Evidence map›Paper›PMID 32171747›Full record

ArticleGastroenterology2020

ABL1, Overexpressed in Hepatocellular Carcinomas, Regulates Expression of NOTCH1 and Promotes Development of Liver Tumors in Mice.

Fang Wang, Wei Hou, Lennox Chitsike, Yingchen Xu, Carlee Bettler, Aldeb Perera, Thomas Bank, Scott J Cotler, Asha Dhanarajan, Mitchell F Denning and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Gastroenterology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
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  6. Identification of ANXA1 as a Novel Upstream Negative Regulator of Notch1 Function in AML.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
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  20. Bioinformatics andFrontiers in endocrinology · 2022
    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

16 authors at 5 institutions in 2 countries.

Fang WangDepartment of Surgery, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois; Department of Cancer Biology, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois.
Wei HouDepartment of Surgery, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois; Department of Cancer Biology, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois.
Lennox ChitsikeDepartment of Surgery, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois; Department of Cancer Biology, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois.
Yingchen XuDepartment of General Surgery, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
Carlee BettlerDepartment of Surgery, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois; Department of Cancer Biology, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois.
Aldeb PereraDepartment of Surgery, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois; Department of Cancer Biology, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois.
Thomas BankDepartment of Surgery, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois; Department of Cancer Biology, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois.
Scott J CotlerDepartment of Medicine, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois.
Asha DhanarajanDepartment of Pathology, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois.
Mitchell F DenningDepartment of Pathology, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois.
Xianzhong DingDepartment of Pathology, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois.
Peter BreslinDepartment of Molecular/Cellular Physiology, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois; Oncology Institute, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois; Department of Biology, Loyola University Chicago Stritch School of Medicine, Northwestern University, Chicago, Illinois.
Wenan QiangDepartment of Obstetrics and Gynecology and Pathology, Northwestern University, Chicago, Illinois.
Jun LiDepartment of Applied and Computational Mathematics and Statistics, University of Notre Dame, Notre Dame, Indiana.
Anthony J KoleskeDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut.
Wei QiuDepartment of Surgery, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois; Department of Cancer Biology, Loyola University Chicago Stritch School of Medicine, Chicago, Illinois. Electronic address: wqiu@luc.edu.
Loyola University Chicago · USNorthwestern University · USBeijing Tongren Hospital · CNUniversity of Notre Dame · USYale University · US

Funding

Molecular mechanisms of focal adhesion kinase in promoting hepatocarcinogenesisR01CA197128 · NCI · LOYOLA UNIVERSITY CHICAGO · PI QIU, WEI · 2015 to 2025
$3.6M
Impact of excitatory synapse maturation on synaptic plasticity and stabilityR01NS105640 · NINDS · YALE UNIVERSITY · PI HIGLEY, MICHAEL JAMES, KOLESKE, ANTHONY J · 2018 to 2022
$2.5M
Control of Dendritic Spine Stability via Regulation of a Stable Actin PoolR01MH115939 · NIMH · YALE UNIVERSITY · PI KOLESKE, ANTHONY J · 2018 to 2022
$2.2M
The role of FAK in hepatocarcinogenesisR03CA184652 · NCI · LOYOLA UNIVERSITY CHICAGO · PI QIU, WEI · 2014 to 2015
$151k
The role of Sirt2 in haptocarcinogenesisR03CA195183 · NCI · LOYOLA UNIVERSITY CHICAGO · PI QIU, WEI · 2015 to 2016
$151k
NCI NIH HHS R01 CA197128NCI NIH HHS R03 CA184652NCI NIH HHS R03 CA195183NIMH NIH HHS R01 MH115939NINDS NIH HHS R01 NS105640
6 · The paper itself

Abstract

BACKGROUND &

aimsWe investigated whether ABL proto-oncogene 1, non-receptor tyrosine kinase (ABL1) is involved in development of hepatocellular carcinoma (HCC).

methodsWe analyzed clinical and gene expression data from The Cancer Genome Atlas. Albumin-Cre (Hep

resultsHCC tissues had higher levels of ABL1 than non-tumor liver tissues, which correlated with shorter survival times of patients. Hep

conclusionsHCC samples have increased levels of ABL1 compared with nontumor liver tissues, and increased levels of ABL1 correlate with shorter survival times of patients. Loss or inhibition of ABL1 reduces proliferation of HCC cells and slows growth of liver tumors in mice. Inhibitors of ABL1 might be used for treatment of HCC.

Indexed as

AnimalsCarcinoma, HepatocellularCell Line, TumorDatasets as TopicDisease Models, AnimalFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansKaplan-Meier EstimateLiverLiver NeoplasmsMaleMicePhosphorylationPrognosisABL1 protein, humanMAS1 protein, humanMYC protein, humannilotinibNOTCH1 protein, humanNotch1 protein, mouseProto-Oncogene MasProto-Oncogene Proteins c-ablProto-Oncogene Proteins c-mycPyrimidinesReceptor, Notch1HepatocarcinogenesisMouse ModelOncogeneSignal Transduction

Identifiers

PMID32171747
PMCPMC7387191
OpenAlexW3011085369

What OpenQuestion holds

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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.