Evidence map›Paper›PMID 40104702›Full record

ArticleTranslational cancer research2025

Low expression of PRTN3 regulates the progression of gastric cancer by inhibition of cell cycle and promotion of apoptosis.

Haoyu Zhu, Fei Wang, Xinran Lu, Hao Wu, Chao Shi, Silvio Matsas, Renata D'Alpino Peixoto, Marcelo Porfirio Sunagua Aruquipa, Chong Tang, Shichun Feng

Abstract read
In one paragraph

Article in Translational cancer research, 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. Review
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

10 authors.

Haoyu Zhu *Department of Gastrointestinal Surgery, Nantong First People Hospital, Medical School of Nantong University, Nantong, China.
Fei Wang *Department of Gastrointestinal Surgery, Nantong First People Hospital, Nantong, China.
Xinran LuDepartment of Gastrointestinal Surgery, Nantong First People Hospital, Medical School of Nantong University, Nantong, China.
Hao WuDepartment of Gastrointestinal Surgery, Nantong First People Hospital, Nantong, China.
Chao ShiDepartment of Pathology, Nantong First People Hospital, Nantong, China.
Silvio MatsasCentro de Estudos e Pesquisas de Hematologia e Oncologia (CEPHO), Santo André, SP, Brazil.
Renata D'Alpino PeixotoDepartment of Medical Oncology, BC Cancer Agency, Vancouver, BC, Canada.
Marcelo Porfirio Sunagua AruquipaDepartment of Gastrointestinal Oncology, Oncoclinicas, São Paulo, SP, Brazil.
Chong TangDepartment of Gastrointestinal Surgery, Nantong First People Hospital, Nantong, China.
Shichun FengDepartment of Gastrointestinal Surgery, Nantong First People Hospital, Nantong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Proteinase 3 (PRTN3) has been linked to the progression of different cancer types. In this study, the expression and cell biological function of PRTN3 were investigated in gastric cancer (GC) to assess its role in GC progression. Methods: The PRTN3 levels in 20 pairs of GC tissues were detected via quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR) and Western blotting, while immunohistochemical staining was used to assess the PRTN3 levels in 47 GC tissue samples. The effects of stable lentivirus-mediated PRTN3 knockdown on GC cell proliferative, cell cycle, and apoptotic activity were evaluated using Cell Counting Kit-8 (CCK-8) and colony formation assays, nude mouse models, and flow cytometry. Results: Elevated levels of PRTN3 messenger RNA (mRNA) and protein were noted in GC tissues, mostly in the cytosol. High PRTN3 levels were positively correlated with GC tumor N staging. Conclusions: Our study found that high expression of PRTN3 is associated with GC tumor N staging. And PRTN3 silencing could regulate GC progression by inhibiting the cell cycle and promoting apoptosis in GC cells, which could be a potential target for GC diagnosis and treatment.

Indexed as

apoptosiscyclegastric cancer (GC)proliferationProteinase 3 (PRTN3)

Identifiers

PMID40104702
PMCPMC11912076

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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.