Pyroptosis-Derived Long Noncoding RNA Profiles Reveal a Novel Signature for Evaluating the Prognosis of Patients With Lung Adenocarcinoma

Author:

Ba Yuhao1,Liu Shutong2,Wei Zhengpan2ORCID,Zhao Nannan3,Qiao Tong4,Ren Yuqing5,Li Lifeng6,Zhang Yuyuan1ORCID,Weng Siyuan1,Xu Hui1,Li Chunwei67,Ge Xiaoyong1,Han Xinwei189ORCID

Affiliation:

1. Department of Interventional Radiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China

2. The Medical School of Zhengzhou University, Zhengzhou University, Zhengzhou, China

3. Department of Neurosurgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China

4. Department of Thoracic Surgery, Henan Provincial People's Hospital, Zhengzhou, China

5. Department of Respiratory Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China

6. Internet Medical and System Applications of National Engineering Laboratory, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China

7. Department of Pharmacy, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China

8. Interventional Institute of Zhengzhou University, Zhengzhou, China

9. Interventional Treatment and Clinical Research Center of Henan Province, Zhengzhou, China

Abstract

PURPOSE Long noncoding RNAs (lncRNAs) were recently implicated in modifying pyroptosis. Nonetheless, pyroptosis-related lncRNAs and their possible clinical relevance persist largely uninvestigated in lung adenocarcinoma (LUAD). MATERIALS AND METHODS A sum of 921 samples were collected from three independent data sets. We obtained pyroptosis-related genes from both the Molecular Signatures Database and relevant literature sources and used four machine learning techniques, comprising stepwise Cox, ridge regression, least absolute shrinkage and selection operator, and random forest. Multiple bioinformatics approaches were used to further investigate the underlying mechanisms. RESULTS In total, 39 differentially expressed pyroptosis genes were identified by comparing normal and tumor samples. Correlation analysis revealed 933 pyroptosis-related lncRNAs. Furthermore, univariate Cox regression determined 11 lncRNAs that exhibited stable associations with prognosis in the three cohorts, which were used to construct the pyroptosis-derived lncRNA signature. After analyzing the optimal results from four machine learning algorithms, we ultimately selected random forest to develop the pyroptosis-derived lncRNA signature. This signature was proven to be an independent prognostic factor and exhibited robust performance in three cohorts. CONCLUSION We provided novel insight and established a pyroptosis-derived lncRNA signature for patients with LUAD, exhibiting strong predictive capabilities in both the training and validation sets.

Publisher

American Society of Clinical Oncology (ASCO)

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