Evidence map›Paper›PMID 20645030›Full record

ArticleMedical oncology (Northwood, London, England)2011

Integrin-targeted paclitaxel nanoliposomes for tumor therapy.

Shuyan Meng, Bo Su, Wei Li, Yongmei Ding, Liang Tang, Wei Zhou, Yin Song, Zhou Caicun

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
  2. Review
  3. Studies of nanoparticle delivery withBioactive materials · 2020
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Interleukin-22 (IL-22) Regulates Apoptosis of Paclitaxel-Resistant Non-Small Cell Lung Cancer Cells Through C-Jun N-Terminal Kinase Signaling Pathway.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. CD44v6-Peptide Functionalized Nanoparticles Selectively Bind to Metastatic Cancer Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2017
    Article
  14. Article
  15. Review
  16. Drug-induced hallucinatory syndrome in a patient with breast cancer after paclitaxel infusion.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2012
    Article
  17. Article
  18. Liposomal nanotherapeutics for cancer treatment: Targeted delivery and immunotherapy.International journal of immunopathology and pharmacology
    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

8 authors at 2 institutions in 1 country.

Shuyan MengCancer Institute of Tongji University School of Medicine, Shanghai Pulmonary Hospital, 507 Zhengmin Road, 200433, Shanghai, China.
Bo Su
Wei Li
Yongmei Ding
Liang Tang
Wei Zhou
Yin Song
Zhou Caicun
Shanghai Pulmonary Hospital · CNTongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A neovessel-targeted PEGylated liposomal formulation of paclitaxel was prepared with the purpose of improving the solubility of paclitaxel and specific targeting ability of this drug to tumor vasculature. AlphaV integrins overexpressed on the surface of new formed tumor vessels were selected to be the targets and their specific ligand, a 12-mer peptide containing a cyclic RGD sequence was used to achieve the goal. After coupled with a KGG-Palmitic acid conjugate, the RGD containing peptide was successfully integrated to the lipid bilayers. Mean particle size of the liposomes was under 100 nm and the drug entrapment efficiency was greater than 95%. Release study showed a much lower release rate of paclitaxel from liposomal formulation than from Cremophor EL-based formulation which indicated that this drug was stable in an entrapped form in vitro. Plasma distribution study showed that liposomal paclitaxel-treated groups obtained higher paclitaxel concentration than Taxol-treated group after 6 h injection. Greater cellular uptake was also found in the integrin-targeted liposomal paclitaxel-treated group compared with Taxol-treated group. Treatment of mice bearing A549 tumors with the integrin-targeted paclitaxel liposomes resulted in a lower tumor microvessel density than Taxol-treated group. Therefore, RGD-based strategy could be used to enhance tumor-specific recognition of nanocarriers. Neovessel-targeted PEGylated paclitaxel liposomes developed in present study might be a more promising drug for cancer treatment.

Indexed as

Integrin alphaVAnimalsAntineoplastic Agents, PhytogenicCell Line, TumorDrug Delivery SystemsFemaleHumansLiposomesMiceMice, NudeNanospheresNeoplasms, ExperimentalPaclitaxelXenograft Model Antitumor AssaysAntineoplastic Agents, PhytogenicIntegrin alphaVLiposomesPaclitaxel

Identifiers

PMID20645030
OpenAlexW1968643207

What OpenQuestion holds

Textmetadata
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.