Evidence map›Paper›PMID 28435247›Full record

ArticleInternational journal of nanomedicine2017

Delivery of curcumin by directed self-assembled micelles enhances therapeutic treatment of non-small-cell lung cancer.

Wen-Ting Zhu, Sheng-Yao Liu, Lei Wu, Hua-Li Xu, Jun Wang, Guo-Xin Ni, Qing-Bing Zeng

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 19% 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, 46 citations in OpenAlex.

  1. Advances in carrier-free nanodrug delivery systems.Drug delivery and translational research · 2026
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  8. Degree-based topological indices and polynomials of hyaluronic acid-curcumin conjugates.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Wen-Ting ZhuBiomaterial Research Center, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.
Sheng-Yao LiuDepartment of Orthopeadics and Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Lei WuBiomaterial Research Center, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.
Hua-Li XuDepartment of Anesthesiology, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Jun WangBiomaterial Research Center, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.
Guo-Xin NiDepartment of Orthopeadics and Traumatology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Qing-Bing ZengBiomaterial Research Center, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.
Southern Medical University · CNFujian Medical University · CNNanfang Hospital · CNZhujiang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt has been widely reported that curcumin (CUR) exhibits anticancer activity and triggers the apoptosis of human A549 non-small-cell lung cancer (NSCLC) cells. However, its application is limited owing to its poor solubility and bioavailability. Therefore, there is an urgent need to develop a new CUR formulation with higher water solubility and better biocompatibility for clinical application in the future. MATERIALS AND

methodsIn this study, CUR-loaded methoxy polyethylene glycol-polylactide (CUR/mPEG-PLA) polymeric micelles were prepared by a thin-film hydration method. Their characteristics and antitumor effects were evaluated subsequently.

resultsThe average size of CUR/mPEG-PLA micelles was 34.9±2.1 nm with its polydispersity index (PDI) in the range of 0.067-0.168. The encapsulation efficiency and drug loading were 90.2%±0.78% and 9.1%±0.07%, respectively. CUR was constantly released from the CUR/mPEG-PLA micelles, and its cellular uptake in A549 cells was significantly increased. It was also found that CUR/mPEG-PLA micelles inhibited A549 cell proliferation, increased the cell cytotoxicity, induced G2/M stage arrest and promoted cell apoptosis. Moreover, the CUR/mPEG-PLA micelles suppressed the migration and invasion of A549 cells more obviously than free CUR. Additionally, CUR/mPEG-PLA micelles inhibited human umbilical vein endothelial cells migration, invasion and corresponding tube formation, implying the antiangiogenesis ability. Its enhanced antitumor mechanism may be related to the reduced expression of vascular endothelial growth factor, matrix metalloproteinase (MMP)-2, MMP-9 and Bcl-2 as well as the increased expression of Bax.

conclusionThe mPEG-PLA copolymer micelles can serve as an efficient carrier for CUR. The CUR/mPEG-PLA micelles have promising clinical potential in treating NSCLC.

Indexed as

MicellesAngiogenesis InhibitorsAntineoplastic Agents, PhytogenicApoptosisBiological AvailabilityCarcinoma, Non-Small-Cell LungCurcuminDrug CarriersDrug Delivery SystemsHumansHuman Umbilical Vein Endothelial CellsLung NeoplasmsPolyestersPolyethylene GlycolsAngiogenesis InhibitorsAntineoplastic Agents, PhytogenicCurcuminDrug Carriersmethoxy poly(ethylene glycol)-poly(lactide)MicellesPolyestersPolyethylene GlycolsA549 cellsangiogenesiscurcuminHUVECsmPEG–PLApolymeric micelles

Identifiers

PMID28435247
PMCPMC5388225
OpenAlexW2605149342

What OpenQuestion holds

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Registered trials

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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.