Evidence map›Paper›PMID 21333700›Full record

ReviewAdvanced drug delivery reviews2011

Prodrugs for improving tumor targetability and efficiency.

Rubi Mahato, Wanyi Tai, Kun Cheng

Abstract readReview
In one paragraph

Review in Advanced drug delivery reviews, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
9.6field-weighted citation impact, top 1% 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

77 citing papers in PubMed, 348 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Localized In Vivo Prodrug Activation Using Radionuclides.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2025
    Article
  11. Review
  12. Article
  13. In vitro evaluation of novel SN-38 prodrug activated by α-rhamnosidase of exogenous enzyme.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2024
    Article
  14. Review
  15. Review
  16. Theranostic Fluorescent Probes.Chemical reviews · 2024
    Review
  17. Article
  18. Designing cytochrome P450 enzymes for use in cancer gene therapy.Frontiers in bioengineering and biotechnology · 2024
    Review
  19. Article
  20. Review

17 more citing papers are in PubMed but not listed here.

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.

Rubi MahatoDivision of Pharmaceutical Sciences, School of Pharmacy, University of Missouri-Kansas City, 2464 Charlotte Street, Kansas City, MO 64108, USA.
Wanyi Tai
Kun Cheng
University of Missouri–Kansas City · US

Funding

Treating Alcoholic Liver Fibrosis by Reversal of Type I CollagenR21AA017960 · NIAAA · UNIVERSITY OF MISSOURI KANSAS CITY · PI CHENG, KUN · 2009 to 2010
$390k
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 1R21CA143683-01NCI NIH HHS R21 CA143683NIAAA NIH HHS 1R21AA017960-01A1NIAAA NIH HHS R21 AA017960
6 · The paper itself

Abstract

As the mainstay in the treatment of various cancers for several decades, chemotherapy is successful but still faces challenges including non-selectivity and high toxicity. Improving the selectivity is therefore a critical step to improve the therapeutic efficacy of chemotherapy. Prodrug is one of the most promising approaches to increase the selectivity and efficacy of a chemotherapy drug. The classical prodrug approach is to improve the pharmaceutical properties (solubility, stability, permeability, irritation, distribution, etc.) via a simple chemical modification. This review will focus on various targeted prodrug designs that have been developed to increase the selectivity of chemotherapy drugs. Various tumor-targeting ligands, transporter-associated ligands, and polymers can be incorporated in a prodrug to enhance the tumor uptake. Prodrugs can also be activated by enzymes that are specifically expressed at a higher level in tumors, leading to a selective anti-tumor effect. This can be achieved by conjugating the enzyme to a tumor-specific antibody, or delivering a vector expressing the enzyme into tumor cells.

Indexed as

ProdrugsAnimalsAntineoplastic AgentsDrug Delivery SystemsDrug DesignHumansLigandsNeoplasmsPolymersAntineoplastic AgentsLigandsPolymersProdrugs

Identifiers

PMID21333700
PMCPMC3132824
OpenAlexW1978556565

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.