Evidence map›Paper›PMID 22790418›Full record

ReviewIntegrative biology : quantitative biosciences from nano to macro2013

Targeted nanoparticles in imaging: paving the way for personalized medicine in the battle against cancer.

Soo J Shin, Jaymes R Beech, Kimberly A Kelly

Abstract readReview
In one paragraph

Review in Integrative biology : quantitative biosciences from nano to macro, 2013. 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
–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

13 citing papers in PubMed.

  1. Review
  2. Exploring innovative strides in radiolabeled nanoparticle progress for multimodality cancer imaging and theranostic applications.Cancer imaging : the official publication of the International Cancer Imaging Society · 2024
    Review
  3. Triggering Immune System With Nanomaterials for Cancer Immunotherapy.Frontiers in bioengineering and biotechnology · 2022
    Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. 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

3 authors.

Soo J ShinDepartment of Biomedical Engineering, University of Virginia School of Engineering and Applied Sciences, PO Box 800759, Health System, Charlottesville, VA 22908, USA.
Jaymes R Beech
Kimberly A Kelly

Funding

BIOTECHNOLOGY TRAINING PROGRAMT32GM008715 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LAURIE, GORDON WILLIAM · 2000 to 2019
$6.6M
Development of Molecularly Targeted Imaging Agents for KRAS activity in vivoR01EB010023 · NIBIB · UNIVERSITY OF VIRGINIA · PI EL-BARDEESY, NABEEL, KELLY, KIMBERLY A. · 2010 to 2013
$1.4M
Development of Molecularly Targeted Imaging Agents for Early Detection of PDACR01CA137071 · NCI · UNIVERSITY OF VIRGINIA · PI KELLY, KIMBERLY A. · 2008 to 2012
$1.3M
NCI NIH HHS R01 CA137071NIBIB NIH HHS R01 EB010023NIGMS NIH HHS T32 GM008715NIGMS NIH HHS T32GM8715-11
6 · The paper itself

Abstract

The way we view cancer has advanced greatly in the past few decades from simplistic approaches to finely honed systems. This transition has been made possible because of advancements on two fronts: the first is the rapidly expanding knowledge base of the mechanisms and characteristics of cancer; the second is innovation in imaging agent design. Rapid advancements in imaging and therapeutic agents are being made through the evolution from one-dimensional molecules to multi-functional nanoparticles. Powerful new agents that have high specificity and minimal toxicity are being developed for in vivo imaging. Here we detail the unique characteristics of cancer that allow differentiation from normal tissue and how they are exploited in nanoparticle imaging development. Firstly, genetic alterations, either endogenous or induced through gene therapy, are one such class of characteristics. Proteomic differences such as overexpressed surface receptors is another targetable feature used for enhanced nanoparticle retention. Increased need for nutrients and specific growth signals to sustain proliferation and angiogenesis are further examples of how cancer can be targeted. Lastly, migration and invasion through a unique microenvironment are two additional traits that are exploitable, due to differences in metalloproteinase concentrations and other factors. These differences are guiding current nanoparticle design to better target, image and treat cancer.

Indexed as

AnimalsAntineoplastic AgentsContrast MediaDiagnostic ImagingHumansNanocapsulesNeoplasmsPrecision MedicineAntineoplastic AgentsContrast MediaNanocapsules

Identifiers

PMID22790418
PMCPMC6943836

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.