Evidence map›Paper›PMID 21354236›Full record

ArticleJournal of hepatology2011

Alpha-fetoprotein-thymidine kinase-luciferase knockin mice: a novel model for dual modality longitudinal imaging of tumorigenesis in liver.

Xincheng Lu, Hong Guo, Joseph Molter, Hui Miao, Lizabeth Gerber, Yiduo Hu, Ellen L Barnes, Hannes Vogel, Zhenghong Lee, Guangbin Luo and 1 more

Abstract read
In one paragraph

Article in Journal of hepatology, 2011. 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
1.2field-weighted citation impact, top 21% 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, 22 citations in OpenAlex.

  1. Article
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  3. Article
  4. Review
  5. Article
  6. Review
  7. PET imaging of oncolytic VSV expressing the mutant HSV-1 thymidine kinase transgene in a preclinical HCC rat model.Molecular therapy : the journal of the American Society of Gene Therapy · 2015
    Article
  8. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Xincheng LuCase Comprehensive Cancer Centre, Case Western Reserve University, Cleveland, OH 44106, USA.
Hong Guo
Joseph Molter
Hui Miao
Lizabeth Gerber
Yiduo Hu
Ellen L Barnes
Hannes Vogel
Zhenghong Lee
Guangbin Luo
Bingcheng Wang
Case Western Reserve University · USMetroHealth Medical Center · USStanford University · USUniversity Hospitals of Cleveland · US

Funding

Quantitative FDG-PET for Imaging Woodchuck HCCR01CA095307 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI LEE, ZHENGHONG · 2003 to 2013
$3.5M
Northeastern Ohio Animal Imaging Resource Center- NOAIRCR24CA110943 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI DUERK, JEFFREY L. · 2004 to 2006
$2.5M
Akt-EphA2 Crosstalk in Glioma InvasionR01CA152371 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MIAO, HUI, WANG, BINGCHENG · 2010 to 2014
$1.6M
EphA2 Agonists as Novel Inhibitors of Tumor ProgressionR01CA092259 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, BINGCHENG · 2002 to 2007
$1.4M
Eph Kinase Signaling In Renal Epithelial CellsR01DK077876 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI WANG, BINGCHENG · 2008 to 2011
$1.4M
Eph Kinase Signaling in Prostate CancerR01CA096533 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, BINGCHENG · 2001 to 2004
$954k
NCI NIH HHS R01 CA092259NCI NIH HHS R01 CA095307NCI NIH HHS R01 CA096533NCI NIH HHS R01 CA152371NCI NIH HHS R01 CA88939NCI NIH HHS R01 CA92259NCI NIH HHS R24 CA110943NIDDK NIH HHS R01 DK077876
6 · The paper itself

Abstract

BACKGROUND &

aimsHepatocellular carcinoma (HCC) is frequently a lethal disease and one of the few malignancies that is still increasing in incidence around the world. Better animal models are highly desired to investigate the molecular basis of HCC and to develop novel therapeutic strategies. Alpha-fetoprotein (Afp) gene is expressed in fetal liver, silenced soon after birth, and highly re-expressed in hepatocellular carcinomas (HCC). We aimed to take advantage of the dramatic re-expression of the Afp gene in HCC to develop a hepatocarcinogenesis reporter (HCR) mouse model for dual-modality, longitudinal in vivo imaging of liver tumor development, and progression.

methodsKnock in mice were established by placing a thymidinekinase (tk)-luciferase (luc) reporter gene cassette under the transcriptional control of the endogenous Afp promoter. DEN, a liver carcinogen, was used to induce liver tumors, which was monitored by both luc-based bioluminescent (BL) and tk-based positron emission tomography (PET) imaging.

resultsThe expression profile of luc was identical to that of the endogenous Afp gene during development. As early as 2 months after the exposure to DEN, BLI revealed multifocal signals in the liver, long before the appearance of histologically apparent neoplastic lesions. By 6 months, BL and PET dual imaging showed strong signals in malignant HCC. By serendipity, a strong BL signal was also detected in adult testes, a previously unknown site of Afp expression.

conclusionsThe HCR model enables longitudinal monitoring of liver tumor development and progression, providing a powerful tool in developing chemoprevention and therapeutic strategies for HCC.

Indexed as

alpha-FetoproteinsAnimalsDiethylnitrosamineDisease Models, AnimalDisease ProgressionFemaleGene Knock-In TechniquesGenes, ReporterHumansLiver Neoplasms, ExperimentalLuciferasesLuminescenceMaleMiceMice, Inbred C3HMice, Inbred C57BLalpha-FetoproteinsDiethylnitrosamineLuciferasesThymidine Kinase

Identifiers

PMID21354236
PMCPMC3465678
OpenAlexW2121962299

What OpenQuestion holds

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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.