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Antiproliferative effects of mesenchymal stem cells carrying Newcastle disease virus and Lactobacillus Casei extract on CT26 Cell line: synergistic effects in cancer therapy

BACKGROUND AND AIMS: Colorectal Cancer (CRC) is a frequent malignancy with a high mortality rate. Specific inherited and environmental influences can affect CRC. Oncolytic viruses and bacteria in treating CRC are one of the innovative therapeutic options. This study aims to determine whether mesench...

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Autores principales: Ghorbani Alvanegh, Akbar, Mirzaei Nodooshan, Majid, Dorostkar, Ruhollah, Ranjbar, Reza, Jalali Kondori, Bahman, Shahriary, Alireza, Parastouei, Karim, Vazifedust, Soheil, Afrasiab, Elmira, Esmaeili Gouvarchinghaleh, Hadi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10391864/
https://www.ncbi.nlm.nih.gov/pubmed/37525229
http://dx.doi.org/10.1186/s13027-023-00521-y
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author Ghorbani Alvanegh, Akbar
Mirzaei Nodooshan, Majid
Dorostkar, Ruhollah
Ranjbar, Reza
Jalali Kondori, Bahman
Shahriary, Alireza
Parastouei, Karim
Vazifedust, Soheil
Afrasiab, Elmira
Esmaeili Gouvarchinghaleh, Hadi
author_facet Ghorbani Alvanegh, Akbar
Mirzaei Nodooshan, Majid
Dorostkar, Ruhollah
Ranjbar, Reza
Jalali Kondori, Bahman
Shahriary, Alireza
Parastouei, Karim
Vazifedust, Soheil
Afrasiab, Elmira
Esmaeili Gouvarchinghaleh, Hadi
author_sort Ghorbani Alvanegh, Akbar
collection PubMed
description BACKGROUND AND AIMS: Colorectal Cancer (CRC) is a frequent malignancy with a high mortality rate. Specific inherited and environmental influences can affect CRC. Oncolytic viruses and bacteria in treating CRC are one of the innovative therapeutic options. This study aims to determine whether mesenchymal stem cells (MSCs) infected with the Newcastle Disease Virus (NDV) in combination with Lactobacillus casei extract (L. casei) have a synergistic effects on CRC cell line growth. MATERIALS AND METHODS: MSCs taken from the bone marrow of BALB/c mice and were infected with the 20 MOI of NDV. Then, using the CT26 cell line in various groups as a single and combined treatment, the anticancer potential of MSCs containing the NDV and L. casei extract was examined. The evaluations considered the CT26 survival and the rate at which LDH, ROS, and levels of caspases eight and nine were produced following various treatments. RESULTS: NDV, MSCs-NDV, and L. casei in alone or combined treatment significantly increased apoptosis percent, LDH, and ROS production compared with the control group (P˂0.05). Also, NDV, in free or capsulated in MSCs, had anticancer effects, but in capsulated form, it had a delay compared with free NDV. The findings proved that L. casei primarily stimulates the extrinsic pathway, while NDV therapy promotes apoptosis through the activation of both intrinsic and extrinsic apoptosis pathways. CONCLUSIONS: The results suggest that MSCs carrying oncolytic NDV in combination with L. casei extract as a potentially effective strategy for cancer immunotherapy by promoting the generation of LDH, ROS, and apoptosis in the microenvironment of the CT26 cell line.
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spelling pubmed-103918642023-08-02 Antiproliferative effects of mesenchymal stem cells carrying Newcastle disease virus and Lactobacillus Casei extract on CT26 Cell line: synergistic effects in cancer therapy Ghorbani Alvanegh, Akbar Mirzaei Nodooshan, Majid Dorostkar, Ruhollah Ranjbar, Reza Jalali Kondori, Bahman Shahriary, Alireza Parastouei, Karim Vazifedust, Soheil Afrasiab, Elmira Esmaeili Gouvarchinghaleh, Hadi Infect Agent Cancer Research BACKGROUND AND AIMS: Colorectal Cancer (CRC) is a frequent malignancy with a high mortality rate. Specific inherited and environmental influences can affect CRC. Oncolytic viruses and bacteria in treating CRC are one of the innovative therapeutic options. This study aims to determine whether mesenchymal stem cells (MSCs) infected with the Newcastle Disease Virus (NDV) in combination with Lactobacillus casei extract (L. casei) have a synergistic effects on CRC cell line growth. MATERIALS AND METHODS: MSCs taken from the bone marrow of BALB/c mice and were infected with the 20 MOI of NDV. Then, using the CT26 cell line in various groups as a single and combined treatment, the anticancer potential of MSCs containing the NDV and L. casei extract was examined. The evaluations considered the CT26 survival and the rate at which LDH, ROS, and levels of caspases eight and nine were produced following various treatments. RESULTS: NDV, MSCs-NDV, and L. casei in alone or combined treatment significantly increased apoptosis percent, LDH, and ROS production compared with the control group (P˂0.05). Also, NDV, in free or capsulated in MSCs, had anticancer effects, but in capsulated form, it had a delay compared with free NDV. The findings proved that L. casei primarily stimulates the extrinsic pathway, while NDV therapy promotes apoptosis through the activation of both intrinsic and extrinsic apoptosis pathways. CONCLUSIONS: The results suggest that MSCs carrying oncolytic NDV in combination with L. casei extract as a potentially effective strategy for cancer immunotherapy by promoting the generation of LDH, ROS, and apoptosis in the microenvironment of the CT26 cell line. BioMed Central 2023-07-31 /pmc/articles/PMC10391864/ /pubmed/37525229 http://dx.doi.org/10.1186/s13027-023-00521-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Ghorbani Alvanegh, Akbar
Mirzaei Nodooshan, Majid
Dorostkar, Ruhollah
Ranjbar, Reza
Jalali Kondori, Bahman
Shahriary, Alireza
Parastouei, Karim
Vazifedust, Soheil
Afrasiab, Elmira
Esmaeili Gouvarchinghaleh, Hadi
Antiproliferative effects of mesenchymal stem cells carrying Newcastle disease virus and Lactobacillus Casei extract on CT26 Cell line: synergistic effects in cancer therapy
title Antiproliferative effects of mesenchymal stem cells carrying Newcastle disease virus and Lactobacillus Casei extract on CT26 Cell line: synergistic effects in cancer therapy
title_full Antiproliferative effects of mesenchymal stem cells carrying Newcastle disease virus and Lactobacillus Casei extract on CT26 Cell line: synergistic effects in cancer therapy
title_fullStr Antiproliferative effects of mesenchymal stem cells carrying Newcastle disease virus and Lactobacillus Casei extract on CT26 Cell line: synergistic effects in cancer therapy
title_full_unstemmed Antiproliferative effects of mesenchymal stem cells carrying Newcastle disease virus and Lactobacillus Casei extract on CT26 Cell line: synergistic effects in cancer therapy
title_short Antiproliferative effects of mesenchymal stem cells carrying Newcastle disease virus and Lactobacillus Casei extract on CT26 Cell line: synergistic effects in cancer therapy
title_sort antiproliferative effects of mesenchymal stem cells carrying newcastle disease virus and lactobacillus casei extract on ct26 cell line: synergistic effects in cancer therapy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10391864/
https://www.ncbi.nlm.nih.gov/pubmed/37525229
http://dx.doi.org/10.1186/s13027-023-00521-y
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