Evidence map›Paper›PMID 38931855›Full record

ReviewPharmaceutics2024

Review of Prodrug and Nanodelivery Strategies to Improve the Treatment of Colorectal Cancer with Fluoropyrimidine Drugs.

Santu Sarkar, Sezgin Kiren, William H Gmeiner

Abstract readReview
In one paragraph

Review in Pharmaceutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Mutant-Selective Binding ofInternational journal of molecular sciences · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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.

Santu SarkarDepartment of Cancer Biology, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
Sezgin KirenDepartment of Chemistry, Winston-Salem State University, Winston-Salem, NC 27110, USA.ORCID 0000-0002-7971-7244
William H GmeinerDepartment of Cancer Biology, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.ORCID 0000-0003-1883-3791

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
Nanodelivery of FP polymers to improve treatment of metastatic colorectal cancerR01CA284083 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI William H. Gmeiner · 2023 to 2026
$2.3M
Improved Treatment of Colorectal Cancer with CF10R42CA254834 · NCI · DEEP CREEK PHARMA, LLC · PI GMEINER, WILLIAM H. · 2023 to 2024
$2.0M
Feasibility of artesunate to improve HPV and cervical precancer treatment outcomes among HIV positive women in LMICsR34CA284983 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MUNGO, CHEMTAI · 2023 to 2025
$739k
NCI NIH HHS P30 CA012197NCI NIH HHS R01 CA284083NCI NIH HHS R34 CA284983NCI NIH HHS R42 CA254834NIH HHS 1R01CA284083-01A1
6 · The paper itself

Abstract

Fluoropyrimidine (FP) drugs are central components of combination chemotherapy regimens for the treatment of colorectal cancer (CRC). FP-based chemotherapy has improved survival outcomes over the last several decades with much of the therapeutic benefit derived from the optimization of dose and delivery. To provide further advances in therapeutic efficacy, next-generation prodrugs and nanodelivery systems for FPs are being developed. This review focuses on recent innovative nanodelivery approaches for FP drugs that display therapeutic promise. We summarize established, clinically useful FP prodrug strategies, including capecitabine, which exploit tumor-specific enzyme expression for optimal anticancer activity. We then describe the use of FP DNA-based polymers (e.g., CF10) for the delivery of activated FP nucleotides as a nanodelivery approach with proven activity in pre-clinical models and with clinical potential. Multiple nanodelivery systems for FP delivery show promise in CRC pre-clinical models and we review advances in albumin-mediated FP delivery, the development of mesoporous silica nanoparticles, emulsion-based nanoparticles, metal nanoparticles, hydrogel-based delivery, and liposomes and lipid nanoparticles that display particular promise for therapeutic development. Nanodelivery of FPs is anticipated to impact CRC treatment in the coming years and to improve survival for cancer patients.

Indexed as

colorectal cancerfluoropyrimidinenanodeliveryprodrugthymidylate synthase

Identifiers

PMID38931855
PMCPMC11206923

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.