Evidence map›Paper›PMID 26831370›Full record

ArticleScientific reports2016

Longitudinal metabolic imaging of hepatocellular carcinoma in transgenic mouse models identifies acylcarnitine as a potential biomarker for early detection.

Jadegoud Yaligar, Wei Wei Teoh, Rashidah Othman, Sanjay Kumar Verma, Beng Hooi Phang, Swee Shean Lee, Who Whong Wang, Han Chong Toh, Venkatesh Gopalan, Kanaga Sabapathy and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
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  4. Acylcarnitine Profiling in Meningiomas with Different NF2 Mutation Statuses.International journal of molecular sciences · 2025
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  16. The Protective Roles of PPARα Activation in Triptolide-Induced Liver Injury.Toxicological sciences : an official journal of the Society of Toxicology · 2019
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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

11 authors at 3 institutions in 1 country.

Jadegoud YaligarLaboratory of Molecular Imaging, Singapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.
Wei Wei TeohLaboratory of Molecular Carcinogenesis, National Cancer Center, Singapore.
Rashidah OthmanLaboratory of Molecular Carcinogenesis, National Cancer Center, Singapore.
Sanjay Kumar VermaLaboratory of Molecular Imaging, Singapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.
Beng Hooi PhangLaboratory of Molecular Carcinogenesis, National Cancer Center, Singapore.
Swee Shean LeeLaboratory of Molecular Imaging, Singapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.
Who Whong WangLaboratory of Cell Therapy and cancer Vaccine, National Cancer Center, Singapore.
Han Chong TohLaboratory of Cell Therapy and cancer Vaccine, National Cancer Center, Singapore.
Venkatesh GopalanLaboratory of Molecular Imaging, Singapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.
Kanaga SabapathyLaboratory of Molecular Carcinogenesis, National Cancer Center, Singapore.
S Sendhil VelanLaboratory of Molecular Imaging, Singapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.
National Cancer Centre Singapore · SGAgency for Science, Technology and Research · SGSingapore Bioimaging Consortium · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cumulative effects of hepatic injury due to hepatitis B virus (HBV) infections and aflatoxin-B1 (AFB1) exposure are the major risk factors of HCC. Understanding early metabolic changes involving these risk factors in an animal model closely resembling human hepatocellular carcinoma (HCC) is critical for biomarker discovery and disease therapeutics. We have used the hepatitis B surface antigen (HBsAg) transgenic mouse model that mimics HBV carriers with and without AFB1 treatment. We investigated early metabolic changes from preneoplastic state to HCC by non-invasive longitudinal imaging in three HCC groups of mice: HBsAg + AFB1(Gp-I), AFB1 alone (Gp-II), HBsAg alone (Gp-III) and a control group (wild-type untreated; Gp-IV). For the first time, we have identified acylcarnitine signals in vivo in the liver prior to the histological manifestation of the tumors in all three groups. Acylcarnitine concentration increased with increase in tumor growth in all HCC mouse models, indicating elevated metabolic activity and increased cell turnover. This was confirmed in a pilot study using human serum from HCC patients, which revealed a higher concentration of acylcarnitine compared with normal subjects. Translational clinical studies can be designed to detect acylcarnitine in patients with high risk factors for HCC.

Indexed as

Molecular ImagingAnimalsBiomarkersCarcinoma, HepatocellularCarnitineDiffusion Magnetic Resonance ImagingDisease Models, AnimalEarly Detection of CancerGene Expression ProfilingHumansLiver NeoplasmsMiceMice, TransgenicTumor BurdenacylcarnitineBiomarkersCarnitine

Identifiers

PMID26831370
PMCPMC4735819
OpenAlexW2414204667

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Registered trials

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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.