Evidence map›Paper›PMID 30484495›Full record

ArticleBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas2018

NOP14 inhibits melanoma proliferation and metastasis by regulating Wnt/β-catenin signaling pathway.

Jingrong Li, Ruihua Fang, Jianqin Wang, Liehua Deng

RetractedErratum issuedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-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

12 citing papers in PubMed, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Jingrong LiDepartment of Dermatology, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Ruihua FangDepartment of Dermatology, Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou, China.
Jianqin WangDepartment of Dermatology, Guangzhou Institute of Dermatology, Guangzhou, China.
Liehua DengDepartment of Dermatology, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Guangzhou Medical University · CNFirst Affiliated Hospital of Jinan University · CNGuangzhou Institute of Dermatology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignant melanoma is an aggressive skin cancer with a high mortality rate. Nucleolar protein 14 (NOP14) has been implicated in cancer development. However, the role of NOP14 in malignant melanoma progression remains largely unclear. In this study, we observed that malignant melanoma tissue showed NOP14 down-regulation compared to melanocytic nevi tissues. Moreover, we observed that NOP14 expression was significantly associated with melanoma tumor thickness and lymph node metastasis. NOP14 overexpression in melanoma cells suppressed proliferation, caused G1 phase arrest, promoted apoptosis, and inhibited melanoma cell migration and invasion. Further investigations revealed that NOP14 overexpression reduced the expression levels of Wnt3a, β-catenin, and GSK-3β of the Wnt/β-catenin pathway. In summary, we demonstrated that NOP14 inhibited melanoma cell proliferation and metastasis by regulating the Wnt/β-catenin signaling pathway.

Indexed as

Apoptosisbeta CateninBlotting, WesternCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansImmunohistochemistryLymphatic MetastasisMaleMelanomaMiddle AgedNuclear ProteinsReverse Transcriptase Polymerase Chain Reactionbeta CateninNOP14 protein, humanNuclear Proteins

Identifiers

PMID30484495
PMCPMC6262753
OpenAlexW2901247462

What OpenQuestion holds

Textmetadata
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.