Your new experience awaits. Try the new design now and help us make it even better

ORIGINAL RESEARCH article

Front. Immunol.

Sec. Cancer Immunity and Immunotherapy

This article is part of the Research TopicNovel Immune Markers and Predictive Models for Diagnosis, Immunotherapy and Prognosis in Lung Cancer​​​​​​​View all articles

DDR1 as a Key Prognostic Biomarker in Non-Small Cell Lung Cancer: Identification, Validation, and Potential Therapeutic Implications

Provisionally accepted
Rencai  LuRencai Lu1,2Lu  QianLu Qian3XueQin  SunXueQin Sun2JianFang  ZhangJianFang Zhang2YeQian  CuiYeQian Cui2HuiMei  SuHuiMei Su4Dongdong  XvDongdong Xv2*ShaoBo  WangShaoBo Wang2*
  • 1Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, China
  • 2Department of Nuclear Medicine, The First People's Hospital of Yunnan Province, Kunming, China
  • 3Department of Pathology, The First People's Hospital of Yunnan Province, Kunming, China
  • 4No.926 Hospital, Joint Logistics Support Force of PLA, Kaiyuan, China

The final, formatted version of the article will be published soon.

Abstract Background: Non-small cell lung cancer (NSCLC) remains the leading cause of cancer-related death, with a limited response to immune checkpoint inhibitors (ICIs). Discoidin domain receptor 1 (DDR1) is a collagen-binding kinase that is implicated in tumor progression and immune escape, but its role in NSCLC is unclear. This study aimed to clarify the clinical significance and therapeutic potential of DDR1 via bioinformatics, machine learning, in vitro experiments, and clinical sample analysis. Materials and Methods: NSCLC patients were stratified by DDR1 expression based on retrospective RNA-seq data from The Cancer Genome Atlas (TCGA); after quality control, 495 lung adenocarcinoma (LUAD) and 481 lung squamous cell carcinoma (LUSC) tumor samples, together with 57 LUAD and 48 LUSC normal samples, were retained for further analysis. The analyses included survival, mutation, immune landscape, drug sensitivity, single-cell heterogeneity, and functional Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses, accounting for the heterogeneity among NSCLC subtypes. A machine learning-based 4-gene prognostic model was constructed and externally validated using two independent datasets: GSE30219

Keywords: discoidin domain receptor 1, Non-small cell lung cancer, bioinformatics, machine learning, Immunotherapy

Received: 22 Aug 2025; Accepted: 17 Nov 2025.

Copyright: © 2025 Lu, Qian, Sun, Zhang, Cui, Su, Xv and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence:
Dongdong Xv, 8421965@qq.com
ShaoBo Wang, wshbo_98@126.com

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.