Evidence map›Paper›PMID 33084485›Full record

ArticleBioengineered2020

A new metabolic signature contributes to disease progression and predicts worse survival in melanoma.

Mengdi Wan, Binyu Zhuang, Xiao Dai, Liang Zhang, Fangqing Zhao, Yan You

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 11 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

6 authors at 1 institution in 1 country.

Mengdi WanDepartment of Dermatology, The Forth Hospital of Harbin Medical University , Harbin, China.
Binyu ZhuangDepartment of Dermatology, The Forth Hospital of Harbin Medical University , Harbin, China.
Xiao DaiDepartment of Dermatology, The Forth Hospital of Harbin Medical University , Harbin, China.
Liang ZhangDepartment of Dermatology, The Forth Hospital of Harbin Medical University , Harbin, China.
Fangqing ZhaoDepartment of Dermatology, The Forth Hospital of Harbin Medical University , Harbin, China.
Yan YouDepartment of Dermatology, The Forth Hospital of Harbin Medical University , Harbin, China.ORCID 0000-0002-2564-828X
Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic reprogramming is a common hallmark of tumor cells and is a crucial mediator of resistance toward anticancer therapies. The pattern of a metabolism-related signature in melanoma remains unknown. Here, we explored the role of a multi-metabolism-related gene signature in melanoma.We used the training and validation sets to develop a multi-metabolism-related gene signature. Cox regression analysis and the least absolute shrinkage and selection operator (LASSO) method were used for constructing a model. The predictive role of the metabolic signature with clinicopathological features of melanoma was also analyzed. Functional analysis of this metabolic signature was also investigated.A ten metabolism-related gene signature was identified and can stratify melanoma into high- and low- risk groups. The signature was correlated with progressive T stage, Breslow thickness, Clark level, and worse survival (all

Indexed as

AdolescentAdultAgedAged, 80 and overBiomarkers, TumorDisease ProgressionGene Expression Regulation, NeoplasticHumansMelanomaMiddle AgedPrognosisProportional Hazards ModelsYoung AdultBiomarkers, TumorimmunemelanomaMetabolismprognosisprogression

Identifiers

PMID33084485
PMCPMC8291831
OpenAlexW3094622670

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.