Evidence map›Paper›PMID 27470938›Full record

ArticleScientific reports2016

Gold Nanoparticle-Mediated Targeted Delivery of Recombinant Human Endostatin Normalizes Tumour Vasculature and Improves Cancer Therapy.

Wei Li, Xiaoxu Zhao, Bin Du, Xin Li, Shuhao Liu, Xiao-Yan Yang, Hui Ding, Wende Yang, Fan Pan, Xiaobo Wu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 115 citations in OpenAlex.

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  8. Advances of medical nanorobots for future cancer treatments.Journal of hematology & oncology · 2023
    Review
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  14. Zonal Intratumoral Delivery of Nanoparticles Guided by Surface Functionalization.Langmuir : the ACS journal of surfaces and colloids · 2022
    Article
  15. Review
  16. Nanotechnology in drug and gene delivery.Naunyn-Schmiedeberg's archives of pharmacology · 2022
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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

12 authors at 2 institutions in 1 country.

Wei LiDepartment of General Surgery, the First Affiliated Hospital of Jinan University, Guangzhou 510632, China.
Xiaoxu ZhaoDepartment of General Surgery, the First Affiliated Hospital of Jinan University, Guangzhou 510632, China.
Bin DuDepartment of Pathology, the First Affiliated Hospital of Jinan University, Guangzhou, 510632, China.
Xin LiDepartment of General Surgery, the First Affiliated Hospital of Jinan University, Guangzhou 510632, China.
Shuhao LiuDepartment of General Surgery, the First Affiliated Hospital of Jinan University, Guangzhou 510632, China.
Xiao-Yan YangDepartment of General Surgery, the First Affiliated Hospital of Jinan University, Guangzhou 510632, China.
Hui DingDepartment of General Surgery, the First Affiliated Hospital of Jinan University, Guangzhou 510632, China.
Wende YangDepartment of General Surgery, the First Affiliated Hospital of Jinan University, Guangzhou 510632, China.
Fan PanDepartment of General Surgery, the First Affiliated Hospital of Jinan University, Guangzhou 510632, China.
Xiaobo WuDepartment of General Surgery, the First Affiliated Hospital of Jinan University, Guangzhou 510632, China.
Li QinDepartment of Histology and Embryology, Medical School of Jinan University, Guangzhou 510632, China.
Yunlong PanDepartment of General Surgery, the First Affiliated Hospital of Jinan University, Guangzhou 510632, China.
First Affiliated Hospital of Jinan University · CNJinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumour vasculature is generally disordered because of the production of excessive angiogenic factors by tumour cells, which results in tumour progression and reduces the effectiveness of radiotherapy or chemotherapy. Transient anti-angiogenic therapies that regulate tumour vascular morphology and function and improve the efficiency of antitumour therapy are under investigation. Recombinant human endostatin (Endostar/rhES) is a vascular angiogenesis-disrupting agent that has been used to treat non-small cell lung cancer (NSCLC) in the clinical setting. In this study, we used gold nanoparticles (AuNPs) as a drug-delivery system (DDS) for targeted tumour delivery of rhES for short therapy, which resulted in transient tumour vascular normalization, reduced permeability and hypoxia, strengthened blood vessel integrity, and increased blood-flow perfusion. Moreover, combination therapy with 5-FU over this timeframe was substantially more effective than 5-FU monotherapy. In conclusion, our research demonstrates the potential use of AuNPs as a drug-delivery platform for transporting rhES into a tumour to induce transient tumour vascular normalization and enhance the antitumour efficacy of cytotoxic drugs.

Indexed as

Angiogenesis InhibitorsAnimalsAntineoplastic AgentsCarcinoma, HepatocellularDisease Models, AnimalDrug CarriersEndostatinsFemaleFluorouracilGoldHeterograftsLiver NeoplasmsMiceNanoparticlesNeoplasm TransplantationNeovascularization, PathologicAngiogenesis InhibitorsAntineoplastic AgentsDrug CarriersEndostatinsFluorouracilGoldRecombinant Proteins

Identifiers

PMID27470938
PMCPMC4965746
OpenAlexW2489212590

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.