalArticleResearchpeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)1413-1420
Number of pages8
JournalMetallomics
Volume9
Issue number10
DOIs
Publication statusPublished - 7 Sept 2017
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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