Evidence map›Paper›PMID 34711645›Full record

ArticleMolecular cancer therapeutics2021

Multimeric Anti-DR5 IgM Agonist Antibody IGM-8444 Is a Potent Inducer of Cancer Cell Apoptosis and Synergizes with Chemotherapy and BCL-2 Inhibitor ABT-199.

Beatrice T Wang, Tasnim Kothambawala, Ling Wang, Thomas J Matthew, Susan E Calhoun, Avneesh K Saini, Maya F Kotturi, Genevive Hernandez, Eric W Humke, Marvin S Peterson and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed, 49 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Understanding IgM Structure and Biology to Engineer New Antibody Therapeutics.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  9. Article
  10. Review
  11. Article
  12. Advances in the study of death receptor 5.Frontiers in pharmacology · 2025
    Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Cancer therapy with antibodies.Nature reviews. Cancer · 2024
    Review
  19. Review
  20. 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

12 authors at 1 institution in 1 country.

Beatrice T WangIGM Biosciences Inc., Mountain View, California.ORCID 0000-0002-5857-8097
Tasnim Kothambawala *IGM Biosciences Inc., Mountain View, California.ORCID 0000-0001-8865-4241
Ling Wang *IGM Biosciences Inc., Mountain View, California.
Thomas J Matthew *IGM Biosciences Inc., Mountain View, California.
Susan E CalhounIGM Biosciences Inc., Mountain View, California.
Avneesh K SainiIGM Biosciences Inc., Mountain View, California.
Maya F KotturiIGM Biosciences Inc., Mountain View, California.ORCID 0000-0002-9387-860X
Genevive HernandezIGM Biosciences Inc., Mountain View, California.ORCID 0000-0001-9226-1889
Eric W HumkeIGM Biosciences Inc., Mountain View, California.ORCID 0000-0002-1137-8557
Marvin S PetersonIGM Biosciences Inc., Mountain View, California.
Angus M SinclairIGM Biosciences Inc., Mountain View, California.ORCID 0000-0002-2467-3301
Bruce A KeytIGM Biosciences Inc., Mountain View, California. bkeyt@igmbio.com.
IGM Biosciences (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Death receptor 5 (DR5) is an attractive target for cancer therapy due to its broad upregulated expression in multiple cancers and ability to directly induce apoptosis. Though anti-DR5 IgG antibodies have been evaluated in clinical trials, limited efficacy has been attributed to insufficient receptor crosslinking. IGM-8444 is an engineered, multivalent agonistic IgM antibody with 10 binding sites to DR5 that induces cancer cell apoptosis through efficient DR5 multimerization. IGM-8444 bound to DR5 with high avidity and was substantially more potent than an IgG with the same binding domains. IGM-8444 induced cytotoxicity in a broad panel of solid and hematologic cancer cell lines but did not kill primary human hepatocytes

Indexed as

AnimalsAntineoplastic AgentsApoptosisBridged Bicyclo Compounds, HeterocyclicCell Line, TumorDisease Models, AnimalFemaleGenes, bcl-2HumansImmunoglobulin MMiceMice, NudeReceptors, TNF-Related Apoptosis-Inducing LigandSulfonamidesAntineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicImmunoglobulin MReceptors, TNF-Related Apoptosis-Inducing LigandSulfonamidesvenetoclax

Identifiers

PMID34711645
PMCPMC9398157
OpenAlexW3209553127

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.