Evidence map›Paper›PMID 26313006›Full record

ArticleOncotarget2015

Small molecule inhibitors of Late SV40 Factor (LSF) abrogate hepatocellular carcinoma (HCC): Evaluation using an endogenous HCC model.

Devaraja Rajasekaran, Ayesha Siddiq, Jennifer L S Willoughby, Jessica M Biagi, Lisa M Christadore, Sarah A Yunes, Rachel Gredler, Nidhi Jariwala, Chadia L Robertson, Maaged A Akiel and 7 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 28 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

17 authors at 3 institutions in 1 country.

Devaraja RajasekaranDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Ayesha SiddiqDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Jennifer L S WilloughbyDepartment of Biology, Center for Chemical Methodology and Library Development at Boston University, Boston, MA 02215, USA.
Jessica M BiagiDepartment of Chemistry, Center for Chemical Methodology and Library Development at Boston University, Boston, MA 02215, USA.
Lisa M ChristadoreDepartment of Chemistry, Center for Chemical Methodology and Library Development at Boston University, Boston, MA 02215, USA.
Sarah A YunesProgram in Molecular Biology, Cell Biology, and Biochemistry, Boston University, Boston, MA 02215, USA.
Rachel GredlerDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Nidhi JariwalaDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Chadia L RobertsonDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Maaged A AkielDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Xue-Ning ShenDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Mark A SublerDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Jolene J WindleDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Scott E SchausDepartment of Chemistry, Center for Chemical Methodology and Library Development at Boston University, Boston, MA 02215, USA.
Paul B FisherDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Ulla HansenDepartment of Biology, Center for Chemical Methodology and Library Development at Boston University, Boston, MA 02215, USA.
Devanand SarkarDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Virginia Commonwealth University · USBoston University · USAlnylam Pharmaceuticals (United States) · US

Funding

SYNTHESIS OF LIBRARIES--LINEAR/POLYKETIDE/POLYPROPIONATEP50GM067041 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI PORCO, JOHN A. · 2002 to 2012
$23.7M
Training Grant in Digestive Diseases and Liver DiseasesT32DK007150 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI SANYAL, ARUN J · 1986 to 2017
$4.2M
The Design and Implementation of Asymmetric Organocatalysis in SynthesisR01GM078240 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI SCHAUS, SCOTT EDWARD · 2007 to 2018
$2.9M
Analysis of a novel regulator of hepatocellular carcinomaR01CA138540 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI SARKAR, DEVANAND · 2010 to 2014
$1.6M
AEG-1: Novel Gene Involved in Malignant GliomaR01CA134721 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B · 2009 to 2013
$1.5M
NCI NIH HHS R01 CA134721NCI NIH HHS R01 CA138540NCI NIH HHS R01 CA138540-01A1NIDDK NIH HHS T32 DK007150NIGMS NIH HHS P50 GM067041NIGMS NIH HHS P50 GM67041NIGMS NIH HHS R01 GM078240
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a lethal malignancy with high mortality and poor prognosis. Oncogenic transcription factor Late SV40 Factor (LSF) plays an important role in promoting HCC. A small molecule inhibitor of LSF, Factor Quinolinone Inhibitor 1 (FQI1), significantly inhibited human HCC xenografts in nude mice without harming normal cells. Here we evaluated the efficacy of FQI1 and another inhibitor, FQI2, in inhibiting endogenous hepatocarcinogenesis. HCC was induced in a transgenic mouse with hepatocyte-specific overexpression of c-myc (Alb/c-myc) by injecting N-nitrosodiethylamine (DEN) followed by FQI1 or FQI2 treatment after tumor development. LSF inhibitors markedly decreased tumor burden in Alb/c-myc mice with a corresponding decrease in proliferation and angiogenesis. Interestingly, in vitro treatment of human HCC cells with LSF inhibitors resulted in mitotic arrest with an accompanying increase in CyclinB1. Inhibition of CyclinB1 induction by Cycloheximide or CDK1 activity by Roscovitine significantly prevented FQI-induced mitotic arrest. A significant induction of apoptosis was also observed upon treatment with FQI. These effects of LSF inhibition, mitotic arrest and induction of apoptosis by FQI1s provide multiple avenues by which these inhibitors eliminate HCC cells. LSF inhibitors might be highly potent and effective therapeutics for HCC either alone or in combination with currently existing therapies.

Indexed as

AnimalsAntineoplastic AgentsApoptosisBenzodioxolesCarcinoma, HepatocellularCell Cycle CheckpointsCell Line, TumorCell ProliferationDiethylnitrosamineDNA-Binding ProteinsDose-Response Relationship, DrugGenes, mycGenetic Predisposition to DiseaseHumansLiver Neoplasms, ExperimentalMice, Transgenic8-(2-ethoxyphenyl)-7,8-dihydro-(1,3)dioxolo(4,5-g)quinolin-6(5H)-oneAntineoplastic AgentsBenzodioxolesDiethylnitrosamineDNA-Binding ProteinsQuinolonesTfcp2 protein, mouseTranscription FactorsapoptosisFQIHCCLSFmitotic arrest

Identifiers

PMID26313006
PMCPMC4694900
OpenAlexW1894085754

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.