Evidence map›Paper›PMID 35456655›Full record

ReviewPharmaceutics2022

Targeted Liposomes: A Nonviral Gene Delivery System for Cancer Therapy.

Marcela Tavares Luiz, Jessyca Aparecida Paes Dutra, Larissa Bueno Tofani, Jennifer Thayanne Cavalcante de Araújo, Leonardo Delello Di Filippo, Juliana Maldonado Marchetti, Marlus Chorilli

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review
  20. 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

7 authors at 2 institutions in 1 country.

Marcela Tavares LuizSchool of Pharmaceutical Science of Ribeirao Preto, University of Sao Paulo (USP), Ribeirao Preto 14040-900, Brazil.
Jessyca Aparecida Paes DutraSchool of Pharmaceutical Science, Sao Paulo State University (UNESP), Araraquara 14800-903, Brazil.
Larissa Bueno TofaniSchool of Pharmaceutical Science, Sao Paulo State University (UNESP), Araraquara 14800-903, Brazil.ORCID 0000-0002-1245-6828
Jennifer Thayanne Cavalcante de AraújoSchool of Pharmaceutical Science, Sao Paulo State University (UNESP), Araraquara 14800-903, Brazil.ORCID 0000-0003-2547-1012
Leonardo Delello Di FilippoSchool of Pharmaceutical Science, Sao Paulo State University (UNESP), Araraquara 14800-903, Brazil.
Juliana Maldonado MarchettiSchool of Pharmaceutical Science of Ribeirao Preto, University of Sao Paulo (USP), Ribeirao Preto 14040-900, Brazil.
Marlus ChorilliSchool of Pharmaceutical Science, Sao Paulo State University (UNESP), Araraquara 14800-903, Brazil.ORCID 0000-0002-6698-0545
Universidade Estadual Paulista (Unesp) · BRUniversidade de Ribeirão Preto · BR

Funding

Coordenação de Aperfeicoamento de Pessoal de Nível Superior 001
6 · The paper itself

Abstract

Cancer is the second most frequent cause of death worldwide, with 28.4 million new cases expected for 2040. Despite de advances in the treatment, it remains a challenge because of the tumor heterogenicity and the increase in multidrug resistance mechanisms. Thus, gene therapy has been a potential therapeutic approach owing to its ability to introduce, silence, or change the content of the human genetic code for inhibiting tumor progression, angiogenesis, and metastasis. For the proper delivery of genes to tumor cells, it requires the use of gene vectors for protecting the therapeutic gene and transporting it into cells. Among these vectors, liposomes have been the nonviral vector most used because of their low immunogenicity and low toxicity. Furthermore, this nanosystem can have its surface modified with ligands (e.g., antibodies, peptides, aptamers, folic acid, carbohydrates, and others) that can be recognized with high specificity and affinity by receptor overexpressed in tumor cells, increasing the selective delivery of genes to tumors. In this context, the present review address and discuss the main targeting ligands used to functionalize liposomes for improving gene delivery with potential application in cancer treatment.

Indexed as

active targetingDNAlipoplexnonviral vectornucleic acidRNA

Identifiers

PMID35456655
PMCPMC9030342
OpenAlexW4224306726

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.