Evidence map›Paper›PMID 36534449›Full record

ArticleAging2022

A nomogram for predicting prognosis of multiple myeloma patients based on a ubiquitin-proteasome gene signature.

Dexiang Ji, Yong Liu, Wenjie Sun, Qing Shi, Guoan Chen, Zhiwang Song, Yanxia Jiang

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Roles of the E3 Ubiquitin Ligase TRIM47 in Inflammation, Organ Injury, and Cancer.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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

7 authors at 2 institutions in 1 country.

Dexiang JiDepartment of Hematology, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
Yong LiuDepartment of Emergency, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
Wenjie SunDepartment of Anesthesiology, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
Qing ShiDepartment of Endocrinology and Metabolism, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
Guoan ChenDepartment of Hematology, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
Zhiwang SongDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
Yanxia JiangDepartment of Endocrinology and Metabolism, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China.
Nanchang University · CNFirst Affiliated Hospital of Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultiple myeloma (MM) is a malignant hematopoietic disease that is usually incurable. However, the ubiquitin-proteasome system (UPS) genes have not yet been established as a prognostic predictor for MM, despite their potential applications in other cancers.

methodsRNA sequencing data and corresponding clinical information were acquired from Multiple Myeloma Research Foundation (MMRF)-COMMPASS and served as a training set (n=787). Validation of the prediction signature were conducted by the Gene Expression Omnibus (GEO) databases (n=1040). To develop a prognostic signature for overall survival (OS), least absolute shrinkage and selection operator regressions, along with Cox regressions, were used.

resultsA six-gene signature, including KCTD12, SIAH1, TRIM58, TRIM47, UBE2S, and UBE2T, was established. Kaplan-Meier survival analysis of the training and validation cohorts revealed that patients with high-risk conditions had a significantly worse prognosis than those with low-risk conditions. Furthermore, UPS-related signature is associated with a positive immune response. For predicting survival, a simple to use nomogram and the corresponding web-based calculator (https://jiangyanxiamm.shinyapps.io/MMprognosis/) were built based on the UPS signature and its clinical features. Analyses of calibration plots and decision curves showed clinical utility for both training and validation datasets.

conclusionsAs a result of these results, we established a genetic signature for MM based on UPS. This genetic signature could contribute to improving individualized survival prediction, thereby facilitating clinical decisions in patients with MM.

Indexed as

Multiple MyelomaNomogramsCarrier ProteinsHumansNeoplasm ProteinsNuclear ProteinsPrognosisProteasome Endopeptidase ComplexTripartite Motif ProteinsUbiquitin-Conjugating EnzymesUbiquitinsCarrier ProteinsNeoplasm ProteinsNuclear ProteinsProteasome Endopeptidase ComplexTRIM47 protein, humanTripartite Motif ProteinsUbe2S protein, humanUBE2T protein, humanUbiquitin-Conjugating EnzymesUbiquitinsmultiple myelomaprognosissignatureubiquitin-proteasome systemvisualization

Identifiers

PMID36534449
PMCPMC9831738
OpenAlexW4311932209

What OpenQuestion holds

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LicenceCC BY
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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.