Evidence map›Paper›PMID 40735792›Full record

ArticleNanomedicine (London, England)2025

Dox-HCl and miR-145 co-delivery through CD44-targeted PEGylated liposomes inhibit Breast Cancer

Chu Xin Ng, Sau Har Lee, Pei Pei Chong

Abstract read
In one paragraph

Article in Nanomedicine (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Chu Xin NgSchool of Biosciences, Faculty of Health and Medical Sciences, Taylor's University, Subang Jaya, Selangor, Malaysia.ORCID 0000-0003-4073-7472
Sau Har LeeSchool of Biosciences, Faculty of Health and Medical Sciences, Taylor's University, Subang Jaya, Selangor, Malaysia.
Pei Pei ChongSchool of Biosciences, Faculty of Health and Medical Sciences, Taylor's University, Subang Jaya, Selangor, Malaysia.ORCID 0000-0002-8229-3593

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThe aim of this study deals with integrating a CD44-targeting short peptide, A6 (KPSSPPEE) onto the PEGylated liposomes to enhance the in vitro anticancer activities of doxorubicin hydrochloride and tumor suppressor miR-145 mimics on triple-negative breast cancer.

methodsA CD44-targeting short peptide, A6 (KPSSPPEE) was integrated onto the optimized PEGylated liposomes, and its effects on cellular uptake, anti-proliferation, and anti-metastasis activities were assessed in triple-negative breast cancer, MDA-MB-231 cells.

resultsThe resulting formulation (A6-PEG-lipo-Dox-miR145) demonstrated enhanced cellular uptake by CD44-expressing MDA-MB-231 cells within 2 h of incubation. In vitro study showed that A6-PEG-lipo-Dox-miR145 exerted a greater anti-proliferative activity with higher selectivity (Dox-HCl IC

conclusionOur findings indicate that the incorporation of A6 peptide represents a simple and straightforward strategy to improve the targetability and therapeutic effects of PEGylated liposome, warranting further investigation.

Indexed as

DoxorubicinHyaluronan ReceptorsMicroRNAsTriple Negative Breast NeoplasmsCell Line, TumorCell ProliferationFemaleHumansLiposomesPeptidesPhosphatidylinositol 3-KinasesPolyethylene GlycolsProto-Oncogene Proteins c-aktSignal TransductionCD44 protein, humanDoxorubicinHyaluronan ReceptorsLiposomesMicroRNAsMIRN145 microRNA, humanPeptidesPhosphatidylinositol 3-KinasesPolyethylene GlycolsProto-Oncogene Proteins c-aktA6-peptidedoxorubicinmiR-145PEGylated liposometargeted therapyTNBC

Identifiers

PMID40735792
PMCPMC12408063

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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.