Hostname: page-component-745bb68f8f-f46jp Total loading time: 0 Render date: 2025-01-12T07:28:30.626Z Has data issue: false hasContentIssue false

Effect of Beta- and Alpha-Carotene Intake on Tumour Formation in the Intestines of APCMin/+ Mice

Published online by Cambridge University Press:  16 December 2024

N. H. Smith
Affiliation:
Human Nutrition & Exercise Research Centre, Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK
C.C. Ojobor
Affiliation:
Human Nutrition & Exercise Research Centre, Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK
L. Huang
Affiliation:
Immune Metabolism Laboratory, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK
K. Brandt
Affiliation:
Human Nutrition & Exercise Research Centre, Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Carotene-rich vegetables like carrots have been consistently associated with lowered cancer risk in observational studies(1). Beta-carotene, a phytochemical found in fruits and vegetables, is known for its antioxidant properties. In rodent trials, supplementation with carrot (containing both carotenes and polyacetylenes) significantly reduced tumour numbers in the APCMin/+ mouse model(2). However, human intervention trials with pure beta-carotene showed more adverse effects than benefits(3). This study aimed to investigate the impact of beta- and alpha-carotene supplementation (without polyacetylenes) on colorectal cancer using the APCMin/+ mouse model, which spontaneously develops intestinal tumours and an enlarged liver(4).

APCMin/+ mice were fed either a daily supplement of 10mg/kg mouse of a polyacetylene-free extract from carrots containing a beta- and alpha-carotene mixture, in a dose corresponding to the beneficial carrot supplementation, or the control diet, with a very low beta-carotene content (providing approx. 0.02mg/kg mouse/day). The 8-week supplementation commenced at 5 weeks of age. Tumour quantification in the small intestines of APCMin/+ mice was performed by histology of the entire small intestine, with one slide per 0.3mm, using the H&E staining method and Imagescope software.

Supplementation with carotenes had no significant effect on the total number of tumours (≥0.5 mm), showing no discernible difference between the control (n = 6) (20.5, 95% CI [14.69, 26.31]) and treatment (n = 8) (24.5, [19.21, 29.79]) group (P = 0.237). However, the liver weight, in % of body weight, showed a significant 25% decrease in the treatment group (n = 7) (4.78 95% CI [4.45, 5.15]) compared to controls (6.42, [5.71, 7.13]) (P<0.0003), reaching a level comparable with wildtype mice (4.48, [4.13, 4.83].

These findings confirm the results from the human intervention trials by indicating that beta- and alpha-carotene do not confer any benefit for cancer prevention, while the decrease in liver weight suggests a potential beneficial effect on another aspect of liver health. Additional research is necessary to fully understand these relationships and uncover the underlying mechanisms behind these results. Specifically, beta-and alpha-carotene from carrots do not provide the reduction in tumour numbers in a mouse model of colon cancer found when feeding the corresponding dose of freeze-dried carrot. However, the carotenes significantly attenuate the liver enlargement also seen in this model.

Type
Abstract
Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of The Nutrition Society

References

Ojobor, CC, O’Brien, GM, Siervo, M et al. (2023) Crit Rev Food Sci Nutr Online doi:10.1080/10408398.2023.2287176.CrossRefGoogle Scholar
Almqbel, M, Seal, CJ & Brandt, K. (2017) Proc Nutr Soc 76, E141.CrossRefGoogle Scholar
Bjelakovic, G, Nikolova, D & Gluud, C (2013) JAMA 310 (11), 11781179.CrossRefGoogle Scholar
Benito, I, Encío, IJ, Milagro, FI et al. (2021) Int J Mol Sci 22, 4906.CrossRefGoogle Scholar