Evidence map›Paper›PMID 32002038›Full record

ArticleOncology letters2020

Upregulation of contactin-1 expression promotes prostate cancer progression.

Boren Wang, Xi Yang, Ting Zhao, Hanghang Du, Tong Wang, Suping Zhong, Bo Yang, Hui Li

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 20% 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, 16 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

8 authors at 1 institution in 1 country.

Boren WangMedical School of Jishou University, Jishou, Hunan 416000, P.R. China.
Xi YangMedical School of Jishou University, Jishou, Hunan 416000, P.R. China.
Ting ZhaoMedical School of Jishou University, Jishou, Hunan 416000, P.R. China.
Hanghang DuMedical School of Jishou University, Jishou, Hunan 416000, P.R. China.
Tong WangMedical School of Jishou University, Jishou, Hunan 416000, P.R. China.
Suping ZhongMedical School of Jishou University, Jishou, Hunan 416000, P.R. China.
Bo YangDepartment of Pathology, First Affiliated Hospital of Jishou University, Jishou, Hunan 416000, P.R. China.
Hui LiDepartment of Microbiology and Immunology, Medical School of Jishou University, Jishou, Hunan 416000, P.R. China.
Jishou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Contactin-1 (CNTN-1) has been reported to serve an oncogenic role in several cancer types. However, detailed mechanisms describing the influence of CNTN-1 in prostate cancer progression have not yet been elucidated. The present study aimed to determine the clinical significance of CNTN-1 expression in prostate cancer progression, and also to investigate the regulatory role of CNTN-1 in the proliferation, migration and invasive ability of prostate cancer cells. The results of the present study indicated that expression levels of CNTN-1 were significantly higher in prostate cancer tissues compared with adjacent normal tissues. Moreover, a high expression level of CNTN-1 was positively correlated with tumor size, stage and metastasis, as well as a poorer prognosis in patients with prostate cancer. Furthermore, CNTN-1-knockdown in prostate cancer cells (using short hairpin RNA) resulted in the significant inhibition of cancer cell proliferation, colony formation, migration and invasiveness. Silencing of CNTN-1 expression also suppressed epithelial-mesenchymal transition in prostate cancer cells via the upregulation of E-cadherin, and the downregulation of N-cadherin and vimentin expression. Inhibition of CNTN-1 expression also reduced the activity of the PI3K/AKT signaling pathway in prostate cancer cells. Thus, it was demonstrated that CNTN-1 expression is upregulated, and plays an oncogenic role, in prostate cancer cells. The results of the current study suggest that CNTN-1 may represent a promising therapeutic target, potentially improving the treatment of patients with prostate cancer.

Indexed as

contactin-1invasionmigrationproliferationprostate cancer

Identifiers

PMID32002038
PMCPMC6960391
OpenAlexW2997180421

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.