Evidence map›Paper›PMID 30464450›Full record

ArticleInternational journal of nanomedicine2018

Peptide T7-modified polypeptide with disulfide bonds for targeted delivery of plasmid DNA for gene therapy of prostate cancer.

Yue Lu, Wenjun Jiang, Xin Wu, Saixu Huang, Zhiyong Huang, Yamin Shi, Qi Dai, Jianming Chen, Fuzheng Ren, Shen Gao

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
  6. Article
  7. Peptide-Assisted Nucleic Acid Delivery Systems on the Rise.International journal of molecular sciences · 2021
    Review
  8. Review
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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

10 authors at 3 institutions in 1 country.

Yue LuShanghai Key Lab New Drug Design, School of Pharmacy, East China University of Science and Technology, Shanghai, People's Republic of China, fzren@ecust.edu.cn.
Wenjun JiangShanghai Key Lab New Drug Design, School of Pharmacy, East China University of Science and Technology, Shanghai, People's Republic of China, fzren@ecust.edu.cn.
Xin WuShanghai Weier Biological Medicine Science and Technology Co. Ltd., Shanghai, People's Republic of China.
Saixu HuangShanghai Key Lab New Drug Design, School of Pharmacy, East China University of Science and Technology, Shanghai, People's Republic of China, fzren@ecust.edu.cn.
Zhiyong HuangShanghai Key Lab New Drug Design, School of Pharmacy, East China University of Science and Technology, Shanghai, People's Republic of China, fzren@ecust.edu.cn.
Yamin ShiDepartment of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, People's Republic of China.
Qi DaiShanghai Key Lab New Drug Design, School of Pharmacy, East China University of Science and Technology, Shanghai, People's Republic of China, fzren@ecust.edu.cn.
Jianming ChenShanghai Weier Biological Medicine Science and Technology Co. Ltd., Shanghai, People's Republic of China.
Fuzheng RenShanghai Key Lab New Drug Design, School of Pharmacy, East China University of Science and Technology, Shanghai, People's Republic of China, fzren@ecust.edu.cn.
Shen GaoDepartment of Pharmaceutics, Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China, liullk@126.com.
East China University of Science and Technology · CNFujian University of Traditional Chinese Medicine · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVectors are essential for successful gene delivery. In the present study, a tumor-targeting cationic gene vector, known as the disulfide cross-linked arginine-aspartic acid peptide modified by HAIYPRH (T7) peptide (CRD-PEG-T7), was designed for targeted delivery of plasmid DNA (pDNA) for gene therapy of prostate cancer (PCa).

methodsThe structure of CRD-PEG-T7 was determined and the cellular uptake efficacy, gene transfection efficacy, cytotoxicity, and the targeting effect of the CRD-PEG-T7-plasmid DNA complex were examined.

resultsThe results demonstrated that the CRD-PEG-T7-plasmid DNA complex was nanosized and had a positively charged surface, good cellular uptake efficacy, minimal cytotoxicity, and a dual-targeting effect as compared with the CRD-PEG-plasmid DNA complex. The peptide T7-modifed new delivery system was able to target the highly expressed transferrin receptor (TfR) on tumor cells with an efficiency four-fold higher than that of the non-modified system.

conclusionThe results above indicatd that the CRD-PEG-T7-plasmid DNA complex may prove to be a promising gene delivery system targeting bone-metastatic tumor.

Indexed as

Genetic TherapyGene Transfer TechniquesAnimalsBenzoxazolesCell DeathCell Line, TumorCell MovementCollagen Type IVDisulfidesDNAEndocytosisHumansMaleMice, Inbred BALB CMice, NudeParticle Size1,1'-((4,4,7,7-tetramethyl)-4,7-diazaundecamethylene)bis-4-(3-methyl-2,3-dihydro(benzo-1,3-oxazole)-2-methylidene)quinoliniumBenzoxazolesCollagen Type IVDisulfidesDNAPeptide FragmentsPolyethylene GlycolsQuinolinium CompoundsTransferrintumstatin (74-98)arginine peptideaspartic acid peptidebone metastasis prostate cancerDNA deliverytumor targeting

Identifiers

PMID30464450
PMCPMC6214593
OpenAlexW2899462096

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.