Evidence map›Paper›PMID 23479511›Full record

ArticleNeoplasia (New York, N.Y.)2013

Anti-HER3 domain 1 and 3 antibodies reduce tumor growth by hindering HER2/HER3 dimerization and AKT-induced MDM2, XIAP, and FoxO1 phosphorylation.

Yassamine Lazrek, Olivier Dubreuil, Véronique Garambois, Nadège Gaborit, Christel Larbouret, Christophe Le Clorennec, Gaelle Thomas, Wilhem Leconet, Marta Jarlier, Martine Pugnière and 8 more

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. HER3 in cancer: from the bench to the bedside.Journal of experimental & clinical cancer research : CR · 2022
    Review
  5. Article
  6. Thirty Years of HER3: From Basic Biology to Therapeutic Interventions.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Examination of HER3 targeting in cancer using monoclonal antibodies.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  19. Article
  20. The HER2 Signaling Network in Breast Cancer--Like a Spider in its Web.Journal of mammary gland biology and neoplasia · 2014
    Review
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

18 authors at 3 institutions in 1 country.

Yassamine LazrekInstitut de Recherche en Cancérologie de Montpellier, INSERM Unit 896, Université Montpellier 1, CRLC Val d'Aurelle Paul Lamarque, Montpellier, France.
Olivier Dubreuil
Véronique Garambois
Nadège Gaborit
Christel Larbouret
Christophe Le Clorennec
Gaelle Thomas
Wilhem Leconet
Marta Jarlier
Martine Pugnière
Nadia Vié
Bruno Robert
Céline Monnet
Khalil Bouayadi
Hakim Kharrat
Philippe Mondon
André Pèlegrin
Thierry Chardès
Université de Montpellier · FRInstitut de Recherche en Cancérologie de Montpellier · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Blockade of the human epidermal growth factor receptor 3 (HER3) and of the downstream phosphatidylinositide 3-kinase (PI3K)/AKT pathway is a prerequisite for overcoming drug resistance and to develop novel treatments for cancers that are not eligible for the currently approved targeted therapies. To this end, we generated specific antibodies (Abs) against domain 1 (D1) and domain 3 (D3) of HER3 that recognize epitopes that do not overlap with the neuregulin-binding site. The fully human H4B-121 Ab and the mouse monoclonal Abs 16D3-C1 and 9F7-F11 inhibited tumor growth in nude mice xenografted with epidermoid, pancreatic, or triple-negative breast cancer cells. The combination of one anti-HER3 Ab and trastuzumab improved tumor growth inhibition in mice xenografted with HER2(low) cancer cell lines, for which trastuzumab alone shows no or moderate efficiency. Ab-induced disruption of tumor growth was associated with G1 cell cycle arrest, proliferation inhibition, and apoptosis of cancer cells. Anti-HER3 Abs blocked HER2/HER3 heterodimerization and HER3 phosphorylation at the cell membrane, leading to inhibition of phosphorylation of the downstream AKT targets murine double minute 2, X-linked inhibitor of apoptosis, and forkhead box O1. This study demonstrates that anti-HER3 D1 and D3 Abs could represent a new option for immunotherapy of pancreatic and triple-negative breast cancers.

Indexed as

Amino Acid SequenceAnimalsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntibody SpecificityApoptosisCell Cycle CheckpointsCell Line, TumorCell ProliferationDimerizationEpitopesErb-b2 Receptor Tyrosine KinasesFemaleForkhead Box Protein O1Forkhead Transcription FactorsHumansAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedEpitopesErb-b2 Receptor Tyrosine KinasesForkhead Box Protein O1Forkhead Transcription FactorsFOXO1 protein, humanProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-mdm2Receptor, ErbB-3TrastuzumabX-Linked Inhibitor of Apoptosis Protein

Identifiers

PMID23479511
PMCPMC3593156
OpenAlexW2129230622

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.