Evidence map›Paper›PMID 39508791›Full record

ArticleBiomolecules & biomedicine2024

Camel milk-derived exosomes as novel nanocarriers for curcumin delivery in lung cancer.

Mohd Saeed, Khalid Alshaghdali, Disha Moholkar, Raghuram Kandimalla, Mohd Adnan Kausar, Farrukh Aqil

Abstract read
In one paragraph

Article in Biomolecules & biomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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.

Mohd SaeedDepartment of Biology, College of Sciences, University of Hail, Hail, Saudi Arabia.
Khalid AlshaghdaliDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, University of Hail, Hail, Saudi Arabia.
Disha MoholkarDepartment of Pharmacology & Toxicology, University of Louisville, Louisville, USA; Brown Cancer Center,Brown Cancer Center, University of Louisville, Louisville, USA.
Raghuram KandimallaDepartment of Pharmacology & Toxicology, University of Louisville, Louisville, USA; Brown Cancer Center, University of Louisville, Louisville, USA.
Mohd Adnan KausarDepartment of Biochemistry, College of Medicine, University of Hail, Hail, Saudi Arabia.
Farrukh AqilBrown Cancer Center, University of Louisville, Louisville, USA; Department of Medicine, University of Louisville, Louisville, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer remains a leading cause of mortality, with non-small cell lung cancer (NSCLC) being a primary contributor to cancer-related deaths. Traditional treatment strategies such as chemotherapy, radiation, and hormone therapy often present challenges, including severe side effects, drug resistance, and toxicity. Recent advancements in nanotechnology aim to enhance the effectiveness of cancer therapies by targeting drugs selectively and specifically to tumor cells. Among these innovations, exosomes, or small extracellular vesicles (sEVs), have emerged as promising carriers for drug delivery due to their natural origin and ability to encapsulate both small molecules and biologics. This study explores the use of exosomes derived from camel milk in Hail, Saudi Arabia, as a vehicle for delivering curcumin (CUR), a polyphenol with known chemopreventive properties but limited bioavailability. Camel milk was processed to isolate exosomes through differential centrifugation, followed by characterization using dynamic light scattering, zeta potential measurements, and Western blot analysis to confirm exosomal markers. The encapsulation of CUR into camel milk-derived exosomes demonstrated a 20% loading efficiency as analyzed by UPLC. In vitro antiproliferative assays revealed that the exosomal formulation of CUR (ExoCUR) significantly enhanced cytotoxicity against drug-sensitive (A549) and taxol-resistant (A549TR) lung cancer cells compared to free CUR. Molecular docking studies and molecular dynamics simulations indicated that CUR has a strong binding affinity for the epidermal growth factor receptor (EGFR), comparable to the established drug gefitinib. Furthermore, CUR effectively downregulated EGFR and STAT3 expression in lung cancer cells, suggesting its potential to disrupt key signaling pathways involved in tumor progression. Our findings highlight the potential of camel milk-derived exosomes as an effective and biocompatible delivery system for CUR, offering a promising strategy to overcome the limitations of current cancer therapies and enhance the therapeutic efficacy of chemopreventive agents.

Indexed as

Antineoplastic AgentsCarcinoma, Non-Small-Cell LungCurcuminDrug CarriersExosomesLung NeoplasmsMilkNanoparticlesA549 CellsAnimalsCamelusCell Line, TumorCell ProliferationDrug Delivery SystemsHumansMolecular Docking SimulationAntineoplastic AgentsCurcuminDrug Carriers

Identifiers

PMID39508791
PMCPMC12499544

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Registered trials

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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.