Evidence map›Paper›PMID 22077464›Full record

ReviewNanomedicine (London, England)2011

Improving delivery and efficacy of nanomedicines in solid tumors: role of tumor priming.

Jie Wang, Ze Lu, Yue Gao, M Guillaume Wientjes, Jessie L-S Au

Abstract readReview
In one paragraph

Review in Nanomedicine (London, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. Effect ofInternational journal of molecular sciences · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. PEG-b-PLA micelles and PLGA-b-PEG-b-PLGA sol-gels for drug delivery.Journal of controlled release : official journal of the Controlled Release Society · 2016
    Review
  16. Nanomedicine of synergistic drug combinations for cancer therapy - Strategies and perspectives.Journal of controlled release : official journal of the Controlled Release Society · 2016
    Review
  17. Review
  18. Article
  19. Review
  20. 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

5 authors.

Jie WangOptimum Therapeutics LLC, The Ohio State University Science Tech Village, Columbus, OH 43212, USA.
Ze Lu
Yue Gao
M Guillaume Wientjes
Jessie L-S Au

Funding

Synergistic chemo-siRNA combination therapyR01CA158300 · NCI · OPTIMUM THERAPEUTICS, LLC · PI AU, JESSIE L.-S., WIENTJES, M GUILLAUME · 2011 to 2015
$1.8M
TARGETING THE CASM ONCOGENE AS A NOVEL THERAPY FOR PANCREATIC CANCERR01CA123159 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI COLE, DAVID J · 2007 to 2011
$1.4M
Capturing dynamic and inter-dependent biointerfaces in nanotechnology designsR01EB015253 · NIBIB · OPTIMUM THERAPEUTICS, LLC · PI AU, JESSIE L.-S., WIENTJES, M GUILLAUME · 2011 to 2014
$1.1M
Tumor-priming Microparticles for Pancreatic CancerR44CA103133 · NCI · OPTIMUM THERAPEUTICS, LLC · PI LU, ZE · 2006 to 2012
$1.1M
Develop a Primary Care Colon Cancer Screening ConsortiumR21CA100553 · NCI · DARTMOUTH COLLEGE · PI DIETRICH, ALLEN J. · 2004 to 2005
$418k
Intraperitoneal Tumor-Targeting Chemo-gene TherapyR43CA134047 · NCI · OPTIMUM THERAPEUTICS, LLC · PI LU, ZE, WANG, JIE · 2008 to 2009
$248k
rTS Signaling Mimetics As Novel Cancer TherapeuticsR43CA121744 · NCI · OPTIMUM THERAPEUTICS, LLC · PI WANG, JIE · 2006 to 2006
$164k
NCI NIH HHS R01 CA123159NCI NIH HHS R01CA123159NCI NIH HHS R01 CA158300NCI NIH HHS R01CA158300NCI NIH HHS R21 CA100553NCI NIH HHS R43 CA121744NCI NIH HHS R43CA121744NCI NIH HHS R43 CA134047NCI NIH HHS R43CA134047NCI NIH HHS R44 CA103133NCI NIH HHS R44CA103133NIBIB NIH HHS R01 EB015253NIBIB NIH HHS R01EB015253
6 · The paper itself

Abstract

Effectiveness of nanomedicines in cancer therapy is limited in part by inadequate delivery and transport in tumor interstitium. This article reviews the experimental approaches to improve nanomedicine delivery and transport in solid tumors. These approaches include tumor vasculature normalization, interstitial fluid pressure modulation, enzymatic extracellular matrix degradation, and apoptosis-inducing tumor priming technology. We advocate the latter approach due to its ease and practicality (accomplished with standard-of-care chemotherapy, such as paclitaxel) and tumor selectivity. Examples of applying tumor priming to deliver nanomedicines and to design drug/RNAi-loaded carriers are discussed.

Indexed as

AnimalsAntineoplastic AgentsApoptosisHumansNanomedicineNeoplasmsPaclitaxelAntineoplastic AgentsPaclitaxel

Identifiers

PMID22077464
PMCPMC3655409

What OpenQuestion holds

Textmetadata
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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.