Evidence map›Paper›PMID 29901861›Full record

ArticleMolecular oncology2018

Rapid proteomic analysis for solid tumors reveals LSD1 as a drug target in an end-stage cancer patient.

Sophia Doll, Maximilian C Kriegmair, Alberto Santos, Michael Wierer, Fabian Coscia, Helen Michele Neil, Stefan Porubsky, Philipp E Geyer, Andreas Mund, Philipp Nuhn and 1 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Molecular oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

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  14. The Proteomic Landscape of Pancreatic Ductal Adenocarcinoma Liver Metastases Identifies Molecular Subtypes and Associations with Clinical Response.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
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  17. Knocking down LSD1 inhibits the stemness features of colorectal cancer stem cells.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020
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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

11 authors at 5 institutions in 2 countries.

Sophia DollDepartment of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, Germany.
Maximilian C KriegmairDepartment of Urology, University Medical Centre Mannheim, University of Heidelberg, Mannheim, Germany.
Alberto SantosNovo Nordisk Foundation Center for Protein Research, Faculty of Health Sciences, University of Copenhagen, Denmark.
Michael WiererDepartment of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, Germany.
Fabian CosciaDepartment of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, Germany.
Helen Michele NeilNovo Nordisk Foundation Center for Protein Research, Faculty of Health Sciences, University of Copenhagen, Denmark.
Stefan PorubskyDepartment of Pathology, University Medical Centre Mannheim, University of Heidelberg, Mannheim, Germany.
Philipp E GeyerDepartment of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, Germany.
Andreas MundNovo Nordisk Foundation Center for Protein Research, Faculty of Health Sciences, University of Copenhagen, Denmark.
Philipp NuhnDepartment of Urology, University Medical Centre Mannheim, University of Heidelberg, Mannheim, Germany.
Matthias MannDepartment of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Martinsried, Germany.
Novo Nordisk Foundation · DKUniversity of Copenhagen · DKUniversity Medical Centre Mannheim · DEHeidelberg University · DEMax Planck Institute of Biochemistry · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent advances in mass spectrometry (MS)-based technologies are now set to transform translational cancer proteomics from an idea to a practice. Here, we present a robust proteomic workflow for the analysis of clinically relevant human cancer tissues that allows quantitation of thousands of tumor proteins in several hours of measuring time and a total turnaround of a few days. We applied it to a chemorefractory metastatic case of the extremely rare urachal carcinoma. Quantitative comparison of lung metastases and surrounding tissue revealed several significantly upregulated proteins, among them lysine-specific histone demethylase 1 (LSD1/KDM1A). LSD1 is an epigenetic regulator and the target of active development efforts in oncology. Thus, clinical cancer proteomics can rapidly and efficiently identify actionable therapeutic options. While currently described for a single case study, we envision that it can be applied broadly to other patients in a similar condition.

Indexed as

ProteomicsUp-RegulationHigh-Throughput Nucleotide SequencingHistone DemethylasesHumansLung NeoplasmsMass SpectrometryMolecular Targeted TherapyPrecision MedicineTime FactorsUrinary Bladder NeoplasmsWorkflowHistone DemethylasesKDM1A protein, humancase studyclinical proteomicsepigeneticsmass spectrometryurachal carcinoma

Identifiers

PMID29901861
PMCPMC6068348
OpenAlexW2807968682

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.