Evidence map›Paper›PMID 27351129›Full record

ArticleOncotarget2016

Inhibition of primary breast tumor growth and metastasis using a neuropilin-1 transmembrane domain interfering peptide.

Alexia Arpel, Coralie Gamper, Caroline Spenlé, Aurore Fernandez, Laurent Jacob, Nadège Baumlin, Patrice Laquerriere, Gertraud Orend, Gérard Crémel, Dominique Bagnard

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.0field-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

22 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Antiviral Peptides as Anti-Influenza Agents.International journal of molecular sciences · 2022
    Review
  4. Neuropilin (NRPs) Related Pathological Conditions and Their Modulators.International journal of molecular sciences · 2022
    Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. FunctionalizedCancers · 2019
    Article
  16. Neuropilins Controlling Cancer Therapy Responsiveness.International journal of molecular sciences · 2019
    Review
  17. Neuropilins in the Context of Tumor Vasculature.International journal of molecular sciences · 2019
    Review
  18. Article
  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

10 authors at 4 institutions in 1 country.

Alexia ArpelINSERM U 1109, MN3T Laboratory, Labex Medalis, Strasbourg University, Strasbourg, France.
Coralie GamperINSERM U 1109, MN3T Laboratory, Labex Medalis, Strasbourg University, Strasbourg, France.
Caroline SpenléINSERM U 1109, MN3T Laboratory, Labex Medalis, Strasbourg University, Strasbourg, France.
Aurore FernandezINSERM U 1109, MN3T Laboratory, Labex Medalis, Strasbourg University, Strasbourg, France.
Laurent JacobINSERM U 1109, MN3T Laboratory, Labex Medalis, Strasbourg University, Strasbourg, France.
Nadège BaumlinINSERM U 1109, MN3T Laboratory, Labex Medalis, Strasbourg University, Strasbourg, France.
Patrice LaquerriereCNRS UMR 7178, Institut Pluridisciplinaire Hubert Curien, Strasbourg University, Strasbourg, France.
Gertraud OrendINSERM U 1109, MN3T Laboratory, Labex Medalis, Strasbourg University, Strasbourg, France.
Gérard CrémelINSERM U 1109, MN3T Laboratory, Labex Medalis, Strasbourg University, Strasbourg, France.
Dominique BagnardINSERM U 1109, MN3T Laboratory, Labex Medalis, Strasbourg University, Strasbourg, France.
Université de Strasbourg · FRInserm · FRCentre National de la Recherche Scientifique · FRInstitut Pluridisciplinaire Hubert Curien · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transmembrane domains (TMD) in membrane receptors play a key role in cell signaling. As previously shown by us a peptide targeting the TMD of neuropilin-1 (MTP-NRP1), blocks cell proliferation, cell migration and angiogenesis in vitro, and decreases glioblastoma growth in vivo. We now explored the clinical potential of MTP-NRP1 on breast cancer models and demonstrate that MTP-NRP1 blocks proliferation of several breast cancer lines including the MDA-MB-231, a triple negative human breast cancer cell line. In models with long term in vivo administration of the peptide, MTP-NRP1 not only reduced tumor volume but also decreased number and size of breast cancer metastases. Strikingly, treating mice before tumors developed protected from metastasis establishment/formation. Overall, our results report that targeting the TMD of NRP1 in breast cancer is a potent new strategy to fight against breast cancer and related metastasis.

Indexed as

Xenograft Model Antitumor AssaysAmino Acid SequenceAnimalsBreast NeoplasmsCell Line, TumorCell ProliferationFemaleHEK293 CellsHumansKaplan-Meier EstimateMCF-7 CellsMiceNeoplasm MetastasisNeuropilin-1PeptidesTumor BurdenNeuropilin-1Peptidesbreast cancermetastasisneuropilin-1peptidetreatment

Identifiers

PMID27351129
PMCPMC5342376
OpenAlexW2419832609

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.