Evidence map›Paper›PMID 32366943›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2020

Blocking thrombospondin-1 signaling via CD47 mitigates renal interstitial fibrosis.

Sohel M Julovi, Barkha Sanganeria, Nikita Minhas, Kedar Ghimire, Brian Nankivell, Natasha M Rogers

Abstract read
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In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

25 citing papers in PubMed, 36 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 2 countries.

Sohel M Julovi *Centre for Transplant and Renal Research, Westmead Institute for Medical Research, Camperdown, NSW, Australia.
Barkha Sanganeria *Centre for Transplant and Renal Research, Westmead Institute for Medical Research, Camperdown, NSW, Australia.
Nikita MinhasCentre for Transplant and Renal Research, Westmead Institute for Medical Research, Camperdown, NSW, Australia.
Kedar GhimireCentre for Transplant and Renal Research, Westmead Institute for Medical Research, Camperdown, NSW, Australia.ORCID http://orcid.org/0000-0002-4672-5256
Brian NankivellCentre for Transplant and Renal Research, Westmead Institute for Medical Research, Camperdown, NSW, Australia.
Natasha M RogersCentre for Transplant and Renal Research, Westmead Institute for Medical Research, Camperdown, NSW, Australia. natasha.rogers@health.nsw.gov.au.
Westmead Institute for Medical Research · AUThe University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute kidney injury triggers a complex cascade of molecular responses that can culminate in maladaptive repair and fibrosis. We have previously reported that the matrix protein thrombospondin-1 (TSP1), binding its high affinity its receptor CD47, promotes acute kidney injury. However, the role of this pathway in promoting fibrosis is less clear. Hypothesizing that limiting TSP1-CD47 signaling is protective against fibrosis, we interrogated this pathway in a mouse model of chronic ischemic kidney injury. Plasma and renal parenchymal expression of TSP1 in patients with chronic kidney disease was also assessed. We found that CD47

Indexed as

Signal TransductionAnimalsCD47 AntigenCells, CulturedDisease Models, AnimalEpithelial CellsFibrosisHumansIschemiaKidneyKidney TubulesMice, Inbred C57BLMice, KnockoutThrombospondin 1CD47 AntigenThrombospondin 1

Identifiers

PMID32366943
OpenAlexW3023103794

What OpenQuestion holds

Textmetadata
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.