Evidence map›Paper›PMID 24892741›Full record

ArticleJournal of drug targeting2014

Cellular uptake and internalization of hyaluronan-based doxorubicin and cisplatin conjugates.

Shuang Cai, Adel Ali B Alhowyan, Qiuhong Yang, W C Melanie Forrest, Yelizaveta Shnayder, M Laird Forrest

Abstract read
In one paragraph

Article in Journal of drug targeting, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
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  7. Current trends of targeted therapy for oral squamous cell carcinoma.Journal of cancer research and clinical oncology · 2022
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  13. Internalized CD44s splice isoform attenuates EGFR degradation by targeting Rab7A.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
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  20. Hyaluronan as a therapeutic target in human diseases.Advanced drug delivery reviews · 2016
    Review
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

6 authors at 2 institutions in 1 country.

Shuang CaiDepartment of Pharmaceutical Chemistry, University of Kansas , Lawrence, KS , USA .
Adel Ali B Alhowyan
Qiuhong Yang
W C Melanie Forrest
Yelizaveta Shnayder
M Laird Forrest
University of Kansas · USHyland Software (United States) · US

Funding

Biomaterials for treatment of head and neck cancerR01CA173292 · NCI · UNIVERSITY OF KANSAS LAWRENCE · PI FORREST, MARCUS LAIRD · 2013 to 2017
$1.4M
NCI NIH HHS R01 CA173292NCI NIH HHS R01-CA173292
6 · The paper itself

Abstract

backgroundHyaluronan (HA) is a ligand for the CD44 receptor which is crucial to cancer cell proliferation and metastasis. High levels of CD44 expression in many cancers have encouraged the development of HA-based carriers for anti-cancer therapeutics. PURPOSE: The objective of this study was to determine whether HA conjugation of anticancer drugs impacts CD44-specific HA-drug uptake and disposition by human head and neck cancer cells.

methodsThe internalization and cellular disposition of hyaluronan-doxorubicin (HA-DOX), hyaluronan-cisplatin (HA-Pt), and hyaluronan-cyanine7 (HA-Cy7) conjugates were investigated by inhibiting endocytosis pathways, and by inhibiting the CD44-mediated internalization pathways that are known to mediate hyaluronan uptake in vitro.

resultsCellular internalization of HA was regulated by CD44 receptors. In mouse xenografts, HA conjugation significantly enhanced tumor cell uptake compared to unconjugated drugs. DISCUSSION: The results suggested that the main mechanism of HA-based conjugate uptake may be active transport via CD44 in conjunction with a clathrin-dependent endocytic pathway. Other HA receptors, hyaluronan-mediated motility receptor (RHAMM) and lymphatic vessel endothelial hyaluronan receptor (LYVE-1), did not play a significant role in conjugate uptake.

conclusionsHA conjugation significantly increased CD44-mediated drug uptake and extended the residence time of drugs in tumor cells.

Indexed as

AnimalsAntineoplastic AgentsCell Culture TechniquesCell Line, TumorCisplatinDoxorubicinDrug CarriersFemaleHumansHyaluronan ReceptorsHyaluronic AcidLigandsMice, SCIDMicroscopy, FluorescenceMolecular StructureNanoconjugatesAntineoplastic AgentsCisplatinDoxorubicinDrug CarriersHyaluronan ReceptorsHyaluronic AcidLigandsNanoconjugatesCD44 receptorscisplatindoxorubicinhyaluronaninternalization mechanism

Identifiers

PMID24892741
PMCPMC4620033
OpenAlexW1986814736

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.