Cargando…
The anticancer effect of saffron in two p53 isogenic colorectal cancer cell lines
BACKGROUND: Saffron extract, a natural product, has been shown to induce apoptosis in several tumor cell lines. Nevertheless, the p53-dependency of saffron’s mechanism of action in colon cancer remains unexplored. MATERIAL AND METHODS: In order to examine saffron’s anti-proliferative and pro-apoptot...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488489/ https://www.ncbi.nlm.nih.gov/pubmed/22640402 http://dx.doi.org/10.1186/1472-6882-12-69 |
_version_ | 1782248621534609408 |
---|---|
author | Bajbouj, Khuloud Schulze-Luehrmann, Jan Diermeier, Stefanie Amin, Amr Schneider-Stock, Regine |
author_facet | Bajbouj, Khuloud Schulze-Luehrmann, Jan Diermeier, Stefanie Amin, Amr Schneider-Stock, Regine |
author_sort | Bajbouj, Khuloud |
collection | PubMed |
description | BACKGROUND: Saffron extract, a natural product, has been shown to induce apoptosis in several tumor cell lines. Nevertheless, the p53-dependency of saffron’s mechanism of action in colon cancer remains unexplored. MATERIAL AND METHODS: In order to examine saffron’s anti-proliferative and pro-apoptotic effects in colorectal cancer cells, we treated two p53 isogenic HCT116 cell lines (HCT wildtype and HCT p53−/−) with different doses of the drug and analyzed cell proliferation and apoptosis in a time-dependent manner. MTT viability and crystal violet assays were performed in order to determine the effective dose of saffron on both cell lines. The cell cycle progress was examined by Flow cytometric analysis. Apoptosis was assessed using Annexin-PI-staining and Western Blotting for caspase 3 and PARP cleavage. Autophagy was determined by Western Blotting of the light chain 3 (LC3)-II and Beclin 1 proteins. The protein content of phospho-H2AX (γH2AX), a sensor of DNA double strand breaks, was also analyzed by Western Blotting. RESULTS: Saffron extract induced a p53-dependent pattern of cell cycle distribution with a full G2/M stop in HCT116 p53 wildtype cells. However, it induced a remarkable delay in S/G2 phase transit with entry into mitosis in HCT116 p53 −/− cells. The apoptotic Pre-G1 cell fraction as well as Annexin V staining and caspase 3 cleavage showed a more pronounced apoptosis induction in HCT116 p53 wildtype cells. Obviously, the significantly higher DNA-damage, reflected by ɣH2AX protein levels in cells lacking p53, was coped by up-regulation of autophagy. The saffron-induced LC3-II protein level was a remarkable indication of the accumulation of autophagosomes, a response to the cellular stress condition of drug treatment. CONCLUSIONS: This is the first study showing the effect of saffron in HCT116 colorectal cancer cells with different p53 status. Saffron induced DNA-damage and apoptosis in both cell lines. However, autophagy has delayed the induction of apoptosis in HCT116 p53 −/− cells. Considering the fact that most tumors show a functional p53 inactivation, further research is needed to elucidate the long-term effects of saffron in p53 −/− tumors. |
format | Online Article Text |
id | pubmed-3488489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34884892012-11-05 The anticancer effect of saffron in two p53 isogenic colorectal cancer cell lines Bajbouj, Khuloud Schulze-Luehrmann, Jan Diermeier, Stefanie Amin, Amr Schneider-Stock, Regine BMC Complement Altern Med Research Article BACKGROUND: Saffron extract, a natural product, has been shown to induce apoptosis in several tumor cell lines. Nevertheless, the p53-dependency of saffron’s mechanism of action in colon cancer remains unexplored. MATERIAL AND METHODS: In order to examine saffron’s anti-proliferative and pro-apoptotic effects in colorectal cancer cells, we treated two p53 isogenic HCT116 cell lines (HCT wildtype and HCT p53−/−) with different doses of the drug and analyzed cell proliferation and apoptosis in a time-dependent manner. MTT viability and crystal violet assays were performed in order to determine the effective dose of saffron on both cell lines. The cell cycle progress was examined by Flow cytometric analysis. Apoptosis was assessed using Annexin-PI-staining and Western Blotting for caspase 3 and PARP cleavage. Autophagy was determined by Western Blotting of the light chain 3 (LC3)-II and Beclin 1 proteins. The protein content of phospho-H2AX (γH2AX), a sensor of DNA double strand breaks, was also analyzed by Western Blotting. RESULTS: Saffron extract induced a p53-dependent pattern of cell cycle distribution with a full G2/M stop in HCT116 p53 wildtype cells. However, it induced a remarkable delay in S/G2 phase transit with entry into mitosis in HCT116 p53 −/− cells. The apoptotic Pre-G1 cell fraction as well as Annexin V staining and caspase 3 cleavage showed a more pronounced apoptosis induction in HCT116 p53 wildtype cells. Obviously, the significantly higher DNA-damage, reflected by ɣH2AX protein levels in cells lacking p53, was coped by up-regulation of autophagy. The saffron-induced LC3-II protein level was a remarkable indication of the accumulation of autophagosomes, a response to the cellular stress condition of drug treatment. CONCLUSIONS: This is the first study showing the effect of saffron in HCT116 colorectal cancer cells with different p53 status. Saffron induced DNA-damage and apoptosis in both cell lines. However, autophagy has delayed the induction of apoptosis in HCT116 p53 −/− cells. Considering the fact that most tumors show a functional p53 inactivation, further research is needed to elucidate the long-term effects of saffron in p53 −/− tumors. BioMed Central 2012-05-28 /pmc/articles/PMC3488489/ /pubmed/22640402 http://dx.doi.org/10.1186/1472-6882-12-69 Text en Copyright ©2012 Bajbouj et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bajbouj, Khuloud Schulze-Luehrmann, Jan Diermeier, Stefanie Amin, Amr Schneider-Stock, Regine The anticancer effect of saffron in two p53 isogenic colorectal cancer cell lines |
title | The anticancer effect of saffron in two p53 isogenic colorectal cancer cell lines |
title_full | The anticancer effect of saffron in two p53 isogenic colorectal cancer cell lines |
title_fullStr | The anticancer effect of saffron in two p53 isogenic colorectal cancer cell lines |
title_full_unstemmed | The anticancer effect of saffron in two p53 isogenic colorectal cancer cell lines |
title_short | The anticancer effect of saffron in two p53 isogenic colorectal cancer cell lines |
title_sort | anticancer effect of saffron in two p53 isogenic colorectal cancer cell lines |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488489/ https://www.ncbi.nlm.nih.gov/pubmed/22640402 http://dx.doi.org/10.1186/1472-6882-12-69 |
work_keys_str_mv | AT bajboujkhuloud theanticancereffectofsaffronintwop53isogeniccolorectalcancercelllines AT schulzeluehrmannjan theanticancereffectofsaffronintwop53isogeniccolorectalcancercelllines AT diermeierstefanie theanticancereffectofsaffronintwop53isogeniccolorectalcancercelllines AT aminamr theanticancereffectofsaffronintwop53isogeniccolorectalcancercelllines AT schneiderstockregine theanticancereffectofsaffronintwop53isogeniccolorectalcancercelllines AT bajboujkhuloud anticancereffectofsaffronintwop53isogeniccolorectalcancercelllines AT schulzeluehrmannjan anticancereffectofsaffronintwop53isogeniccolorectalcancercelllines AT diermeierstefanie anticancereffectofsaffronintwop53isogeniccolorectalcancercelllines AT aminamr anticancereffectofsaffronintwop53isogeniccolorectalcancercelllines AT schneiderstockregine anticancereffectofsaffronintwop53isogeniccolorectalcancercelllines |