Evidence map›Paper›PMID 32205858›Full record

ArticleLaboratory investigation; a journal of technical methods and pathology2020

Altered glycosylation of glycodelin in endometrial carcinoma.

Laura C Hautala, Poh-Choo Pang, Aristotelis Antonopoulos, Annukka Pasanen, Cheuk-Lun Lee, Philip C N Chiu, William S B Yeung, Mikko Loukovaara, Ralf Bützow, Stuart M Haslam and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Laboratory investigation; a journal of technical methods and pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

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  11. Tumor reversion: a dream or a reality.Biomarker research · 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

12 authors at 3 institutions in 3 countries.

Laura C HautalaDepartment of Clinical Chemistry, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Poh-Choo PangDepartment of Life Sciences, Imperial College London, London, UK.
Aristotelis AntonopoulosDepartment of Life Sciences, Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-1592-4092
Annukka PasanenDepartment of Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Cheuk-Lun LeeDepartment of Obstetrics and Gynaecology, The University of Hong Kong, Hong Kong SAR, China.
Philip C N ChiuDepartment of Obstetrics and Gynaecology, The University of Hong Kong, Hong Kong SAR, China.
William S B YeungDepartment of Obstetrics and Gynaecology, The University of Hong Kong, Hong Kong SAR, China.
Mikko LoukovaaraDepartment of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Ralf BützowDepartment of Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Stuart M HaslamDepartment of Life Sciences, Imperial College London, London, UK.
Anne DellDepartment of Life Sciences, Imperial College London, London, UK.
Hannu KoistinenDepartment of Clinical Chemistry, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. hannu.k.koistinen@helsinki.fi.ORCID http://orcid.org/0000-0003-0926-3109
University of Helsinki · FIImperial College London · GBUniversity of Hong Kong · HK

Funding

Biotechnology and Biological Sciences Research Council BB/K016164/1
6 · The paper itself

Abstract

Glycodelin is a major glycoprotein expressed in reproductive tissues, like secretory and decidualized endometrium. It has several reproduction related functions that are dependent on specific glycosylation, but it has also been found to drive differentiation of endometrial carcinoma cells toward a less malignant phenotype. Here we aimed to elucidate whether the glycosylation and function of glycodelin is altered in endometrial carcinoma as compared with a normal endometrium. We carried out glycan structure analysis of glycodelin expressed in HEC-1B human endometrial carcinoma cells (HEC-1B Gd) by mass spectrometry glycomics strategies. Glycans of HEC-1B Gd were found to comprise a typical mixture of high-mannose, hybrid, and complex-type N-glycans, often containing undecorated LacNAc (Galβ1-4GlcNAc) antennae. However, several differences, as compared with previously reported glycan structures of normal human decidualized endometrium-derived glycodelin isoform, glycodelin-A (GdA), were also found. These included a lower level of sialylation and more abundant poly-LacNAc antennae, some of which are fucosylated. This allowed us to select lectins that showed different binding to these classes of glycodelin. Despite the differences in glycosylation between HEC-1B Gd and GdA, both showed similar inhibitory activity on trophoblast cell invasion and peripheral blood mononuclear cell proliferation. For the detection of cancer associated glycodelin, we established a novel in situ proximity-ligation based histochemical staining method using a specific glycodelin antibody and UEAI lectin. We found that the UEAI reactive glycodelin was abundant in endometrial carcinoma, but virtually absent in normal endometrial tissue even when glycodelin was strongly expressed. In conclusion, we established a histochemical staining method for the detection of endometrial carcinoma-associated glycodelin and showed that this specific glycodelin is exclusively expressed in cancer, not in normal endometrium. Similar methods can be used for studies of other glycoproteins.

Indexed as

Endometrial NeoplasmsGlycodelinUterine NeoplasmsCarbohydrate SequenceCell Line, TumorFemaleGlycomicsGlycosylationHumansLectinsMass SpectrometryPlacentaPregnancyGlycodelinLectins

Identifiers

PMID32205858
PMCPMC7312397
OpenAlexW3012695622

What OpenQuestion holds

Textmetadata
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.