Evidence map›Paper›PMID 32258098›Full record

ArticleBioMed research international2019

STC2 Is a Potential Prognostic Biomarker for Pancreatic Cancer and Promotes Migration and Invasion by Inducing Epithelial-Mesenchymal Transition.

Chen Lin, Lina Sun, Shenglei Huang, Xiangqun Weng, Zhixian Wu

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2019. 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
3.3field-weighted citation impact, top 8% 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, 33 citations in OpenAlex.

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  9. Stanniocalcin 2 (STC2): a universal tumour biomarker and a potential therapeutical target.Journal of experimental & clinical cancer research : CR · 2022
    Review
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  18. Solasodine, Isolated fromDrug design, development and therapy · 2021
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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 1 institution in 1 country.

Chen LinDepartment of General Surgery, Fuzhou General Hospital (Dongfang Hospital), Xiamen University, Fuzhou, Fujian 350025, China.ORCID https://orcid.org/0000-0002-6453-7996
Lina SunDepartment of Presbyatrics, Fuzhou General Hospital (Dongfang Hospital), Xiamen University, Fuzhou, Fujian 350025, China.ORCID https://orcid.org/0000-0002-5035-0848
Shenglei HuangDepartment of Hepatobiliary Disease, Fuzhou General Hospital (Dongfang Hospital), Xiamen University, Fuzhou, Fujian 350025, China.ORCID https://orcid.org/0000-0001-5269-6319
Xiangqun WengDepartment of General Practice, Fuzhou General Hospital (Dongfang Hospital), Xiamen University, Fuzhou, Fujian 350025, China.ORCID https://orcid.org/0000-0001-6403-3694
Zhixian WuDepartment of Hepatobiliary Disease, Fuzhou General Hospital (Dongfang Hospital), Xiamen University, Fuzhou, Fujian 350025, China.ORCID https://orcid.org/0000-0002-0708-6770
Xiamen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant expression of stanniocalcin 2 (STC2) is implicated in cancer development. STC2 acts as a tumor promoter to drive some cancers. However, its contribution to the development of pancreatic cancer remains unclear. This study showed that the expression of STC2 was significantly upregulated in pancreatic cancer tissues. Moreover, its expression was positively correlated with tumor size and lymph node metastasis and negatively correlated with 5-year survival rate of pancreatic cancer patients. Additionally, the expression levels of STC2 were a novel biomarker for predicting overall survival rate after surgery. Furthermore, overexpression of STC2 could promote the proliferation, migration, and invasion of pancreatic cancer cell lines, while knocking down of STC2 led to antiproliferation and antimetastasis activities. Further mechanistic investigations revealed that the expression of STC2 could significantly promote the epithelial-mesenchymal transition (EMT) in pancreatic cancer cells. These data indicated that the overexpression of STC2 in pancreatic cancer contributes to the metastasis through the promotion of EMT, suggesting that STC2 is a potential prognostic biomarker and therapeutic target for pancreatic cancer.

Indexed as

Biomarkers, TumorCell MovementNeoplastic ProcessesAgedCell Line, TumorCell ProliferationEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticGlycoproteinsHEK293 CellsHumansIntercellular Signaling Peptides and ProteinsLymphatic MetastasisMaleMiddle AgedBiomarkers, TumorGlycoproteinsIntercellular Signaling Peptides and ProteinsSTC2 protein, human

Identifiers

PMID32258098
PMCPMC7099867
OpenAlexW2957388330

What OpenQuestion holds

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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 OpenQuestion graph.