# Flavones and Aminoflavones Increase the Cytotoxicity of NK Cells in Human Non‐Small Cell Lung Cancer

**Authors:** Ping‐Chih Hsu, Chih‐Cheng Chien, Yang‐Je Cheng, Chuan‐Hsin Chang, Tzenge‐Lien Shih

PMC · DOI: 10.1111/jcmm.71055 · Journal of Cellular and Molecular Medicine · 2026-02-13

## TL;DR

This study shows that aminoflavone 8 boosts the ability of NK cells to kill lung cancer cells without harming normal cells.

## Contribution

The study identifies aminoflavone 8 as a novel compound that enhances NK cell cytotoxicity against lung cancer.

## Key findings

- Aminoflavone 8 increases NK-92MI cell cytotoxicity against A549 lung cancer cells.
- Aminoflavone 8 inhibits STAT3 phosphorylation in both cancer and NK cells.
- Aminoflavone 8 combined with NK cells shows synergistic anti-tumor effects in mice.

## Abstract

Natural flavonoids (flavones) and synthetic aminoflavones are known for their anti‐cancer properties; however, their immunomodulation ability has been largely unexplored. This study determined that synthetic flavones and aminoflavones modulate the cytotoxicity of natural killer (NK) cells against lung cancer cells. Notably, flavones 2, 3, and 6 and aminoflavone 8 were shown to increase the cytotoxicity of NK‐92MI cells against A549 lung cancer cells without adversely affecting MRC5 normal cells. Aminoflavone 8 enhanced NK‐92MI cell cytotoxicity, as evidenced by the elevated expression of cytotoxic effectors, such as IFN‐γ, perforin, and granzyme B. Aminoflavone 8 also inhibited STAT3 phosphorylation in A549 lung cancer and NK‐92MI cells under co‐culture conditions. Moreover, aminoflavone 8 exhibited anti‐tumour effects in a lung cancer xenograft mouse model. Combined therapy with aminoflavone 8 and NK‐92MI cells had synergistic anti‐tumour effects without liver or kidney toxicity. Our analysis revealed that the amino group in the C6 position of aminoflavone 8 was crucial to the enhanced cytotoxicity of NK cells. These findings suggest that aminoflavone 8 can potentiate NK cell cytotoxicity against lung cancer cells, highlighting its potential as a novel therapeutic agent for the treatment of lung cancer.

## Linked entities

- **Proteins:** IFNG (interferon gamma), PRF1 (perforin 1), STAT3 (signal transducer and activator of transcription 3)
- **Diseases:** lung cancer (MONDO:0005138), non-small cell lung cancer (MONDO:0005233)

## Full-text entities

- **Genes:** STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, GZMB (granzyme B) [NCBI Gene 3002] {aka C11, CCPI, CGL-1, CGL1, CSP-B, CSPB}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** Non-Small Cell Lung Cancer (MESH:D002289), cancer (MESH:D009369), lung cancer (MESH:D008175), Cytotoxicity (MESH:D064420), liver or kidney toxicity (MESH:D056486)
- **Chemicals:** Aminoflavone 8 (-), Flavones (MESH:D047309), flavonoids (MESH:D005419), Aminoflavones (MESH:C413760)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12904836/full.md

## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12904836/full.md

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Source: https://tomesphere.com/paper/PMC12904836