Titel
Comparison of Radiation Response between 2D and 3D Cell Culture Models of Different Human Cancer Cell Lines
Autor*in
Bernadette Barta
Ludwig Boltzmann Institute Applied Diagnostics
Autor*in
Marcus Hacker
Department of Biomedical Imaging and Image-Guided Therapy, Division of Nuclear Medicine, Medical University of Vienna
... show all
Abstract
Radiation therapy is one of the most effective tools in cancer therapy. However, success varies individually, necessitating improved understanding of radiobiology. Three-dimensional (3D) tumor spheroids are increasingly gaining attention, being a superior in vitro cancer model compared to 2D cell cultures. This in vitro study aimed at comparing radiation responses in 2D and 3D cell culture models of different human cancer cell lines (PC-3, LNCaP and T-47D) irradiated with varying doses (1, 2, 4, 6, 8 or 20 Gy) of X-ray beams. Radiation response was analyzed by growth analysis, various cell viability assays (e.g., clonogenic assay, resazurin assay) and amount of DNA damage (γH2AX Western Blot). Results showed decreasing cell proliferation with the increase of radiation doses for all cell lines in monolayers and spheroids of LNCaP and T-47D. However, significantly lower radiosensitivity was detected in spheroids, most pronounced in PC-3, evincing radiation resistance of PC-3 spheroids up to 8 Gy and significant growth inhibition only by a dose escalation of 20 Gy. Cell line comparison showed highest radiosensitivity in LNCaP, followed by T-47D and PC-3 in 2D, whereas, in 3D, T-47D showed highest sensitivity. The results substantiate the significant differences in radiobiological response to X-rays between 2D and 3D cell culture models.
Stichwort
radiobiologyradiation oncologyradiosensitivityexternal photon beam (X-ray)therapyhuman cancer cell lines (PC-3, LNCaP, T-47D)multicellular tumor spheroids (3D)clonogenic assayresazurin assayγH2AX
Objekt-Typ
Sprache
Englisch [eng]
Persistent identifier
https://phaidra.univie.ac.at/o:2045402
Erschienen in
Titel
Cells
Band
12
Ausgabe
3
ISSN
2073-4409
Erscheinungsdatum
2023
Seitenanfang
360
Verlag
MDPI AG
Erscheinungsdatum
2023
Zugänglichkeit
Rechteangabe
© 2023 by the authors

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