Coadministration of auraptene and radiotherapy; a novel modality against colon carcinoma cells in vitro and in vivo. (2nd August 2020)

• Record Type: Journal Article
• Authors: Salari, Hamide; Afkhami-Poostchi, Amin; Soleymanifard, Shokouhozaman; Nakhaei-Rad, Saeideh; Merajifar, Elahe; Iranshahi, Mehrdad; Matin, Maryam M.; Rassouli, Fatemeh B.
• Is Part Of: International journal of radiation biology. Volume 96:Number 8(2020)
• Page Start: 1051
• Page End: 1059
• Publication Date: 2020-08-02
• Subjects: Auraptene -- Ionizing radiation -- radiosensitizer colon carcinoma -- combinatorial approach; Radiation -- Physiological effect -- Periodicals; Radiobiology -- Periodicals; 571.45
• DOI: 10.1080/09553002.2020.1770359
• Languages: English
• ISSNs: 0955-3002

Abstract

Abstract: Background: Use of ionizing radiation (IR) is a common therapeutic modality for patients with colon carcinoma, although resistance of cancer cells and unintended toxicity reduce clinical outcomes. Purpose: To enhance radioresponse of colon cancer cells, we designed a novel approach using auraptene (AUR) in combination with ionizing radiation (IR). Methods: For in vitro studies, CT26 cells were pretreated with AUR and irradiated at different doses. Then, cell viability was evaluated by alamarBlue assay, and the mechanism of cell death was elucidated using annexin V-PI. To determine efficacy of our combined therapeutic modality in vivo, AUR was injected intraperitoneally to murine models of colon carcinoma followed by IR, and then quantitative measurements and histopathological examinations were performed. For molecular analyses, real time PCR and Western blot were carried out. Results: Assessment of cell viability indicated significant enhancement of IR effects by AUR that was also confirmed by increased number of apoptotic cells. In vivo studies further demonstrated improved outcome in IR, since significant regression in tumor size was observed after administration of AUR + IR. Molecular analyses revealed down regulation of Cyclin D1 and CD44, along with involvement of PI3K-AKT-mTORC signaling pathway and Caspase-3 in observed combinatorial effects. Conclusion: Taken together, current findings support our previous reports on sensitizing effects of AUR and that AUR could be used as a promising adjunct to IR in cancer treatment.