Evidence map›Paper›PMID 23024757›Full record

ArticlePloS one2012

Soluble MICA and a MICA variation as possible prognostic biomarkers for HBV-induced hepatocellular carcinoma.

Vinod Kumar, Paulisally Hau Yi Lo, Hiromi Sawai, Naoya Kato, Atsushi Takahashi, Zhenzhong Deng, Yuji Urabe, Hamdi Mbarek, Katsushi Tokunaga, Yasuhito Tanaka and 11 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 3 pooled it
3.2field-weighted citation impact, top 8% 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

56 citing papers in PubMed, 3 syntheses or guidelines pooled it, 93 citations in OpenAlex.

  1. Pooled it
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  9. Associations between MICA and MICB Genetic Variants, Protein Levels, and Colorectal Cancer: Atherosclerosis Risk in Communities (ARIC).Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2023
    Article
  10. Study of the association between aClinical and experimental hepatology · 2022
    Article
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  15. MHC Variants Associated With SymptomaticFrontiers in immunology · 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

21 authors at 5 institutions in 1 country.

Vinod KumarLaboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan. koichima@ims.u-tokyo.ac.jp
Paulisally Hau Yi Lo
Hiromi Sawai
Naoya Kato
Atsushi Takahashi
Zhenzhong Deng
Yuji Urabe
Hamdi Mbarek
Katsushi Tokunaga
Yasuhito Tanaka
Masaya Sugiyama
Masashi Mizokami
Ryosuke Muroyama
Ryosuke Tateishi
Masao Omata
Kazuhiko Koike
Chizu Tanikawa
Naoyuki Kamatani
Michiaki Kubo
Yusuke Nakamura
Koichi Matsuda
The University of Tokyo · JPNational Center for Global Health and Medicine · JPRIKEN · JPRIKEN Center for Integrative Medical Sciences · JPNagoya City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MHC class I polypeptide-related chain A (MICA) molecule is induced in response to viral infection and various types of stress. We recently reported that a single nucleotide polymorphism (SNP) rs2596542 located in the MICA promoter region was significantly associated with the risk for hepatitis C virus (HCV)-induced hepatocellular carcinoma (HCC) and also with serum levels of soluble MICA (sMICA). In this study, we focused on the possible involvement of MICA in liver carcinogenesis related to hepatitis B virus (HBV) infection and examined correlation between the MICA polymorphism and the serum sMICA levels in HBV-induced HCC patients. The genetic association analysis revealed a nominal association with an SNP rs2596542; a G allele was considered to increase the risk of HBV-induced HCC (P = 0.029 with odds ratio of 1.19). We also found a significant elevation of sMICA in HBV-induced HCC cases. Moreover, a G allele of SNP rs2596542 was significantly associated with increased sMICA levels (P = 0.009). Interestingly, HCC patients with the high serum level of sMICA (>5 pg/ml) exhibited poorer prognosis than those with the low serum level of sMICA (≤5 pg/ml) (P = 0.008). Thus, our results highlight the importance of MICA genetic variations and the significance of sMICA as a predictive biomarker for HBV-induced HCC.

Indexed as

Polymorphism, Single NucleotideAdultAgedBiomarkers, TumorCarcinoma, HepatocellularFemaleHepatitis B virusHistocompatibility Antigens Class IHumansLiver NeoplasmsMaleMiddle AgedMinisatellite RepeatsNeovascularization, PathologicPrognosisBiomarkers, TumorHistocompatibility Antigens Class IMHC class I-related chain A

Identifiers

PMID23024757
PMCPMC3443094
OpenAlexW2052095307

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LicenceCC BY
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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.