Evidence map›Paper›PMID 33376323›Full record

ArticleInternational journal of nanomedicine2020

Aptamer-Functionalized Dendrimer Delivery of Plasmid-Encoding lncRNA

Zongguang Tai, Jinyuan Ma, Jianing Ding, Huijun Pan, Rongrong Chai, Congcong Zhu, Zhen Cui, Zhongjian Chen, Quangang Zhu

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 51 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

9 authors at 1 institution in 1 country.

Zongguang Tai *Shanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai 200443, People's Republic of China.ORCID 0000-0001-5603-745X
Jinyuan Ma *Shanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai 200443, People's Republic of China.
Jianing Ding *Shanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai 200443, People's Republic of China.
Huijun PanShanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai 200443, People's Republic of China.
Rongrong ChaiShanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai 200443, People's Republic of China.
Congcong ZhuShanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai 200443, People's Republic of China.
Zhen CuiShanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai 200443, People's Republic of China.
Zhongjian ChenShanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai 200443, People's Republic of China.
Quangang ZhuShanghai Skin Disease Hospital, Tongji University School of Medicine, Shanghai 200443, People's Republic of China.
Tongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe clinical management of patients with castration-resistant prostate cancer (CRPC) is difficult. However, novel treatment methods are gradually being introduced. Considering the adverse effects of traditional treatments, recent studies have investigated gene therapy as a method to combat CRPC; but, the application of long non-coding (lnc) RNA in gene therapy remains scarce, despite their promise. Therefore, it is imperative to develop a system that can efficiently deliver lncRNA for the treatment of CRPC. Here, we investigated the efficacy of a delivery system by introducing the plasmid-encoding tumor suppressor lncRNA MATERIALS AND

methodsAn EpDT3 aptamer-linked poly(amidoamine) (PAMAM) dendrimer targeting EpCAM was used to deliver pMEG3 in CRPC cells. The PAMAM-PEG-EpDT3/pMEG3 nanoparticles (NPs) were tested using in vitro cellular assays including cellular uptake, entry, and CCK-8 measurement, and tumor growth inhibition, histological assessment, and safety evaluations in in vivo animal models.

resultsThe EpDT3 aptamer promoted endocytosis of PAMAM and PAMAM-PEG-EpDT3/pMEG3 NPs in CRPC cells. PAMAM-PEG-EpDT3/pMEG3 NPs exhibited a significant anti-CRPC effect, both in vivo and in vitro, when compared to that of unfunctionalized PAMAM-PEG/pMEG3 NPs.

conclusionPAMAM-PEG-EpDT3/pMEG3 NPs can potentially improve gene therapy in CRPC cells.

Indexed as

AnimalsAptamers, NucleotideCell Line, TumorDendrimersDrug CarriersGenetic TherapyHumansMaleNanoparticlesPlasmidsPolyethylene GlycolsProstatic Neoplasms, Castration-ResistantRNA, Long NoncodingAptamers, NucleotideDendrimersDrug CarriersMEG3 non-coding RNA, humanPEG-PAMAMPolyethylene GlycolsRNA, Long Noncodingcastration-resistant prostate cancerdendrimergene therapylong non-coding RNA MEG3

Identifiers

PMID33376323
PMCPMC7759727
OpenAlexW3112819706

What OpenQuestion holds

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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.