Evidence map›Paper›PMID 29201626›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2017

Rod-Shaped Active Drug Particles Enable Efficient and Safe Gene Delivery.

Xiaofei Xin, Xue Pei, Xin Yang, Yaqi Lv, Li Zhang, Wei He, Lifang Yin

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Macropinocytosis as a cell entry route for peptide-functionalized and bystander nanoparticles.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Review
  13. 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
  14. Article
  15. Article
  16. Article
  17. "Locked" cancer cells are more sensitive to chemotherapy.Bioengineering & translational medicine · 2019
    Article
  18. Article
  19. Review
  20. Oral Nonviral Gene Delivery for Chronic Protein Replacement Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2018
    Article
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

7 authors at 1 institution in 1 country.

Xiaofei XinDepartment of Pharmaceutics, School of Pharmacy China Pharmaceutical University Nanjing 210009 P. R. China.
Xue PeiDepartment of Pharmaceutics, School of Pharmacy China Pharmaceutical University Nanjing 210009 P. R. China.
Xin YangDepartment of Pharmaceutics, School of Pharmacy China Pharmaceutical University Nanjing 210009 P. R. China.
Yaqi LvDepartment of Pharmaceutics, School of Pharmacy China Pharmaceutical University Nanjing 210009 P. R. China.
Li ZhangDepartment of Pharmaceutics, School of Pharmacy China Pharmaceutical University Nanjing 210009 P. R. China.
Wei HeDepartment of Pharmaceutics, School of Pharmacy China Pharmaceutical University Nanjing 210009 P. R. China.
Lifang YinDepartment of Pharmaceutics, School of Pharmacy China Pharmaceutical University Nanjing 210009 P. R. China.ORCID 0000-0002-2825-3136
China Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Efficient microRNAs (miRNA) delivery into cells is a promising strategy for disease therapy, but is a major challenge because the available conventional nonviral vectors have significant drawbacks. In particular, after these vectors are entrapped in lysosomes, the escape efficiency of genes from lysosomes into the cytosol is less than 2%. Here, a novel approach for lethal-7a (let-7a) replacement therapy using rod-shaped active pure drug nanoparticles (≈130 nm in length, PNPs) with a dramatically high drug-loading of ≈300% as vectors is reported. Importantly, unlike other vectors, the developed PNPs/let-7a complexes (≈178 nm, CNPs) can enter cells and bypass the lysosomal route to localize to the cytosol, achieving efficient intracellular delivery of let-7a and a 50% reduction in expression of the target protein (KRAS). Also, CNPs prolong the

Indexed as

caveolar pathwaygene therapymetastatic breast cancerrod‐shaped drug particlessafety

Identifiers

PMID29201626
PMCPMC5700648
OpenAlexW2751323893

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.