Evidence map›Paper›PMID 25473281›Full record

ArticleInternational journal of nanomedicine2014

Study on the prostate cancer-targeting mechanism of aptamer-modified nanoparticles and their potential anticancer effect in vivo.

Xin Wu, Zongguang Tai, Quangang Zhu, Wei Fan, Baoyue Ding, Wei Zhang, Lijuan Zhang, Chong Yao, Xiaoyu Wang, Xueying Ding and 5 more

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. In vivo gene delivery mediated by non-viral vectors for cancer therapy.Journal of controlled release : official journal of the Controlled Release Society · 2020
    Review
  12. Delivery of therapeutic miRNA using polymer-based formulation.Drug delivery and translational research · 2019
    Review
  13. Article
  14. Diagnosis of prostate cancer via nanotechnological approach.International journal of nanomedicine · 2015
    Review
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

15 authors at 6 institutions in 1 country.

Xin WuDepartment of Pharmaceutics, Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China ; Department of Pharmaceutics, Shanghai First People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.
Zongguang TaiDepartment of Pharmaceutics, Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.
Quangang ZhuDepartment of Pharmaceutics, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, People's Republic of China.
Wei FanDepartment of Pharmaceutics, The 425th Hospital of PLA, Sanya, People's Republic of China.
Baoyue DingDepartment of Pharmaceutics, Medical College of Jiaxing University, Jiaxing, People's Republic of China.
Wei ZhangDepartment of Pharmaceutics, Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China ; Department of Pharmaceutics, The 522nd Hospital of PLA, Luoyang, People's Republic of China.
Lijuan ZhangDepartment of Pharmaceutics, Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.
Chong YaoDepartment of Pharmaceutics, Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.
Xiaoyu WangDepartment of Pharmaceutics, Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.
Xueying DingDepartment of Pharmaceutics, Shanghai First People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.
Qin LiDepartment of Pharmaceutics, Shanghai First People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.
Xiaoyu LiDepartment of Pharmaceutics, Shanghai First People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.
Gaolin LiuDepartment of Pharmaceutics, Shanghai First People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.
Jiyong LiuDepartment of Pharmaceutics, Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.
Shen GaoDepartment of Pharmaceutics, Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.
Changhai Hospital · CNSecond Military Medical University · CNShanghai First People's Hospital · CN82th Hospital of Pla · CNJiaxing University · CNShanghai University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ligand-mediated prostate cancer (PCa)-targeting gene delivery is one of the focuses of research in recent years. Our previous study reported the successful preparation of aptamer-modified nanoparticles (APT-NPs) in our laboratory and demonstrated their PCa-targeting ability in vitro. However, the mechanism underlying this PCa-targeting effect and their anticancer ability in vivo have not yet been elucidated. The objective of this study was to assess the feasibility of using APT-NPs to deliver micro RNA (miRNA) systemically to PCa cells, to testify their tumor-targeting efficiency, and to observe their biodistribution after systemic administration to a xenograft mouse model of PCa. In addition, the effect of APT depletion and endocytosis inhibitors on cellular uptake was also evaluated quantitatively in LNCaP cells to explore the internalization mechanism of APT-NPs. Finally, blood chemistry, and renal and liver function parameters were measured in the xenograft mouse model of PCa to see whether APT-NPs had any demonstrable toxicity in mice in vivo. The results showed that APT-NPs prolonged the survival duration of the PCa tumor-bearing mice as compared with the unmodified NPs. In addition, they had a potential PCa-targeting effect in vivo. In conclusion, this research provides a prototype for the safe and efficient delivery of miRNA expression vectors to PCa cells, which may prove useful for preclinical and clinical studies on the treatment of PCa.

Indexed as

AnimalsAntigens, SurfaceAntineoplastic AgentsAptamers, NucleotideBody WeightDrug CarriersGlutamate Carboxypeptidase IIMaleMiceMice, Inbred BALB CMice, NudeMicroRNAsNanoparticlesProstatic NeoplasmsXenograft Model Antitumor AssaysAntigens, SurfaceAntineoplastic AgentsAptamers, NucleotideDrug CarriersFOLH1 protein, humanGlutamate Carboxypeptidase IIMicroRNAsaptamermiRNApolyamidoamineprostate cancerprostate-specific membrane antigentargeted delivery

Identifiers

PMID25473281
PMCPMC4247134
OpenAlexW1990627889

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.