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In vitro antitumor effects of AHR ligands aminoflavone (AFP 464) and benzothiazole (5F 203) in human renal carcinoma cells

Luzzani, Gabriela A.; Callero, Mariana A.; Kuruppu, Anchala I.; Trapani, Valentina; Flumian, Carolina; Todaro, Laura; Bradshaw, Tracey D.; Loaiza Perez, Andrea I.

In vitro antitumor effects of AHR ligands aminoflavone (AFP 464) and benzothiazole (5F 203) in human renal carcinoma cells Thumbnail


Authors

Gabriela A. Luzzani

Mariana A. Callero

Anchala I. Kuruppu

Valentina Trapani

Carolina Flumian

Laura Todaro

Tracey D. Bradshaw

Andrea I. Loaiza Perez



Abstract

We investigated activity and mechanism of action of two AhR ligand antitumor agents, AFP 464 and 5F 203 on human renal cancer cells, specifically examining their effects on cell cycle progression, apoptosis, and migration. TK-10, SN12C, Caki-1, and ACHN human renal cancer cell lines were treated with AFP 464 and 5F 203. We evaluated cytotoxicity by MTS assays, cell cycle arrest, and apoptosis by flow cytometry and corroborated a mechanism of action involving AhR signal transduction activation. Changes in migration properties by wound healing assays were investigated: 5F 203-sensitive cells show decreased migration after treatment, therefore, we measured c-Met phosphorylation by Western blot in these cells. A 5F 203 induced a decrease in cell viability which was more marked than AFP 464. This cytotoxicity was reduced after treatment with the AhR inhibitor α-NF for both compounds indicating AhR signaling activation plays a role in the mechanism of action. A 5F 203 is sequestered by TK-10 cells and induces CYP1A1 expression; 5F 203 potently inhibited migration of TK-10, Caki-1, and SN12C cells, and inhibited c-Met receptor phosphorylation in TK-10 cells. AhR ligand antitumor agents AFP 464 and 5F 203 represent potential new candidates for the treatment of renal cancer. A 5F 203 only inhibited migration of sensitive cells and c-Met receptor phosphorylation in TK-10 cells. c-Met receptor signal transduction is important in migration and metastasis. Therefore, we consider that 5F 203 offers potential for the treatment of metastatic renal carcinoma.

Citation

Luzzani, G. A., Callero, M. A., Kuruppu, A. I., Trapani, V., Flumian, C., Todaro, L., …Loaiza Perez, A. I. (in press). In vitro antitumor effects of AHR ligands aminoflavone (AFP 464) and benzothiazole (5F 203) in human renal carcinoma cells. Journal of Cellular Biochemistry, https://doi.org/10.1002/jcb.26114

Journal Article Type Article
Acceptance Date May 3, 2017
Online Publication Date Jun 12, 2017
Deposit Date Sep 26, 2017
Publicly Available Date Sep 26, 2017
Journal Journal of Cellular Biochemistry
Print ISSN 0730-2312
Electronic ISSN 1097-4644
Publisher Wiley
Peer Reviewed Peer Reviewed
DOI https://doi.org/10.1002/jcb.26114
Keywords AFP 464; 5F 203; AhR; Human renal cancer
Public URL https://nottingham-repository.worktribe.com/output/865545
Publisher URL https://doi.org/10.1002/jcb.26114
Additional Information This is the peer reviewed version of the following article: Luzzani, G. A., Callero, M. A., Kuruppu, A. I., Trapani, V., Flumian, C., Todaro, L., Bradshaw, T. D. and Loaiza Perez, A. I. (2017), In Vitro Antitumor Effects of AHR Ligands Aminoflavone (AFP 464) and Benzothiazole (5F 203) in Human Renal Carcinoma Cells. J. Cell. Biochem.. doi:10.1002/jcb.26114, which has been published in final form at https://doi.org/10.1002/jcb.26114. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
Contract Date Sep 26, 2017

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