Evidence map›Paper›PMID 22114188›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Targeted drug delivery to tumor vasculature by a carbohydrate mimetic peptide.

Shingo Hatakeyama, Kazuhiro Sugihara, Toshiaki K Shibata, Jun Nakayama, Tomoya O Akama, Naoaki Tamura, Shuk-Man Wong, Andrey A Bobkov, Yutaka Takano, Chikara Ohyama and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. 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
3.6field-weighted citation impact, top 6% 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, 96 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Vasculature organotropism in drug delivery.Advanced drug delivery reviews · 2023
    Review
  5. Review
  6. Designed Multifunctional Peptides for Intracellular Targets.Antibiotics (Basel, Switzerland) · 2022
    Review
  7. Synergetic Enhancement of Tumor Double-Targeted MRI Nano-Probe.International journal of molecular sciences · 2022
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Targeting Tumors with Small Molecule Peptides.Current cancer drug targets · 2016
    Review
  18. Article
  19. Review
  20. 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

12 authors at 4 institutions in 2 countries.

Shingo HatakeyamaTumor Microenvironment Program, Cancer Center, Sanford-Burnham Medical Research Institute, La Jolla, CA 92037, USA.
Kazuhiro Sugihara
Toshiaki K Shibata
Jun Nakayama
Tomoya O Akama
Naoaki Tamura
Shuk-Man Wong
Andrey A Bobkov
Yutaka Takano
Chikara Ohyama
Minoru Fukuda
Michiko N Fukuda
Sanford Burnham Prebys Medical Discovery Institute · USHamamatsu University School of Medicine · JPHirosaki University · JPShinshu University · JP

Funding

THE A(1,3)FUCOSYLTRANSFERASE GENES AND SELECTIN LIGAND EXPRESSIONP01CA071932 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI FUKUDA, MINORU · 1996 to 2012
$15.5M
NCI NIH HHS P01 CA071932NCI NIH HHS P01CA071932
6 · The paper itself

Abstract

Although numerous carbohydrates play significant roles in mammalian cells, carbohydrate-based drug discovery has not been explored due to the technical difficulty of chemically synthesizing complex carbohydrate structures. Previously, we identified a series of carbohydrate mimetic peptides and found that a 7-mer peptide, designated I-peptide, inhibits hematogenous carbohydrate-dependent cancer cell colonization. During analysis of the endothelial surface receptor for I-peptide, we found that I-peptide bound to annexin 1 (Anxa1). Because Anxa1 is a highly specific tumor vasculature surface marker, we hypothesized that an I-peptide-like peptide could target anticancer drugs to the tumor vasculature. This study identifies IFLLWQR peptide, designated IF7, as homing to tumors. When synthetic IF7 peptide was conjugated to fluorescent Alexa 488 (A488) and injected intravenously into tumor-bearing mice, IF7-A488 targeted tumors within minutes. IF7 conjugated to the potent anticancer drug SN-38 and injected intravenously into nude mice carrying human colon HCT116 tumors efficiently suppressed tumor growth at low dosages with no apparent side effects. These results suggest that IF7 serves as an efficient drug delivery vehicle by targeting Anxa1 expressed on the surface of tumor vasculature. Given its extremely specific tumor-targeting activity, IF7 may represent a clinically relevant vehicle for anticancer drugs.

Indexed as

Amino Acid SequenceAnimalsAnnexin A1Antineoplastic Combined Chemotherapy ProtocolsCamptothecinCarbohydratesCell Line, TumorDrug Delivery SystemsHCT116 CellsHumansHydrazinesInjections, IntravenousIrinotecanLuminescent MeasurementsMiceMice, Inbred C57BLAlexa 488 hydrazideAnnexin A1CamptothecinCarbohydratesHydrazinesIrinotecanPeptides

Identifiers

PMID22114188
PMCPMC3241764
OpenAlexW2023344421

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.