Evidence map›Paper›PMID 41656379›Full record

ArticleScientific reports2026

MUC14 suppresses lung adenocarcinoma via integrin α8β6/PI3K/AKT/MAPK modulating cisplatin response and immunity.

Xiaoqing Li, Ming Li, Shizhuan Huang, Zhihua Zhang, Chen Xing, Shan Yu, Guiping Han

Abstract read
In one paragraph

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

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Xiaoqing LiDepartment of Pathology, Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Ming LiDepartment of Pathology, Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Shizhuan HuangDepartment of Hepatic Surgery, Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Zhihua ZhangDepartment of Hepatic Surgery, Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Chen XingDepartment of Pathology, Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, Heilongjiang, China.
Shan YuDepartment of Pathology, Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, Heilongjiang, China. yushan@hrbmu.edu.cn.
Guiping HanDepartment of Pathology, Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, Heilongjiang, China. 600400@hrbmu.edu.cn.

Funding

Basic scientific research expenses for scientific research projects of universities of Heilongjiang province 2023-KYYWF-0182
6 · The paper itself

Abstract

MUC14/Endomucin, a transmembrane mucin, is a potential prognostic biomarker in malignancies. This study aimed to elucidate the functional impact of MUC14 on tumor proliferation, migration, immune microenvironment modulation, and cisplatin response in lung adenocarcinoma (LUAD), and investigate its molecular mechanisms. LUAD cell lines with MUC14 overexpression (MUC14-OE) or silencing were constructed. Malignant behaviors were assessed via CCK-8, Transwell, and colony formation assays. Immune cell infiltration was quantified by CD3+/CD8 + immunohistochemistry. Subcutaneous xenograft and tail-vein metastasis murine models evaluated in vivo tumor progression and cisplatin responsiveness. Mechanisms were characterized using FRET and western blotting. Multiplatform bioinformatics analysis of public databases correlated MUC14 expression with clinical outcomes, immune infiltration, and chemotherapy response. MUC14-OE inhibited LUAD cell proliferation, migration, colony formation, and adhesion, while silencing promoted these phenotypes. MUC14 expression positively correlated with CD3+/CD8 + T-cell infiltration. In vivo, MUC14-OE suppressed subcutaneous tumor growth, lung metastasis, and enhanced cisplatin efficacy. Mechanistically, MUC14 inhibited integrin α8β6 clustering, suppressing PI3K/AKT and MAPK/ERK signaling. Cisplatin sensitization involved JNK/c-Jun pathway activation. This study establishes MUC14 as a multifunctional tumor suppressor in LUAD. It inhibits integrin α8β6-mediated PI3K/AKT and MAPK/ERK signaling to suppress tumor growth, promotes CD8+ T-cell infiltration, and augments cisplatin sensitivity via the JNK/c-Jun pathway. These findings nominate MUC14 as a prognostic biomarker and therapeutic target, suggesting combinatorial strategies integrating immunotherapy and chemotherapy.

Indexed as

Adenocarcinoma of LungCisplatinIntegrinsLung NeoplasmsAnimalsAntineoplastic AgentsCD146 AntigenCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMicePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktAntineoplastic AgentsCD146 AntigenCisplatinIntegrinsMCAM protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktCisplatinImmunotherapyIntegrinLung adenocarcinomaMUC14

Identifiers

PMID41656379
PMCPMC12948968

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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.