Evidence map›Paper›PMID 19720291›Full record

ArticleNuclear medicine and biology2009

Bifunctional phage-based pretargeted imaging of human prostate carcinoma.

Jessica R Newton-Northup, Said D Figueroa, Thomas P Quinn, Susan L Deutscher

Open access · greenAbstract read
In one paragraph

Article in Nuclear medicine and biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.8field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. T7 Phage as an Emerging Nanobiomaterial with Genetically Tunable Target Specificity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Review
  3. Review
  4. Article
  5. Cytotoxic Tumor-Targeting Peptides From In Vivo Phage Display.Combinatorial chemistry & high throughput screening · 2016
    Article
  6. Addressing challenges of heterogeneous tumor treatment through bispecific protein-mediated pretargeted drug delivery.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Landscape phage ligands for PC3 prostate carcinoma cells.Protein engineering, design & selection : PEDS · 2010
    Article
  13. 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.

Jessica R Newton-NorthupDepartment of Biochemistry, University of Missouri, Columbia, MO 65211, USA. newtonj@missouri.edu
Said D Figueroa
Thomas P Quinn
Susan L Deutscher
University of Missouri · USHarry S. Truman Memorial Veterans' Hospital · US

Funding

CENTER FOR SINGLE PHOTON-EMITTING CANCER IMAGING AGENTSP50CA103130 · NCI · UNIVERSITY OF MISSOURI-COLUMBIA · PI VOLKERT, WYNN A · 2003 to 2007
$9.8M
NCI NIH HHS P50 CA103130NCI NIH HHS P50 CA103130-01
6 · The paper itself

Abstract

introductionTwo-step and three-step pretargeting systems utilizing biotinylated prostate tumor-homing bacteriophage (phage) and (111)In-radiolabeled streptavidin or biotin were developed for use in cancer radioimaging. The in vivo selected prostate carcinoma-specific phage (G1) displaying up to five copies of the peptide IAGLATPGWSHWLAL was the focus of the present study.

methodsThe ability of G1 phage to extravasate and target prostate tumor cells was investigated using immunohistochemistry. G1 phages were biotinylated, streptavidin was conjugated to diethylenetriaminepentaacetic acid (DTPA) and biotin was conjugated to 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA). Biodistribution studies and single-photon emission computed tomography (SPECT)/CT imaging of xenografted PC-3 tumors via two-step pretargeted (111)In-labeled streptavidin and three-step pretargeted (111)In-labeled biotin were performed in SCID mice to determine the optimal pretargeting method.

resultsThe ability of G1 phage to extravasate the vasculature and bind directly to human PC-3 prostate carcinoma tumor cells in vivo was demonstrated via immunocytochemical analysis. Comparative biodistribution studies of the two-step and three-step pretargeting strategies indicated increased PC-3 human prostate carcinoma tumor uptake in SCID mice of 4.34+/-0.26 %ID g(-1) at 0.5 h postinjection of (111)In-radiolabeled biotin (utilized in a three-step protocol) compared to 0.67+/-0.06 %ID g(-1) at 24 h postinjection of (111)In radiolabeled streptavidin (employed in a two-step protocol). In vivo SPECT/CT imaging of xenografted PC-3 tumors in SCID mice with the three-step pretargeting method was superior to that of the two-step pretargeting method, and, importantly, blocking studies demonstrated specificity of tumor uptake of (111)In-labeled biotin in the three-step pretargeting scheme.

conclusionThis study demonstrates the use of multivalent bifunctional phage in a three-step pretargeting system for prostate cancer radioimaging.

Indexed as

Amino Acid SequenceAnimalsBacteriophagesCell Line, TumorExtravasation of Diagnostic and Therapeutic MaterialsHumansImmunohistochemistryMaleMiceMolecular Sequence DataNanoparticlesPeptidesProstatic NeoplasmsTomography, Emission-Computed, Single-PhotonTomography, X-Ray ComputedPeptides

Identifiers

PMID19720291
PMCPMC2739128
OpenAlexW2005864110

What OpenQuestion holds

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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.