携带新城疫病毒和干酪乳杆菌提取物的间充质干细胞对CT26细胞系的抗增殖作用:在肿瘤治疗中的协同作用。

IF 3.1 2区 医学 Q3 IMMUNOLOGY
Akbar Ghorbani Alvanegh, Majid Mirzaei Nodooshan, Ruhollah Dorostkar, Reza Ranjbar, Bahman Jalali Kondori, Alireza Shahriary, Karim Parastouei, Soheil Vazifedust, Elmira Afrasiab, Hadi Esmaeili Gouvarchinghaleh
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引用次数: 1

摘要

背景与目的:结直肠癌(Colorectal Cancer, CRC)是一种常见的恶性肿瘤,死亡率高。特定的遗传和环境影响可影响结直肠癌。溶瘤病毒和细菌治疗结直肠癌是一种创新的治疗选择。本研究旨在确定感染新城疫病毒(NDV)的间充质干细胞(MSCs)与干酪乳杆菌提取物(L. casei)联合对结直肠癌细胞系生长是否具有协同作用。材料和方法:骨髓间充质干细胞取自BALB/c小鼠骨髓,经20 MOI NDV感染。然后,以不同组的CT26细胞系作为单一和联合处理,检测含有NDV和干酪乳杆菌提取物的MSCs的抗癌潜力。评估考虑了CT26的存活率以及LDH、ROS和caspases 8和9的水平在不同治疗后的产生率。结果:与对照组相比,NDV、MSCs-NDV和干酪乳杆菌单独或联合治疗显著增加细胞凋亡率、LDH和ROS生成(P小于0.05)。同时,游离NDV和被包裹在MSCs中的NDV也有抗癌作用,但被包裹的NDV比游离NDV有延迟作用。研究结果证明,干酪乳杆菌主要刺激外源性通路,而NDV治疗通过激活内源性和外源性凋亡通路促进细胞凋亡。结论:结果表明,携带溶瘤性NDV的MSCs与干酪乳杆菌提取物联合使用可促进CT26细胞系微环境中LDH、ROS的产生和细胞凋亡,可能是一种有效的癌症免疫治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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 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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来源期刊
Infectious Agents and Cancer
Infectious Agents and Cancer ONCOLOGY-IMMUNOLOGY
CiteScore
5.80
自引率
2.70%
发文量
54
期刊介绍: Infectious Agents and Cancer is an open access, peer-reviewed online journal that encompasses all aspects of basic, clinical, epidemiological and translational research providing an insight into the association between chronic infections and cancer. The journal welcomes submissions in the pathogen-related cancer areas and other related topics, in particular: • HPV and anogenital cancers, as well as head and neck cancers; • EBV and Burkitt lymphoma; • HCV/HBV and hepatocellular carcinoma as well as lymphoproliferative diseases; • HHV8 and Kaposi sarcoma; • HTLV and leukemia; • Cancers in Low- and Middle-income countries. The link between infection and cancer has become well established over the past 50 years, and infection-associated cancer contribute up to 16% of cancers in developed countries and 33% in less developed countries. Preventive vaccines have been developed for only two cancer-causing viruses, highlighting both the opportunity to prevent infection-associated cancers by vaccination and the gaps that remain before vaccines can be developed for other cancer-causing agents. These gaps are due to incomplete understanding of the basic biology, natural history, epidemiology of many of the pathogens that cause cancer, the mechanisms they exploit to cause cancer, and how to interrupt progression to cancer in human populations. Early diagnosis or identification of lesions at high risk of progression represent the current most critical research area of the field supported by recent advances in genomics and proteomics technologies.
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