Evidence map›Paper›PMID 21075152›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2011

Tumor-targeted delivery of liposome-encapsulated doxorubicin by use of a peptide that selectively binds to irradiated tumors.

Amanda Lowery, Halina Onishko, Dennis E Hallahan, Zhaozhong Han

Open access · greenAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 88 citations in OpenAlex.

  1. Liposomal DoxorubicinCurrent drug delivery · 2024
    Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  6. Evaluation of NanotargetedInternational journal of molecular sciences · 2021
    Article
  7. Review
  8. PEGylated peptide to TIP1 is a novel targeting agent that binds specifically to various cancers in vivo.Journal of controlled release : official journal of the Controlled Release Society · 2019
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Tumor-targeting peptides from combinatorial libraries.Advanced drug delivery reviews · 2017
    Review
  14. Article
  15. Article
  16. Chemically enhanced radiotherapy: visions for the future.Annals of translational medicine · 2016
    Review
  17. Article
  18. Article
  19. Smart nanosystems: Bio-inspired technologies that interact with the host environment.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Review
  20. Nanotechnology in radiation oncology.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 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

4 authors at 2 institutions in 1 country.

Amanda LoweryDepartment of Radiation Oncology, School of Medicine, Vanderbilt University, Nashville, TN 37232, United States.
Halina Onishko
Dennis E Hallahan
Zhaozhong Han
Vanderbilt University · USWashington University in St. Louis · US

Funding

Vanderbilt In Vivo Cellular and Molecular Imaging CenterP50CA128323 · NCI · VANDERBILT UNIVERSITY · PI SHYR, YU · 2008 to 2012
$6.8M
Lysophospholipids in Radiation Induced Signal Transduction in Malignant GliomasR01CA140220 · NCI · WASHINGTON UNIVERSITY · PI HALLAHAN, DENNIS E · 2010 to 2014
$1.7M
Pharmacodynamic Assessment of RTK Inhibitors in CancerR01CA112385 · NCI · WASHINGTON UNIVERSITY · PI HALLAHAN, DENNIS E · 2005 to 2009
$1.3M
Roles of TIP-1 in Cancer RadiotherapyR01CA127482 · NCI · VANDERBILT UNIVERSITY · PI HAN, ZHAOZHONG · 2008 to 2011
$1.1M
NCI NIH HHS P50 CA128323NCI NIH HHS R01 CA112385NCI NIH HHS R01CA112385NCI NIH HHS R01 CA127482NCI NIH HHS R01CA127482NCI NIH HHS R01 CA140220
6 · The paper itself

Abstract

Tumor-targeted drug delivery improves anti-tumor efficacy and reduces systemic toxicity by limiting bioavailability of cytotoxic drugs to within tumors. Targeting reagents, such as peptides or antibodies recognizing molecular targets over-expressed within tumors, have been used to improve liposome-encapsulated drug accumulation within tumors and resulted in enhanced tumor growth control. In this report, we expand the scope of targeting reagents by showing that one peptide, HVGGSSV which was isolated from an in vivo screening of phage-displayed peptide library due to its selective binding within irradiated tumors, enabled highly selective tumor-targeted delivery of liposome-encapsulated doxorubicin and resulted in enhanced cytotoxicity within tumors. Targeting liposomes (TL) and non-targeting liposomes (nTL) were labeled with Alexa Fluor 750. Biodistribution of the liposomes within tumor-bearing mice was studied with near infrared (NIR) imaging. In the single dose pharmacokinetic study, the liposomal doxorubicin has an extended circulation half life as compared to the free doxorubicin. Targeting liposomes partitioned to the irradiated tumors and improved drug deposition and retention within tumors. The tumor-targeted delivery of doxorubicin improved tumor growth control as indicated with reduced tumor growth rate and tumor cell proliferation, enhanced tumor blood vessel destruction, and increased treatment-associated apoptosis and necrosis of tumor cells. Collectively, the results demonstrated the remarkable capability of the HVGGSSV peptide in radiation-guided drug delivery to tumors.

Indexed as

AnimalsAntibiotics, AntineoplasticDoxorubicinHumansLiposomesLungLung NeoplasmsMiceMice, Inbred C57BLMice, NudePeptidesAntibiotics, AntineoplasticDoxorubicinLiposomesPeptides

Identifiers

PMID21075152
PMCPMC3044774
OpenAlexW2014269617

What OpenQuestion holds

Textmetadata
LicenceTDM
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.