Evidence map›Paper›PMID 31287944›Full record

ReviewThe FEBS journal2019

C-type lectin domain group 14 proteins in vascular biology, cancer and inflammation.

Kabir A Khan, Jack L McMurray, Fiyaz Mohammed, Roy Bicknell

Open access · hybridAbstract readReview
In one paragraph

Review in The FEBS journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 79 citations in OpenAlex.

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  19. Clinicopathological association of CD93 expression in gastric adenocarcinoma.Journal of cancer research and clinical oncology · 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

4 authors at 3 institutions in 2 countries.

Kabir A KhanBiological Sciences Platform, Sunnybrook Research Institute, Toronto, Canada.ORCID 0000-0001-8453-3485
Jack L McMurrayCancer Immunology and Immunotherapy Centre, Institute of Immunology and Immunotherapy, University of Birmingham, UK.
Fiyaz MohammedCancer Immunology and Immunotherapy Centre, Institute of Immunology and Immunotherapy, University of Birmingham, UK.
Roy BicknellInstitutes of Cardiovascular Sciences and Biomedical Research, College of Medical and Dental Sciences, University of Birmingham, UK.
University of Birmingham · GBNIHR Birmingham Biomedical Research Centre · GBSunnybrook Health Science Centre · CA

Funding

Canadian Institute of Health ResearchMedical Research CouncilWellcome Trust 099266/Z/12/Z
6 · The paper itself

Abstract

The C-type lectin domain (CTLD) group 14 family of transmembrane glycoproteins consist of thrombomodulin, CD93, CLEC14A and CD248 (endosialin or tumour endothelial marker-1). These cell surface proteins exhibit similar ectodomain architecture and yet mediate a diverse range of cellular functions, including but not restricted to angiogenesis, inflammation and cell adhesion. Thrombomodulin, CD93 and CLEC14A can be expressed by endothelial cells, whereas CD248 is expressed by vasculature associated pericytes, activated fibroblasts and tumour cells among other cell types. In this article, we review the current literature of these family members including their expression profiles, interacting partners, as well as established and speculated functions. We focus primarily on their roles in the vasculature and inflammation as well as their contributions to tumour immunology. The CTLD group 14 family shares several characteristic features including their ability to be proteolytically cleaved and engagement of some shared extracellular matrix ligands. Each family member has strong links to tumour development and in particular CD93, CLEC14A and CD248 have been proposed as attractive candidate targets for cancer therapy.

Indexed as

AnimalsAntigens, CDAntigens, NeoplasmCell Adhesion MoleculesEndothelium, VascularHumansLectins, C-TypeMembrane GlycoproteinsNeoplasmsNeovascularization, PhysiologicReceptors, ComplementThrombomodulinAntigens, CDAntigens, NeoplasmCD248 protein, humanCell Adhesion MoleculesCLEC14A protein, humancomplement 1q receptorLectins, C-TypeMembrane GlycoproteinsReceptors, ComplementThrombomodulincancerCD248CD93CLEC14AC-type lectinextracellular matrixgroup XIVimmuno-oncologythrombomodulinvascular targeting

Identifiers

PMID31287944
PMCPMC6852297
OpenAlexW2961903560

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.