Evidence map›Paper›PMID 35469167›Full record

ReviewJHEP reports : innovation in hepatology2022

Lipid alterations in chronic liver disease and liver cancer.

Bichitra Paul, Monika Lewinska, Jesper B Andersen

Open access · goldAbstract readReview
In one paragraph

Review in JHEP reports : innovation in hepatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 207 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
207citing papers in PubMed, 1 pooled it
46.6field-weighted citation impact, top 1% 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

207 citing papers in PubMed, 1 synthesis or guideline pooled it, 294 citations in OpenAlex.

  1. Pooled it
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  7. Defective efferocytosis in diabetes: molecular mechanisms and emerging therapeutic strategies.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
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  11. bioRxiv : the preprint server for biology · 2026
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147 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Bichitra PaulBiotech Research & Innovation Center (BRIC), Department of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Monika LewinskaBiotech Research & Innovation Center (BRIC), Department of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Jesper B AndersenBiotech Research & Innovation Center (BRIC), Department of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
University of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipids are a complex and diverse group of molecules with crucial roles in many physiological processes, as well as in the onset, progression, and maintenance of cancers. Fatty acids and cholesterol are the building blocks of lipids, orchestrating these crucial metabolic processes. In the liver, lipid alterations are prevalent as a cause and consequence of chronic hepatitis B and C virus infections, alcoholic hepatitis, and non-alcoholic fatty liver disease and steatohepatitis. Recent developments in lipidomics have also revealed that dynamic changes in triacylglycerols, phospholipids, sphingolipids, ceramides, fatty acids, and cholesterol are involved in the development and progression of primary liver cancer. Accordingly, the transcriptional landscape of lipid metabolism suggests a carcinogenic role of increasing fatty acids and sterol synthesis. However, limited mechanistic insights into the complex nature of the hepatic lipidome have so far hindered the development of effective therapies.

Indexed as

ACC, acetyl-CoA carboxylaseACLY, ATP citrate lyaseALD, alcohol-related liver diseaseBAs, bile acidsCCA, cholangiocarcinomaCer, ceramide(s)cholangiocarcinomaCPT, carnitine palmitoyltransferaseDNL, de novo lipogenesisELOV1-6, elongation of very-long-chain fatty acidsFABP, fatty acid-binding proteinFADS2, fatty acid desaturase 2FA, fatty acidFAO, fatty acid oxidationFASN, fatty acid synthaseFXR, farnesoid X receptorHCC, hepatocellular carcinomahepatocellular carcinomaHMGCR, 3-hydroxy-3-methyl-glutaryl-coenzyme A reductaseHSCs, hepatic stellate cellsLA, linoleic acidlipidomicsLPC, lysophosphatidylcholineLXR, liver X receptormetabolomicsMUFA, monounsaturated fatty acidNAFLD, non-alcoholic fatty liver diseaseNASH, non-alcoholic steatohepatitisNon-alcoholic fatty liver diseasePC, phosphatidylcholinePPARs, peroxisome proliferator-activated receptorsPSC, primary sclerosing cholangitisPUFA, polyunsaturated fatty acidS1P, sphingosine-1-phosphateSCD, stearoyl-CoA desaturaseSE, sterol estersSFA, saturated fatty acidSM, sphingomyelinSREBP, sterol regulatory element-binding proteinTERT, telomerase reverse transcriptaseTG, triglyceridesTLR, Toll-like receptor

Identifiers

PMID35469167
PMCPMC9034302
OpenAlexW4220874523

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.