Dissecting multi drug resistance in head and neck cancer cells using multicellular tumor spheroids.
Mohammad AzharuddinKarin RobergAshis Kumar DharaMayur Vilas JainPadraig DarcyJorma HinkulaNigel K H SlaterHirak Kumar PatraPublished in: Scientific reports (2019)
One of the hallmarks of cancers is their ability to develop resistance against therapeutic agents. Therefore, developing effective in vitro strategies to identify drug resistance remains of paramount importance for successful treatment. One of the ways cancer cells achieve drug resistance is through the expression of efflux pumps that actively pump drugs out of the cells. To date, several studies have investigated the potential of using 3-dimensional (3D) multicellular tumor spheroids (MCSs) to assess drug resistance; however, a unified system that uses MCSs to differentiate between multi drug resistance (MDR) and non-MDR cells does not yet exist. In the present report we describe MCSs obtained from post-diagnosed, pre-treated patient-derived (PTPD) cell lines from head and neck squamous cancer cells (HNSCC) that often develop resistance to therapy. We employed an integrated approach combining response to clinical drugs and screening cytotoxicity, monitoring real-time drug uptake, and assessing transporter activity using flow cytometry in the presence and absence of their respective specific inhibitors. The report shows a comparative response to MDR, drug efflux capability and reactive oxygen species (ROS) activity to assess the resistance profile of PTPD MCSs and two-dimensional (2D) monolayer cultures of the same set of cell lines. We show that MCSs provide a robust and reliable in vitro model to evaluate clinical relevance. Our proposed strategy can also be clinically applicable for profiling drug resistance in cancers with unknown resistance profiles, which consequently can indicate benefit from downstream therapy.
Keyphrases
- induced apoptosis
- cell cycle arrest
- reactive oxygen species
- flow cytometry
- multidrug resistant
- endoplasmic reticulum stress
- cell death
- poor prognosis
- signaling pathway
- oxidative stress
- stem cells
- dna damage
- bone marrow
- drug induced
- low grade
- binding protein
- single cell
- mesenchymal stem cells
- single molecule
- human health
- newly diagnosed
- cell therapy