Evidence map›Paper›PMID 37506150›Full record

ArticleImmunity, inflammation and disease2023

PABPC1 promotes cell proliferation and metastasis in pancreatic adenocarcinoma by regulating COL12A1 expression.

Weijie Yao, Yanrong Yao, Wen He, Chengsi Zhao, Di Liu, Genwang Wang, Zuozheng Wang

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

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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

11 citing papers in PubMed, 17 citations in OpenAlex.

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  7. The Multifaced Role of Collagen in Cancer Development and Progression.International journal of molecular sciences · 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

7 authors at 1 institution in 1 country.

Weijie YaoDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Yanrong YaoDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Wen HeDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Chengsi ZhaoDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Di LiuDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Genwang WangDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Zuozheng WangDepartment of Hepatobiliary Surgery, General Hospital of Ningxia Medical University, Yinchuan, China.ORCID 0000-0002-3834-1404
Ningxia Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe expression of cytoplasmic poly (A) binding protein-1 (PABPC1) has been reported in multiple cancer types. This protein is known to modulate cancer progression. However, the effects of PABPC1 expression in pancreatic adenocarcinoma (PAAD) have not been investigated. Here, we investigate the regulatory targets and molecular mechanisms of PABPC1 in PAAD.

methodsPABPC1 and collagen type XII α1 chain (COL12A1) expression in PAAD and their role in tumor prognosis and tumor stage were investigated using The Cancer Genome Atlas database analysis. After silencing PABPC1, messenger RNA sequencing and Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were performed. The expression of differentially expressed genes (DEGs), cell viability, apoptosis, and cell migration and invasion were explored using reverse transcription-quantitative polymerase chain reaction, Cell Counting Kit-8 assay, flow cytometry assay, and transwell assay, respectively. The relationship between PABPC1 and COL12A1 expression was assessed by Pearson's correlation analysis. The regulatory function of COL12A1 in PABPC1-affected BXPC3 cell behavior was studied after COL12A1 was overexpressed.

resultsPABPC1 and COL12A1 expression was upregulated in patients with PAAD and was linked to poor prognosis. Four hundred and seventy-four DEGs were observed in BXPC3 cells after PABPC1 silencing. GO and KEGG analyses revealed that the top 10 DEGs were enriched in cell adhesion pathways. Additionally, PABPC1 silencing inhibited cell viability, migration, and invasion and accelerated apoptosis in BXPC3 cells. PABPC1 silencing increased AZGP1 and ARHGAP30 expression and decreased CAV1 and COL12A1 expression in BXPC3 cells. PABPC1 positively mediated COL12A1 expression, whereas PABPC1 knockdown induced the inhibition of BXPC3 cell proliferation, migration, and invasion.

conclusionThe results of this study indicate that PABPC1 may function as a tumor promoter in PAAD, accelerating BXPC3 cell proliferation and metastasis by regulating COL12A1 expression.

Indexed as

AdenocarcinomaPancreatic NeoplasmsCell ProliferationCollagen Type XIIGTPase-Activating ProteinsHumansPoly(A)-Binding Protein IPrognosisARHGAP30 protein, humanCOL12A1 protein, humanCollagen Type XIIGTPase-Activating ProteinsPoly(A)-Binding Protein Icell metastasiscollagen type XII α1 chain (COL12A1)PABPC1pancreatic adenocarcinoma

Identifiers

PMID37506150
PMCPMC10336663
OpenAlexW4384068294

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LicenceCC BY
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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.