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微免疫疗法药物2LMIREG中的活性物质在两种结肠癌细胞系中显示出体外抗氧化特性。

Active Substances from the Micro-Immunotherapy Medicine 2LMIREG Display Antioxidative Properties In Vitro in Two Colorectal Cancer Cell Lines.

作者信息

Garcia-Sureda Laura, Jacques Camille, Pons Daniel G, Sastre-Serra Jorge, Oliver Jordi, Floris Ilaria

机构信息

Preclinical Research Department, Labo'life España, 07330 Consell, Spain.

Preclinical Research Department, Labo'life France, Pescalis-Les Magnys, 79320 Moncoutant-sur-Sevre, France.

出版信息

Life (Basel). 2025 May 6;15(5):743. doi: 10.3390/life15050743.

DOI:10.3390/life15050743
PMID:40430171
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12112867/
Abstract

Mitochondria play a crucial role in oxidative stress control and reactive oxygen species (ROS) generation, impacting many cellular processes. Dysregulated mitochondria are linked to diseases such as colorectal cancer (CRC), known for its aggressiveness. Since ROS plays a role in tumor growth and metastasis, there is considerable interest in developing therapies that target these reactives. This study investigates the effects of some active substances from the micro-immunotherapy (MI) medicine 2LMIREG on mitochondrial metabolism parameters in two CRC-derived cell lines. HT-29 and the metastasis-derived SW620 cell lines, which heavily rely on ROS for proliferation, were used to evaluate the effects of the tested active substances. Cellular viability and various mitochondrial metabolism parameters were measured: ROS production, mitochondrial mass index, and mitochondrial DNA levels. In both cell lines, the tested MI formulation reduced cellular viability as well as ROS production compared to the vehicle used as a control. The treatment also appeared to increase the mitochondrial mass index without affecting mitochondrial DNA levels in the two CRC models. Altogether, these preliminary results report for the first time the mitochondria-related effects of some actives from 2LMIREG in two CRC cell models and open perspectives for further in-depth metabolism-based studies.

摘要

线粒体在氧化应激控制和活性氧(ROS)生成中发挥着关键作用,影响着许多细胞过程。失调的线粒体与诸如结直肠癌(CRC)这类以侵袭性著称的疾病相关联。由于ROS在肿瘤生长和转移中起作用,因此开发针对这些活性物质的疗法备受关注。本研究调查了微免疫疗法(MI)药物2LMIREG中的一些活性物质对两种CRC衍生细胞系中线粒体代谢参数的影响。HT - 29细胞系以及转移衍生的SW620细胞系严重依赖ROS进行增殖,被用于评估受试活性物质的效果。测量了细胞活力和各种线粒体代谢参数:ROS生成、线粒体质量指数和线粒体DNA水平。在两种细胞系中,与用作对照的赋形剂相比,受试的MI制剂降低了细胞活力以及ROS生成。在这两种CRC模型中,该处理似乎还增加了线粒体质量指数,而不影响线粒体DNA水平。总之,这些初步结果首次报道了2LMIREG中的一些活性物质在两种CRC细胞模型中与线粒体相关的作用,并为进一步基于代谢的深入研究开辟了前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/12112867/5066b0af7a74/life-15-00743-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/12112867/5c2e557082bf/life-15-00743-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/12112867/b6d93764bb6c/life-15-00743-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/12112867/178c464c4d7b/life-15-00743-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/12112867/5066b0af7a74/life-15-00743-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/12112867/5c2e557082bf/life-15-00743-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/12112867/b6d93764bb6c/life-15-00743-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/12112867/178c464c4d7b/life-15-00743-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a906/12112867/5066b0af7a74/life-15-00743-g004.jpg

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本文引用的文献

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ATP Inhibition for Starvation/Mild Photothermal/Photodynamic Synergy Therapy Using Polypeptide Nanoparticles Conjugating 2-Deoxy-D-Glucose and Dye under NIR Phototheranostic Strategy.基于近红外光疗策略的多肽纳米载体连接 2-脱氧-D-葡萄糖和染料用于饥饿/温和光热/光动力协同治疗的 ATP 抑制作用
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Actives from the Micro-Immunotherapy Medicine 2LMIREG Reduce the Expression of Cytokines and Immune-Related Markers Including Interleukin-2 and HLA-II While Modulating Oxidative Stress and Mitochondrial Function.
微免疫疗法药物2LMIREG中的活性成分可降低细胞因子和免疫相关标志物(包括白细胞介素-2和HLA-II)的表达,同时调节氧化应激和线粒体功能。
J Inflamm Res. 2024 Feb 21;17:1161-1181. doi: 10.2147/JIR.S445053. eCollection 2024.
4
Reigniting hope in cancer treatment: the promise and pitfalls of IL-2 and IL-2R targeting strategies.重新点燃癌症治疗的希望:IL-2 和 IL-2R 靶向策略的前景与挑战。
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A Sequential Micro-Immunotherapy Medicine Increases Collagen Deposition in Human Gingival Fibroblasts and in an Engineered 3D Gingival Model under Inflammatory Conditions.序贯微免疫疗法药物在炎症条件下增加人牙龈成纤维细胞胶原沉积和工程化 3D 牙龈模型中的胶原沉积。
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