Evidence map›Paper›PMID 38114532›Full record

ArticleScientific reports2023

KRT13 and UPK1B for differential diagnosis between metastatic lung carcinoma from oral squamous cell carcinoma and lung squamous cell carcinoma.

Hiroyuki Goda, Koh-Ichi Nakashiro, Yoshifumi Sano, Tomoko Adachi, Norihiko Tokuzen, Nobuyuki Kuribayashi, Satoshi Hino, Daisuke Uchida

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. KRT13 Drives Pancreatic Cancer Malignancy Via the PI3K/AKT-PPARG Axis While Enhancing Sensitivity to Navitoclax.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Article
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  3. Article
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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

8 authors.

Hiroyuki GodaDepartment of Oral and Maxillofacial Surgery, Ehime University Graduate School of Medicine, Toon, Japan. hiro9832@m.ehime-u.ac.jp.
Koh-Ichi NakashiroDepartment of Oral and Maxillofacial Surgery, Ehime University Graduate School of Medicine, Toon, Japan.
Yoshifumi SanoDepartment of Cardiovascular and Thoracic Surgery, Ehime University Graduate School of Medicine, Toon, Japan.
Tomoko AdachiDepartment of Oral and Maxillofacial Surgery, Ehime University Graduate School of Medicine, Toon, Japan.
Norihiko TokuzenDepartment of Oral and Maxillofacial Surgery, Ehime University Graduate School of Medicine, Toon, Japan.
Nobuyuki KuribayashiDepartment of Oral and Maxillofacial Surgery, Ehime University Graduate School of Medicine, Toon, Japan.
Satoshi HinoDepartment of Oral and Maxillofacial Surgery, Ehime University Graduate School of Medicine, Toon, Japan.
Daisuke UchidaDepartment of Oral and Maxillofacial Surgery, Ehime University Graduate School of Medicine, Toon, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral squamous cell carcinomas unusually show distant metastasis to the lung after primary treatment, which can be difficult to differentiate from primary squamous cell carcinoma of the lung. While the location and number of tumor nodules is helpful in diagnosing cases, differential diagnosis may be difficult even with histopathological examination. Therefore, we attempted to identify molecules that can facilitate accurate differential diagnosis. First, we performed a comprehensive gene expression analysis using microarray data for OSCC-LM and LSCC, and searched for genes showing significantly different expression levels. We then identified KRT13, UPK1B, and nuclear receptor subfamily 0, group B, member 1 (NR0B1) as genes that were significantly upregulated in LSCC and quantified the expression levels of these genes by real-time quantitative RT-PCR. The expression of KRT13 and UPK1B proteins were then examined by immunohistochemical staining. While OSCC-LM showed no KRT13 and UPK1B expression, some tumor cells of LSCC showed KRT13 and UPK1B expression in 10 of 12 cases (83.3%). All LSCC cases were positive for at least one of these markers. Thus, KRT13 and UPK1B might contribute in differentiating OSCC-LM from LSCC.

Indexed as

Carcinoma, Non-Small-Cell LungCarcinoma, Squamous CellHead and Neck NeoplasmsLung NeoplasmsMouth NeoplasmsDiagnosis, DifferentialGene Expression Regulation, NeoplasticHumansKeratin-13LungSquamous Cell Carcinoma of Head and NeckUroplakin IbKeratin-13KRT13 protein, humanUPK1B protein, humanUroplakin Ib

Identifiers

PMID38114532
PMCPMC10730515

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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.