Evidence map›Paper›PMID 41214651›Full record

ArticleBMC veterinary research2025

PRC1, CDCA3, and CDC20 are upregulated and Treg numbers are decreased in canine massive hepatocellular carcinoma.

Toshiyuki Tanaka, Tomoki Motegi, Yasumasa Iimori, Hideo Akiyoshi

Abstract read
In one paragraph

Article in BMC veterinary research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. 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

4 authors.

Toshiyuki Tanaka *Laboratory of Veterinary Advanced Diagnosis and Treatment, School of Veterinary Science, Osaka Metropolitan University, Osaka, Japan.
Tomoki Motegi *Laboratory of Veterinary Molecular Pathophysiology Treatment, Cooperative Department of Veterinary Medicine, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Tokyo, Japan.
Yasumasa IimoriPurdue University School of Veterinary Medicine, West Lafayette, IN, USA.
Hideo AkiyoshiNeovets Veterinary Referral Center, Osaka, Japan. hideo.akiyoshi@gmail.com.

Funding

Japan Society for the Promotion of Science 22K05991
6 · The paper itself

Abstract

backgroundThe mechanisms underlying the development and prognosis of hepatocellular carcinoma (HCC) differ between dogs and humans. Although genetic alterations can cause carcinogenesis, the genetic alterations in canine HCC may differ from those observed in human HCC. In humans, various signaling pathways, oncogenes, and tumor suppressor genes are associated with HCC oncogenesis. Immune cells have been reported to be associated with prognosis. In canine HCC, the genes related to oncogenesis and prognosis remain unclear. Therefore, in this study, we used RNA sequencing to comprehensively evaluate abnormally expressed genes and infer immune cell composition in canine HCC.

resultsFourteen dogs histopathologically diagnosed with HCC and four dogs with normal livers (NL) were included in this study. No HCC recurrence or metastasis was observed. A total of 260 differentially expressed genes were identified in dogs with HCC compared to those in NL dogs. Among them, 119 were downregulated and 141 were upregulated in HCC. Among the ontology and oncogenic signature gene sets, PRC1, CDCA3, and CDC20 were upregulated in the top 20 genes. Regulatory T cells (Treg) levels were decreased in the livers of dogs with HCC compared to those in normal livers.

conclusionsPRC1, CDCA3, and CDC20 were upregulated and were identified as candidate oncogenic genes in canine massive HCC. Downregulation of Tregs may be associated with prognosis in canine massive HCC.

Indexed as

Carcinoma, HepatocellularCdc20 ProteinsCell Cycle ProteinsDog DiseasesLiver NeoplasmsT-Lymphocytes, RegulatoryAnimalsDogsFemaleGene Expression Regulation, NeoplasticMaleUp-RegulationCdc20 ProteinsCell Cycle ProteinsDogLiverOncogeneOncogenic mechanismRNA sequence

Identifiers

PMID41214651
PMCPMC12604188

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LicenceCC BY-NC-ND
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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.