Evidence map›Paper›PMID 32306508›Full record

ArticleJournal of cellular and molecular medicine2020

A five-mRNA signature associated with post-translational modifications can better predict recurrence and survival in cervical cancer.

Mingyi Ju, Aoshuang Qi, Jia Bi, Lan Zhao, Longyang Jiang, Qiang Zhang, Qian Wei, Qiutong Guan, Xueping Li, Lin Wang and 2 more

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Transcriptomic identification and developmental mapping ofTurkish journal of biology = Turk biyoloji dergisi · 2026
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  10. A novel lncRNA-mRNA-miRNA signature predicts recurrence and disease-free survival in cervical cancer.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2021
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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

12 authors.

Mingyi JuDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, Liaoning, China.ORCID 0000-0002-4084-3358
Aoshuang QiDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, Liaoning, China.
Jia BiDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, Liaoning, China.
Lan ZhaoDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, Liaoning, China.
Longyang JiangDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, Liaoning, China.
Qiang ZhangDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, Liaoning, China.
Qian WeiDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, Liaoning, China.
Qiutong GuanDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, Liaoning, China.
Xueping LiDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, Liaoning, China.
Lin WangDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, Liaoning, China.
Minjie WeiDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, Liaoning, China.
Lin ZhaoDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang City, Liaoning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High mortality of patients with cervical cancer (CC) stresses the imperative of prognostic biomarkers for CC patients. Additionally, the vital status of post-translational modifications (PTMs) in the progression of cancers has been reported by numerous researches. Therefore, the purpose of this research was to dig a prognostic signature correlated with PTMs for CC. We built a five-mRNA (GALNTL6, ARSE, DPAGT1, GANAB and FURIN) prognostic signature associated with PTMs to predict both disease-free survival (DFS) (hazard ratio [HR] = 3.967, 95% CI = 1.985-7.927; P < .001) and overall survival (HR = 2.092, 95% CI = 1.138-3.847; P = .018) for CC using data from The Cancer Genome Atlas database. Then, the robustness of the signature was validated using GSE44001 and the Human Protein Atlas (HPA) database. CIBERSORT algorithm analysis displayed that activated CD4 memory T cell was also an independent indicator for DFS (HR = 0.426, 95% CI = 0.186-0.978; P = .044) which could add additional prognostic value to the signature. Collectively, the PTM-related signature and activated CD4 memory T cell can provide new avenues for the prognostic predication of CC. These findings give further insights into effective treatment strategies for CC, providing opportunities for further experimental and clinical validations.

Indexed as

Gene Expression ProfilingGene Expression Regulation, NeoplasticCD4-Positive T-LymphocytesDatabases, GeneticFemaleHumansImmunologic MemoryKaplan-Meier EstimateLymphocyte ActivationMiddle AgedMolecular Sequence AnnotationNeoplasm Recurrence, LocalPrognosisProgression-Free SurvivalProtein Processing, Post-TranslationalReproducibility of ResultsRNA, Messengeractivated CD4 memory T cellbiomarkerscervical cancerpost-translational modificationstumour-infiltrating immune cells

Identifiers

PMID32306508
PMCPMC7294153

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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.