Evidence map›Paper›PMID 17600129›Full record

ArticleThe American journal of pathology2007

Molecular changes in the vasculature of injured tissues.

Tero A H Järvinen, Erkki Ruoslahti

Abstract read
In one paragraph

Article in The American journal of pathology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
–field-weighted citation impact
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

47 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Molecular ZIP codes in targeted drug delivery.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Review
  9. Article
  10. Article
  11. Review
  12. Exposed CendR Domain in Homing Peptide Yields Skin-Targeted Therapeutic in Epidermolysis Bullosa.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    Article
  13. Carbonic Anhydrase VI in Skin Wound Healing Study onInternational journal of molecular sciences · 2020
    Article
  14. Review
  15. Article
  16. Review
  17. Bacteriophage-based biomaterials for tissue regeneration.Advanced drug delivery reviews · 2019
    Review
  18. Review
  19. Article
  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

2 authors.

Tero A H JärvinenCancer Research Center, Burnham Institute for Medical Research, La Jolla, CA, USA.
Erkki Ruoslahti

Funding

Tumor Microenvironment and Cancer ImmunologyP30CA030199 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI Michael Jackson · 1985 to 2026
$107.2M
Tumor Therapy/Annihilation Using a Smart NanoPlatform (SNaP)U54CA119335 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ESENER, SADIK · 2005 to 2010
$21.2M
VASCULAR TARGETING WITH PHAGE LIBRARIESP01CA082713 · NCI · BURNHAM INSTITUTE FOR MEDICAL RESEARCH · PI RUOSLAHTI, ERKKI · 2000 to 2004
$9.3M
NCI NIH HHS CA 119335NCI NIH HHS CA 30199NCI NIH HHS CA 82713NCI NIH HHS P01 CA082713NCI NIH HHS P30 CA030199NCI NIH HHS U54 CA119335
6 · The paper itself

Abstract

We have explored molecular specialization of the vasculature of regenerating wound tissue in the skin and tendons to identify a different repertoire of markers from that obtained by studying tumor vasculature. We screened a phage-displayed peptide library for peptides that home to wounds in mice and identified two peptides that selectively target phage to skin and tendon wounds: CARSKNKDC (CAR) and CRKDKC (CRK). CAR is homologous to heparin-binding sites in various proteins and binds to cell surface heparan sulfate and heparin. CRK is similar to a segment in thrombospondin type 1 repeat. Intravenously injected CAR and CRK phage, as well as fluorescein-labeled CAR and CRK peptides, selectively accumulated at wound sites, where they partially co-localized with blood vessels. The CAR peptide showed a preference for early stages of wound healing, whereas the CRK favored wounds at later stages of healing. The CAR peptide was internalized into the target cells and delivered the fluorescent label into the cell nuclei. These results identify new molecular markers in wound tissues and show that the expression of these markers in wound vasculature changes as healing progresses. The peptides recognizing these markers may be useful in delivering treatments into regenerating tissues.

Indexed as

Peptide LibraryAmino Acid SequenceAnimalsBacteriophagesCHO CellsCricetinaeCricetulusMiceMice, Inbred BALB CMicroscopy, FluorescenceNeovascularization, PathologicOligopeptidesRatsRats, Sprague-DawleySkinTendon InjuriesOligopeptidesPeptide Library

Identifiers

PMID17600129
PMCPMC1934529

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.