Evidence map›Paper›PMID 28122357›Full record

ArticleOncotarget2017

Activation of Akt by SC79 protects myocardiocytes from oxygen and glucose deprivation (OGD)/re-oxygenation.

Koulong Zheng, Qing Zhang, Gang Lin, Yefei Li, Zhenqiang Sheng, Jue Wang, Liang Chen, Hui-He Lu

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
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  9. Review
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  11. FGF20-FGFR1 signaling through MAPK and PI3K controls sensory progenitor differentiation in the organ of Corti.Developmental dynamics : an official publication of the American Association of Anatomists · 2021
    Article
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  17. Circular RNA Involved in the Protective Effect ofFrontiers in pharmacology · 2020
    Article
  18. Article
  19. SC79, the AKT Activator Protects Cerebral Ischemia in a Rat Model of Ischemia/Reperfusion Injury.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  20. Protective Effects the Akt Activator SC79 in Hepatic Ischemia-Reperfusion Injury.Medical science monitor : international medical journal of experimental and clinical research · 2018
    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

8 authors at 3 institutions in 1 country.

Koulong ZhengDepartment of Cardiology, The Second Affiliated Hospital of Nantong University, Nantong, China.
Qing ZhangDepartment of Cardiology, The Second Affiliated Hospital of Nantong University, Nantong, China.
Gang LinDepartment of Cardiology, The Second Affiliated Hospital of Nantong University, Nantong, China.
Yefei LiDepartment of Cardiology, The Second Affiliated Hospital of Nantong University, Nantong, China.
Zhenqiang ShengDepartment of Cardiology, The Second Affiliated Hospital of Nantong University, Nantong, China.
Jue WangDepartment of Cardiology, The Second Affiliated Hospital of Nantong University, Nantong, China.
Liang ChenDepartment of Cardiology, The Second Affiliated Hospital of Nantong University, Nantong, China.
Hui-He LuDepartment of Cardiology, The Second Affiliated Hospital of Nantong University, Nantong, China.
Second Affiliated Hospital of Nantong UniversityAffiliated Hospital of Nantong University · CNNantong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SC79 is a novel Akt activator. The current study tested its potential effect against oxygen and glucose deprivation (OGD)/re-oxygenation-induced myocardial cell death. We showed that SC79 activated Akt and protected H9c2 myocardial cells and primary murine myocardiocytes from OGD/re-oxygenation. Reversely, Akt inhibitor MK-2206 or Akt1 shRNA knockdown almost completely abolished SC79-mediated myocardial cytoprotection. SC79 treatment in H9c2 cells inhibited OGD/re-oxygenation-induced programmed necrosis pathway, evidenced by mitochondrial depolarization and cyclophilin D-p53-ANT-1 (adenine nucleotide translocator 1) association. Further, SC79 activated Akt downstream NF-E2-related factor 2 (NRF2) signaling to suppress OGD/re-oxygenation-induced reactive oxygen species (ROS) production. Reversely, NRF2 shRNA knockdown in H9c2 cells largely attenuated SC79-induced ROS scavenging ability and cytoprotection against OGD/re-oxygenation. Together, we conclude that activation of Akt by SC79 protects myocardial cells from OGD/re-oxygenation.

Indexed as

AcetatesAnimalsBenzopyransCells, CulturedCytoprotectionEnzyme ActivationGene Expression Regulation, EnzymologicGlucoseHeterocyclic Compounds, 3-RingMiceMice, Inbred C57BLMyocytes, CardiacNecrosisNF-E2-Related Factor 2OxygenProtective AgentsAcetatesAKT activator SC79BenzopyransGlucoseHeterocyclic Compounds, 3-RingMK 2206NF-E2-Related Factor 2OxygenProtective AgentsProto-Oncogene Proteins c-aktReactive Oxygen SpeciesAktischemic heart diseasesmyocardial cellsoxygen glucose deprivation (OGD)SC79

Identifiers

PMID28122357
PMCPMC5362459
OpenAlexW2582965162

What OpenQuestion holds

Textmetadata
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.