Evidence map›Paper›PMID 27143875›Full record

ArticleInternational journal of nanomedicine2016

Novel walnut peptide-selenium hybrids with enhanced anticancer synergism: facile synthesis and mechanistic investigation of anticancer activity.

Wenzhen Liao, Rong Zhang, Chenbo Dong, Zhiqiang Yu, Jiaoyan Ren

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Review
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  12. Article
  13. Fucoxanthin Prevents 6-OHDA-Induced Neurotoxicity by Targeting Keap1.Oxidative medicine and cellular longevity · 2021
    Article
  14. Small Molecule Oligopeptides Isolated from Walnut (Molecules (Basel, Switzerland) · 2018
    Article
  15. Article
  16. Review
  17. Polyphenols fromMedChemComm · 2018
    Article
  18. Nano-selenium and its nanomedicine applications: a critical review.International journal of nanomedicine · 2018
    Review
  19. Article
  20. Article
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.

Wenzhen LiaoCollege of Light Industry and Food Sciences, South China University of Technology, Guangzhou, Guangdong, People's Republic of China.
Rong ZhangCollege of Light Industry and Food Sciences, South China University of Technology, Guangzhou, Guangdong, People's Republic of China.
Chenbo DongCivil and Environmental Engineering, Rice University, Houston, TX, USA.
Zhiqiang YuSchool of Pharmaceutical Science, Guangdong Provincial Key Laboratory of New Drug Screening, Southern Medical University, Guangzhou, Guangdong, People's Republic of China.
Jiaoyan RenCollege of Light Industry and Food Sciences, South China University of Technology, Guangzhou, Guangdong, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This contribution reports a facile synthesis of degreased walnut peptides (WP1)-functionalized selenium nanoparticles (SeNPs) hybrids with enhanced anticancer activity and a detailed mechanistic evaluation of its superior anticancer activity. Structural and chemical characterizations proved that SeNPs are effectively capped with WP1 via physical absorption, resulting in a stable hybrid structure with an average diameter of 89.22 nm. A panel of selected human cancer cell lines demonstrated high susceptibility toward WP1-SeNPs and displayed significantly reduced proliferative behavior. The as-synthesized WP1-SeNPs exhibited excellent selectivity between cancer cells and normal cells. The targeted induction of apoptosis in human breast adenocarcinoma cells (MCF-7) was confirmed by the accumulation of arrested S-phase cells, nuclear condensation, and DNA breakage. Careful investigations revealed that an extrinsic apoptotic pathway can be attributed to the cell apoptosis and the same was confirmed by activation of the Fas-associated with death domain protein and caspases 3, 8, and 9. In addition, it was also understood that intrinsic apoptotic pathways including reactive oxygen species generation, as well as the reduction in mitochondrial membrane potential, are also involved in the WP1-SeNP-induced apoptosis. This suggested the involvement of multiple apoptosis pathways in the anticancer activity. Our results indicated that WP1-SeNP hybrids with Se core encapsulated in a WP1 shell could be a highly effective method to achieve anticancer synergism. Moreover, the great potential exhibited by WP1-SeNPs could make them an ideal candidate as a chemotherapeutic agent for human cancers, especially for breast cancer.

Indexed as

Antineoplastic AgentsApoptosisBlotting, WesternBreast NeoplasmsCell Line, TumorFemaleHumansJuglansMembrane Potential, MitochondrialNanoparticlesPeptide FragmentsSelenium CompoundsSignal TransductionAntineoplastic AgentsPeptide FragmentsSelenium Compoundsantiproliferative activityapoptosishuman cancer cell linesselenium nanoparticleswalnut peptides

Identifiers

PMID27143875
PMCPMC4841427

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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.