Evidence map›Paper›PMID 36952469›Full record

ArticlePloS one2023

FOXP1 inhibits pancreatic cancer growth by transcriptionally regulating IRF1 expression.

Le Wang, Ping Luo, Zhiwen Yang, Xiaoming Zhong, Changxue Ji

Open access · goldFull text read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

9 citing papers in PubMed, 7 citations in OpenAlex.

  1. FOXP1 exacerbates allergic rhinitis progression by mediating ferroptosis in nasal mucosal epithelial cells via transcriptional regulation of SDHAF2.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
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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

5 authors at 3 institutions in 1 country.

Le WangGraduate School, Medical College, Nanchang University, Nanchang, Jiangxi Province, China.
Ping LuoDepartment of Breast Surgery, Nanchang Third Hospital, Nanchang, China.
Zhiwen YangDepartment of Pharmacy, Songjiang District Central Hospital, Shanghai, China.
Xiaoming ZhongGraduate School, Medical College, Nanchang University, Nanchang, Jiangxi Province, China.
Changxue JiDepartment of Vascular Interventional Radiology, Songjiang District Central Hospital, Shanghai, China.ORCID 0000-0002-7372-0311
Nanchang University · CNSongjiang District Central Hospital · CNThird Hospital of Nanchang · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

FOXP1, known as a Forkhead-box (FOX) family protein, plays an important role in human tumorigenesis. However, the function and molecular mechanism of FOXP1 in pancreatic cancer (PC) remain unclear. Here, we report that PC patients with FOXP1 overexpression had a higher survival rate compared to patients with low- FOXP1 expression. Additionally, high expression of FOXP1 can markedly inhibit the growth of pancreatic cancer in vivo and in vitro, whereas low expression of FOXP1 effectively promoted the tumorigenesis. Mechanistically, FOXP1 could directly bind the IRF1 promoter, which triggered the transcriptional activity of IRF1. Taken together, FOXP1 suppressed PC growth via IRF1-dependent manner, serving as a potential prognostic biomarker for patients with PC.

Indexed as

Pancreatic NeoplasmsRepressor ProteinsCarcinogenesisForkhead Transcription FactorsHumansInterferon Regulatory Factor-1Promoter Regions, GeneticForkhead Transcription FactorsFOXP1 protein, humanInterferon Regulatory Factor-1IRF1 protein, humanRepressor Proteins

Identifiers

PMID36952469
PMCPMC10035899
OpenAlexW4360609234

What Socratic holds

Textfull text, public
LicenceCC BY
measurements read27
identifiers read8
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.