Evidence map›Paper›PMID 29046806›Full record

ArticleBiomarker research2017

Development of a fully automated chemiluminescence immunoassay for urine monomeric laminin-γ2 as a promising diagnostic tool of non-muscle invasive bladder cancer.

Masatoshi Nakagawa, Takashi Karashima, Masayuki Kamada, Eisaku Yoshida, Toru Yoshimura, Masanori Nojima, Keiji Inoue, Taro Shuin, Motoharu Seiki, Naohiko Koshikawa

Open access · goldAbstract read
In one paragraph

Article in Biomarker research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 12 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

10 authors at 5 institutions in 1 country.

Masatoshi Nakagawa *Diagnostic Division, Abbott Japan Co. Ltd., Chiba, Japan.
Takashi Karashima *Department of Urology, Kochi Medical School, Kochi, Japan.
Masayuki KamadaDepartment of Urology, Kochi Medical School, Kochi, Japan.
Eisaku YoshidaDiagnostic Division, Abbott Japan Co. Ltd., Chiba, Japan.
Toru YoshimuraDiagnostic Division, Abbott Japan Co. Ltd., Chiba, Japan.
Masanori NojimaCenter for Translational Research, Institute of Medical Science Hospital, University of Tokyo, Tokyo, Japan.
Keiji InoueDepartment of Urology, Kochi Medical School, Kochi, Japan.
Taro ShuinDepartment of Urology, Kochi Medical School, Kochi, Japan.
Motoharu SeikiDivision of Cancer Cell Research, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Naohiko KoshikawaDivision of Cancer Cell Research, Kanagawa Cancer Center Research Institute, 2-3-2 Nakao, Yokohama, 241-8515 Japan.ORCID 0000-0002-4539-888X
Kochi Medical School Hospital · JPAbbott (Japan) · JPKanagawa Prefectural Hospital Organization · JPKanazawa University · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMonomeric laminin-γ2 in urine is a potential biomarker for bladder cancer. However, the current detection system uses an antibody that cannot discriminate between monomeric laminin-γ2 and the heterotrimeric γ2 chain of laminin-332, which may cause false-positive reactions. The present study aimed to develop a fully automated chemiluminescence immunoassay system using a specific monoclonal antibody against monomeric laminin-γ2.

methodsIn total, 237 urine specimens (84 from patients with bladder cancer, 48 from patients with benign urological disease, and 105 from healthy donors) were collected, and monomeric laminin-γ2 values in the urine were measured using a fully automated chemiluminescence immunoassay.

resultsThe results revealed that laminin-γ2 values in patients with benign urological disease were comparable to those of healthy donors and that the chemiluminescence immunoassay's lower limit of detection was 10 pg/mL (approximately 20-fold better than the sandwich enzyme-linked immunosorbent assay's limit of 200 pg/mL). Moreover, the chemiluminescence immunoassay demonstrated that patients with bladder cancer, including non-muscle invasive bladder cancer (≤pT1), had higher laminin-γ2 values than patients with benign urological disease or healthy donors.

conclusionsThese results suggest that urine monomeric laminin-γ2 may be a promising biomarker to diagnose cases of non-muscle invasive bladder cancer using a fully automated chemiluminescence immunoassay system.

Indexed as

Chemiluminescence immunoassay (CLIA)Monomeric laminin-γ2Non-muscle invasive bladder cancer (NMIBC)Urine biomarker

Identifiers

PMID29046806
PMCPMC5640956
OpenAlexW2760950262

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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.