Evidence map›Paper›PMID 37366601›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2023

Lipophilic statins inhibit YAP coactivator transcriptional activity in HCC cells through Rho-mediated modulation of actin cytoskeleton.

Jihane N Benhammou, Bo Qiao, Arthur Ko, James Sinnett-Smith, Joseph R Pisegna, Enrique Rozengurt

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 10 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 1 country.

Jihane N BenhammouVatche and Tamar Manoukian Division of Digestive Diseases, University of California, Los Angeles, California, United States.ORCID 0000-0003-2442-5145
Bo QiaoVatche and Tamar Manoukian Division of Digestive Diseases, University of California, Los Angeles, California, United States.
Arthur KoCenter for Genetic Medicine Research, Childrens National Research Institute, Washington, District of Columbia, United States.
James Sinnett-SmithVatche and Tamar Manoukian Division of Digestive Diseases, University of California, Los Angeles, California, United States.ORCID 0000-0003-0074-7270
Joseph R PisegnaVatche and Tamar Manoukian Division of Digestive Diseases, University of California, Los Angeles, California, United States.
Enrique RozengurtVatche and Tamar Manoukian Division of Digestive Diseases, University of California, Los Angeles, California, United States.ORCID 0000-0002-7838-9170
University of California, Los Angeles · USChildren's National · US

Funding

UCLA Clinical Translational Science InstituteUL1TR001881 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ARLEEN F. BROWN, ARASH NAEIM · 2016 to 2026
$118.1M
Project 3: Role of the pancreatic fibroinflammatory microenvironment in obesity-promoted pancreatic cancerP01CA236585 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI EIBL, GUIDO ERWIN MICHAEL · 2020 to 2024
$5.6M
Targeting YAP with statins to prevent antibody-mediated transplant rejectionR21AI156592 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI REED, ELAINE F, ROZENGURT, JUAN ENRIQUE · 2021 to 2022
$444k
Interaction between Chronic Stress and Obesity in Pancreatic Cancer ProgressionR21CA258125 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI EIBL, GUIDO ERWIN MICHAEL, ROZENGURT, JUAN ENRIQUE · 2022 to 2023
$397k
BLRD VA I01 BX003801Foundation for the National Institutes of Health (FNIH) P01CA236585Foundation for the National Institutes of Health (FNIH) R21AI156592Foundation for the National Institutes of Health (FNIH) R21CA258125HHS | NIH | National Center for Advancing Translational Sciences (NCATS) UL1TR001881NCATS NIH HHS UL1 TR001881NCI NIH HHS P01 CA236585NCI NIH HHS R21 CA258125NIAID NIH HHS R21 AI156592
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the third leading cause of liver-related death. Lipophilic statins have been associated with a decrease in HCC incidence, raising the possibility of their use as chemoprevention agents. The Yes-associated protein (YAP) and transcriptional coactivator with PDZ-binding motif (TAZ) have emerged as an important pro-oncogenic mechanism in HCC. Statins modulate YAP/TAZ in other solid tumors, but few studies have assessed their mechanisms in HCC. We aimed to delineate how lipophilic statins regulate YAP protein localization by interrogating the mevalonate pathway in a stepwise manner using pharmacological and genetical approaches in HCC cells. Huh7 and Hep3B HCC cells were treated with the lipophilic statins cerivastatin and atorvastatin. YAP protein localization was determined using quantitative immunofluorescence (IF) imaging. The gene expression of

Indexed as

Carcinoma, HepatocellularHydroxymethylglutaryl-CoA Reductase InhibitorsLiver NeoplasmsYAP-Signaling ProteinsActin CytoskeletonAdaptor Proteins, Signal TransducingHumansMevalonic Acidrho GTP-Binding ProteinsAdaptor Proteins, Signal TransducingHydroxymethylglutaryl-CoA Reductase InhibitorsMevalonic Acidrho GTP-Binding ProteinsYAP1 protein, humanYAP-Signaling Proteinschemopreventionhepatocellular carcinomastatinYAP

Identifiers

PMID37366601
PMCPMC10511177
OpenAlexW4382182598

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.