Evidence map›Paper›PMID 29729190›Full record

ArticleHepatology (Baltimore, Md.)2018

Baicalein Targets GTPase-Mediated Autophagy to Eliminate Liver Tumor-Initiating Stem Cell-Like Cells Resistant to mTORC1 Inhibition.

Raymond Wu, Ramachandran Murali, Yasuaki Kabe, Samuel W French, Yi-Ming Chiang, Siyu Liu, Linda Sher, Clay C Wang, Stan Louie, Hidekazu Tsukamoto

Abstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 81 citations in OpenAlex.

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  11. Liver cancer wars: plant-derived polyphenols strike back.Medical oncology (Northwood, London, England) · 2024
    Review
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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

10 authors at 4 institutions in 2 countries.

Raymond WuSouthern California Research Center for ALPD and Cirrhosis and Department of Pathology, Keck School of Medicine of the University of Southern California, Los Angeles, California.
Ramachandran MuraliDepartment of Biomedical Sciences, Cedars Sinai Medical Center, Los Angeles, California.
Yasuaki KabeDepartment of Biochemistry, Keio University of School of Medicine, Tokyo, Japan.
Samuel W FrenchHarbor-UCLA Medical Center, Torrance, California.
Yi-Ming ChiangSchool of Pharmacy, University of Southern California, Los Angeles, California.
Siyu LiuSchool of Pharmacy, University of Southern California, Los Angeles, California.
Linda SherDepartment of Surgery, Keck School of Medicine of the University of Southern California, Los Angeles, California.
Clay C WangSchool of Pharmacy, University of Southern California, Los Angeles, California.
Stan LouieSchool of Pharmacy, University of Southern California, Los Angeles, California.
Hidekazu TsukamotoSouthern California Research Center for ALPD and Cirrhosis and Department of Pathology, Keck School of Medicine of the University of Southern California, Los Angeles, California.
University of Southern California · USCedars-Sinai Medical Center · USHarbor–UCLA Medical Center · USKeio University · JP

Funding

The Southernearch Center for ALPD and CirrhosisP50AA011999 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Tatiana Kisseleva · 1999 to 2026
$45.8M
USC RESEARCH CENTER FOR LIVER DISEASES: PILOT PROGRAMSP30DK048522 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI STILES, BANGYAN · 1995 to 2020
$21.8M
Nuclear Receptors in Liver Health and DiseaseP20GM103549 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI JAESCHKE, HARTMUT W. · 2012 to 2015
$8.1M
NON-PARENCHYMAL LIVER CELL CORER24AA012885 · NIAAA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TSUKAMOTO, HIDEKAZU · 2001 to 2025
$8.1M
Pilot Grants ProgramP30GM118247 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI WEINMAN, STEVEN A · 2016 to 2020
$5.5M
Molecular Mechanisms of Stellate Cell Activation in Liver FibrosisI01BX001991 · VA · VA GREATER LOS ANGELES HEALTHCARE SYSTEM · PI HIDEKAZU TSUKAMOTO · 2014 to 2026
–
BLRD VA I01 BX001991NIAAA NIH HHS P50 AA011999NIAAA NIH HHS R24 AA012885NIDDK NIH HHS P30 DK048522NIGMS NIH HHS P20 GM103549NIGMS NIH HHS P30 GM118247
6 · The paper itself

Abstract

Drug resistance is a major problem in the treatment of liver cancer. Mammalian Target of Rapamycin 1 (mTORC1) inhibitors have been tested for the treatment of liver cancer based on hyperactive mTOR in this malignancy. However, their clinical trials showed poor outcome, most likely due to their ability to upregulate CD133 and promote chemoresistance. The CD133

Indexed as

AnimalsAutophagyCell Line, TumorDrug Resistance, NeoplasmEnzyme InhibitorsFlavanonesGTP PhosphohydrolasesHumansLiverLiver NeoplasmsMechanistic Target of Rapamycin Complex 1MiceMonomeric GTP-Binding ProteinsNeoplastic Stem CellsSignal TransductionXenograft Model Antitumor AssaysbaicaleinEnzyme InhibitorsFlavanonesGTP PhosphohydrolasesMechanistic Target of Rapamycin Complex 1Monomeric GTP-Binding ProteinsSAR1B protein, human

Identifiers

PMID29729190
PMCPMC6204108
OpenAlexW2799271130

What OpenQuestion holds

Textmetadata
LicenceTDM
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.