Evidence map›Paper›PMID 35077861›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2022

Antitumor activity of a lectibody targeting cancer-associated high-mannose glycans.

Young Jun Oh, Matthew W Dent, Angela R Freels, Qingwen Zhou, Carlito B Lebrilla, Michael L Merchant, Nobuyuki Matoba

Open access · greenAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Chimerolectins: Classification, structural architecture, and functional perspectives.Protein science : a publication of the Protein Society · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Metabolomic differences between exanthematous drug eruption and infectious mononucleosis.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2024
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Lectin Drug Conjugates Targeting High Mannose N-Glycans.Chembiochem : a European journal of chemical biology · 2022
    Article
  17. Targeting glycans for CAR therapy: The advent of sweet CARs.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Review
  18. Review
  19. Extending Janus lectins architecture: Characterization and application to protocells.Computational and structural biotechnology journal · 2022
    Article
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

7 authors at 2 institutions in 1 country.

Young Jun OhUofL Health - Brown Cancer Center, University of Louisville School of Medicine, 505 S. Hancock Street, Louisville, KY 40202, USA.
Matthew W DentUofL Health - Brown Cancer Center, University of Louisville School of Medicine, 505 S. Hancock Street, Louisville, KY 40202, USA; Department of Pharmacology and Toxicology, University of Louisville School of Medicine, Louisville, KY, USA.
Angela R FreelsUofL Health - Brown Cancer Center, University of Louisville School of Medicine, 505 S. Hancock Street, Louisville, KY 40202, USA.
Qingwen ZhouDepartment of Chemistry, University of California Davis, Davis, CA 95616, USA.
Carlito B LebrillaDepartment of Chemistry, University of California Davis, Davis, CA 95616, USA.
Michael L MerchantDivision of Nephrology and Hypertension, Department of Medicine, University of Louisville School of Medicine, KY, USA.
Nobuyuki MatobaUofL Health - Brown Cancer Center, University of Louisville School of Medicine, 505 S. Hancock Street, Louisville, KY 40202, USA; Department of Pharmacology and Toxicology, University of Louisville School of Medicine, Louisville, KY, USA; Center for Predictive Medicine, University of Louisville School of Medicine, Louisville, KY, USA. Electronic address: n.matoba@louisville.edu.
University of Louisville · USUniversity of California, Davis · US

Funding

Role of oxidized linoleic acid metabolites in the pathogenesis of alcoholic liver diseaseP20GM113226 · NIGMS · UNIVERSITY OF LOUISVILLE · PI GHARE, SMITA S · 2016 to 2025
$24.1M
The Role of Nutrition in the Development/Progression of Alcohol-Induced Organ InjuryP50AA024337 · NIAAA · UNIVERSITY OF LOUISVILLE · PI SHIRISH S BARVE · 2016 to 2026
$17.9M
University of Louisville Center for Integrative Environmental Health SciencesP30ES030283 · NIEHS · UNIVERSITY OF LOUISVILLE · PI J CHRISTOPHER STATES · 2020 to 2026
$10.0M
UOFL ENVIRONMENTAL HEALTH SCIENCES TRAINING PROGRAMT32ES011564 · NIEHS · UNIVERSITY OF LOUISVILLE · PI David W Hein, John Pierce Wise · 2004 to 2026
$7.1M
PILOT PROJECT PROGRAMP30GM106396 · NIGMS · UNIVERSITY OF LOUISVILLE · PI EATON, JOHN W · 2013 to 2017
$5.4M
Investigation of a lectibody targeting tumor-associated oligomannose glycansR21CA216447 · NCI · UNIVERSITY OF LOUISVILLE · PI MATOBA, NOBUYUKI · 2018 to 2019
$359k
NCI NIH HHS R21 CA216447NIAAA NIH HHS P50 AA024337NIEHS NIH HHS P30 ES030283NIEHS NIH HHS T32 ES011564NIGMS NIH HHS P20 GM113226NIGMS NIH HHS P30 GM106396
6 · The paper itself

Abstract

Aberrant protein glycosylation is a hallmark of cancer, but few drugs targeting cancer glycobiomarkers are currently available. Here, we showed that a lectibody consisting of the high-mannose glycan-binding lectin Avaren and human immunoglobulin G1 (IgG1) Fc (AvFc) selectively recognizes a range of cell lines derived from lung, breast, colon, and blood cancers at nanomolar concentrations. Binding of AvFc to the non-small cell lung cancer (NSCLC) cell lines A549 and H460 was characterized in detail. Co-immunoprecipitation proteomics analysis revealed that epidermal growth factor receptor (EGFR) and insulin-like growth factor 1 receptor (IGF1R) are among the lectibody's common targets in these cells. AvFc blocked the activation of EGFR and IGF1R by their respective ligands in A549 cells and inhibited the migration of A549 and H460 cells upon stimulation with EGF and IGF1. Furthermore, AvFc induced potent Fc-mediated cytotoxic effects and significantly restricted A549 and H460 tumor growth in severe combined immunodeficiency (SCID) mice. Immunohistochemistry analysis of primary lung tissues from NSCLC patients demonstrated that AvFc preferentially binds to tumors over adjacent non-tumor tissues. Our findings provide evidence that increased abundance of high-mannose glycans in the glycocalyx of cancer cells can be a druggable target, and AvFc may provide a new tool to probe and target this tumor-associated glycobiomarker.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAnimalsCell Line, TumorErbB ReceptorsHumansMannoseMicePolysaccharidesErbB ReceptorsMannosePolysaccharidesavarenepidermal growth factor receptorhigh mannose glycaninsulin-like growth factor 1 receptorlectibodynon-small cell lung cancertumor-associated carbohydrate antigen

Identifiers

PMID35077861
PMCPMC9077314
OpenAlexW4225987499

What OpenQuestion holds

Textmetadata
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.