Cargando…

Radiosensitizer Effect of β-Apopicropodophyllin against Colorectal Cancer via Induction of Reactive Oxygen Species and Apoptosis

β-apopicropodophyllin (APP), a derivative of podophyllotoxin (PPT), has been identified as a potential anti-cancer drug. This study tested whether APP acts as an anti-cancer drug and can sensitize colorectal cancer (CRC) cells to radiation treatment. APP exerted an anti-cancer effect against the CRC...

Descripción completa

Detalles Bibliográficos
Autores principales: Kwon, Jin-Hee, Lee, Na-Gyeong, Kang, A-Ram, Song, Jie-Young, Hwang, Sang-Gu, Um, Hong-Duck, Kim, Joon, Park, Jong Kuk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8708374/
https://www.ncbi.nlm.nih.gov/pubmed/34948311
http://dx.doi.org/10.3390/ijms222413514
_version_ 1784622668866125824
author Kwon, Jin-Hee
Lee, Na-Gyeong
Kang, A-Ram
Song, Jie-Young
Hwang, Sang-Gu
Um, Hong-Duck
Kim, Joon
Park, Jong Kuk
author_facet Kwon, Jin-Hee
Lee, Na-Gyeong
Kang, A-Ram
Song, Jie-Young
Hwang, Sang-Gu
Um, Hong-Duck
Kim, Joon
Park, Jong Kuk
author_sort Kwon, Jin-Hee
collection PubMed
description β-apopicropodophyllin (APP), a derivative of podophyllotoxin (PPT), has been identified as a potential anti-cancer drug. This study tested whether APP acts as an anti-cancer drug and can sensitize colorectal cancer (CRC) cells to radiation treatment. APP exerted an anti-cancer effect against the CRC cell lines HCT116, DLD-1, SW480, and COLO320DM, with IC50 values of 7.88 nM, 8.22 nM, 9.84 nM, and 7.757 nM, respectively, for the induction of DNA damage. Clonogenic and cell counting assays indicated that the combined treatment of APP and γ-ionizing radiation (IR) showed greater retardation of cell growth than either treatment alone, suggesting that APP sensitized CRC cells to IR. Annexin V–propidium iodide (PI) assays and immunoblot analysis showed that the combined treatment of APP and IR increased apoptosis in CRC cells compared with either APP or IR alone. Results obtained from the xenograft experiments also indicated that the combination of APP and IR enhanced apoptosis in the in vivo animal model. Apoptosis induction by the combined treatment of APP and IR resulted from reactive oxygen species (ROS). Inhibition of ROS by N-acetylcysteine (NAC) restored cell viability and decreased the induction of apoptosis by APP and IR in CRC cells. Taken together, these results indicate that a combined treatment of APP and IR might promote apoptosis by inducing ROS in CRC cells.
format Online
Article
Text
id pubmed-8708374
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-87083742021-12-25 Radiosensitizer Effect of β-Apopicropodophyllin against Colorectal Cancer via Induction of Reactive Oxygen Species and Apoptosis Kwon, Jin-Hee Lee, Na-Gyeong Kang, A-Ram Song, Jie-Young Hwang, Sang-Gu Um, Hong-Duck Kim, Joon Park, Jong Kuk Int J Mol Sci Article β-apopicropodophyllin (APP), a derivative of podophyllotoxin (PPT), has been identified as a potential anti-cancer drug. This study tested whether APP acts as an anti-cancer drug and can sensitize colorectal cancer (CRC) cells to radiation treatment. APP exerted an anti-cancer effect against the CRC cell lines HCT116, DLD-1, SW480, and COLO320DM, with IC50 values of 7.88 nM, 8.22 nM, 9.84 nM, and 7.757 nM, respectively, for the induction of DNA damage. Clonogenic and cell counting assays indicated that the combined treatment of APP and γ-ionizing radiation (IR) showed greater retardation of cell growth than either treatment alone, suggesting that APP sensitized CRC cells to IR. Annexin V–propidium iodide (PI) assays and immunoblot analysis showed that the combined treatment of APP and IR increased apoptosis in CRC cells compared with either APP or IR alone. Results obtained from the xenograft experiments also indicated that the combination of APP and IR enhanced apoptosis in the in vivo animal model. Apoptosis induction by the combined treatment of APP and IR resulted from reactive oxygen species (ROS). Inhibition of ROS by N-acetylcysteine (NAC) restored cell viability and decreased the induction of apoptosis by APP and IR in CRC cells. Taken together, these results indicate that a combined treatment of APP and IR might promote apoptosis by inducing ROS in CRC cells. MDPI 2021-12-16 /pmc/articles/PMC8708374/ /pubmed/34948311 http://dx.doi.org/10.3390/ijms222413514 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kwon, Jin-Hee
Lee, Na-Gyeong
Kang, A-Ram
Song, Jie-Young
Hwang, Sang-Gu
Um, Hong-Duck
Kim, Joon
Park, Jong Kuk
Radiosensitizer Effect of β-Apopicropodophyllin against Colorectal Cancer via Induction of Reactive Oxygen Species and Apoptosis
title Radiosensitizer Effect of β-Apopicropodophyllin against Colorectal Cancer via Induction of Reactive Oxygen Species and Apoptosis
title_full Radiosensitizer Effect of β-Apopicropodophyllin against Colorectal Cancer via Induction of Reactive Oxygen Species and Apoptosis
title_fullStr Radiosensitizer Effect of β-Apopicropodophyllin against Colorectal Cancer via Induction of Reactive Oxygen Species and Apoptosis
title_full_unstemmed Radiosensitizer Effect of β-Apopicropodophyllin against Colorectal Cancer via Induction of Reactive Oxygen Species and Apoptosis
title_short Radiosensitizer Effect of β-Apopicropodophyllin against Colorectal Cancer via Induction of Reactive Oxygen Species and Apoptosis
title_sort radiosensitizer effect of β-apopicropodophyllin against colorectal cancer via induction of reactive oxygen species and apoptosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8708374/
https://www.ncbi.nlm.nih.gov/pubmed/34948311
http://dx.doi.org/10.3390/ijms222413514
work_keys_str_mv AT kwonjinhee radiosensitizereffectofbapopicropodophyllinagainstcolorectalcancerviainductionofreactiveoxygenspeciesandapoptosis
AT leenagyeong radiosensitizereffectofbapopicropodophyllinagainstcolorectalcancerviainductionofreactiveoxygenspeciesandapoptosis
AT kangaram radiosensitizereffectofbapopicropodophyllinagainstcolorectalcancerviainductionofreactiveoxygenspeciesandapoptosis
AT songjieyoung radiosensitizereffectofbapopicropodophyllinagainstcolorectalcancerviainductionofreactiveoxygenspeciesandapoptosis
AT hwangsanggu radiosensitizereffectofbapopicropodophyllinagainstcolorectalcancerviainductionofreactiveoxygenspeciesandapoptosis
AT umhongduck radiosensitizereffectofbapopicropodophyllinagainstcolorectalcancerviainductionofreactiveoxygenspeciesandapoptosis
AT kimjoon radiosensitizereffectofbapopicropodophyllinagainstcolorectalcancerviainductionofreactiveoxygenspeciesandapoptosis
AT parkjongkuk radiosensitizereffectofbapopicropodophyllinagainstcolorectalcancerviainductionofreactiveoxygenspeciesandapoptosis