Evidence map›Paper›PMID 36684109›Full record

ArticleBioengineering & translational medicine2023

Pin1/YAP pathway mediates matrix stiffness-induced epithelial-mesenchymal transition driving cervical cancer metastasis via a non-Hippo mechanism.

Long Yang, Jingwen Li, Guangchao Zang, Sijie Song, Zhengwen Sun, Xinyue Li, Yuanzhu Li, Zhenhong Xie, Guangyuan Zhang, Ni Gui and 4 more

Open access · goldAbstract read
In one paragraph

Article in Bioengineering & translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.2field-weighted citation impact, top 7% of its field
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

20 citing papers in PubMed, 31 citations in OpenAlex.

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  17. The molecular mechanisms of peptidyl-prolylFrontiers in pharmacology · 2024
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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

14 authors at 1 institution in 1 country.

Long YangLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.
Jingwen LiLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.
Guangchao ZangLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.
Sijie SongLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.
Zhengwen SunLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.
Xinyue LiLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.
Yuanzhu LiLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.
Zhenhong XieLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.
Guangyuan ZhangLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.
Ni GuiLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.
Shu ZhuLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.
Tingting ChenLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.
Yikui CaiLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.
Yinping ZhaoLaboratory of Tissue and Cell Biology Lab Teaching & Management Center, Chongqing Medical University Yuzhong District, Chongqing China.ORCID https://orcid.org/0000-0002-4801-364X
Chongqing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer metastasis is an important cause of death in cervical cancer. Previous studies have shown that epithelial-mesenchymal transition (EMT) of tumors promotes its invasive and metastatic capacity. Alterations in the extracellular matrix (ECM) and mechanical signaling are closely associated with cancer cell metastasis. However, it is unclear how matrix stiffness as an independent cue triggers EMT and promotes cervical cancer metastasis. Using collagen-coated polyacrylamide hydrogel models and animal models, we investigated the effect of matrix stiffness on EMT and metastasis in cervical cancer. Our data showed that high matrix stiffness promotes EMT and migration of cervical cancer hela cell lines in vitro and in vivo. Notably, we found that matrix stiffness regulates yes-associated protein (YAP) activity via PPIase non-mitotic a-interaction 1 (Pin1) with a non-Hippo mechanism. These data indicate that matrix stiffness of the tumor microenvironment positively regulates EMT in cervical cancer through the Pin1/YAP pathway, and this study deepens our understanding of cervical cancer biomechanics and may provide new ideas for the treatment of cervical cancer.

Indexed as

epithelial–mesenchymal transitionextracellular matrix stiffnessPPIase non‐mitotic a‐interaction 1yes‐associated protein

Identifiers

PMID36684109
PMCPMC9842039
OpenAlexW4283773787

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.