Evidence map›Paper›PMID 33982666›Full record

ArticleAging2021

TRIM14 regulates melanoma malignancy via PTEN/PI3K/AKT and STAT3 pathways.

Jiangyan Chen, Lin Huang, Jin Quan, Debing Xiang

Open access · greenAbstract read
In one paragraph

Article in Aging, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 24 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

4 authors at 1 institution in 1 country.

Jiangyan ChenDepartment of Oncology, Jiangjin Central Hospital of Chongqing, Chongqing, China.
Lin HuangDepartment of Dermatology, Jiangjin Central Hospital of Chongqing, Chongqing, China.
Jin QuanDepartment of Oncology, Jiangjin Central Hospital of Chongqing, Chongqing, China.
Debing XiangDepartment of Oncology, Jiangjin Central Hospital of Chongqing, Chongqing, China.
Jiangjin Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanoma is one of the most aggressive cancers with poor overall survival. To date, there are still few effective methods for the treatment of melanoma. TRIM14 was previously reported to be an important oncogene in many tumors. Nevertheless, the roles of TRIM14 in melanoma remain unknown. In this study, we found that TRIM14 was abnormally upregulated in melanoma cell lines. Knockdown of TRIM14 suppressed melanoma cell proliferation, migration, invasion, epithelial-mesenchymal transition, and melanin synthesis. Overexpression of TRIM14 had opposite effects on the cellular functions of melanoma cell lines. Further study revealed that TRIM14 knockdown increased PTEN protein levels, which in turn inactivated AKT and STAT3 pathways. Moreover, blocking AKT or STAT3 pathway with a specific inhibitor could partially reverse the promotion of melanoma malignancy mediated by TRIM14 overexpression. In addition,

Indexed as

Cell ProliferationCutaneous Malignant MelanomaEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansIntracellular Signaling Peptides and ProteinsMelanomaProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseSkin NeoplasmsSTAT3 Transcription FactorTripartite Motif ProteinsIntracellular Signaling Peptides and ProteinsProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanSTAT3 protein, humanSTAT3 Transcription FactorTRIM14 protein, humanTripartite Motif ProteinsAKTmelanomaSTAT3TRIM14

Identifiers

PMID33982666
PMCPMC8148494
OpenAlexW3162216723

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.