Phumuzile Dube, Bernice Monchusi, Mutsa M Takundwa, Vanelle L Kenmogne, Austin Malise, Deepak B Thimiri Govinda Raj
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引用次数: 0
Abstract
This protocol outlines a detailed method for performing drug sensitivity testing (DST) on HeLa cells, focusing on both single-drug and combination-drug screening to assess cell viability. DST is integral to cancer research and functional precision medicine, providing insight into individual drug responses and facilitating the optimization of drug combinations. The protocol includes preparing and maintaining HeLa cell cultures, seeding in 96-well plates, and performing single and combination drug treatments using a low-throughput screening approach. These drug treatments aim to evaluate therapeutic effectiveness, enhance understanding of synergistic interactions, and identify optimal combinations that could minimize toxicity while overcoming resistance. Data analysis uses open-source tools, including the BREEZE pipeline and Synergy-Finder, allowing for precise analysis of cell viability and drug interactions. This protocol provides a robust, reproducible framework for DST in cancer research, applicable to other cell lines, patient samples, and various drug types/classes. The critical role of DST in improving clinical treatment strategies through precise, scalable drug response analysis is demonstrated.
期刊介绍:
For over 20 years, biological scientists have come to rely on the research protocols and methodologies in the critically acclaimed Methods in Molecular Biology series. The series was the first to introduce the step-by-step protocols approach that has become the standard in all biomedical protocol publishing. Each protocol is provided in readily-reproducible step-by-step fashion, opening with an introductory overview, a list of the materials and reagents needed to complete the experiment, and followed by a detailed procedure that is supported with a helpful notes section offering tips and tricks of the trade as well as troubleshooting advice.