Evidence map›Paper›PMID 24878184›Full record

ReviewJournal of controlled release : official journal of the Controlled Release Society2014

Prostate cancer relevant antigens and enzymes for targeted drug delivery.

Ashutosh Barve, Wei Jin, Kun Cheng

Abstract readReview
In one paragraph

Review in Journal of controlled release : official journal of the Controlled Release Society, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

45 citing papers in PubMed, 109 citations in OpenAlex.

  1. Review
  2. Review
  3. [Recent advances in antibody-drug conjugates for metastatic castration-resistant prostate cancer].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2025
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Preclinical Evaluation of a Novel High-Affinity Radioligand [International journal of molecular sciences · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. The GRPR Antagonist [Diagnostics (Basel, Switzerland) · 2023
    Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  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

3 authors at 1 institution in 1 country.

Ashutosh BarveDivision of Pharmaceutical Sciences, School of Pharmacy, University of Missouri-Kansas City, Kansas City 64108, USA.
Wei JinDivision of Pharmaceutical Sciences, School of Pharmacy, University of Missouri-Kansas City, Kansas City 64108, USA.
Kun ChengDivision of Pharmaceutical Sciences, School of Pharmacy, University of Missouri-Kansas City, Kansas City 64108, USA. Electronic address: chengkun@umkc.edu.
University of Missouri–Kansas City · US

Funding

Targeted delivery of PCBP2 siRNA for treating alcoholic liver fibrosisR01AA021510 · NIAAA · UNIVERSITY OF MISSOURI KANSAS CITY · PI CHENG, KUN · 2012 to 2022
$3.8M
Targeted delivery of IKKalpha siRNA to prostate cancer cellsR21CA143683 · NCI · UNIVERSITY OF MISSOURI KANSAS CITY · PI CHENG, KUN · 2010 to 2011
$365k
NCI NIH HHS 1R21CA143683NCI NIH HHS R21 CA143683NIAAA NIH HHS 1R01AA021510NIAAA NIH HHS R01 AA021510
6 · The paper itself

Abstract

Chemotherapy is one of the most widely used approaches in combating advanced prostate cancer, but its therapeutic efficacy is usually insufficient due to poor specificity and associated toxicity. Lack of targeted delivery to prostate cancer cells is also the primary obstacles in achieving feasible therapeutic effect of other promising agents including peptide, protein, and nucleic acid. Consequently, there remains a critical need for strategies to increase the selectivity of anti-prostate cancer agents. This review will focus on various prostate cancer-relevant antigens and enzymes that could be exploited for prostate cancer targeted drug delivery. Among various targeting strategies, active targeting is the most advanced approach to specifically deliver drugs to their designated cancer cells. In this approach, drug carriers are modified with targeting ligands that can specifically bind to prostate cancer-specific antigens. Moreover, there are several specific enzymes in the tumor microenvironment of prostate cancer that can be exploited for stimulus-responsive drug delivery systems. These systems can specifically release the active drug in the tumor microenvironment of prostate cancer, leading to enhanced tumor penetration efficiency.

Indexed as

Drug Delivery SystemsAnimalsAntigens, NeoplasmBiomarkers, TumorHumansMaleProstatic NeoplasmsAntigens, NeoplasmBiomarkers, TumorHER2Prostate cancerPSAPSCAPSMATumor microenvironment

Identifiers

PMID24878184
PMCPMC4079732
OpenAlexW2030845523

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.