Evidence map›Paper›PMID 37929660›Full record

ArticleJournal of cellular and molecular medicine2024

PIN1P1 is activated by CREB1 and promotes gastric cancer progression via interacting with YBX1 and upregulating PIN1.

Ya-Wen Wang, Wen-Jie Zhu, Ran-Ran Ma, Ya-Ru Tian, Xu Chen, Peng Gao

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Ya-Wen WangDepartment of Pathology, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Wen-Jie ZhuDepartment of Pathology, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Ran-Ran MaDepartment of Pathology, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Ya-Ru TianDepartment of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Science, Jinan, Shandong, China.
Xu ChenDepartment of Pathology, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Peng GaoDepartment of Pathology, Qilu Hospital of Shandong University, Jinan, Shandong, China.ORCID 0000-0002-4721-0887
Shandong University · CNShandong Tumor Hospital · CN

Funding

National Natural Science Foundation of China 81802406National Natural Science Foundation of China 81902698Natural Science Foundation of Shandong Province ZR2019BH034Natural Science Foundation of Shandong Province ZR2019BH061Natural Science Foundation of Shandong Province ZR2020LZL009
6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) play critical roles in the carcinogenesis and progression of cancers. However, the role and mechanism of the pseudogene lncRNA PIN1P1 in gastric carcinoma remain unclear. The expression and effects of lncRNA PIN1P1 in gastric cancer were investigated. The transcriptional regulation of CREB1 on PIN1P1 was determined by ChIP and luciferase assays. The mechanistic model of PIN1P1 in gastric cancer was further explored by RNA pull-down, RIP and western blot analysis. PIN1P1 was overexpressed in gastric cancer tissues, and upregulated PIN1P1 predicted poor prognosis in patients. CREB1 was directly combined with the promoter region of PIN1P1 to promote the transcription of PIN1P1. CREB1-mediated enhanced proliferation, migration and invasion could be partially reversed by downregulation of PIN1P1. Overexpressed PIN1P1 promoted the proliferation, migration and invasion of gastric cancer cells, whereas decreased PIN1P1 showed the opposite effects. PIN1P1 directly interacted with YBX1 and promoted YBX1 protein expression, leading to upregulation of PIN1, in which E2F1 may be involved. Silencing of YBX1 during PIN1P1 overexpression could partially rescue PIN1 upregulation. PIN1, the parental gene of PIN1P1, was elevated in gastric cancer tissues, and its upregulation was correlated with poor patient outcomes. PIN1 facilitated gastric cancer cell proliferation, migration and invasion. To sum up, CREB1-activated PIN1P1 could promote gastric cancer progression through YBX1 and upregulating PIN1, suggesting that it is a potential target for gastric cancer.

Indexed as

RNA, Long NoncodingStomach NeoplasmsCell Line, TumorCell MovementCell ProliferationCyclic AMP Response Element-Binding ProteinGene Expression Regulation, NeoplasticHumansNIMA-Interacting Peptidylprolyl IsomeraseY-Box-Binding Protein 1CREB1 protein, humanCyclic AMP Response Element-Binding ProteinNIMA-Interacting Peptidylprolyl IsomerasePIN1 protein, humanRNA, Long NoncodingY-Box-Binding Protein 1YBX1 protein, humanCREB1gastric cancerlncRNAPIN1PIN1P1pseudogeneYBX1

Identifiers

PMID37929660
PMCPMC10805483
OpenAlexW4388421129

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.