Evidence map›Paper›PMID 26617690›Full record

ArticleInternational journal of clinical and experimental pathology2015

Up-regulation of AKAP13 and MAGT1 on cytoplasmic membrane in progressive hepatocellular carcinoma: a novel target for prognosis.

Patamaporn Molee, Poom Adisakwattana, Onrapak Reamtong, Songsak Petmitr, Thaniya Sricharunrat, Nantana Suwandittakul, Urai Chaisri

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-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

15 citing papers in PubMed, 21 citations in OpenAlex.

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  7. Enhanced Efficacy and Increased Long-Term Toxicity of CNS-Directed, AAV-Based Combination Therapy for Krabbe Disease.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
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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

7 authors at 2 institutions in 1 country.

Patamaporn MoleeDepartment of Tropical Pathology, Faculty of Tropical Medicine, Mahidol University Bangkok 10400, Thailand.
Poom AdisakwattanaDepartment of Helminthology, Faculty of Tropical Medicine, Mahidol University Bangkok 10400, Thailand.
Onrapak ReamtongDepartment of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine, Mahidol University Bangkok 10400, Thailand.
Songsak PetmitrDepartment of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine, Mahidol University Bangkok 10400, Thailand.
Thaniya SricharunratPathology Unit, Chulabhorn Hospital Bangkok 10210, Thailand.
Nantana SuwandittakulDepartment of Helminthology, Faculty of Tropical Medicine, Mahidol University Bangkok 10400, Thailand.
Urai ChaisriDepartment of Tropical Pathology, Faculty of Tropical Medicine, Mahidol University Bangkok 10400, Thailand.
Mahidol Oxford Tropical Medicine Research Unit · THMahidol University · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is one of the most common cancers and is associated with high mortality worldwide. The current gold standards for HCC surveillance are detection of serum α-fetoprotein (AFP) and ultrasonography; however, non-specificity of AFP and ultrasonography has frequently been reported. Therefore, alternative tools, especially novel specific tumor markers, are required. In this study, cytoplasmic membrane proteins were isolated from phorbol 12-myristate 13-acetate (PMA)-induced invasive HepG2 cells and identified using nano-scale liquid chromatographic tandem mass spectrometry (NLC-MS/MS) with comparison to non-treated controls. The results showed that two proteins, magnesium transporter protein 1 (MAGT1) and A-kinase anchor protein 13 (AKAP13), were highly expressed in PMA-treated HepG2 cells. This up-regulation was confirmed by real-time RT-PCR, western blot analysis, and immunofluorescent staining studies. Furthermore, evaluation of MAGT1 and AKAP13 expression in clinical HCC tissues by immunohistochemistry suggested that both proteins were strongly expressed in tumor tissues with significantly higher average immunoreactive scores of Remmele and Stegner (IRS) than in non-tumor tissues (P ≤ 0.005). In conclusion, the expression levels of MAGT1 and AKAP13 in HCC may be potential biomarkers for the diagnosis and prognosis of this cancer.

Indexed as

AgedA Kinase Anchor ProteinsBiomarkers, TumorBlotting, WesternCarcinoma, HepatocellularCation Transport ProteinsCell MembraneChromatography, LiquidFemaleFluorescent Antibody TechniqueHep G2 CellsHumansImmunohistochemistryLiver NeoplasmsMaleMembrane ProteinsAKAP13 protein, humanA Kinase Anchor ProteinsBiomarkers, TumorCation Transport ProteinsMagT1 protein, humanMembrane ProteinsMinor Histocompatibility AntigensProto-Oncogene ProteinsAKAP13cytoplasmic membrane proteinsHepatocellular carcinomaimmunohistochemistryMAGT1proteomics

Identifiers

PMID26617690
PMCPMC4637775
OpenAlexW2419459620

What OpenQuestion holds

Textmetadata
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.