Functional, Pharmacogenomic, and Immune Landscapes of Long Non‐Coding RNAs in Cancer

Long non-coding RNAs (lncRNAs) are emerging as key regulators in cancer, with significant potential as diagnostic, prognostic, and therapeutic targets. Here, this work systematically analyzes lncRNA associations with targeted therapies and immunotherapies across 33 cancer types using The Cancer Genome Atlas (TCGA) and real-world datasets. This work identifies 53,173 lncRNA-pathway associations, millions of lncRNA-drug response associations (via CancerRxTissue and VAEN), and extensive correlations with immune checkpoints and infiltration. This work further identifies 69 lncRNAs associated with immunotherapy response and 2,611 differentially expressed lncRNAs between low and high objective response rate (ORR) groups. Additionally, two lncRNAs are correlated with immune-related adverse events (irAEs), and 1,376 lncRNAs exhibited expression differences between cancers with low and high irAE risk. To facilitate further research, this work develops PILNC (https://hanlaboratory.com/PILNC), a comprehensive web portal enabling exploration of lncRNA associations with cancer pathways, drug responses, immune features, and immunotherapy outcomes.

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Publication Details

Journal
Advanced Science
Published
2025-11-21
DOI
https://doi.org/10.1002/advs.202513414
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
0.00

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article

Functional, Pharmacogenomic, and Immune Landscapes of Long Non‐Coding RNAs in Cancer

Chunru Lin, Yamei Chen, Mei Luo, Leng Han et al.
Advanced Science
Cancer-related molecular mechanisms research
article

Functional, Pharmacogenomic, and Immune Landscapes of Long Non‐Coding RNAs in Cancer

Chunru Lin, Yamei Chen, Mei Luo, Leng Han, Chengxuan Chen, Lifei Ma, Runhao Wang, Stephanie Ding, Lixia Diao, Wenbo Li, H. J. Yang, Yuan Liu, Yong Zang, Bora Lim, Liuqing Yang, James Wengler
article en

Abstract

Long non-coding RNAs (lncRNAs) are emerging as key regulators in cancer, with significant potential as diagnostic, prognostic, and therapeutic targets. Here, this work systematically analyzes lncRNA associations with targeted therapies and immunotherapies across 33 cancer types using The Cancer Genome Atlas (TCGA) and real-world datasets. This work identifies 53,173 lncRNA-pathway associations, millions of lncRNA-drug response associations (via CancerRxTissue and VAEN), and extensive correlations with immune checkpoints and infiltration. This work further identifies 69 lncRNAs associated with immunotherapy response and 2,611 differentially expressed lncRNAs between low and high objective response rate (ORR) groups. Additionally, two lncRNAs are correlated with immune-related adverse events (irAEs), and 1,376 lncRNAs exhibited expression differences between cancers with low and high irAE risk. To facilitate further research, this work develops PILNC (https://hanlaboratory.com/PILNC), a comprehensive web portal enabling exploration of lncRNA associations with cancer pathways, drug responses, immune features, and immunotherapy outcomes.

Advanced ScienceVol. 13(6)
The Graduate Center, CUNY (US), The University of Texas MD Anderson Cancer Center (US), Prevention Institute (US), Indiana University Bloomington (US), Indiana University School of Medicine, Indiana University – Purdue University Indianapolis (US), The University of Texas Health Science Center at Houston (US)
National Science Foundation, National Institutes of Health, School of Medicine, Indiana University, Office of Advanced Cyberinfrastructure
Openalex Percentile: Top 57%
Cancer-related molecular mechanisms research
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