Evidence map›Paper›PMID 21751810›Full record

ArticleJournal of the American Chemical Society2011

Catechol polymers for pH-responsive, targeted drug delivery to cancer cells.

Jing Su, Feng Chen, Vincent L Cryns, Phillip B Messersmith

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
15.8field-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

74 citing papers in PubMed, 438 citations in OpenAlex.

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  11. Diffusion-Based 3D Bioprinting Strategies.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
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14 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

4 authors at 2 institutions in 1 country.

Jing SuBiomedical Engineering Department, Northwestern University, Evanston, Illinois 60208, USA.
Feng Chen
Vincent L Cryns
Phillip B Messersmith
Northwestern University · USRobert H. Lurie Comprehensive Cancer Center of Northwestern University

Funding

Theranostic Magnetic Nanostructures for the Molecular Imaging of CancerU54CA151880 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MIRKIN, CHAD A. · 2010 to 2014
$11.5M
Biologically Inspired Polymer AdhesivesR37DE014193 · NIDCR · UNIVERSITY OF CALIFORNIA BERKELEY · PI MESSERSMITH, PHILLIP B · 2006 to 2015
$3.5M
Tumor Targeted Nanobins for the Treatment of Metastatic Breast and Ovarian CancerU01CA151461 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI O'HALLORAN, THOMAS V · 2010 to 2014
$2.2M
Bioadhesive Polymer Hydrogels: Basic and Applied StudiesR01DE014193 · NIDCR · NORTHWESTERN UNIVERSITY · PI MESSERSMITH, PHILLIP B · 2002 to 2005
$1.2M
NCI NIH HHS U01 CA151461NCI NIH HHS U54 CA151880NIDCR NIH HHS DE014193NIDCR NIH HHS R01 DE014193NIDCR NIH HHS R37 DE014193
6 · The paper itself

Abstract

A novel cell-targeting, pH-sensitive polymeric carrier was employed in this study for delivery of the anticancer drug bortezomib (BTZ) to cancer cells. Our strategy is based on facile conjugation of BTZ to catechol-containing polymeric carriers that are designed to be taken up selectively by cancer cells through cell surface receptor-mediated mechanisms. The polymer used as a building block in this study was poly(ethylene glycol), which was chosen for its ability to reduce nonspecific interactions with proteins and cells. The catechol moiety was exploited for its ability to bind and release borate-containing therapeutics such as BTZ in a pH-dependent manner. In acidic environments, such as in cancer tissue or the subcellular endosome, BTZ dissociates from the polymer-bound catechol groups to liberate the free drug, which inhibits proteasome function. A cancer-cell-targeting ligand, biotin, was presented on the polymer carriers to facilitate targeted entry of drug-loaded polymer carriers into cancer cells. Our study demonstrated that the cancer-targeting drug-polymer conjugates dramatically enhanced cellular uptake, proteasome inhibition, and cytotoxicity toward breast carcinoma cells in comparison with nontargeting drug-polymer conjugates. The pH-sensitive catechol-boronate binding mechanism provides a chemoselective approach for controlling the release of BTZ in targeted cancer cells, establishing a concept that may be applied in the future toward other boronic acid-containing therapeutics to treat a broad range of diseases.

Indexed as

Drug Delivery SystemsAntineoplastic AgentsBoronic AcidsBortezomibCatecholsCell DeathCell Line, TumorCell ProliferationCell SurvivalDose-Response Relationship, DrugDrug CarriersDrug Screening Assays, AntitumorHumansHydrogen-Ion ConcentrationMolecular StructurePolymersAntineoplastic AgentsBoronic AcidsBortezomibcatecholCatecholsDrug CarriersPolymersProteasome Endopeptidase ComplexProteasome InhibitorsPyrazines

Identifiers

PMID21751810
PMCPMC3149454
OpenAlexW2092319622

What OpenQuestion holds

Textmetadata
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.