Evidence map›Paper›PMID 42292412›Full record

ReviewFrontiers in immunology2026

Tumor-immune crosstalk in lung cancer: emerging roles of long non-coding RNAs.

Upasna Madan, Riitta Lahesmaa, Anil K Thotakura

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Upasna MadanTurku Bioscience Center, University of Turku and Åbo Akademi University, Turku, Finland.
Riitta LahesmaaTurku Bioscience Center, University of Turku and Åbo Akademi University, Turku, Finland.
Anil K ThotakuraImmuno-Oncology, Oncology Research, Orion Pharma, Turku, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer, primarily non-small cell lung cancer (NSCLC), remains one of the leading contributors to cancer-related mortality worldwide. The tumor immune microenvironment (TIME) critically influences tumor progression, metastasis, prognosis, and therapeutic responses. Emerging evidence highlights the significant role of long non-coding RNAs (lncRNAs) in mediating tumor-immune interactions, thereby underscoring their potential as biomarkers and therapeutic targets. This review synthesizes current knowledge of lncRNAs expressed by immune and tumor cells in NSCLC. Immune cell-derived lncRNAs regulate the differentiation and function of specific immune cell subsets; tumor cell-derived lncRNAs modulate immune checkpoint molecules, immune evasion pathways, and immune cell infiltration and polarization. Collectively, these lncRNAs shape anti-tumor immunity and therapy responses. We provide an overview of their expression, prognostic relevance, functional effects, and underlying molecular mechanisms, classified by level of evidence spanning clinical, preclinical, and in silico studies. We then discuss convergent regulatory nodes shared across lncRNAs, lncRNA-mediated immune checkpoint inhibitor response and resistance, and therapeutic targeting strategies. Finally, we highlight emerging technological frontiers for lncRNA profiling in the TIME, alongside key limitations and future directions of the field.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsRNA, Long NoncodingTumor MicroenvironmentAnimalsBiomarkers, TumorGene Expression Regulation, NeoplasticHumansBiomarkers, TumorRNA, Long Noncodingbiomarkerlong non coding RNANSCLCPD-L1tumor immune microenvironment

Identifiers

PMID42292412
PMCPMC13260236

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.