Evidence map›Paper›PMID 41461671›Full record

ArticleScientific reports2025

The claudin family characteristics in pan-cancer and the role of claudin12 in the malignant progression of lung adenocarcinoma.

Pei Gao, Yan Wu, Yuxin Bian, Yixuan Liu, Weixin Jing

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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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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

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Pei GaoDepartment of Biology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi, 830017, China.
Yan WuDepartment of Biology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi, 830017, China.
Yuxin BianClinical Laboratory Center, the Fourth Affiliated Hospital of Xinjiang Medical University, Urumqi, 830001, China.
Yixuan LiuDepartment of Biology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi, 830017, China.
Weixin JingDepartment of Biology, School of Basic Medical Sciences, Xinjiang Medical University, Urumqi, 830017, China. jing@xjmu.edu.cn.

Funding

Natural Science Foundation of Xinjiang Uygur Autonomous Region 2022D01C200Xinjiang Medical University Doctoral Research Initiation Fund XJMUYJ20210603
6 · The paper itself

Abstract

Claudins (CLDNs), pivotal components of tight junctions (TJs), are integral to epithelial barrier function, cell polarity, and paracellular permeability as well as in tumor initiation and development. Among the histological subtypes of lung cancer, lung adenocarcinoma (LUAD) predominates and is frequently diagnosed at an advanced stage, contributing to its dismal 5-year survival rate and posing a significant threat to patient survival. In this work, the expression, prognosis and diagnostic of CLDNs in pan-cancer were analyzed using bioinformatics. In particular, the relationship between claudin12 (CLDN12) and the expression, prognosis and clinical stage in LUAD was paid attention to, and the diagnostic efficiency of CLDN12 was evaluated by receiver operator characteristic curve. The PPI network was constructed using STRING database, followed by Cytoscape-assisted hub gene identification. Functional enrichment analyses (GO and KEGG) were conducted to elucidate potential signaling pathways linked to CLDN12. These results showed that CLDNs were differentially expressed in pan-cancer, and were valuable for the prognosis and diagnosis of tumors. Specifically, CLDN12 was significantly upregulated in LUAD, correlating with advanced tumor stage, lymph nodes metastasis, and poor survival outcomes. In vitro functional assays revealed that CLDN12 knockdown suppressed LUAD cell proliferation, migration, and invasion while promoting cell apoptosis. In summary, CLDN12 may serve as a promising biomarker for LUAD detection and a potential therapeutic target.

Indexed as

Adenocarcinoma of LungClaudinsLung NeoplasmsApoptosisBiomarkers, TumorCell Line, TumorCell MovementCell ProliferationDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMalePrognosisProtein Interaction MapsBiomarkers, TumorClaudinsClaudin 12InvasionLung adenocarcinomaMigrationPan-cancer

Identifiers

PMID41461671
PMCPMC12749535

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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.