Evidence map›Paper›PMID 29355035›Full record

ArticleDrug delivery2018

Simultaneous targeting therapy for lung metastasis and breast tumor by blocking the NF-κB signaling pathway using Celastrol-loaded micelles.

Yue Zhao, Yanan Tan, Tingting Meng, Xuan Liu, Yun Zhu, Yun Hong, Xiqin Yang, Hong Yuan, Xuan Huang, Fuqiang Hu

Open access · goldAbstract read
In one paragraph

Article in Drug delivery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
8.9field-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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Degradation-Based Protein Profiling: A Case Study of Celastrol.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. The role of RNA mInternational journal of biological sciences · 2021
    Review
  11. Review
  12. Article
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  14. Article
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  16. Article
  17. 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

10 authors at 3 institutions in 1 country.

Yue Zhaoa Ocean College , Zhejiang University , Zhoushan , China.
Yanan Tana Ocean College , Zhejiang University , Zhoushan , China.
Tingting Mengb College of Pharmaceutical Science , Zhejiang University , Hangzhou , China.
Xuan Liub College of Pharmaceutical Science , Zhejiang University , Hangzhou , China.
Yun Zhua Ocean College , Zhejiang University , Zhoushan , China.
Yun Hongc The First Affiliated Hospital, College of Pharmaceutical Medicine , Zhejiang University , Hangzhou , China.
Xiqin Yangb College of Pharmaceutical Science , Zhejiang University , Hangzhou , China.
Hong Yuanb College of Pharmaceutical Science , Zhejiang University , Hangzhou , China.
Xuan Huangd Department of Pharmacy, School of Medicine Science , Jiaxing University , Zhejiang , China.
Fuqiang Hua Ocean College , Zhejiang University , Zhoushan , China.
Zhejiang University · CNZhejiang Ocean University · CNJiaxing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastasis is one of the major obstacles for successful therapy of breast tumor. To inhibit the metastasis and growth of breast tumor simultaneously, a Celastrol (Cela) loaded glucolipid-like conjugates (CSOSA/Cela) with αvβ3-ligand Tetraiodothyroacetic acid (TET) modification (TET-CSOSA/Cela) were established to block nuclear factor-kappa B (NF-κB) signaling pathway. The distribution of TET-CSOSA was remarkably increased in lung metastasis and primary tumor of 4T1 tumor-bearing mice by means of αvβ3 receptor-mediated interaction. The results demonstrated that TET-CSOSA/Cela significantly suppressed Bcl-2 activation of lung metastatic cells and reduced MMP-9 expression of 4T1 breast tumor cells by blocking NF-κB. The inhibitory rates of TET-CSOSA/Cela against lung metastasis and primary tumor were raised to 90.72 and 81.15%, compared to those of Celastrol (72.15 and 46.40%), respectively. All results demonstrated the αvβ3 receptor targeted TET-CSOSA/Cela micelles exhibited great potential in treating lung metastasis and primary tumor simultaneously via blocking NF-κB signaling pathway.

Indexed as

AnimalsAntineoplastic AgentsBreast NeoplasmsCell Line, TumorFemaleHumansIntegrin alphaVbeta3Lung NeoplasmsMiceMice, Inbred BALB CMicellesNeoplasm MetastasisNF-kappa BPentacyclic TriterpenesSignal TransductionThyroxineAntineoplastic AgentscelastrolIntegrin alphaVbeta3MicellesNF-kappa BPentacyclic Triterpenestetraiodothyroacetic acidThyroxineTriterpenesbreast tumordrug delivery systemmetastasisSimultaneous targetingtetraiodothyroacetic acid

Identifiers

PMID29355035
PMCPMC6058533
OpenAlexW2791457767

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.