Evidence map›Paper›PMID 29426376›Full record

ArticleOncology research2019

Silencing of NADPH Oxidase 4 Attenuates Hypoxia Resistance in Neuroblastoma Cells SH-SY5Y by Inhibiting PI3K/Akt-Dependent Glycolysis.

Ting Yu, Lei Li, Wenyan Liu, Bailiu Ya, Hongju Cheng, Qing Xin

Open access · hybridAbstract read
In one paragraph

Article in Oncology research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. NOX Family: Regulators of Reactive Oxygen Species Balance in Tumor Cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Review
  2. Article
  3. Article
  4. Model for predicting prognosis and immunotherapy based on CDJournal of cancer research and clinical oncology · 2023
    Article
  5. Review
  6. Article
  7. NOX Dependent ROS Generation and Cell Metabolism.International journal of molecular sciences · 2023
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Inhibiting the Activity of NADPH Oxidase in Cancer.Antioxidants & redox signaling · 2020
    Article
  15. Article
  16. 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

6 authors at 1 institution in 1 country.

Ting YuDepartment of Physiology, Jining Medical University, Jining, Shandong, P.R. China.
Lei LiDepartment of Diagnosis, Jining Medical University, Jining, Shandong, P.R. China.
Wenyan LiuDepartment of Physiology, Jining Medical University, Jining, Shandong, P.R. China.
Bailiu YaDepartment of Physiology, Jining Medical University, Jining, Shandong, P.R. China.
Hongju ChengDepartment of Physiology, Jining Medical University, Jining, Shandong, P.R. China.
Qing XinDepartment of Physiology, Jining Medical University, Jining, Shandong, P.R. China.
Jining Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypoxia-induced chemoresistance is a major obstacle in the development of effective cancer therapy. In our study, the reversal abilities of NADPH oxidase 4 (NOX4) silence on hypoxia resistance and the potential mechanism were investigated. Our data showed that the expression of NOX4 was upregulated in human neuroblastoma cells SH-SY5Y under hypoxia condition time dependently. Knockdown of NOX4 expression by siRNA inhibited glycolysis induced by hypoxia through decreasing the expression of glycolysis-related proteins (HIF-1α, LDHA, and PDK1), decreasing glucose uptake, lactate production, and ROS production, while increasing mitochondria membrane potential. Moreover, NOX4 silence inhibited cell growth under hypoxia condition through suppressing cell proliferation and proliferation-related proteins (Ki-67 and PCNA) compared with the hypoxia 24 h + siRNA NC group. Further, Western blot experiments exhibited that NOX4 siRNA could downregulate the rate of p-Akt/Akt. Treatment with PI3K/Akt signaling activator IGF-1 blocked, while treatment with Akt inhibitor perifosine enhanced the inhibitory effect of si-NOX4 on glycolysis and cell growth. In summary, knockdown of NOX4 had the ability of reversing hypoxia resistance, and the major mechanism is considered to be the inhibition of glycolysis and cell growth via the PI3K/Akt signaling pathway. Therefore, NOX4 could be a novel target against hypoxia resistance in neuroblastoma.

Indexed as

Cell Line, TumorCell ProliferationDrug Resistance, NeoplasmGene SilencingGlycolysisHumansHypoxiaInsulin-Like Growth Factor IMembrane Potential, MitochondrialNADPH Oxidase 4NeuroblastomaNeuronsPhosphatidylinositol 3-KinasesPhosphorylcholineProto-Oncogene Proteins c-aktRNA, Small InterferingInsulin-Like Growth Factor INADPH Oxidase 4NOX4 protein, humanperifosinePhosphatidylinositol 3-KinasesPhosphorylcholineProto-Oncogene Proteins c-aktRNA, Small Interfering

Identifiers

PMID29426376
PMCPMC7848326
OpenAlexW2792827060

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.