| Literature DB >> 34989923 |
Shilpaa Mukundan1, Jordan Bell2, Matthew Teryek1, Charles Hernandez2, Andrea C Love2, Biju Parekkadan1,3, Leo Li-Ying Chan4.
Abstract
Tumor spheroid models have proven useful in the study of cancer cell responses to chemotherapeutic compounds by more closely mimicking the 3-dimensional nature of tumors in situ. Their advantages are often offset, however, by protocols that are long, complicated, and expensive. Efforts continue for the development of high-throughput assays that combine the advantages of 3D models with the convenience and simplicity of traditional 2D monolayer methods. Herein, we describe the development of a breast cancer spheroid image cytometry assay using T47D cells in Aggrewell™400 spheroid plates. Using the Celigo® automated imaging system, we developed a method to image and individually track thousands of spheroids within the Aggrewell™400 microwell plate over time. We demonstrate the use of calcein AM and propidium iodide staining to study the effects of known anti-cancer drugs Doxorubicin, Everolimus, Gemcitabine, Metformin, Paclitaxel and Tamoxifen. We use the image cytometry results to quantify the fluorescence of calcein AM and PI as well as spheroid size in a dose dependent manner for each of the drugs. We observe a dose-dependent reduction in spheroid size and find that it correlates well with the viability obtained from the CellTiter96® endpoint assay. The image cytometry method we demonstrate is a convenient and high-throughput drug-response assay for breast cancer spheroids under 400 μm in diameter, and may lay a foundation for investigating other three-dimensional spheroids, organoids, and tissue samples.Entities:
Keywords: Aggrewell™400; Celigo; High-throughput screening; Image cytometry; Tumor spheroid
Mesh:
Substances:
Year: 2022 PMID: 34989923 DOI: 10.1007/s10895-021-02881-3
Source DB: PubMed Journal: J Fluoresc ISSN: 1053-0509 Impact factor: 2.217