Evidence map›Paper›PMID 35199059›Full record

ArticleCell reports. Physical science2022

Targeted disruption of tumor vasculature via polyphenol nanoparticles to improve brain cancer treatment.

Fuyao Liu, Bin Peng, Miao Li, Junning Ma, Gang Deng, Shenqi Zhang, Wendy C Sheu, Pan Zou, Haoan Wu, Jun Liu and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Physical science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
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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

13 authors at 1 institution in 1 country.

Fuyao LiuDepartment of Neurosurgery, Yale University, New Haven, CT 06510, USA.
Bin PengDepartment of Neurosurgery, Yale University, New Haven, CT 06510, USA.
Miao LiDepartment of Neurosurgery, Yale University, New Haven, CT 06510, USA.
Junning MaDepartment of Neurosurgery, Yale University, New Haven, CT 06510, USA.
Gang DengDepartment of Neurosurgery, Yale University, New Haven, CT 06510, USA.
Shenqi ZhangDepartment of Neurosurgery, Yale University, New Haven, CT 06510, USA.
Wendy C SheuDepartment of Biomedical Engineering, Yale University, New Haven, CT 06510, USA.
Pan ZouDepartment of Neurosurgery, Yale University, New Haven, CT 06510, USA.
Haoan WuDepartment of Neurosurgery, Yale University, New Haven, CT 06510, USA.
Jun LiuDepartment of Neurosurgery, Yale University, New Haven, CT 06510, USA.
Ann T ChenDepartment of Biomedical Engineering, Yale University, New Haven, CT 06510, USA.
Farrah S MohammedDepartment of Biomedical Engineering, Yale University, New Haven, CT 06510, USA.
Jiangbing ZhouDepartment of Neurosurgery, Yale University, New Haven, CT 06510, USA.
Yale University · US

Funding

Ex vivo analysis of human brain tumor cells in a microvascular niche modelR01CA245313 · NCI · YALE UNIVERSITY · PI FAN, RONG, ZHOU, JIANGBING · 2020 to 2024
$2.6M
Systemic gene therapy for glioblastomaR01NS095817 · NINDS · YALE UNIVERSITY · PI ZHOU, JIANGBING · 2016 to 2020
$1.8M
Convergent Graduate Training in Engineering, Physics and BiologyT32EB019941 · NIBIB · YALE UNIVERSITY · PI O'HERN, COREY · 2016 to 2020
$998k
NCI NIH HHS R01 CA245313NIBIB NIH HHS T32 EB019941NINDS NIH HHS R01 NS095817
6 · The paper itself

Abstract

Despite being effective for many other solid tumors, traditional anti-angiogenic therapy has been shown to be insufficient for the treatment of malignant glioma. Here, we report the development of polyphenol nanoparticles (NPs), which not only inhibit the formation of new vessels but also enable targeted disruption of the existing tumor vasculature. The NPs are synthesized through a combinatory iron-coordination and polymer-stabilization approach, which allows for high drug loading and intrinsic tumor vessel targeting. We study a lead NP consisting of quercetin and find that the NP after intravenous administration preferentially binds to VEGFR2, which is overexpressed in tumor vasculature. We demonstrate that the binding is mediated by quercetin, and the interaction of NPs with VEGFR2 leads to disruption of the existing tumor vasculature and inhibition of new vessel development. As a result, systemic treatment with the NPs effectively inhibits tumor growth and increases drug delivery to tumors.

Identifiers

PMID35199059
PMCPMC8863382
OpenAlexW4200279139

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.