Evidence map›Paper›PMID 40504175›Full record

ArticleCancer science2025

Implication of KLHL Gene Family Member KLHL5 in Colorectal Cancer Progression and Prognosis.

Konomu Uno, Hirotada Nishie, Hiromi Hiyoshi, Kyosuke Habu, Jun Nakayama, Sota Tate, Tomohisa Sakaue, Eiji Kubota, Mamoru Tanaka, Takaya Shimura and 3 more

Abstract read
In one paragraph

Article in Cancer science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Konomu UnoDepartment of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID https://orcid.org/0009-0006-2164-5205
Hirotada NishieDepartment of Gastroenterology, Nagoya City University Midori Municipal Hospital, Nagoya, Japan.
Hiromi HiyoshiDepartment of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Kyosuke HabuDepartment of Biochemistry and Molecular Genetics, Ehime University Graduate School of Medicine, Ehime, Japan.
Jun NakayamaDepartment of Oncogenesis and Growth Regulation, Research Institute, Osaka International Cancer Institute, Osaka, Japan.ORCID https://orcid.org/0000-0001-8844-4295
Sota TateDepartment of Biochemistry and Molecular Genetics, Ehime University Graduate School of Medicine, Ehime, Japan.
Tomohisa SakaueDepartment of Biochemistry and Molecular Genetics, Ehime University Graduate School of Medicine, Ehime, Japan.
Eiji KubotaDepartment of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Mamoru TanakaDepartment of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID https://orcid.org/0000-0001-8416-5774
Takaya ShimuraDepartment of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID https://orcid.org/0000-0002-6048-0021
Hiromi KataokaDepartment of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID https://orcid.org/0000-0001-9491-0723
Takashi JohDepartment of Gastroenterology, Gamagori Municipal Hospital, Gamagori, Japan.
Shigeki HigashiyamaDepartment of Biochemistry and Molecular Genetics, Ehime University Graduate School of Medicine, Ehime, Japan.ORCID https://orcid.org/0000-0002-2417-3921

Funding

Japan Society for the Promotion of Science 17K09357
6 · The paper itself

Abstract

The KLHL gene family member KLHL5, which is a constituent factor of the RING E3 ubiquitin ligase complex, is expressed in various types of cancers and plays a role in cancer pathophysiology. In this study, we identified KLHL5 as a potential biomarker for predicting the prognosis of colorectal cancer (CRC) from 42 KLHL family genes using transcriptome profiles generated by RNA-seq analysis of The Cancer Genome Atlas colorectal adenocarcinoma (TCGA-COAD). We further investigated the implication of KLHL5 in CRC using pathological examination and bioinformatics analyses. Clinicopathological analyses revealed that KLHL5 was more highly expressed in CRC than in adjacent normal mucosa, and its expression level increased concomitantly with the CRC stage (p < 0.05). KLHL5 expression was associated with poor prognostic factors such as depth of invasion (p < 0.001), lymphovascular invasion (p = 0.029), and lymph node metastasis (p = 0.025). Notably, KLHL5 exhibited heterogeneous expression within the tumor, with pronounced expression observed at the invasive front of the tumor (p < 0.0001). Through bioinformatics analyses, we determined that elevated KLHL5 expression in CRC is significantly associated with poor prognosis. Furthermore, analysis from the Gene Expression Omnibus database indicated that KLHL5 expression was more pronounced in the common molecular subtype (CMS) 4 CRC, which is characterized as highly advanced, and the overall and recurrence-free survival rates were poor compared to other CMS groups. Our findings indicate that KLHL5 plays a pivotal role in the progression and development of CRC, and can be used as a potential biomarker and therapeutic target for CRC treatment.

Indexed as

Biomarkers, TumorColorectal NeoplasmsAgedComputational BiologyDisease ProgressionFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansLymphatic MetastasisMaleMiddle AgedPrognosisTranscriptomeBiomarkers, Tumoradenocarcinomabiomarkerscolorectal neoplasmspathologytranscriptome

Identifiers

PMID40504175
PMCPMC12400045

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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.