[Ferroptosis-related long non-coding RNA to predict the clinical outcome of non-small cell lung cancer after radiotherapy].

Objective: To construct a long non-coding RNA (lncRNA) model based on ferroptosis and predict the prognosis of non-small cell lung cancer (NSCLC) patients after radiotherapy, to develop a comprehensive framework that integrates genomic data with clinical outcomes, and to identify lncRNA associated with ferroptosis and evaluate their predictive power for patient survival and progression-free survival following radiotherapy.

Methods: This study commenced by acquiring standardized transcriptome data from primary tumors and normal tissues, along with corresponding clinical information, from the cancer genome atlas (TCGA) database. This dataset provided a robust foundation for identifying differentially expressed genes (DEGs) related to ferroptosis. These analyses helped pinpoint specific pathways and biological processes involved in ferroptosis, such as glutathione metabolism, lipid signaling, oxidative stress, and reactive oxygen species (ROS) metabolism. Subsequently, univariate and multivariate Cox regression analyses were conducted to construct a predictive model based on lncRNA associated with ferroptosis. The goal was to differentiate between the high-risk and low-risk groups of NSCLC patients who had undergone radiotherapy. By incorporating these lncRNA into the model, we aimed to provide a more accurate prediction of patient outcomes. The performance of the model was validated by comparing the survival rates and progression-free survival between the high-risk and low-risk groups. Additionally, differences in gene expression patterns and pathway activities between these two groups were examined to further validate the model's effectiveness.

Results: Our analysis revealed that the differentially expressed genes related to ferroptosis were significantly enriched in several key pathways, including ferroptosis itself, glutathione metabolism, lipid signaling, and processes involving oxidative stress and ROS metabolism. Based on these findings, we constructed a prognostic model using 14 lncRNA that showed strong associations with ferroptosis. Further data analysis demonstrated that these lncRNA could independently predict the prognosis of NSCLC patients after radiotherapy. Specifically, age, stage, and gender were used as clinical pathological variables, and the results indicated that the high-risk group of NSCLC patients had a poorer prognosis following radiotherapy. This finding underscores the potential of the model to serve as a valuable tool for predicting prognosis for NSCLC patients undergoing radiotherapy.

Conclusion: The risk model developed in this study can independently predict the prognosis of NSCLC patients after radiotherapy. This model provides a solid basis for understanding the role of ferroptosis-related lncRNA in the prognosis of NSCLC patients following radiotherapy. Furthermore, it offers clinical guidance for combining radiotherapy with ferroptosis-targeted treatments, potentially improving therapeutic outcomes for NSCLC patients. The integration of genomic and clinical data in this study highlights the importance of personalized medicine approaches in oncology, paving the way for more precise and effective treatment strategies.