Evidence map›Paper›PMID 40841384›Full record

ArticleScientific reports2025

Genomic analysis identifies TJP3 as a prognostic marker for radiotherapy and chemoradiotherapy in oral squamous cell carcinoma.

Su Kyung Kuk, Jae Il Lee, Jong-Ho Lee, Ik-Jae Kwon, Kang Mi Pang

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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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

The trial behind it

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Su Kyung KukDivision of Biomedical Informatics, College of Medicine, Seoul National University, 101 Daehak-ro, Jongno-gu, Seoul, 03080, Republic of Korea.
Jae Il LeeDepartment of Oral Pathology, School of Dentistry, Seoul National University, 101 Daehak-ro, Jongno-gu, Seoul, 03080, Republic of Korea.
Jong-Ho LeeOral Oncology Clinic, National Cancer Center, 323 Ilsan-ro, Ilsandong-gu, Goyang-si, 10408, Gyeonggi-do, Republic of Korea.
Ik-Jae KwonDepartment of Oral and Maxillofacial Surgery, Dental Research Institute, School of Dentistry, Seoul National University, 101 Daehak-ro, Jongno-gu, Seoul, 03080, Korea. ijkwon@snu.ac.kr.
Kang Mi PangDepartment of Oral Anatomy and Dental Research Institute, School of Dentistry, Seoul National University, 101 Daehak-ro, Jongno-gu, Seoul, 03080, Republic of Korea. pkm81@snu.ac.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study analyzed somatic mutations and differentially expressed genes in primary oral squamous cell carcinoma (OSCC) tumors to identify prognostic markers for radiotherapy (RT) and concurrent chemo-radiation therapy (CCRT). We used longitudinal whole-exome sequencing (WES) data from a patient who developed radiation-induced sarcoma (RIS) after CCRT with public datasets (TCGA and GSE41613) to identify genes associated with 24-month overall survival (OS). Candidates were further refined using Cox regression for OS. Twenty-two prognostic genes were identified and validated in WES data, functioning as indicators of RT and CCRT resistance. In patients with poor outcomes within 24 months post-RT, CLTCL1, RGL3 and H3C12 showed significant prognostic value in multivariate Cox analyses, while SLC35G5, GARS1 and JPH3 were identified as prognostic markers for CCRT. Limited overlap was observed between RT and CCRT, with TJP3 being the only common gene. RNA-seq data from the GSE217645 revealed that TJP3 exhibited significantly altered expression between radiosensitive and radioresistant cell lines (p = 0.037). RT-related genes were predominantly found in primary tumors, whereas CCRT-related genes were distributed across primary tumor, inflamed granulation tissue, inflammatory myofibroblastic proliferation and RIS. These findings provide insights into molecular mechanisms underlying RT and CCRT resistance, supporting future directions in precision medicine.

Indexed as

Biomarkers, TumorCarcinoma, Squamous CellMouth NeoplasmsAgedCell Line, TumorChemoradiotherapyExome SequencingFemaleGene Expression Regulation, NeoplasticGenomicsHumansMaleMiddle AgedMutationPrognosisBiomarkers, TumorConcurrent chemo-radiation therapyOral squamous cell carcinomaPrecision medicineRadiation induced sarcomaRadiotherapy

Identifiers

PMID40841384
PMCPMC12371094

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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.