Evidence map›Paper›PMID 24711740›Full record

ArticleTheScientificWorldJournal2014

4-Hydroxy-2-nonenal induces apoptosis by inhibiting AKT signaling in human osteosarcoma cells.

Guang-rong Ji, Nai-chun Yu, Xiang Xue, Zong-guang Li

Open access · goldAbstract read
In one paragraph

Article in TheScientificWorldJournal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

  1. ExploringMolecules (Basel, Switzerland) · 2026
    Article
  2. Lipid Peroxidation-Related Redox Signaling in Osteosarcoma.International journal of molecular sciences · 2024
    Review
  3. Impact of ROS-Dependent Lipid Metabolism on Psoriasis Pathophysiology.International journal of molecular sciences · 2022
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. 4-hydroxynonenal-mediated signaling and aging.Free radical biology & medicine · 2017
    Review
  10. Article
  11. Review
  12. Review
  13. 4-Hydroxy-2-nonenal: a critical target in oxidative stress?American journal of physiology. Cell physiology · 2016
    Review
  14. Review
  15. 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

4 authors at 1 institution in 1 country.

Guang-rong JiDepartment of Orthopaedics, The 2nd Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Nai-chun YuDepartment of Orthopaedics, The 2nd Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Xiang XueDepartment of Orthopaedics, The 2nd Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Zong-guang LiDepartment of Orthopaedics, The 2nd Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The onset of lipid peroxidation within cellular membranes is associated with changes in their physiochemical properties and enzymatic dysfunction of the membrane environment. There are increasing bodies of evidence indicating that aldehydic molecules generated endogenously during the process of lipid peroxidation are causally involved in most of the pathophysiological effects associated with oxidative stress in cells and tissues. 4-Hydroxy-2-nonenal (4-HNE), among them, is believed to be largely responsible for cytopathological effects observed during oxidative stress in vivo and has achieved the status of one of the best recognized and most studied of the cytotoxic products of lipid peroxidation. Here, we reported that 4-HNE treatment may induce cell death in MG63 human osteosarcoma cells. The 4-HNE treatment could activate caspase-3 and alter the Bax/Bcl-2 apoptotic signaling. All these changes are due to the inhibition of AKT activity by 4-HNE treatment, and we also found that the p70S6K activity, downstream factors of AKT, was also blocked by 4-HNE. Our results revealed the molecular mechanism of how 4-HNE induces cell death in MG63 human osteosarcoma cells, which contributes to the clinical treatment of cancer therapy.

Indexed as

AldehydesAntineoplastic AgentsApoptosisbcl-2-Associated X ProteinBone NeoplasmsCaspase 3Cell DeathCell Line, TumorCysteine Proteinase InhibitorsHumansOsteosarcomaProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-bcl-2Signal Transduction4-hydroxy-2-nonenalAldehydesAntineoplastic Agentsbcl-2-Associated X ProteinCaspase 3Cysteine Proteinase InhibitorsProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-bcl-2

Identifiers

PMID24711740
PMCPMC3953651
OpenAlexW2048971550

What OpenQuestion holds

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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.