Evidence map›Paper›PMID 36632508›Full record

ReviewBioactive materials2023

Functionalized liposomes for targeted breast cancer drug delivery.

Janske Nel, Kamil Elkhoury, Émilie Velot, Arnaud Bianchi, Samir Acherar, Grégory Francius, Ali Tamayol, Stéphanie Grandemange, Elmira Arab-Tehrany

Abstract readReview
In one paragraph

Review in Bioactive materials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing 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

81 citing papers in PubMed.

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21 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

9 authors.

Janske NelUniversité de Lorraine, LIBio, F-54000, Nancy, France.
Kamil ElkhouryLAAS-CNRS, F-31400, Toulouse, France.
Émilie VelotUniversité de Lorraine, CNRS, IMoPA, F-54000, Nancy, France.
Arnaud BianchiUniversité de Lorraine, CNRS, IMoPA, F-54000, Nancy, France.
Samir AcherarUniversité de Lorraine, CNRS, LCPM, F-54000, Nancy, France.
Grégory FranciusUniversité de Lorraine, CNRS, LCPME, F-54000, Nancy, France.
Ali TamayolDepartment of Biomedical Engineering, University of Connecticut Health Center, Farmington, CT, 06030, USA.
Stéphanie GrandemangeUniversité de Lorraine, CNRS, CRAN, F-54000, Nancy, France.
Elmira Arab-TehranyUniversité de Lorraine, LIBio, F-54000, Nancy, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the exceptional progress in breast cancer pathogenesis, prognosis, diagnosis, and treatment strategies, it remains a prominent cause of female mortality worldwide. Additionally, although chemotherapies are effective, they are associated with critical limitations, most notably their lack of specificity resulting in systemic toxicity and the eventual development of multi-drug resistance (MDR) cancer cells. Liposomes have proven to be an invaluable drug delivery system but of the multitudes of liposomal systems developed every year only a few have been approved for clinical use, none of which employ active targeting. In this review, we summarize the most recent strategies in development for actively targeted liposomal drug delivery systems for surface, transmembrane and internal cell receptors, enzymes, direct cell targeting and dual-targeting of breast cancer and breast cancer-associated cells, e.g., cancer stem cells, cells associated with the tumor microenvironment, etc.

Indexed as

Anti-cancer agentsBreast cancerLiposomesReceptor-targeted drug deliverySurface functionalizationTargeted drug delivery

Identifiers

PMID36632508
PMCPMC9812688

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.