Evidence map›Paper›PMID 19687214›Full record

ArticleProceedings of the American Thoracic Society2009

Targeting and imaging signature caveolar molecules in lungs.

Kerri A Massey, Jan E Schnitzer

Abstract read
In one paragraph

Article in Proceedings of the American Thoracic Society, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Polymeric nanoparticles in development for treatment of pulmonary infectious diseases.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2016
    Review
  6. Article
  7. Article
  8. Challenges in design and characterization of ligand-targeted drug delivery systems.Journal of controlled release : official journal of the Controlled Release Society · 2012
    Review
  9. Antioxidant protection by PECAM-targeted delivery of a novel NADPH-oxidase inhibitor to the endothelium in vitro and in vivo.Journal of controlled release : official journal of the Controlled Release Society · 2012
    Article
  10. Article
  11. Assessing the barriers to image-guided drug delivery.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology
    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

2 authors.

Kerri A MasseyProteogenomics Research Institute for Systems Medicine, 11107 Roselle St., San Diego, CA 92121, USA.
Jan E Schnitzer

Funding

Targeting Vessels in TumorsP01CA104898 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TALAMINI, MARK A · 2005 to 2009
$13.8M
Mapping Vascular Proteome for Organ Targeting in VivoR01HL074063 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SCHNITZER, JAN EUGENIUSZ · 2005 to 2009
$3.8M
Nanotechnology Platform for Targeting Solid TumorsR01CA119378 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TALAMINI, MARK A · 2005 to 2009
$3.6M
TISSUE TARGETING TO ENDOTHELIUM AND ITS CAVEOLAER01HL058216 · NHLBI · SIDNEY KIMMEL CANCER CENTER · PI SCHNITZER, JAN EUGENIUSZ · 1998 to 2006
$2.8M
Targeting Caveolae in Breast TumorsR01CA083989 · NCI · SIDNEY KIMMEL CANCER CENTER · PI SCHNITZER, JAN EUGENIUSZ · 2002 to 2006
$2.2M
MOLECULAR BASIS OF CAPILLARY PERMEABILITYR01HL052766 · NHLBI · SIDNEY KIMMEL CANCER CENTER · PI SCHNITZER, JAN EUGENIUSZ · 1994 to 2004
$2.2M
Technology/Map Endothelial Targets/Human Renal TumorsR33CA118602 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TALAMINI, MARK A · 2006 to 2008
$2.1M
Role and Utility of Annexins in Endothelium of Solid TumR01CA115215 · NCI · SIDNEY KIMMEL CANCER CENTER · PI SCHNITZER, JAN EUGENIUSZ · 2004 to 2008
$2.1M
Proteomic Resource for Basic &Clinical Cancer ResearchR24CA095893 · NCI · SIDNEY KIMMEL CANCER CENTER · PI SCHNITZER, JAN EUGENIUSZ · 2002 to 2006
$1.9M
NCI NIH HHS P01CA104898NCI NIH HHS R01CA083989NCI NIH HHS R01CA115215NCI NIH HHS R01CA119378NCI NIH HHS R24CA095893NCI NIH HHS R33CA118602NHLBI NIH HHS R01HL052766NHLBI NIH HHS R01HL058216NHLBI NIH HHS R01HL074063
6 · The paper itself

Abstract

A major goal of molecular medicine is to target imaging agents or therapeutic compounds to a single organ. Targeting imaging agents to a single organ could facilitate the high-resolution, in vivo imaging of molecular events. In addition, genetic and acquired diseases primary to a single organ, such as cystic fibrosis, tuberculosis, lung cancer, pulmonary fibrosis, pulmonary hypertension, and acute respiratory distress syndrome, could be specifically targeted in the lung. By targeting and concentrating imaging agents or therapeutics to the lungs, deleterious side effects can be avoided with greater efficacy at much lower dosages. Pathologic changes can be identified earlier and followed over time. In addition, therapeutics that have been abandoned due to toxicities may find renewed utility when coupled with specific targeting agents such as antibodies. To achieve these goals, distinct molecular signatures must be found for each organ or disease-state.

Indexed as

Molecular ImagingBiomarkersCaveolaeEndothelium, VascularHumansLungLung DiseasesLung NeoplasmsMass SpectrometryProteomeBiomarkersProteome

Identifiers

PMID19687214
PMCPMC2731802

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.