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Dual-jet transition cold atmospheric plasma suppresses colon cancer stem cells via matrix metalloproteinase regulation.

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Cancer treatment and research communications 📖 저널 OA 19.8% 2023: 0/1 OA 2024: 0/1 OA 2025: 1/15 OA 2026: 23/104 OA 2023~2026 2026 Vol.46() p. 101096
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Soulat A, Mohsenpour T, Roshangar L

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Colon cancer stem cells (CCSCs) are critical drivers of tumor progression, metastasis, and therapeutic resistance, largely mediated by matrix metalloproteinases (MMPs).

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  • p-value p < 0.0001

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APA Soulat A, Mohsenpour T, Roshangar L (2026). Dual-jet transition cold atmospheric plasma suppresses colon cancer stem cells via matrix metalloproteinase regulation.. Cancer treatment and research communications, 46, 101096. https://doi.org/10.1016/j.ctarc.2026.101096
MLA Soulat A, et al.. "Dual-jet transition cold atmospheric plasma suppresses colon cancer stem cells via matrix metalloproteinase regulation.." Cancer treatment and research communications, vol. 46, 2026, pp. 101096.
PMID 41592439 ↗

Abstract

Colon cancer stem cells (CCSCs) are critical drivers of tumor progression, metastasis, and therapeutic resistance, largely mediated by matrix metalloproteinases (MMPs). This study investigates the therapeutic potential of a novel dual-jet transition cold atmospheric plasma (DJTCAP) system to modulateMMP expression and reduce CCSC viability. HT29-derived CCSCs were cultured in 3D Matrigel and exposed to three sequential plasma jets generated by a custom DJTCAP device, applied either via direct irradiation or plasma-activated medium for 120- or 240-seconds using helium or argon.MMP-1, -2, -3, -7, -9, and -14 expression was measured by RT-PCR, and cell viability was assessed using the MTT assay. DJTCAP treatment significantly downregulated allMMPs (p < 0.0001), with the most pronounced effects and cytotoxicity observed following 240-second helium exposure, which consistently outperformed argon. Plasma diagnostics confirmed efficient energy utilization (<1 W) and high generation of reactive oxygen and nitrogen species (RONS), suggesting a RONS-mediated mechanism of action. These results demonstrate that DJTCAP selectively suppressesMMP expression and reduces CCSC viability, highlighting its potential as a safe, energy-efficient, and targeted therapy for metastatic and treatment-resistant colorectal cancer.

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