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The comparative anti-cancer effects of krill oil and oxaliplatin in an orthotopic mouse model of colorectal cancer
BACKGROUND: Our in vitro studies demonstrated that krill oil (KO) has anti-cancer potential. This study aimed to compare the anti-cancer effects of KO with a commonly used chemotherapeutic drug, oxaliplatin and to identify the molecular mechanisms associated with KO supplementation in a mouse model...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892734/ https://www.ncbi.nlm.nih.gov/pubmed/35236377 http://dx.doi.org/10.1186/s12986-022-00646-8 |
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author | Jayathilake, Abilasha Gayani Hassanzadeganroudsari, Majid Jovanovska, Valentina Luwor, Rodney Brain Nurgali, Kulmira Su, Xiao Qun |
author_facet | Jayathilake, Abilasha Gayani Hassanzadeganroudsari, Majid Jovanovska, Valentina Luwor, Rodney Brain Nurgali, Kulmira Su, Xiao Qun |
author_sort | Jayathilake, Abilasha Gayani |
collection | PubMed |
description | BACKGROUND: Our in vitro studies demonstrated that krill oil (KO) has anti-cancer potential. This study aimed to compare the anti-cancer effects of KO with a commonly used chemotherapeutic drug, oxaliplatin and to identify the molecular mechanisms associated with KO supplementation in a mouse model of colorectal cancer (CRC). METHODS: Thirty-six male Balb/c mice were randomly divided into six groups. Five groups received standard chow diet supplemented with KO (150 g/kg)), corn oil (150 g/kg), KO combined with ½ dose of oxaliplatin (1.5 mg/kg body weight/3 times per week), corn oil combined with ½ dose of oxaliplatin (1.5 mg/kg body weight/3 times per week), or a full dose of oxaliplatin (3 mg/kg body weight/3 times per week). The control (sham) group received a standard chow diet. Treatments started three weeks before and continued for three weeks after orthotopic CRC induction. The number of metastases, tumour weight and volume were quantified ex-vivo. The expression of cytochrome c, cleaved caspase-9 and -3, DNA damage, PD-L1, PD-L2 and HSP-70 were determined. RESULTS: A significant reductions in the weight and volume of tumours were observed in mice treated with KO and KO plus a ½ dose of oxaliplatin compared to the sham group, similar to oxaliplatin-treated mice. KO, and KO plus ½ dose of oxaliplatin significantly increased the expression of cytochrome c, cleaved caspase-9 and -3, and DNA damage and decreased expression of PD-L1, PD-L2 and HSP-70 in tumour tissues compared to the sham group. CONCLUSIONS: The in vivo anti-cancer effects of KO are comparable with oxaliplatin. Thus, dietary KO supplementation has a great potential as a therapeutic/adjunctive agent for CRC treatment. |
format | Online Article Text |
id | pubmed-8892734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88927342022-03-10 The comparative anti-cancer effects of krill oil and oxaliplatin in an orthotopic mouse model of colorectal cancer Jayathilake, Abilasha Gayani Hassanzadeganroudsari, Majid Jovanovska, Valentina Luwor, Rodney Brain Nurgali, Kulmira Su, Xiao Qun Nutr Metab (Lond) Research BACKGROUND: Our in vitro studies demonstrated that krill oil (KO) has anti-cancer potential. This study aimed to compare the anti-cancer effects of KO with a commonly used chemotherapeutic drug, oxaliplatin and to identify the molecular mechanisms associated with KO supplementation in a mouse model of colorectal cancer (CRC). METHODS: Thirty-six male Balb/c mice were randomly divided into six groups. Five groups received standard chow diet supplemented with KO (150 g/kg)), corn oil (150 g/kg), KO combined with ½ dose of oxaliplatin (1.5 mg/kg body weight/3 times per week), corn oil combined with ½ dose of oxaliplatin (1.5 mg/kg body weight/3 times per week), or a full dose of oxaliplatin (3 mg/kg body weight/3 times per week). The control (sham) group received a standard chow diet. Treatments started three weeks before and continued for three weeks after orthotopic CRC induction. The number of metastases, tumour weight and volume were quantified ex-vivo. The expression of cytochrome c, cleaved caspase-9 and -3, DNA damage, PD-L1, PD-L2 and HSP-70 were determined. RESULTS: A significant reductions in the weight and volume of tumours were observed in mice treated with KO and KO plus a ½ dose of oxaliplatin compared to the sham group, similar to oxaliplatin-treated mice. KO, and KO plus ½ dose of oxaliplatin significantly increased the expression of cytochrome c, cleaved caspase-9 and -3, and DNA damage and decreased expression of PD-L1, PD-L2 and HSP-70 in tumour tissues compared to the sham group. CONCLUSIONS: The in vivo anti-cancer effects of KO are comparable with oxaliplatin. Thus, dietary KO supplementation has a great potential as a therapeutic/adjunctive agent for CRC treatment. BioMed Central 2022-03-02 /pmc/articles/PMC8892734/ /pubmed/35236377 http://dx.doi.org/10.1186/s12986-022-00646-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Jayathilake, Abilasha Gayani Hassanzadeganroudsari, Majid Jovanovska, Valentina Luwor, Rodney Brain Nurgali, Kulmira Su, Xiao Qun The comparative anti-cancer effects of krill oil and oxaliplatin in an orthotopic mouse model of colorectal cancer |
title | The comparative anti-cancer effects of krill oil and oxaliplatin in an orthotopic mouse model of colorectal cancer |
title_full | The comparative anti-cancer effects of krill oil and oxaliplatin in an orthotopic mouse model of colorectal cancer |
title_fullStr | The comparative anti-cancer effects of krill oil and oxaliplatin in an orthotopic mouse model of colorectal cancer |
title_full_unstemmed | The comparative anti-cancer effects of krill oil and oxaliplatin in an orthotopic mouse model of colorectal cancer |
title_short | The comparative anti-cancer effects of krill oil and oxaliplatin in an orthotopic mouse model of colorectal cancer |
title_sort | comparative anti-cancer effects of krill oil and oxaliplatin in an orthotopic mouse model of colorectal cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892734/ https://www.ncbi.nlm.nih.gov/pubmed/35236377 http://dx.doi.org/10.1186/s12986-022-00646-8 |
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