两级转移冷大气等离子体作为针对结肠癌干细胞的独特治疗策略

IF 3.1 Q2 PHARMACOLOGY & PHARMACY Advanced pharmaceutical bulletin Pub Date : 2024-03-17 DOI:10.34172/apb.2024.041
Abolfazl Soulat, Taghi mohsenpour, Leila Roshangar, H. Naghshara
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引用次数: 0

摘要

这项研究采用一种名为 TS-TCAP 的创新型冷大气等离子体 (CAP) 透射法,研究了在三维培养环境中诱导结肠癌干细胞 (CCSC) 细胞凋亡的问题。TS-TCAP是一种部分或完全电离的非热性气态混合物,由光子、带电粒子、中性粒子和自由基组成,已在癌症治疗等生物医学应用中得到广泛应用。TS-TCAP 通过连续的两步传输过程影响 CCSCs,促进活性氧和氮物种(RONS)的有效传输。使用 qrt-ELISA、Annexin V 和 qrt-PCR 程序分别评估了经 TS-TCAP 处理的 CCSCs 的关键细胞因子,包括 IL-6 和 IL-8 的分泌和表达水平、凋亡细胞数量以及 BAX、BCL-2 和 KI-67 蛋白的表达。用TS-TCAP处理CCSCs的结果显示,凋亡细胞数量显著增加(p值<0.0001),IL-6和IL-8的分泌和基因表达减少(p值<0.0001),同时BCL-2和BAX基因表达也发生了有利的变化(p值<0.0001)。此外,还观察到 KI-67 表达明显减少,与 CCSCs 增殖减少相关(p 值 <0.0001)。这项研究还强调了 TS-TCAP 的抗癌潜力,展示了它在降低 CCSCs 存活率方面的功效。不过,还需要进一步的临床前和临床试验来全面评估 CAP 的疗效、安全性以及与其他疗法的潜在协同作用。总之,TS-TCAP是一种治疗CCSCs的有前途的替代疗法,有待进一步研究和完善。
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A Two-Stage Transferred Cold Atmospheric Plasma as a Unique Therapeutic Strategy for Targeting Colon Cancer Stem Cells
The study examines the induction of apoptosis in colon cancer stem cells (CCSCs) within a 3D culture setting, employing an innovative cold atmospheric plasma (CAP) transmission method known as TS-TCAP. TS-TCAP is a partially or fully ionized non-thermal gaseous mixture that comprises photons, charged and neutral particles, and free radicals, which has gained traction in biomedical applications such as cancer therapy. TS-TCAP impacts CCSCs via a continuous, two-step transport process, facilitating the efficient delivery of reactive oxygen and nitrogen species (RONS). The key cellular factors of CCSCs impacted by TS-TCAP treatment, encompassing the secretion and expression levels of IL-6 and IL-8, apoptotic cell count, and expression of BAX, BCL-2, and KI-67 proteins, were evaluated using qrt-ELISA, Annexin V, and qrt-PCR procedures, respectively. The outcomes of CCSCs treatment with TS-TCAP reveal a notable rise in the number of apoptotic cells (p value <0.0001), diminished secretion, and gene expression of IL-6 and IL-8 (p-value < 0.0001), accompanied by favorable alterations in BCL-2 and BAX gene expression (p value <0.0001). Additionally, a notable decrease in KI-67 expression was observed, correlating with a reduction in CCSCs proliferation (p value <0.0001). As well, this study underscores the anti-cancer potential of TS-TCAP, showcasing its efficacy in reducing CCSCs survival rates. However, further pre-clinical and clinical trials are necessary to evaluate CAP's efficacy, safety, and potential synergistic effects with other therapies thoroughly. Overall, TS-TCAP presents a promising alternative for CCSCs treatment, pending further investigation and refinement.
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来源期刊
Advanced pharmaceutical bulletin
Advanced pharmaceutical bulletin PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
2.80%
发文量
51
审稿时长
12 weeks
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