Evidence map›Paper›PMID 32130072›Full record

ReviewAmerican journal of physiology. Cell physiology2020

The role of the sphingolipid pathway in liver fibrosis: an emerging new potential target for novel therapies.

Yuval Ishay, Dean Nachman, Tawfik Khoury, Yaron Ilan

Abstract readReview
PubMed Publisher
In one paragraph

Review in American journal of physiology. Cell physiology, 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
2.0field-weighted citation impact, top 13% 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, 40 citations in OpenAlex.

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  13. Sphingolipids: drivers of cardiac fibrosis and atrial fibrillation.Journal of molecular medicine (Berlin, Germany) · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Yuval IshayDepartment of Internal Medicine A, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Dean NachmanDepartment of Internal Medicine A, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Tawfik KhouryGastroenterology and Liver Units, Department of Medicine, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Yaron IlanGastroenterology and Liver Units, Department of Medicine, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.ORCID 0000-0003-0802-1220
Hadassah Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sphingolipids (SL) are a family of bioactive lipids and a major cellular membrane structural component. SLs include three main compounds: ceramide (Cer), sphingosine (Sp), and sphingosine-1-phosphate (S-1P), all of which have emerging roles in biological functions in cells, especially in the liver. They are under investigation in various liver diseases, including cirrhosis and end-stage liver disease. In this review, we provide an overview on the role of SLs in liver pathobiology and focus on their potential role in the development of hepatic fibrosis. We describe recent evidence and suggest SLs are a promising potential therapeutic target for the treatment of liver disease and fibrosis.

Indexed as

AnimalsCell ProliferationEnzyme InhibitorsExtracellular MatrixHepatic Stellate CellsHumansKupffer CellsLiverLiver CirrhosisPhosphotransferases (Alcohol Group Acceptor)Signal TransductionSphingolipidsSphingosine KinaseEnzyme InhibitorsPhosphotransferases (Alcohol Group Acceptor)SphingolipidsSphingosine Kinaseinflammationliver fibrosissphingolipidssphingosine kinase

Identifiers

PMID32130072
OpenAlexW3010015465

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.