Evidence map›Paper›PMID 29464002›Full record

ArticleTheranostics2018

MiR-205-5p and miR-342-3p cooperate in the repression of the E2F1 transcription factor in the context of anticancer chemotherapy resistance.

Xin Lai, Shailendra K Gupta, Ulf Schmitz, Stephan Marquardt, Susanne Knoll, Alf Spitschak, Olaf Wolkenhauer, Brigitte M Pützer, Julio Vera

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Theranostics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07356466 (Clinical Efficacy of Pucotenlimab Combined With Lenvatinib and SOX Versus SOX Alone in Patients With HER2-Negative Advanced Gastric or Gastroesophageal Junction Adenocarcinoma), which is not on this map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 6% 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.

NCT07356466 early_phase1enrolling by invitationnot on this mapstarted 2025, after this paper: background citation

Clinical Efficacy of Pucotenlimab Combined With Lenvatinib and SOX Versus SOX Alone in Patients With HER2-Negative Advanced Gastric or Gastroesophageal Junction Adenocarcinoma: A Single-Center Randomized Controlled Trial

TypeinterventionalSponsorFujian Medical UniversityRan2025 to 2030Enrolled100ConditionsGastric (Stomach) CancerArmsPucotenlimab Combined with Lenvatinib, Oxaliplatin plus S-1 regimen
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 citations in OpenAlex.

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  11. Advanced computational predictive models of miRNA-mRNA interaction efficiency.Computational and structural biotechnology journal · 2024
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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

9 authors at 5 institutions in 4 countries.

Xin LaiLaboratory of Systems Tumour Immunology, Department of Dermatology, Friedrich-Alexander-University of Erlangen-Nürnberg (FAU) and Universitätsklinikum Erlangen, Erlangen, Germany.
Shailendra K GuptaDepartment of Systems Biology and Bioinformatics, University of Rostock, Rostock, Germany.
Ulf SchmitzGene & Stem Cell Therapy Program, Centenary Institute, University of Sydney, Camperdown, Australia.
Stephan MarquardtInstitute of Experimental Gene Therapy and Cancer Research, Rostock University Medical Centre, Rostock, Germany.
Susanne KnollInstitute of Experimental Gene Therapy and Cancer Research, Rostock University Medical Centre, Rostock, Germany.
Alf SpitschakInstitute of Experimental Gene Therapy and Cancer Research, Rostock University Medical Centre, Rostock, Germany.
Olaf WolkenhauerDepartment of Systems Biology and Bioinformatics, University of Rostock, Rostock, Germany.
Brigitte M PützerInstitute of Experimental Gene Therapy and Cancer Research, Rostock University Medical Centre, Rostock, Germany.
Julio VeraLaboratory of Systems Tumour Immunology, Department of Dermatology, Friedrich-Alexander-University of Erlangen-Nürnberg (FAU) and Universitätsklinikum Erlangen, Erlangen, Germany.
University of Rostock · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEStellenbosch University · ZAUniversitätsklinikum Erlangen · DEUniversity of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High rates of lethal outcome in tumour metastasis are associated with the acquisition of invasiveness and chemoresistance. Several clinical studies indicate that E2F1 overexpression across high-grade tumours culminates in unfavourable prognosis and chemoresistance in patients. Thus, fine-tuning the expression of E2F1 could be a promising approach for treating patients showing chemoresistance.

Indexed as

Down-RegulationDrug Resistance, NeoplasmCell Line, TumorE2F1 Transcription FactorHumansMicroRNAsModels, TheoreticalMolecular Dynamics SimulationNucleic Acid ConformationProtein BindingRNA, MessengerE2F1 protein, humanE2F1 Transcription FactorMicroRNAsMIR205, humanMIRN342 microRNA, humanRNA, MessengerChemotherapy resistanceE2F1Kinetic modelling.MicroRNAMolecular dynamics simulation

Identifiers

PMID29464002
PMCPMC5817113
OpenAlexW2782791713

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.