Evidence map›Paper›PMID 28724284›Full record

ArticleCancer research and treatment2018

Inter-alpha Inhibitor H4 as a Potential Biomarker Predicting the Treatment Outcomes in Patients with Hepatocellular Carcinoma.

Eun-Jung Lee, Seung-Hyun Yang, Kyoung-Jin Kim, Hyejung Cha, Seo Jin Lee, Ji-Hye Kim, Junkyu Song, Kyung-Hee Chun, Jinsil Seong

Open access · diamondAbstract read
In one paragraph

Article in Cancer research and treatment, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 30% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 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

9 authors at 2 institutions in 1 country.

Eun-Jung LeeDepartment of Radiation Oncology, Yonsei University Health System, Seoul, Korea.
Seung-Hyun YangDepartment of Radiation Oncology, Yonsei University Health System, Seoul, Korea.
Kyoung-Jin KimDepartment of Radiation Oncology, Yonsei University Health System, Seoul, Korea.
Hyejung ChaDepartment of Radiation Oncology, Yonsei University Health System, Seoul, Korea.
Seo Jin LeeDepartment of Radiation Oncology, Yonsei University Health System, Seoul, Korea.
Ji-Hye KimDepartment of Radiation Oncology, Yonsei University Health System, Seoul, Korea.
Junkyu SongDepartment of Biochemistry and Molecular Biology, Yonsei University College of Medicine, Seoul, Korea.
Kyung-Hee ChunDepartment of Biochemistry and Molecular Biology, Yonsei University College of Medicine, Seoul, Korea.
Jinsil SeongDepartment of Radiation Oncology, Yonsei University Health System, Seoul, Korea.
Yonsei University Health System · KRYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEarly prediction of treatment outcomes represents an essential step towards increased treatment efficacy and survival in patients with hepatocellular carcinoma (HCC). In this study, we performed two-dimensional electrophoresis (2-DE) followed by protein profiling to identify biomarkers predictive of therapeutic outcomes in patients with HCC who received liver-directed therapy (LDTx) involving local radiotherapy (RT), and studied the underlying mechanisms of the identified proteins. MATERIALS AND

methods2-DE analysis was conducted by pooling sera from patients with a good or poor prognosis; serum proteomic profiles of the two groups were compared and analyzed using matrixassisted laser desorption/ionization time-of-flight mass spectrometry. Identified proteins were confirmed via enzyme-linked immunosorbent assay. An invasion assay was performed after overexpression and knockdown of target protein in Huh7 cells.

resultsLevels of inter-alpha inhibitor H4 (ITIH4), fibrinogen gamma chain, keratin 9/1 complex, carbonic anhydrase I, and carbonmonoxyhemoglobin S were changed by more than 4-fold in response to LDTx. In particular, pre-LDTx ITIH4 expression was more than 5-fold higher in patients with a good prognosis, compared to patients with a poor prognosis. The migration ability of Huh7 cells was significantly suppressed and enhanced by ITIH4 overexpression and knockdown, respectively. The tumors of patients with HCC and a good prognosis expressed high levels of ITIH4, compared to those of patients with a poor prognosis.

conclusionTaken together, ITIH4 may be a potential therapeutic target that could inhibit cancer metastasis, as well as a prognostic marker for patients with HCC who are receiving LDTx.

Indexed as

AdultAgedBiomarkers, TumorBlood ProteinsCarcinoma, HepatocellularCell Line, TumorCell MovementChemoradiotherapyElectrophoresis, Gel, Two-DimensionalFemaleFluorouracilGene Expression Regulation, NeoplasticGlycoproteinsHumansInfusions, Intra-ArterialLiver NeoplasmsBiomarkers, TumorBlood ProteinsFluorouracilGlycoproteinsITIH4 protein, humanProteinase Inhibitory Proteins, SecretoryBiomarkersHepatocellular carcinomaITIH4Liver-directed therapyPrognosis

Identifiers

PMID28724284
PMCPMC6056950
OpenAlexW2734949938

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.