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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

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          Abstract

          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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          Most cited references54

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          Epidemiology of colorectal cancer: incidence, mortality, survival, and risk factors

          According to GLOBOCAN 2018 data, colorectal cancer (CRC) is the third most deadly and fourth most commonly diagnosed cancer in the world. Nearly 2 million new cases and about 1 million deaths are expected in 2018. CRC incidence has been steadily rising worldwide, especially in developing countries that are adopting the “western” way of life. Obesity, sedentary lifestyle, red meat consumption, alcohol, and tobacco are considered the driving factors behind the growth of CRC. However, recent advances in early detection screenings and treatment options have reduced CRC mortality in developed nations, even in the face of growing incidence. Genetic testing and better family history documentation can enable those with a hereditary predisposition for the neoplasm to take preventive measures. Meanwhile, the general population can reduce their risk by lowering their red meat, alcohol, and tobacco consumption and raising their consumption of fibre, wholesome foods, and certain vitamins and minerals.
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            Roles of the immune system in cancer: from tumor initiation to metastatic progression

            In this review, Gonzelez et al. provide an update of recent accomplishments, unifying concepts, and futures challenges to study tumor-associated immune cells, with an emphasis on metastatic carcinomas. The presence of inflammatory immune cells in human tumors raises a fundamental question in oncology: How do cancer cells avoid the destruction by immune attack? In principle, tumor development can be controlled by cytotoxic innate and adaptive immune cells; however, as the tumor develops from neoplastic tissue to clinically detectable tumors, cancer cells evolve different mechanisms that mimic peripheral immune tolerance in order to avoid tumoricidal attack. Here, we provide an update of recent accomplishments, unifying concepts, and future challenges to study tumor-associated immune cells, with an emphasis on metastatic carcinomas.
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              Comprehensive review of targeted therapy for colorectal cancer

              Colorectal cancer (CRC) is among the most lethal and prevalent malignancies in the world and was responsible for nearly 881,000 cancer-related deaths in 2018. Surgery and chemotherapy have long been the first choices for cancer patients. However, the prognosis of CRC has never been satisfying, especially for patients with metastatic lesions. Targeted therapy is a new optional approach that has successfully prolonged overall survival for CRC patients. Following successes with the anti-EGFR (epidermal growth factor receptor) agent cetuximab and the anti-angiogenesis agent bevacizumab, new agents blocking different critical pathways as well as immune checkpoints are emerging at an unprecedented rate. Guidelines worldwide are currently updating the recommended targeted drugs on the basis of the increasing number of high-quality clinical trials. This review provides an overview of existing CRC-targeted agents and their underlying mechanisms, as well as a discussion of their limitations and future trends.
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                Author and article information

                Contributors
                alvanegh@yahoo.com
                majid.mirzaei.n.67@gmail.com
                r.dorost@yahoo.com
                ranjbarre@gmail.com
                bahmanjalali2010@gmail.com
                shahriary961@gmail.com
                parastouei@gmail.com
                vazifedust71@yahoo.com
                eafrasiabb@gmail.com
                h.smaili69@yahoo.com
                Journal
                Infect Agent Cancer
                Infect Agent Cancer
                Infectious Agents and Cancer
                BioMed Central (London )
                1750-9378
                31 July 2023
                31 July 2023
                2023
                : 18
                : 46
                Affiliations
                [1 ]GRID grid.411521.2, ISNI 0000 0000 9975 294X, Human Genetics Research Center, , Baqiyatallah University of Medical Sciences, ; Tehran, Iran
                [2 ]GRID grid.411521.2, ISNI 0000 0000 9975 294X, Applied Virology Research Center, , Baqiyatallah University of Medical Sciences, ; Tehran, Iran
                [3 ]GRID grid.411521.2, ISNI 0000 0000 9975 294X, Molecular Biology Research Center, Systems Biology and Poisonings Institute, , Baqiyatallah University of Medical Sciences, ; Tehran, Iran
                [4 ]GRID grid.411521.2, ISNI 0000 0000 9975 294X, Department of Anatomical Sciences, Faculty of Medicine, , Baqiyatallah University of Medical Sciences, ; Tehran, Iran
                [5 ]GRID grid.411521.2, ISNI 0000 0000 9975 294X, Baqiyatallah Research Center for Gastroenterology and Liver Diseases (BRCGL), , Baqiyatallah University of Medical Sciences, ; Tehran, Iran
                [6 ]GRID grid.411521.2, ISNI 0000 0000 9975 294X, Chemical Injuries Research Center, Systems Biology and Poisonings Institute, , Baqiyatallah University of Medical Sciences, ; Tehran, Iran
                [7 ]GRID grid.411521.2, ISNI 0000 0000 9975 294X, Health Research Center, Life Style Institute, , Baqiyatallah University of Medical Sciences, ; Tehran, Iran
                [8 ]GRID grid.419420.a, ISNI 0000 0000 8676 7464, Department of Medical Biotechnology, , National Institute of Genetic Engineering and Biotechnology (NIGEB), ; Tehran, Iran
                Author information
                http://orcid.org/0000-0001-8958-4812
                http://orcid.org/0000-0002-8180-1031
                http://orcid.org/0000-0002-2574-1150
                http://orcid.org/0000-0001-8593-1514
                http://orcid.org/0000-0002-6134-9965
                http://orcid.org/0000-0003-3240-9591
                http://orcid.org/0000-0002-8087-663X
                http://orcid.org/0000-0002-8185-6323
                http://orcid.org/0000-0001-8562-2295
                Article
                521
                10.1186/s13027-023-00521-y
                10391864
                37525229
                d243767d-e475-4de5-ba93-76a49c511d89
                © The Author(s) 2023

                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/. The Creative Commons Public Domain Dedication waiver ( http://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.

                History
                : 19 January 2023
                : 13 July 2023
                Categories
                Research
                Custom metadata
                © BioMed Central Ltd., part of Springer Nature 2023

                Oncology & Radiotherapy
                colorectal cancer,mesenchymal stem cells,newcastle disease virus,lactobacillus casei

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