Cargando…

Effects of concomitant use of THC and irinotecan on tumour growth and biochemical markers in a syngeneic mouse model of colon cancer

Clinical treatment with the antineoplastic drug irinotecan (IRI) is often hindered by side effects that significantly reduce the quality of life of treated patients. Due to the growing public support for products with Δ(9)-tetrahydrocannabinol (THC), even though relevant scientific literature does n...

Descripción completa

Detalles Bibliográficos
Autores principales: Žunec, Suzana, Karačonji, Irena Brčić, Čatalinac, Martin, Jurič, Andreja, Katić, Anja, Kozina, Goran, Micek, Vedran, Neuberg, Marijana, Vrdoljak, Ana Lucić
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10549892/
https://www.ncbi.nlm.nih.gov/pubmed/37791673
http://dx.doi.org/10.2478/aiht-2023-74-3765
_version_ 1785115420680781824
author Žunec, Suzana
Karačonji, Irena Brčić
Čatalinac, Martin
Jurič, Andreja
Katić, Anja
Kozina, Goran
Micek, Vedran
Neuberg, Marijana
Vrdoljak, Ana Lucić
author_facet Žunec, Suzana
Karačonji, Irena Brčić
Čatalinac, Martin
Jurič, Andreja
Katić, Anja
Kozina, Goran
Micek, Vedran
Neuberg, Marijana
Vrdoljak, Ana Lucić
author_sort Žunec, Suzana
collection PubMed
description Clinical treatment with the antineoplastic drug irinotecan (IRI) is often hindered by side effects that significantly reduce the quality of life of treated patients. Due to the growing public support for products with Δ(9)-tetrahydrocannabinol (THC), even though relevant scientific literature does not provide clear evidence of their high antitumour potential, some cancer patients take unregistered preparations containing up to 80 % THC. This study was conducted on a syngeneic colorectal cancer mouse model to test the efficiency and safety of concomitant treatment with IRI and THC. Male BALB/c mice subcutaneously injected with CT26 cells were receiving 60 mg/kg of IRI intraperitoneally on day 1 and 5 of treatment and/or 7 mg/kg of THC by gavage a day for 7 days. Treatment responses were evaluated based on changes in body, brain, and liver weight, tumour growth, blood cholinesterase activity, and oxidative stress parameters. Irinotecan’s systemic toxicity was evidenced by weight loss and high oxidative stress. The important finding of this study is that combining THC with IRI diminishes IRI efficiency in inhibiting tumour growth. However, further studies, focused on more subtle molecular methods in tumour tissue and analytical analysis of IRI and THC distribution in tumour-bearing mice, are needed to prove our observations.
format Online
Article
Text
id pubmed-10549892
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Sciendo
record_format MEDLINE/PubMed
spelling pubmed-105498922023-10-05 Effects of concomitant use of THC and irinotecan on tumour growth and biochemical markers in a syngeneic mouse model of colon cancer Žunec, Suzana Karačonji, Irena Brčić Čatalinac, Martin Jurič, Andreja Katić, Anja Kozina, Goran Micek, Vedran Neuberg, Marijana Vrdoljak, Ana Lucić Arh Hig Rada Toksikol Original Article Clinical treatment with the antineoplastic drug irinotecan (IRI) is often hindered by side effects that significantly reduce the quality of life of treated patients. Due to the growing public support for products with Δ(9)-tetrahydrocannabinol (THC), even though relevant scientific literature does not provide clear evidence of their high antitumour potential, some cancer patients take unregistered preparations containing up to 80 % THC. This study was conducted on a syngeneic colorectal cancer mouse model to test the efficiency and safety of concomitant treatment with IRI and THC. Male BALB/c mice subcutaneously injected with CT26 cells were receiving 60 mg/kg of IRI intraperitoneally on day 1 and 5 of treatment and/or 7 mg/kg of THC by gavage a day for 7 days. Treatment responses were evaluated based on changes in body, brain, and liver weight, tumour growth, blood cholinesterase activity, and oxidative stress parameters. Irinotecan’s systemic toxicity was evidenced by weight loss and high oxidative stress. The important finding of this study is that combining THC with IRI diminishes IRI efficiency in inhibiting tumour growth. However, further studies, focused on more subtle molecular methods in tumour tissue and analytical analysis of IRI and THC distribution in tumour-bearing mice, are needed to prove our observations. Sciendo 2023-09-30 /pmc/articles/PMC10549892/ /pubmed/37791673 http://dx.doi.org/10.2478/aiht-2023-74-3765 Text en © 2023 Suzana Žunec et al., published by Sciendo https://creativecommons.org/licenses/by-nc-nd/3.0/This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
spellingShingle Original Article
Žunec, Suzana
Karačonji, Irena Brčić
Čatalinac, Martin
Jurič, Andreja
Katić, Anja
Kozina, Goran
Micek, Vedran
Neuberg, Marijana
Vrdoljak, Ana Lucić
Effects of concomitant use of THC and irinotecan on tumour growth and biochemical markers in a syngeneic mouse model of colon cancer
title Effects of concomitant use of THC and irinotecan on tumour growth and biochemical markers in a syngeneic mouse model of colon cancer
title_full Effects of concomitant use of THC and irinotecan on tumour growth and biochemical markers in a syngeneic mouse model of colon cancer
title_fullStr Effects of concomitant use of THC and irinotecan on tumour growth and biochemical markers in a syngeneic mouse model of colon cancer
title_full_unstemmed Effects of concomitant use of THC and irinotecan on tumour growth and biochemical markers in a syngeneic mouse model of colon cancer
title_short Effects of concomitant use of THC and irinotecan on tumour growth and biochemical markers in a syngeneic mouse model of colon cancer
title_sort effects of concomitant use of thc and irinotecan on tumour growth and biochemical markers in a syngeneic mouse model of colon cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10549892/
https://www.ncbi.nlm.nih.gov/pubmed/37791673
http://dx.doi.org/10.2478/aiht-2023-74-3765
work_keys_str_mv AT zunecsuzana effectsofconcomitantuseofthcandirinotecanontumourgrowthandbiochemicalmarkersinasyngeneicmousemodelofcoloncancer
AT karaconjiirenabrcic effectsofconcomitantuseofthcandirinotecanontumourgrowthandbiochemicalmarkersinasyngeneicmousemodelofcoloncancer
AT catalinacmartin effectsofconcomitantuseofthcandirinotecanontumourgrowthandbiochemicalmarkersinasyngeneicmousemodelofcoloncancer
AT juricandreja effectsofconcomitantuseofthcandirinotecanontumourgrowthandbiochemicalmarkersinasyngeneicmousemodelofcoloncancer
AT katicanja effectsofconcomitantuseofthcandirinotecanontumourgrowthandbiochemicalmarkersinasyngeneicmousemodelofcoloncancer
AT kozinagoran effectsofconcomitantuseofthcandirinotecanontumourgrowthandbiochemicalmarkersinasyngeneicmousemodelofcoloncancer
AT micekvedran effectsofconcomitantuseofthcandirinotecanontumourgrowthandbiochemicalmarkersinasyngeneicmousemodelofcoloncancer
AT neubergmarijana effectsofconcomitantuseofthcandirinotecanontumourgrowthandbiochemicalmarkersinasyngeneicmousemodelofcoloncancer
AT vrdoljakanalucic effectsofconcomitantuseofthcandirinotecanontumourgrowthandbiochemicalmarkersinasyngeneicmousemodelofcoloncancer