Evidence map›Paper›PMID 22798260›Full record

ArticlePharmaceutical research2012

Mechanisms of tumor vascular priming by a nanoparticulate doxorubicin formulation.

Tista Roy Chaudhuri, Robert D Arnold, Jun Yang, Steven G Turowski, Yang Qu, Joseph A Spernyak, Richard Mazurchuk, Donald E Mager, Robert M Straubinger

Open access · greenAbstract read
In one paragraph

Article in Pharmaceutical research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Dual-Hit Strategy for Therapeutic Targeting of Pancreatic Cancer in Patient-Derived Xenograft Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Improving the distribution of Doxil® in the tumor matrix by depletion of tumor hyaluronan.Journal of controlled release : official journal of the Controlled Release Society · 2014
    Article
  8. A robust and quantitative method for tracking liposome contents after intravenous administration.Journal of controlled release : official journal of the Controlled Release Society · 2014
    Article
  9. Article
  10. 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

9 authors at 3 institutions in 1 country.

Tista Roy ChaudhuriDepartment of Pharmaceutical Sciences, University at Buffalo, State University of New York, 445 Kapoor Hall, Buffalo, New York 14214-8033, USA.
Robert D Arnold
Jun Yang
Steven G Turowski
Yang Qu
Joseph A Spernyak
Richard Mazurchuk
Donald E Mager
Robert M Straubinger
University at Buffalo, State University of New York · USRoswell Park Comprehensive Cancer Center · USAuburn University · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
Drug carrier of blood/tumor/brain permeabilityR01CA107570 · NCI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI STRAUBINGER, ROBERT M · 2004 to 2008
$1.6M
NCI NIH HHS P30 CA016056NCI NIH HHS P30-CA016056NCI NIH HHS R01 CA107570NCI NIH HHS R01-CA107570
6 · The paper itself

Abstract

purposeTumor vascular normalization by antiangiogenic agents may increase tumor perfusion but reestablish vascular barrier properties in CNS tumors. Vascular priming via nanoparticulate carriers represents a mechanistically distinct alternative. This study investigated mechanisms by which sterically-stabilized liposomal doxorubicin (SSL-DXR) modulates tumor vascular properties.

methodsFunctional vascular responses to SSL-DXR were investigated in orthotopic rat brain tumors using deposition of fluorescent permeability probes and dynamic contrast-enhanced magnetic resonance imaging. Microvessel density and tumor burden were quantified by immunohistochemistry (CD-31) and quantitative RT-PCR (VE-cadherin).

resultsAdministration of SSL-DXR (5.7 mg/kg iv) initially (3-4 days post-treatment) decreased tumor vascular permeability, k(trans) (vascular exchange constant), vascular endothelial cell content, microvessel density, and deposition of nanoparticulates. Tumor vasculature became less chaotic. Permeability and perfusion returned to control values 6-7 days post-treatment, but intratumor SSL-DXR depot continued to effect tumor vascular endothelial compartment 7-10 days post-treatment, mediating enhanced permeability.

conclusionsSSL-DXR ultimately increased tumor vascular permeability, but initially normalized tumor vasculature and decreased tumor perfusion, permeability, and nanoparticulate deposition. These temporal changes in vascular integrity resulting from a single SSL-DXR dose have important implications for the design of combination therapies incorporating nanoparticle-based agents for tumor vascular priming.

Indexed as

AnimalsAntibiotics, AntineoplasticBrainBrain NeoplasmsCapillary PermeabilityDoxorubicinLiposomesMaleNeovascularization, PathologicRatsRats, Inbred F344Rats, Sprague-DawleyAntibiotics, AntineoplasticDoxorubicinLiposomes

Identifiers

PMID22798260
PMCPMC3631713
OpenAlexW2048395537

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.