Evidence map›Paper›PMID 28842588›Full record

ArticleScientific reports2017

Cancer-targeted Nucleic Acid Delivery and Quantum Dot Imaging Using EGF Receptor Aptamer-conjugated Lipid Nanoparticles.

Min Woo Kim, Hwa Yeon Jeong, Seong Jae Kang, Moon Jung Choi, Young Myoung You, Chan Su Im, Tae Sup Lee, In Ho Song, Chang Gun Lee, Ki-Jong Rhee and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 75 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Min Woo KimDepartment of Biomedical Laboratory Science, Yonsei University, Wonju, Republic of Korea.
Hwa Yeon JeongDepartment of Biomedical Laboratory Science, Yonsei University, Wonju, Republic of Korea.
Seong Jae KangDepartment of Biomedical Laboratory Science, Yonsei University, Wonju, Republic of Korea.
Moon Jung ChoiDepartment of Biomedical Laboratory Science, Yonsei University, Wonju, Republic of Korea.
Young Myoung YouDepartment of Biomedical Laboratory Science, Yonsei University, Wonju, Republic of Korea.
Chan Su ImDepartment of Biomedical Laboratory Science, Yonsei University, Wonju, Republic of Korea.
Tae Sup LeeDivision of RI-Convergence Research, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea.
In Ho SongDivision of RI-Convergence Research, Korea Institute of Radiological and Medical Sciences, Seoul, Republic of Korea.
Chang Gun LeeDepartment of Biomedical Laboratory Science, Yonsei University, Wonju, Republic of Korea.
Ki-Jong RheeDepartment of Biomedical Laboratory Science, Yonsei University, Wonju, Republic of Korea.ORCID 0000-0001-5130-2728
Yeon Kyung LeeCenter for Theragnosis, Biomedical Research Institute, Korea Institute of Science and Technology, Seoul, Republic of Korea.
Yong Serk ParkDepartment of Biomedical Laboratory Science, Yonsei University, Wonju, Republic of Korea. parkys@yonsei.ac.kr.
Yonsei University · KRKorea Institute of Radiological and Medical Sciences · KRKorea Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Co-application of fluorescent quantum dot nanocrystals and therapeutics has recently become a promising theranostic methodology for cancer treatment. We developed a tumor-targeted lipid nanocarrier that demonstrates notable efficacy in gene delivery as well as tumor bio-imaging. Coupling of aptamer molecules against the EGF receptor (EGFR) to the distal termini of lipid nanoparticles provided the carrier with tumor-specific recognition capability. The cationic lipid component, referred to as O,O'-dimyristyl-N-lysyl glutamate (DMKE), was able to effectively complex with anionic small-interfering RNA (siRNA). The hydrophobic quantum dots (Q-dots) were effectively incorporated in hydrophobic lipid bilayers at an appropriate Q-dot to lipid ratio. In this study, we optimized the liposomal formula of aptamer-conjugated liposomes containing Q-dots and siRNA molecules (Apt-QLs). The anti-EGFR Apt-QLs exhibited remarkable EGFR-dependent siRNA delivery as well as fluorescence imaging, which were analyzed in cultured cancer cells and tumor xenografts in mice. These results imply that the formulation of Apt-QLs could be widely utilized as a carrier for tumor-directed gene delivery and bio-imaging.

Indexed as

Aptamers, NucleotideGene Transfer TechniquesMolecular ImagingNanoparticlesQuantum DotsAnimalsCell Line, TumorDisease Models, AnimalDrug Delivery SystemsErbB ReceptorsHeterograftsHumansLipidsLiposomesMiceMicroscopy, FluorescenceAptamers, NucleotideErbB ReceptorsLipidsLiposomes

Identifiers

PMID28842588
PMCPMC5573382
OpenAlexW2750078485

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.