Evidence map›Paper›PMID 32066783›Full record

ArticleScientific reports2020

Study of glycosylation of prostate-specific antigen secreted by cancer tissue-originated spheroids reveals new candidates for prostate cancer detection.

Hiroko Ideo, Jumpei Kondo, Taisei Nomura, Norio Nonomura, Masahiro Inoue, Junko Amano

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 40 citations in OpenAlex.

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  13. Pro-Survival Factor EDEM3 Confers Therapy Resistance in Prostate Cancer.International journal of molecular sciences · 2022
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  20. Mass Spectrometry-Based Glycoproteomics and Prostate Cancer.International journal of molecular sciences · 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

6 authors at 5 institutions in 1 country.

Hiroko IdeoLaboratory of glycobiology, The Noguchi Institute, Tokyo, 173-0033, Japan.
Jumpei KondoDepartment of Clinical Bio-resource Research and Development, Graduate School of Medicine, Kyoto University, Kyoto, 606-8501, Japan.
Taisei NomuraAnimal Models of Human Diseases, National Institutes of Biomedical Innovation, Health and Nutrition, Osaka, 567-0085, Japan.
Norio NonomuraDepartment of Urology, Osaka University Graduate School of Medicine, Osaka, 565-0871, Japan.
Masahiro InoueDepartment of Clinical Bio-resource Research and Development, Graduate School of Medicine, Kyoto University, Kyoto, 606-8501, Japan.
Junko AmanoLaboratory of glycobiology, The Noguchi Institute, Tokyo, 173-0033, Japan. amano@noguchi.or.jp.
Noguchi Institute · JPKyoto University · JPNational Institute of Biomedical Innovation, Health and Nutrition · JPOsaka Medical Center for Cancer and Cardiovascular Diseases · JPOsaka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate-specific antigen (PSA) is the most frequently used biomarker for the screening of prostate cancer. Understanding the structure of cancer-specific glycans can help us improve PSA assay. In the present study, we analysed the glycans of PSA obtained from culture medium containing cancer tissue-originated spheroids (CTOS) which have similar characteristics as that of the parent tumour to explore the new candidates for cancer-related glycoforms of PSA. The glycan profile of PSA from CTOS was determined by comparing with PSA from normal seminal plasma and cancer cell lines (LNCaP and 22Rv1) using lectin chromatography and mass spectrometry. PSA from CTOS was mostly sialylated and the content of Wisteria floribunda agglutinin reactive glycan (LacdiNAc) was similar to that of PSA derived from seminal plasma and 22Rv1. Conversely, concanavalin A (Con A)-unbound PSA was definitely detected from the three cancer origins but was almost negligible in seminal PSA. Two novel types of PSA were elucidated in the Con A-unbound fraction: one is a high molecular weight PSA with highly branched N-glycans, and the other is a low molecular weight PSA without N-glycans. Furthermore, the existence of Lewis X antigen group on PSA was indicated. These PSAs will be candidates for new cancer-related markers.

Indexed as

Protein Processing, Post-TranslationalBiomarkers, TumorCarbohydrate SequenceCell Line, TumorChromatography, AffinityConcanavalin ACulture Media, ConditionedGlycopeptidesGlycosylationHumansLewis X AntigenMalePlant LectinsPolysaccharidesProstateProstate-Specific AntigenBiomarkers, TumorConcanavalin ACulture Media, ConditionedDatura stramonium lectinGlycopeptidesLewis X AntigenPlant LectinsPolysaccharidesProstate-Specific AntigenReceptors, N-Acetylglucosaminewisteria lectin

Identifiers

PMID32066783
PMCPMC7026178
OpenAlexW3006487802

What OpenQuestion holds

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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.