Evidence map›Paper›PMID 33806580›Full record

ArticleDiagnostics (Basel, Switzerland)2021

Validating METCAM/MUC18 as a Novel Biomarker to Predict the Malignant Potential of Prostate Cancer at an Early Stage by Using a Modified Gold Nanoparticles-Based Lateral Flow Immunoassay.

Jui-Chuang Wu, Yin-Huan Chuang, Yu-Chun Wei, Chia-Chi Hsieh, Yuan-Hung Pong, Yenn-Rong Su, Vincent F-S Tsai, Guang-Jer Wu

Open access · goldAbstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. METCAM/MUC18 is a Biomarker and Therapeutic Target for Prostate Cancer.Asian Pacific journal of cancer prevention : APJCP · 2025
    Article
  2. Review
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

8 authors at 4 institutions in 2 countries.

Jui-Chuang WuBiochemical Engineering Laboratory, Department of Chemical Engineering, Chung Yuan Christian University, Chung-li District, Taoyuan City 32023, Taiwan.
Yin-Huan ChuangBiochemical Engineering Laboratory, Department of Chemical Engineering, Chung Yuan Christian University, Chung-li District, Taoyuan City 32023, Taiwan.
Yu-Chun WeiBiochemical Engineering Laboratory, Department of Chemical Engineering, Chung Yuan Christian University, Chung-li District, Taoyuan City 32023, Taiwan.
Chia-Chi HsiehBiochemical Engineering Laboratory, Department of Chemical Engineering, Chung Yuan Christian University, Chung-li District, Taoyuan City 32023, Taiwan.
Yuan-Hung PongDepartment of Urology, Ten Chen General Hospital, Yang-Mei District, Taoyuan City 326, Taiwan.ORCID 0000-0001-7319-7834
Yenn-Rong SuDepartment of Urology, National Taiwan University Hospital Hsin-Chu Branch, Hsin-Chu City 300, Taiwan.
Vincent F-S TsaiDepartment of Urology, Ten Chen General Hospital, Yang-Mei District, Taoyuan City 326, Taiwan.
Guang-Jer WuCancer Metastasis Laboratory, Department of Bioscience Technology, Chung Yuan Christian University, Chung-li District, Taoyuan City 32023, Taiwan.ORCID 0000-0003-1485-9169
Chung Yuan Christian University · TWTen Chen Hospital · TWEmory University · USNational Taiwan University Hospital · TW

Funding

National Science Council NSC-101-2320-B-033-003
6 · The paper itself

Abstract

(1) Background: To further validate METCAM/MUC18 as a diagnostic biomarker for prostate cancer, a modified Lateral Flow Immune Assay (LFIA) with increased sensitivity and specificity was designed by taking advantage of the extremely high affinity between biotin and streptavidin and used. (2) Methods: The combination of a commercial biotinylated rabbit antibody (EPP11278), or the home-made biotinylated chicken antibody, and the nano-gold conjugated home-made chicken antibody or a commercial rabbit antibody (EPP11278), had the higher sensitivity and specificity in this modified LFIA to establish calibration curves from the two recombinant METCAM/MUC18 proteins and were used for determining METCAM/MUC18 concentrations in serum specimens from normal individuals, benign prostatic hyperplasia (BPH) patients, prostatic intraepithelial neoplasia (PIN) patients, prostate cancer patients with various Gleason scores, and treated patients. (3) Results: Data obtained by this modified LFIA were statistically better than traditional LFIA and prostate-specific antigen (PSA) test. Interestingly, serum METCAM/MUC18 concentrations were higher in pre-malignant PIN patients than prostate cancer patients and both were higher than normal individuals, BPH patients, and treated patients. Serum METCAM/MUC18 concentrations were directly proportional to most serum PSA. (4) Conclusions: Elevated serum METCAM/MUC18 concentrations may be used for predicting the malignant potential of prostate cancer at an early premalignant (PIN) stage, which is not achievable by the current PSA test.

Indexed as

biomarkerbiosensorbiotinylated antibodieshuman serummalignant potentialMETCAM/MUC18modified LFIAnano-gold conjugated antibodiesprostate cancerstreptavidin

Identifiers

PMID33806580
PMCPMC8000444
OpenAlexW3134706708

What OpenQuestion holds

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LicenceCC BY
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.