Evidence map›Paper›PMID 27486320›Full record

ArticleInternational journal of nanomedicine2016

Cerium oxide nanoparticles inhibit the migration and proliferation of gastric cancer by increasing DHX15 expression.

Yu-Feng Xiao, Jian-Mei Li, Su-Min Wang, Xin Yong, Bo Tang, Meng-Meng Jie, Hui Dong, Xiao-Chao Yang, Shi-Ming Yang

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 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Nanoceria: an innovative strategy for cancer treatment.Cellular and molecular life sciences : CMLS · 2023
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Molecular targeted treatment and drug delivery system for gastric cancer.Journal of cancer research and clinical oncology · 2021
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. 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

9 authors.

Yu-Feng XiaoDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, People's Republic of China.
Jian-Mei LiSchool of Biomedical Engineering, Third Military Medical University, Chongqing, People's Republic of China.
Su-Min WangDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, People's Republic of China.
Xin YongDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, People's Republic of China.
Bo TangDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, People's Republic of China.
Meng-Meng JieDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, People's Republic of China.
Hui DongDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, People's Republic of China.
Xiao-Chao YangSchool of Biomedical Engineering, Third Military Medical University, Chongqing, People's Republic of China.
Shi-Ming YangDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University, Chongqing, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer is one of the leading causes of tumor-related deaths in the world. Current treatment options do not satisfy doctors and patients, and new therapies are therefore needed. Cerium oxide nanoparticles (CNPs) have been studied as a potential therapeutic approach for treating many diseases. However, their effects on human gastric cancer are currently unknown. Therefore, in this study, we aimed to characterize the effects of CNPs on human gastric cancer cell lines (MKN28 and BGC823). Gastric cancer cells were cocultured with different concentrations of CNPs, and proliferation and migration were measured both in vitro and in vivo. We found that CNPs inhibited the migration of gastric cancer cells when applied at different concentrations, but only a relatively high concentration (10 µg/mL) of CNPs suppressed proliferation. Furthermore, we found that CNPs increased the expression of DHX15 and its downstream signaling pathways. We therefore provide evidence showing that CNPs may be a promising approach to suppress malignant activity of gastric cancer by increasing the expression of DHX15.

Indexed as

AnimalsCell Line, TumorCell MovementCell ProliferationCeriumGene Expression Regulation, NeoplasticHumansMaleMice, NudeNanoparticlesNeoplasm MetastasisRNA HelicasesStomach Neoplasmsceric oxideCeriumDHX15 protein, humanRNA Helicasescerium oxide nanoparticlesDHX15gastric cancerp38

Identifiers

PMID27486320
PMCPMC4956072

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.