Evidence map›Paper›PMID 41796250›Full record

ArticleNPJ precision oncology2026

Pulmonary surfactant protein D reduces lung cancer progression associated with decreased IL-4/STAT6 signaling.

Ali Mohammadi, Mohammed Inayatullah, Anders Schlosser, Bartosz Pilecki, Niels Marcussen, Seyda Ünsal, Behzad Mansoori, Behzad Baradaran, Yousef Tallouzi, Morten Frier Gjerstorff and 5 more

Abstract read
In one paragraph

Article in NPJ precision oncology, 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

15 authors.

Ali MohammadiDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Mohammed InayatullahDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Anders SchlosserDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Bartosz PileckiDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Niels MarcussenDepartment of Pathology, Research Unit of Pathology, University Hospital of Southern Denmark, Aabenraa, Denmark.
Seyda ÜnsalDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Behzad MansooriDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Behzad BaradaranImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Yousef TallouziDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Morten Frier GjerstorffDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Jonas GraversenDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Kim RavnskjærDepartment of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.
Vijay K TiwariDepartment of Molecular Medicine, University of Southern Denmark, Odense, Denmark.
Mikkel G Terp *Department of Molecular Medicine, University of Southern Denmark, Odense, Denmark. mterp@health.sdu.dk.
Grith Lykke Sorensen *Department of Molecular Medicine, University of Southern Denmark, Odense, Denmark. glsorensen@health.sdu.dk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary surfactant protein D (SP-D) is an innate immune molecule implicated in lung cancer, where its expression correlates with improved survival and reduced tumor growth. Despite its relevance to lung pathobiology, the transcriptional programs regulated by SP-D and their role in cancer progression and metastasis remain poorly understood. Through integrative analysis of multimodal human data we demonstrate that the SP-D gene (SFTPD) expression is reduced to near absence in metastatic non-small cell lung cancer (NSCLC) tissue, linking its loss to metastatic progression. SFTPD overexpression in A549 lung adenocarcinoma cells significantly decreased tumor growth and metastasis in vivo, and intranasal SP-D protein administration reduced lung tumor burden. Mechanistically, SP-D suppressed several signaling pathways, including IL-4/STAT6 signaling. Analysis of clinical lung tumor samples confirmed that SFTPD expression is associated with reduced IL-4/STAT6 signaling, and patients with low SFTPD expression and elevated IL-4 signaling in their tumors showed the poorest disease-free survival. Our findings demonstrate that SP-D interacts with NSCLC cells to suppress lung cancer progression, in part by blocking of the IL-4/STAT6 signaling pathway.

Identifiers

PMID41796250
PMCPMC13099962

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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.