Evidence map›Paper›PMID 9664085›Full record

ArticleThe Journal of clinical investigation1998

Molecular heterogeneity of the vascular endothelium revealed by in vivo phage display.

D Rajotte, W Arap, M Hagedorn, E Koivunen, R Pasqualini, E Ruoslahti

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 145 papers.

0numbers the graph read from it
0cells of the map it votes in
145citing papers in PubMed
17.7field-weighted citation impact, top 1% 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

145 citing papers in PubMed, 457 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Ceramide as an endothelial cell surface receptor and a lung-specific lipid vascular target for circulating ligands.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  7. Article
  8. Cardiomyocyte Targeting Peptide to Deliver Amiodarone.bioRxiv : the preprint server for biology · 2023
    Article
  9. Review
  10. Review
  11. Molecular ZIP codes in targeted drug delivery.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Review
  12. Review
  13. Molecular analysis of vascular gene expression.Research and practice in thrombosis and haemostasis · 2022
    Article
  14. T7 Phage as an Emerging Nanobiomaterial with Genetically Tunable Target Specificity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

85 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 3 countries.

D RajotteResearch Center, The Burnham Institute, 10901 North Torrey Pines Road, La Jolla, California 92037, USA.
W Arap
M Hagedorn
E Koivunen
R Pasqualini
E Ruoslahti
Spanish Oncology Genitourinary Group · ESDiscovery Institute · USSanford Burnham Prebys Medical Discovery Institute · USUniversity of Helsinki · FI

Funding

Tumor Microenvironment and Cancer ImmunologyP30CA030199 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI Maximiliano A DAngelo · 1985 to 2026
$107.2M
TISSUE TARGETING WITH PHAGE LIBRARIESR01CA074238 · NCI · BURNHAM INSTITUTE FOR MEDICAL RESEARCH · PI RUOSLAHTI, ERKKI I · 1997 to 2001
$572k
NCI NIH HHS CA 30199NCI NIH HHS CA 74238
6 · The paper itself

Abstract

Vascular beds are known to differ in structure and metabolic function, but less is known about their molecular diversity. We have studied organ-specific molecular differences of the endothelium in various tissues by using in vivo screening of peptide libraries expressed on the surface of a bacteriophage. We report here that targeting of a large number of tissues with this method yielded, in each case, phage that homed selectively to the targeted organ. Different peptide motifs were recovered from each of these tissues. The enrichment in homing to the target organs relative to an unselected phage was 3-35-fold. Peptide sequences that conferred selective phage homing to the vasculature of lung, skin, and pancreas were characterized in detail. Immunohistochemistry showed that the phage localized in the blood vessels of their target organ. When tested, the phage homing was blocked in the presence of the cognate peptide. By targeting several tissues and by showing that specific homing could be achieved in each case, we provide evidence that organ- and tissue-specific molecular heterogeneity of the vasculature is a general, perhaps even universal, phenomenon. Our results also show that these molecular differences can serve as molecular addresses.

Indexed as

BacteriophagesPeptide LibraryAnimalsEndothelium, VascularFemaleGenetic VectorsMiceMice, Inbred BALB CMice, NudePeptidesRatsRecombinant Fusion ProteinsPeptide LibraryPeptidesRecombinant Fusion Proteins

Identifiers

PMID9664085
PMCPMC508902
OpenAlexW2015615249

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.