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Enrichment for Chemoresistant Ovarian Cancer Stem Cells from Human Cell Lines
Published on: September 10, 2014
Tracking carboplatin chemoresistance in ovarian cancer by scanning electrochemical microscopy
Roy Daou1, Mengzhen Lyu1, Katherine Bazin1
1Laboratory for Bioanalytics and Electrochemical Sensing, Department of Chemistry, Faculty of Science, University of Manitoba 144 Dysart Road R3T 2N2 Winnipeg Manitoba Canada sabine.kuss@umanitoba.ca.
Abstract:
Drug resistance in cancer presents a significant challenge in oncology, contributing to most chemotherapy failures. Early detection of drug resistance is crucial for improving treatment outcomes. Ovarian cancer is often treated with platinum-based drugs, such as carboplatin (CBDCA), but unfortunately, resistance to these compounds is common. The exact mechanisms behind platinum-based drug-resistance remain unclear. This research demonstrates the use of scanning electrochemical microscopy (SECM) to track the cellular response to chemotherpeutic exposure through the quantification of glutathione, a cellular antioxidant, as a biomarker for cellular drug resistance. In the presence of the redox mediator ferrocenemethanol, SECM successfully tracks differential cell redox behaviours in CBDCA-susceptible and CBDCA-resistant ovarian cancer cell models in response to chemotherapeutic exposure. The presented study highlights the potential of using electrochemistry to detect and quantify chemoresistance in cell samples within minutes.

