# Time-Resolved Oxygen Dynamics Reveals Redox-Selective Apoptosis Induced by Cold Atmospheric Plasma in HT-29 Colorectal Cancer Cells

**Authors:** Hamideh Mohammadi, Kamal Hajisharifi, Esmaeil Heydari, Hassan Mehdian, Sara Emadi, Yuri Akishev, Svetlana A. Ermolaeva, Augusto Stancampiano, Eric Robert

PMC · DOI: 10.3390/antiox15020209 · Antioxidants · 2026-02-04

## TL;DR

Cold plasma treatment selectively kills cancer cells by triggering redox reactions, and changes in oxygen levels can predict treatment success.

## Contribution

The study provides mechanistic validation of the Bauer redox model and identifies early oxygen dynamics as predictive markers for plasma therapy efficacy.

## Key findings

- A delayed surge in extracellular singlet oxygen was observed in dying cancer cells 10–20 minutes after CAP treatment.
- Intracellular ROS levels correlated strongly with extracellular singlet oxygen dynamics and cell viability loss.
- Early oxygen dynamics after CAP exposure can serve as predictive markers for treatment efficacy.

## Abstract

Cold atmospheric plasma (CAP) has emerged as a promising anticancer approach because of its ability to selectively eliminate malignant cells. Among the proposed mechanisms of this selectivity, the Bauer theory emphasizes the synergistic action of plasma-derived hydrogen peroxide (H2O2) and nitrite (NO2−), leading to the transient generation of primary singlet oxygen (1O2). This early event inactivates membrane-bound catalase, allowing tumor cell-derived H2O2 and peroxynitrite to initiate a self-amplifying cycle that produces secondary 1O2, as a hallmark of CAP selectivity. To test this hypothesis, in this work, we monitored extracellular dissolved oxygen (DO) dynamics in HT-29 colorectal cancer cells treated with an argon plasma jet using time-resolved phosphorescence lifetime spectroscopy. Temporal variations in DO likely reflect the cumulative effect of rapid 1O2 production and its reactions with cells. A delayed surge in extracellular 1O2 was observed specifically in dying cancer cells within the 10–20 min window predicted by the model. Intracellular ROS imaging confirmed a strong correlation between intracellular ROS, extracellular 1O2 dynamics, and viability loss. Together, these results provide mechanistic validation of Bauer’s redox model and suggest that early oxygen dynamics after CAP exposure can serve as predictive markers for treatment efficacy in plasma or photodynamic therapies.

## Linked entities

- **Chemicals:** hydrogen peroxide (PubChem CID 784), nitrite (PubChem CID 946), singlet oxygen (PubChem CID 159832), peroxynitrite (PubChem CID 104806)
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** CAT (catalase) [NCBI Gene 847], NOX1 (NADPH oxidase 1) [NCBI Gene 27035] {aka GP91-2, MOX1, NOH-1, NOH-1L, NOH1}, AQP8 (aquaporin 8) [NCBI Gene 343] {aka AQP-8}, AQP3 (aquaporin 3 (Gill blood group)) [NCBI Gene 360] {aka AQP-3, GIL}, CYCS (cytochrome c, somatic) [NCBI Gene 54205] {aka CYC, HCS, THC4}
- **Diseases:** cytotoxic (MESH:D064420), CAP (MESH:D000067390), Colorectal Cancer (MESH:D015179), necrosis (MESH:D009336), Cancer (MESH:D009369), mitochondrial dysfunction (MESH:D028361), injury to (MESH:D014947), hypoxia (MESH:D000860), colorectal adenocarcinoma (MESH:D003110)
- **Chemicals:** T1 (MESH:C103828), MTT (MESH:C070243), nitrite (MESH:D009573), sodium sulfate (MESH:C012036), penicillin (MESH:D010406), ruthenium (MESH:D012428), Cold Plasma (MESH:D058626), Cold Atmospheric Plasma (-), superoxide (MESH:D013481), Propidium iodide (MESH:D011419), H2O2 (MESH:D006861), ROS (MESH:D017382), Ar (MESH:D001128), DMSO (MESH:D004121), cobalt chloride (MESH:C018021), glucose (MESH:D005947), RNS (MESH:D011886), PBS (MESH:D007854), KCl (MESH:D011189), OH (MESH:C031356), lipids (MESH:D008055), sodium butyrate (MESH:D020148), peroxynitrite (MESH:D030421), CO2 (MESH:D002245), PDMS (MESH:C013830), 2',7'-Dichlorodihydrofluorescein diacetate (MESH:C110400), streptomycin (MESH:D013307), nitrogen (MESH:D009584), EDTA (MESH:D004492), NO2- (MESH:D009585), formazan (MESH:D005562), Oxygen (MESH:D010100), phosphate (MESH:D010710), PI (MESH:D010716), singlet oxygen (MESH:D026082), Acridine (MESH:D000166), metal (MESH:D008670), acridine orange (MESH:D000165), platinum (MESH:D010984), hydroxyl radicals (MESH:D017665), cholesterol (MESH:D002784), DCF (MESH:C037631), DCFH-DA (MESH:C029569), water (MESH:D014867), palladium (MESH:D010165), tetrazolium salt (MESH:D013778)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** HT-29 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0320)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12938700/full.md

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938700/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938700/full.md

---
Source: https://tomesphere.com/paper/PMC12938700