| Literature DB >> 24758920 |
Angelika Walzl1, Christine Unger2, Nina Kramer2, Daniela Unterleuthner1, Martin Scherzer1, Markus Hengstschläger1, Dagmar Schwanzer-Pfeiffer3, Helmut Dolznig4.
Abstract
Spheroid-based cellular screening approaches represent a highly physiologic experimental setup to identify novel anticancer drugs and an innovative preclinical model to reduce the high failure rate of anticancer compounds in clinical trials. The resazurin reduction (RR) assay, known as the alamarBlue or CellTiter-Blue assay, is frequently used to determine cell viability/proliferation capacity in eukaryotic cells. Whether this assay is applicable to assess viability in multicellular spheroids has not been evaluated. We analyzed the RR assay to measure cytotoxic and/or cytostatic responses in tumor cell spheroids compared with conventional 2D cultures. We found that tight cell-cell interactions in compact spheroids hamper resazurin uptake and its subsequent reduction to resorufin, leading to lowered reduction activity in relation to the actual cellular health/cell number. Treatment with staurosporine disrupted close cell-cell contacts, which increased resazurin reduction compared with untreated controls. Loss of tight junctions by trypsinization or addition of EGTA or EDTA restored high resazurin reduction rates in untreated spheroids. In conclusion, the RR assay is unsuited to quantitatively measure cellular health/cell number in compact spheroids. However, it can be used to distinguish between cytotoxic versus cytostatic compounds in spheroids. Restoration of the correlation of cell viability/number to resazurin reduction capacity can be achieved by disruption of tight junctions.Entities:
Keywords: 3D cell culture; cellular screening; rezazurin to resorufin reduction assay; spheroid
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Year: 2014 PMID: 24758920 DOI: 10.1177/1087057114532352
Source DB: PubMed Journal: J Biomol Screen ISSN: 1087-0571