Evidence map›Paper›PMID 38732153›Full record

ArticleInternational journal of molecular sciences2024

JMJD6 Autoantibodies as a Potential Biomarker for Inflammation-Related Diseases.

Bo-Shi Zhang, Xiao-Meng Zhang, Masaaki Ito, Satoshi Yajima, Kimihiko Yoshida, Mikiko Ohno, Eiichiro Nishi, Hao Wang, Shu-Yang Li, Masaaki Kubota and 14 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
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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

24 authors.

Bo-Shi ZhangDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.ORCID 0009-0006-5817-9586
Xiao-Meng ZhangDepartment of Biochemistry and Genetics, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Masaaki ItoDepartment of Clinical Oncology, Graduate School of Medicine, Toho University, Tokyo 143-8541, Japan.
Satoshi YajimaDepartment of Gastroenterological Surgery, Graduate School of Medicine, Toho University, Tokyo 143-8541, Japan.
Kimihiko YoshidaDepartment of Gastroenterological Surgery, Graduate School of Medicine, Toho University, Tokyo 143-8541, Japan.
Mikiko OhnoDepartment of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Eiichiro NishiDepartment of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Hao WangDepartment of Biochemistry and Genetics, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.ORCID 0000-0003-2169-1712
Shu-Yang LiDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Masaaki KubotaDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Yoichi YoshidaDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Tomoo MatsutaniDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Seiichiro MineDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Toshio MachidaDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Minoru TakemotoDepartment of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Hiroki YamagataDepartment of Diabetes, Metabolism and Endocrinology, School of Medicine, International University of Health and Welfare, Chiba 286-8686, Japan.
Aiko HayashiDepartment of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Koutaro YokoteDepartment of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Yoshio KobayashiDepartment of Cardiovascular Medicine, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Hirotaka TakizawaPort Square Kashiwado Clinic, Kashiwado Memorial Foundation, Chiba 260-0025, Japan.
Hideyuki KurodaMedical Project Division, Research Development Center, Fujikura Kasei Co., Saitama 340-0203, Japan.
Hideaki ShimadaDepartment of Clinical Oncology, Graduate School of Medicine, Toho University, Tokyo 143-8541, Japan.
Yasuo IwadateDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Takaki HiwasaDepartment of Neurological Surgery, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.

Funding

Japan Science and Technology Agency 14657335Japan Science and Technology Agency JPMJSP2109Japan Society for the Promotion of Science 17K16626Japan Society for the Promotion of Science 19K09451Japan Society for the Promotion of Science 20H03449Japan Society for the Promotion of Science 20K07810Japan Society for the Promotion of Science 20K08445Japan Society for the Promotion of Science 20K17953Japan Society for the Promotion of Science 21K19437Japan Society for the Promotion of Science 22K07273Japan Society for the Promotion of Science 22K09227Japan Society for the Promotion of Science 22K19428
6 · The paper itself

Abstract

Inflammation is closely associated with cerebrovascular diseases, cardiovascular diseases, diabetes, and cancers, and it is accompanied by the development of autoantibodies in the early stage of inflammation-related diseases. Hence, it is meaningful to discover novel antibody biomarkers targeting inflammation-related diseases. In this study, Jumonji C-domain-containing 6 (JMJD6) was identified by the serological identification of antigens through recombinant cDNA expression cloning. In particular, JMJD6 is an antigen recognized in serum IgG from patients with unstable angina pectoris (a cardiovascular disease). Then, the serum antibody levels were examined using an amplified luminescent proximity homogeneous assay-linked immunosorbent assay and a purified recombinant JMJD6 protein as an antigen. We observed elevated levels of serum anti-JMJD6 antibodies (s-JMJD6-Abs) in patients with inflammation-related diseases such as ischemic stroke, acute myocardial infarction (AMI), diabetes mellitus (DM), and cancers (including esophageal cancer, EC; gastric cancer; lung cancer; and mammary cancer), compared with the levels in healthy donors. The s-JMJD6-Ab levels were closely associated with some inflammation indicators, such as C-reactive protein and intima-media thickness (an atherosclerosis index). A better postoperative survival status of patients with EC was observed in the JMJD6-Ab-positive group than in the negative group. An immunohistochemical analysis showed that JMJD6 was highly expressed in the inflamed mucosa of esophageal tissues, esophageal carcinoma tissues, and atherosclerotic plaques. Hence, JMJD6 autoantibodies may reflect inflammation, thereby serving as a potential biomarker for diagnosing specific inflammation-related diseases, including stroke, AMI, DM, and cancers, and for prediction of the prognosis in patients with EC.

Indexed as

AutoantibodiesBiomarkersInflammationJumonji Domain-Containing Histone DemethylasesAdultAgedDiabetes MellitusFemaleHumansMaleMiddle AgedNeoplasmsAutoantibodiesBiomarkersJMJD6 protein, humanJumonji Domain-Containing Histone Demethylasesacute myocardial infarctionatherosclerosisautoantibodydiabetes mellitusesophageal cancerinflammationischemic strokeJMJD6

Identifiers

PMID38732153
PMCPMC11084951

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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.