Evidence map›Paper›PMID 37028592›Full record

ReviewThe American journal of pathology2023

The Dynamic Role of Endoplasmic Reticulum Stress in Chronic Liver Disease.

Kaitlyn G Jackson, Grayson W Way, Jing Zeng, Marissa K Lipp, Huiping Zhou

Open access · hybridAbstract readReview
In one paragraph

Review in The American journal of pathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Kaitlyn G JacksonDepartment of Microbiology and Immunology, Virginia Commonwealth University School of Medicine, Richmond, Virginia.
Grayson W WayDepartment of Microbiology and Immunology, Virginia Commonwealth University School of Medicine, Richmond, Virginia; Center for Clinical and Translational Research, Virginia Commonwealth University School of Medicine, Richmond, Virginia.
Jing ZengDepartment of Microbiology and Immunology, Virginia Commonwealth University School of Medicine, Richmond, Virginia; Department of Gastroenterology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Marissa K LippDepartment of Microbiology and Immunology, Virginia Commonwealth University School of Medicine, Richmond, Virginia.
Huiping ZhouDepartment of Microbiology and Immunology, Virginia Commonwealth University School of Medicine, Richmond, Virginia; Central Virginia Veterans Healthcare System, Richmond, Virginia. Electronic address: huiping.zhou@vcuhealth.org.
Virginia Commonwealth University · USShanghai Jiao Tong University · CN

Funding

Regulation of Hepatic SphK2 by Bile Acids: Effects on Lipid MetabolismR01DK057543 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI HYLEMON, PHILLIP B, ZHOU, HUIPING ROSE · 2001 to 2015
$4.4M
Sphingolipids in alcoholic liver diseaseR01AA030180 · NIAAA · VIRGINIA COMMONWEALTH UNIVERSITY · PI PHILLIP B HYLEMON, HUIPING ZHOU · 2023 to 2026
$2.1M
Bile Acid and Sphingosine-1-phosphate Receptor-mediated Signaling in CholestasisR01DK104893 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI HYLEMON, PHILLIP B, ZHOU, HUIPING ROSE · 2016 to 2020
$2.0M
Sphingosine-1 phosphate signaling in alcoholic liver diseaseR21AA026629 · NIAAA · VIRGINIA COMMONWEALTH UNIVERSITY · PI ZHOU, HUIPING ROSE · 2019 to 2020
$407k
The role of sphingosine kinase 2 in mitochondrial dysfunction and NAFLDF31DK135372 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI JACKSON, KAITLYN GEORGENE · 2023 to 2024
$75k
BLRD VA I01 BX005730BLRD VA IK6 BX004477BLRD VA IS1 BX004777BLRD VA IS1 BX005517NIAAA NIH HHS R01 AA030180NIAAA NIH HHS R21 AA026629NIDDK NIH HHS F31 DK135372NIDDK NIH HHS R01 DK057543NIDDK NIH HHS R01 DK104893
6 · The paper itself

Abstract

Chronic liver disease (CLD) is a major worldwide public health threat, with an estimated prevalence of 1.5 billion individuals with CLD in 2020. Chronic activation of endoplasmic reticulum (ER) stress-related pathways is recognized as substantially contributing to the pathologic progression of CLD. The ER is an intracellular organelle that folds proteins into their correct three-dimensional shapes. ER-associated enzymes and chaperone proteins highly regulate this process. Perturbations in protein folding lead to misfolded or unfolded protein accumulation in the ER lumen, resulting in ER stress and concomitant activation of the unfolded protein response (UPR). The adaptive UPR is a set of signal transduction pathways evolved in mammalian cells that attempts to reestablish ER protein homeostasis by reducing protein load and increasing ER-associated degradation. However, maladaptive UPR responses in CLD occur due to prolonged UPR activation, leading to concomitant inflammation and cell death. This review assesses the current understanding of the cellular and molecular mechanisms that regulate ER stress and the UPR in the progression of various liver diseases and the potential pharmacologic and biological interventions that target the UPR.

Indexed as

Endoplasmic Reticulum StressLiver DiseasesAnimalsHumansMammalsMolecular ChaperonesSignal TransductionUnfolded Protein ResponseMolecular Chaperones

Identifiers

PMID37028592
PMCPMC10548273
OpenAlexW4362602761

What Socratic 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 Socratic graph.