Evidence map›Paper›PMID 36943663›Full record

ReviewMolecular and cellular biochemistry2024

Emerging role of lipophagy in liver disorders.

Bismillah Nazeer, Muhammad Babar Khawar, Muhammad Usman Khalid, Syeda Eisha Hamid, Mussarat Rafiq, Muddasir Hassan Abbasi, Nadeem Sheikh, Ahmad Ali, Hooriya Fatima, Sadia Ahmad

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular and cellular biochemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Functional role of autophagy in testicular and ovarian steroidogenesis.Frontiers in cell and developmental biology · 2024
    Review
  6. Article
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

10 authors at 4 institutions in 2 countries.

Bismillah Nazeer *Molecular Medicine and Cancer Therapeutics Lab, Department of Zoology, Faculty of Sciences, University of Central Punjab, Lahore, Pakistan.
Muhammad Babar Khawar *Applied Molecular Biology and Biomedicine Lab, Department of Zoology, University of Narowal, Narowal, Pakistan. babarkhawar@yahoo.com.ORCID http://orcid.org/0000-0002-1812-0591
Muhammad Usman Khalid *Molecular Medicine and Cancer Therapeutics Lab, Department of Zoology, Faculty of Sciences, University of Central Punjab, Lahore, Pakistan.
Syeda Eisha Hamid *Molecular Medicine and Cancer Therapeutics Lab, Department of Zoology, Faculty of Sciences, University of Central Punjab, Lahore, Pakistan.
Mussarat Rafiq *Cell and Molecular Biology Lab, Institute of Zoology, University of the Punjab, Lahore, Pakistan.
Muddasir Hassan AbbasiDepartment of Zoology, University of Okara, Okara, Pakistan. dr.muddasir@uo.edu.pk.
Nadeem SheikhCell and Molecular Biology Lab, Institute of Zoology, University of the Punjab, Lahore, Pakistan. Nadeem.zool@pu.edu.pk.
Ahmad AliMolecular Medicine and Cancer Therapeutics Lab, Department of Zoology, Faculty of Sciences, University of Central Punjab, Lahore, Pakistan.
Hooriya FatimaMolecular Medicine and Cancer Therapeutics Lab, Department of Zoology, Faculty of Sciences, University of Central Punjab, Lahore, Pakistan.
Sadia AhmadMolecular Medicine and Cancer Therapeutics Lab, Department of Zoology, Faculty of Sciences, University of Central Punjab, Lahore, Pakistan.
University of Central Punjab · PKUniversity of the Punjab · PKShowa University · JPUniversity of Okara · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipophagy is a selective degradation of lipids by a lysosomal-mediated pathway, and dysregulation of lipophagy is linked with the pathological hallmark of many liver diseases. Downregulation of lipophagy in liver cells results in abnormal accumulation of LDs (Lipid droplets) in hepatocytes which is a characteristic feature of several liver pathologies such as nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH). Contrarily, upregulation of lipophagy in activated hepatic stellate cells (HSCs) is associated with hepatic fibrosis and cirrhosis. Lipid metabolism reprogramming in violent cancer cells contributes to the progression of liver cancer. In this review, we have summarized the recent studies focusing on various components of the lipophagic machinery that can be modulated for their potential role as therapeutic agents against a wide range of liver diseases.

Indexed as

LiverNon-alcoholic Fatty Liver DiseaseAutophagyHumansLipid MetabolismLiver CirrhosisHSCsLipophagyNAFLDNASHTherapeutic agents

Identifiers

PMID36943663
OpenAlexW4328048350

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.