Evidence map›Paper›PMID 42424412›Full record

ArticlePloS one2026

Compressive stress inhibits proliferation in AsPC-1 pancreatic cancer cells and reduction of Myc protein.

Fuko Miyake, Seiichiro Ishihara, Naomi Ando, Shoichiro Tange, Atsushi Enomoto, Hisashi Haga

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Fuko MiyakeDivision of Soft Matter, Graduate School of Life Science, Hokkaido University, Sapporo, Hokkaido, Japan.
Seiichiro IshiharaDepartment of Advanced Transdisciplinary Sciences, Faculty of Advanced Life Science, Hokkaido University, Sapporo, Hokkaido, Japan.ORCID https://orcid.org/0009-0000-6148-449X
Naomi AndoDivision of Soft Matter, Graduate School of Life Science, Hokkaido University, Sapporo, Hokkaido, Japan.
Shoichiro TangeDivision of Medical Genome Sciences, Department of Genomic and Preventive Medicine, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.
Atsushi EnomotoDepartment of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
Hisashi HagaDepartment of Advanced Transdisciplinary Sciences, Faculty of Advanced Life Science, Hokkaido University, Sapporo, Hokkaido, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer cells grow in confined tumor microenvironments and push the surrounding tissue, which reacts and exposes them to compressive stress. Previous studies have revealed that compressive stress inhibits proliferation in breast and colorectal cancer cells. It has been reported that pancreatic tumors accumulate compressive stress in vivo, but it is not well understood whether compressive stress regulates proliferation in pancreatic cancer cells. Therefore, the effect of compressive stress on the proliferation of human pancreatic cancer cells was investigated in this study. We found that the growth of compressed AsPC-1 human pancreatic cancer cells was slower than that of uncompressed cells. Furthermore, the protein expression of Myc was reduced in compressed cells, which inhibited their proliferation. In addition, the expression of Snail, which is correlated with poor prognosis in pancreatic cancer patients, was promoted by compressive stress and the inhibition of Myc. These results suggest that compressive stress inhibits proliferation and triggers Snail expression via the reduction of Myc protein in AsPC-1 pancreatic cancer cells.

Indexed as

Cell ProliferationPancreatic NeoplasmsProto-Oncogene Proteins c-mycStress, MechanicalCell Line, TumorGene Expression Regulation, NeoplasticHumansSnail Family Transcription FactorsTranscription FactorsMYC protein, humanProto-Oncogene Proteins c-mycSnail Family Transcription FactorsTranscription Factors

Identifiers

PMID42424412
PMCPMC13349192

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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.