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Investigation of the protective and therapeutic effects of Lactobacillus casei and Saccharomyces cerevisiae in a breast cancer mouse model

INTRODUCTION: The development of novel strategies for cancer therapy is crucial to improve standard treatment protocols. AIM: This study aimed to determine the protective and therapeutic effects of heat-killed preparations of Lactobacillus casei and Saccharomyces cerevisiae in a breast cancer mouse...

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Autores principales: Baraka, Kholoud, Abozahra, Rania, Helmy, Maged Wasfy, El Meniawy, Nada Salah El Dine, Abdelhamid, Sarah M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AIMS Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329878/
https://www.ncbi.nlm.nih.gov/pubmed/35974992
http://dx.doi.org/10.3934/microbiol.2022016
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author Baraka, Kholoud
Abozahra, Rania
Helmy, Maged Wasfy
El Meniawy, Nada Salah El Dine
Abdelhamid, Sarah M
author_facet Baraka, Kholoud
Abozahra, Rania
Helmy, Maged Wasfy
El Meniawy, Nada Salah El Dine
Abdelhamid, Sarah M
author_sort Baraka, Kholoud
collection PubMed
description INTRODUCTION: The development of novel strategies for cancer therapy is crucial to improve standard treatment protocols. AIM: This study aimed to determine the protective and therapeutic effects of heat-killed preparations of Lactobacillus casei and Saccharomyces cerevisiae in a breast cancer mouse model. METHODS: Forty-two female BALB/c mice (7–8 weeks old) were divided into six groups (seven mice per group). Four groups were injected with 10(7) Ehrlich ascites tumor (EAT) cells suspended in phosphate-buffered saline (PBS) subcutaneously into the left side of the mammary fat pad. Tumor growth was monitored weekly until all animals developed a palpable tumor. The tumor-bearing mice in the experimental groups received heat-killed L. casei or S. cerevisiae three times per week for 35 days. The mice in the control group received PBS. The remaining two groups received heated L. casei or S. cerevisiae and then were injected with EAT cells. After 35 days, all mice were sacrificed to determine the immune response. RESULTS: Animals that received heated S. cerevisiae exhibited the lowest rate of tumor growth compared with the other groups. TGF-β and IL-4 secretion was increased in all mice, whereas the secretion of INF-γ and IL-10 was decreased in breast tissues. Moreover, at the histopathological level, the volume of viable tumor in the control group was higher than in the treated groups. CONCLUSION: Supplementary treatment with S. cerevisiae resulted in the best outcome in the breast cancer model compared with other treated and vaccinated groups.
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spelling pubmed-93298782022-08-15 Investigation of the protective and therapeutic effects of Lactobacillus casei and Saccharomyces cerevisiae in a breast cancer mouse model Baraka, Kholoud Abozahra, Rania Helmy, Maged Wasfy El Meniawy, Nada Salah El Dine Abdelhamid, Sarah M AIMS Microbiol Research Article INTRODUCTION: The development of novel strategies for cancer therapy is crucial to improve standard treatment protocols. AIM: This study aimed to determine the protective and therapeutic effects of heat-killed preparations of Lactobacillus casei and Saccharomyces cerevisiae in a breast cancer mouse model. METHODS: Forty-two female BALB/c mice (7–8 weeks old) were divided into six groups (seven mice per group). Four groups were injected with 10(7) Ehrlich ascites tumor (EAT) cells suspended in phosphate-buffered saline (PBS) subcutaneously into the left side of the mammary fat pad. Tumor growth was monitored weekly until all animals developed a palpable tumor. The tumor-bearing mice in the experimental groups received heat-killed L. casei or S. cerevisiae three times per week for 35 days. The mice in the control group received PBS. The remaining two groups received heated L. casei or S. cerevisiae and then were injected with EAT cells. After 35 days, all mice were sacrificed to determine the immune response. RESULTS: Animals that received heated S. cerevisiae exhibited the lowest rate of tumor growth compared with the other groups. TGF-β and IL-4 secretion was increased in all mice, whereas the secretion of INF-γ and IL-10 was decreased in breast tissues. Moreover, at the histopathological level, the volume of viable tumor in the control group was higher than in the treated groups. CONCLUSION: Supplementary treatment with S. cerevisiae resulted in the best outcome in the breast cancer model compared with other treated and vaccinated groups. AIMS Press 2022-05-16 /pmc/articles/PMC9329878/ /pubmed/35974992 http://dx.doi.org/10.3934/microbiol.2022016 Text en © 2022 the Author(s), licensee AIMS Press https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) )
spellingShingle Research Article
Baraka, Kholoud
Abozahra, Rania
Helmy, Maged Wasfy
El Meniawy, Nada Salah El Dine
Abdelhamid, Sarah M
Investigation of the protective and therapeutic effects of Lactobacillus casei and Saccharomyces cerevisiae in a breast cancer mouse model
title Investigation of the protective and therapeutic effects of Lactobacillus casei and Saccharomyces cerevisiae in a breast cancer mouse model
title_full Investigation of the protective and therapeutic effects of Lactobacillus casei and Saccharomyces cerevisiae in a breast cancer mouse model
title_fullStr Investigation of the protective and therapeutic effects of Lactobacillus casei and Saccharomyces cerevisiae in a breast cancer mouse model
title_full_unstemmed Investigation of the protective and therapeutic effects of Lactobacillus casei and Saccharomyces cerevisiae in a breast cancer mouse model
title_short Investigation of the protective and therapeutic effects of Lactobacillus casei and Saccharomyces cerevisiae in a breast cancer mouse model
title_sort investigation of the protective and therapeutic effects of lactobacillus casei and saccharomyces cerevisiae in a breast cancer mouse model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9329878/
https://www.ncbi.nlm.nih.gov/pubmed/35974992
http://dx.doi.org/10.3934/microbiol.2022016
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