# Single-Cell Sequencing Reveals the Role of Radiation-Induced Stemness-Responsive Cancer Cells in the Development of Radioresistance

**Authors:** Zheng Shi, Cuilan Hu, Jiadi Liu, Wei Cheng, Xiaohua Chen, Xiongxiong Liu, Yanyu Bao, Haidong Tian, Boyi Yu, Feifei Gao, Fei Ye, Xiaodong Jin, Chao Sun, Qiang Li

PMC · DOI: 10.3390/ijms26041433 · International Journal of Molecular Sciences · 2025-02-08

## TL;DR

This study uses single-cell sequencing to show how cancer cells become resistant to radiation therapy by developing stem-like traits early in treatment.

## Contribution

The paper identifies a novel subpopulation of cancer cells that respond to radiation by enhancing stemness and reprogramming metabolism, driven by the EGFR-Hippo signaling pathway.

## Key findings

- Radiation-induced stemness-responsive cancer cells emerge early in radiotherapy and contribute to radioresistance.
- These cells undergo metabolic reprogramming and differentiate into more malignant phenotypes.
- The EGFR-Hippo signaling pathway activation drives stemness responses and radioresistance development.

## Abstract

Increased stemness of cancer cells exacerbates radioresistance, thereby greatly limiting the efficacy of radiotherapy. In order to study the changes in cancer cell stemness during radiotherapy, we established a radioresistance model of human non-small cell lung cancer A549 cells and obtained A549 radioresistant cells (A549-RR). We sampled the cells at different time points during the modeling process and investigated the heterogeneity of each group of cells using single-cell sequencing. Cells in the early stages of fractionated irradiation were found to be significantly up-regulated in stemness, and a subpopulation of cells producing this response was screened and referred to as “radiation-induced stemness-responsive cancer cells”. They were undergoing stemness response, energy metabolism reprogramming, and progressively differentiating into cells with more diverse and malignant phenotypes in order to attenuate the killing effect of radiation. Furthermore, we demonstrated that such responses might be driven by the activation of the EGFR-Hippo signaling pathway axis, which also plays a crucial role in the development of radioresistance. Our study reveals the dynamic evolution of cell subpopulation in cancer cells during fractionated radiotherapy; the early stage of irradiation can determine the destiny of the radiation-induced stemness-responsive cancer cells. The activation of stemness-like phenotypes during the development of radioresistance is not the result of dose accumulation but occurs during the early stage of radiotherapy with relatively low-dose irradiation. The degree of the radiation-induced stemness response of cancer cells mediated by the EGFR-Hippo signaling pathway might be a potential predictor of the efficacy of radiotherapy and the development of radioresistance.

## Linked entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956], hpo (hippo) [NCBI Gene 37247]
- **Diseases:** non-small cell lung cancer (MONDO:0005233)

## Full-text entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** Cancer (MESH:D009369), non-small cell lung cancer (MESH:D002289)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** A549 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023)

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11855645/full.md

## References

72 references — full list in the complete paper: https://tomesphere.com/paper/PMC11855645/full.md

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Source: https://tomesphere.com/paper/PMC11855645