Evidence map›Paper›PMID 30242913›Full record

ArticleMolecular carcinogenesis2019

PADI4 stimulates esophageal squamous cell carcinoma tumor growth and up-regulates CA9 expression.

Chunyan Liu, Junyi Tang, Chang Li, Guangbo Pu, Dongxia Yang, Xiaotian Chang

Open access · hybridAbstract read
In one paragraph

Article in Molecular carcinogenesis, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
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  9. PADI3 induces cell cycle arrestCancer biology & medicine · 2019
    Article
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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.

Chunyan LiuMedical Research Center of Shandong Qianfoshan Hospital, Shandong University, Jinan, Shandong, P. R. China.
Junyi TangMedical Research Center of Shandong Qianfoshan Hospital, Shandong University, Jinan, Shandong, P. R. China.
Chang LiTengzhou People's Central Hospital, Tengzhou, Shandong, P. R. China.
Guangbo PuTengzhou People's Central Hospital, Tengzhou, Shandong, P. R. China.
Dongxia YangMedical Research Center of Shandong Qianfoshan Hospital, Shandong University, Jinan, Shandong, P. R. China.
Xiaotian ChangMedical Research Center of Shandong Qianfoshan Hospital, Shandong University, Jinan, Shandong, P. R. China.ORCID 0000-0002-7639-7740
Shandong University · CNTengzhou Central People's Hospital · CN

Funding

The National Natural Science Foundation of China Basic Research Program of China 81702440The National Natural Science Foundation of China Basic Research Program of China No. 81802422The Natural Science Foundation of Shandong Province ZR2015HL059The Projects of Medical and Health Technology Development Program in Shandong Province 2014WS0360The Shandong Provincial Key R & D programs 2014GSF118135The Shandong Provincial Key R & D programs 2015GGH3180819The Shandong Provincial Key R & D programs 2017GSF218102The Shandong Provincial Key R & D programs GG201703080038
6 · The paper itself

Abstract

An increasing amount of evidence indicates that peptidylarginine deiminase isoform 4 (PADI4) plays an important role in tumorigenesis. However, the effects of PADI4 on tumor-bearing mice are unknown, and no studies have investigated this tumorigenic pathway in an animal model. In the present study, ECA109 cells originating from esophageal squamous cell carcinoma (ESCC) were transfected with PADI4-expressing lentivirus and were injected into BALB/c nude mice. Tumor size and weight were significantly increased in the mouse tumors established with PADI4-overexpressing ECA109 cells. PCR array analysis revealed increased CA9 expression in ECA109 cells transfected with a PADI4-expressing plasmid, while decreased CA9 expression levels were detected in cells transfected with anti-PADI4 siRNA. Furthermore, up-regulation of CA9 expression was detected in mouse tumors established with PADI4-overexpressing cells. Immunohistochemistry detected the increased expression and co-localization of PADI4 and CA9 in ESCC tissues compared with adjacent non-tumor tissues and normal tissue controls. These results were verified using Western blotting. Cell proliferation significantly increased or decreased in ECA109 and EC9706 (another ESCC-originating cell line) cells transfected with a PADI4-expressing plasmid or anti-PADI4 siRNA, respectively. The above findings suggest that increased PADI4 expression in ESCC stimulates tumor growth and up-regulates CA9 expression, which is known to promote metastatic properties in tumor cells.

Indexed as

Cell ProliferationGene Expression Regulation, NeoplasticAnimalsAntigens, NeoplasmApoptosisBiomarkers, TumorCarbonic Anhydrase IXCarcinoma, Squamous CellEsophageal NeoplasmsHumansMiceMice, Inbred BALB CMice, NudePrognosisProtein-Arginine DeiminasesProtein-Arginine Deiminase Type 4Antigens, NeoplasmBiomarkers, TumorCA9 protein, humanCarbonic Anhydrase IXPADI4 protein, humanpeptidylarginine deiminase 4, mouseProtein-Arginine DeiminasesProtein-Arginine Deiminase Type 4carbonic anhydrase 9 (CA9)esophageal squamous cell carcinoma (ESCC)peptidylarginine deiminase isoform 4 (PADI4)

Identifiers

PMID30242913
PMCPMC6588094
OpenAlexW2890922981

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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 OpenQuestion graph.