Evidence map›Paper›PMID 32696621›Full record

SynthesisThe journal of pathology. Clinical research2020

An evaluation of the tumour endothelial marker CLEC14A as a therapeutic target in solid tumours.

Joseph Robinson, Katharine Whitworth, Elizabeth Jinks, Zsuzsanna Nagy, Roy Bicknell, Steven P Lee

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in The journal of pathology. Clinical research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 16 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 2 institutions in 1 country.

Joseph RobinsonInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
Katharine WhitworthInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
Elizabeth JinksInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
Zsuzsanna NagyInstitute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.
Roy BicknellInstitute of Cardiovascular Sciences, University of Birmingham, Birmingham, UK.
Steven P LeeInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.ORCID 0000-0001-7391-2404
University of Birmingham · GBWarren Spring Laboratory · GB

Funding

Cell and Gene Therapy Catapult, UKMedical Research Council, UK
6 · The paper itself

Abstract

Earlier studies identified the transmembrane cell surface C-type lectin CLEC14A as a putative tumour endothelial marker. For CLEC14A to progress as a vascular target in solid tumours an in-depth analysis of CLEC14A expression in human healthy and tumour tissue is needed. It is here shown that an analysis of 5332 RNA expression profiles in the public domain confirmed high expression of CLEC14A in tumour compared to healthy human tissue. It is further shown by immunohistochemistry that CLEC14A protein is absent, or expressed at a very low level, in healthy human and primate tissue. In contrast, CLEC14A is expressed on the vasculature of a range of human solid tumours, with particularly high expression in more than half of renal cell carcinomas. Elevated levels of CLEC14A transcripts were identified in some non-cancer pathologies; such comorbidities may need to be excluded from trials of therapies targeting this marker. It is further shown that, as CLEC14A expression can be induced by the absence of shear stress, it is imperative that freshly collected as opposed to aged or post-mortem tissue be analysed. We conclude that CLEC14A is a promising target to enable development of novel anti-cancer therapies for solid tumours.

Indexed as

Neovascularization, PathologicAngiogenesis InhibitorsAnimalsBiomarkers, TumorCell Adhesion MoleculesDatabases, GeneticEndothelial CellsHumansImmunohistochemistryLectins, C-TypeMacaca fascicularisMolecular Targeted TherapyNeoplasmsUp-RegulationAngiogenesis InhibitorsBiomarkers, TumorCell Adhesion MoleculesCLEC14A protein, humanLectins, C-Typecancerchimeric antigen receptorCLEC14Aimmunohistochemistryrenal cell carcinomatumour endothelial marker

Identifiers

PMID32696621
PMCPMC7578301
OpenAlexW3044451210

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.