Evidence map›Paper›PMID 32296050›Full record

ArticleSignal transduction and targeted therapy2020

Fibronectin-targeted dual-acting micelles for combination therapy of metastatic breast cancer.

Zhuoran Gong, Min Chen, Qiushi Ren, Xiuli Yue, Zhifei Dai

Open access · goldAbstract read
In one paragraph

Article in Signal transduction and targeted therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 69 citations in OpenAlex.

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  10. Photoactivatable nanoagonists chemically programmed for pharmacokinetic tuning and in situ cancer vaccination.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

5 authors at 2 institutions in 1 country.

Zhuoran GongDepartment of Biomedical Engineering, College of Engineering, Peking University, Beijing, 100871, China.ORCID http://orcid.org/0000-0002-7195-0527
Min ChenDepartment of Biomedical Engineering, College of Engineering, Peking University, Beijing, 100871, China.
Qiushi RenDepartment of Biomedical Engineering, College of Engineering, Peking University, Beijing, 100871, China.
Xiuli YueSchool of Environment, Harbin Institute of Technology, Harbin, 150090, China. xiulidx@163.com.
Zhifei DaiDepartment of Biomedical Engineering, College of Engineering, Peking University, Beijing, 100871, China. zhifei.dai@pku.edu.cn.
Peking University · CNHarbin Institute of Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stage IV breast cancer, which has a high risk of invasion, often develops into metastases in distant organs, especially in the lung, and this could threaten the lives of women. Thus, the development of more advanced therapeutics that can efficiently target metastatic foci is crucial. In this study, we built an dual-acting therapeutic strategy using micelles with high stability functionalized with fibronectin-targeting CREKA peptides encapsulating two slightly soluble chemotherapy agents in water, doxorubicin (D) and vinorelbine (V), which we termed C-DVM. We found that small C-DVM micelles could efficiently codeliver drugs into 4T1 cells and disrupt microtubule structures. C-DVM also exhibited a powerful ability to eradicate and inhibit invasion of 4T1 cells. Moreover, an in vivo pharmacokinetics study showed that C-DVM increased the drug circulation half-life and led to increased enrichment of drugs in lung metastatic foci after 24 h. Moreover, dual-acting C-DVM treatment led to 90% inhibition of metastatic foci development and reduced invasion of metastases. C-DVM could potentially be used as a targeted treatment for metastasis and represents a new approach with higher therapeutic efficacy than conventional chemotherapy for stage IV breast cancer that could be used in the future.

Indexed as

Molecular Targeted TherapyAntineoplastic AgentsBreast NeoplasmsCell Line, TumorCombined Modality TherapyDoxorubicinFemaleFibronectinsHumansMicellesNanoparticlesNeoplasm MetastasisNeoplasm StagingOligopeptidesVinorelbineAntineoplastic Agentscysteinyl-arginyl-glutamyl-lysyl-alanylDoxorubicinFibronectinsFN1 protein, humanMicellesOligopeptidesVinorelbine

Identifiers

PMID32296050
PMCPMC7005157
OpenAlexW3005119440

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.