Evidence map›Paper›PMID 30111774›Full record

ArticleScientific reports2018

Novel monoclonal antibody L2A5 specifically targeting sialyl-Tn and short glycans terminated by alpha-2-6 sialic acids.

Liliana R Loureiro, Diana P Sousa, Dylan Ferreira, Wengang Chai, Luís Lima, Carina Pereira, Carla B Lopes, Viviana G Correia, Lisete M Silva, Chunxia Li and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

36 citing papers in PubMed, 54 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

16 authors at 7 institutions in 4 countries.

Liliana R LoureiroUCIBIO-REQUIMTE, Department of Life Sciences, Faculty of Science and Technology, NOVA University of Lisbon, Lisbon, 2829, Portugal.ORCID 0000-0002-7150-6354
Diana P SousaUCIBIO-REQUIMTE, Department of Life Sciences, Faculty of Science and Technology, NOVA University of Lisbon, Lisbon, 2829, Portugal.ORCID 0000-0003-3474-5417
Dylan FerreiraExperimental Pathology and Therapeutics Group, IPO-Porto Research Center, Portuguese Institute of Oncology of Porto, Porto, 4200, Portugal.
Wengang ChaiGlycosciences Laboratory - Department of Medicine, Imperial College London, London, W12 0NN, United Kingdom.
Luís LimaExperimental Pathology and Therapeutics Group, IPO-Porto Research Center, Portuguese Institute of Oncology of Porto, Porto, 4200, Portugal.
Carina PereiraCINTESIS - Center for Health Technology and Services Research, University of Porto, Porto, 4200, Portugal.
Carla B LopesJoaquim Chaves Saúde, Anatomical Pathology Laboratory, Lisboa, 1170, Portugal.
Viviana G CorreiaUCIBIO-REQUIMTE, Department of Chemistry, Faculty of Science and Technology, NOVA University of Lisbon, Lisbon, 2829, Portugal.
Lisete M SilvaGlycosciences Laboratory - Department of Medicine, Imperial College London, London, W12 0NN, United Kingdom.
Chunxia LiKey Laboratory of Marine Drugs of Ministry of Education, and Shandong Provincial Key Laboratory of Glycoscience and Glycoengineering, School of Medicine and Pharmacy, Ocean University of China, Qingdao, 266003, China.
Lúcio Lara SantosExperimental Pathology and Therapeutics Group, IPO-Porto Research Center, Portuguese Institute of Oncology of Porto, Porto, 4200, Portugal.
José Alexandre FerreiraExperimental Pathology and Therapeutics Group, IPO-Porto Research Center, Portuguese Institute of Oncology of Porto, Porto, 4200, Portugal.ORCID 0000-0002-0097-6148
Ana BarbasiBET, Instituto de Biologia Experimental e Tecnológica, Oeiras, 2780, Portugal.ORCID 0000-0002-6245-8549
Angelina S PalmaGlycosciences Laboratory - Department of Medicine, Imperial College London, London, W12 0NN, United Kingdom.
Carlos NovoUCIBIO-REQUIMTE, Department of Life Sciences, Faculty of Science and Technology, NOVA University of Lisbon, Lisbon, 2829, Portugal. cnovo@ihmt.unl.pt.
Paula A VideiraUCIBIO-REQUIMTE, Department of Life Sciences, Faculty of Science and Technology, NOVA University of Lisbon, Lisbon, 2829, Portugal. p.videira@fct.unl.pt.ORCID 0000-0001-5987-2485
University of Lisbon · PTUniversidade do Porto · PTClovis Oncology (United Kingdom) · GBAlliant International University · USHospital de Santa Cruz · PTInstituto Português de Oncologia Francisco Gentil · PTOcean University of China · CN

Funding

Wellcome Trust
6 · The paper itself

Abstract

Incomplete O-glycosylation is a feature associated with malignancy resulting in the expression of truncated glycans such as the sialyl-Tn (STn) antigen. Despite all the progress in the development of potential anti-cancer antibodies, their application is frequently hindered by low specificities and cross-reactivity. In this study, a novel anti-STn monoclonal antibody named L2A5 was developed by hybridoma technology. Flow cytometry analysis showed that L2A5 specifically binds to sialylated structures on the cell surface of STn-expressing breast and bladder cancer cell lines. Moreover, immunoblotting assays demonstrated reactivity to tumour-associated O-glycosylated proteins, such as MUC1. Tumour recognition was further observed using immunohistochemistry assays, which demonstrated a high sensitivity and specificity of L2A5 mAb towards cancer tissue, using bladder and colorectal cancer tissues. L2A5 staining was exclusively tumoural, with a remarkable reactivity in invasive and metastasis sites, not detectable by other anti-STn mAbs. Additionally, it stained 20% of cases of triple-negative breast cancers, suggesting application in diseases with unmet clinical needs. Finally, the fine specificity was assessed using glycan microarrays, demonstrating a highly specific binding of L2A5 to core STn antigens and additional ability to bind 2-6-linked sialyl core-1 probes. In conclusion, this study describes a novel anti-STn antibody with a unique binding specificity that can be applied for cancer diagnostic and future development of new antibody-based therapeutic applications.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, Tumor-Associated, CarbohydrateBreast NeoplasmsCell Line, TumorFemaleGlycosylationHumansHybridomasMiceMice, Inbred BALB CNeoplasm ProteinsPolysaccharidesSialic AcidsUrinary Bladder NeoplasmsAntibodies, MonoclonalAntigens, Tumor-Associated, CarbohydrateNeoplasm ProteinsPolysaccharidesSialic Acidssialosyl-Tn antigen

Identifiers

PMID30111774
PMCPMC6093877
OpenAlexW2887954794

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.