Evidence map›Paper›PMID 27517753›Full record

ArticleOncotarget2016

SC79 protects retinal pigment epithelium cells from UV radiation via activating Akt-Nrf2 signaling.

Yi-Qing Gong, Wei Huang, Ke-Ran Li, Yuan-Yuan Liu, Guo-Fan Cao, Cong Cao, Qin Jiang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
11.0field-weighted citation impact, top 1% 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

50 citing papers in PubMed, 80 citations in OpenAlex.

  1. A renaissance in targeting the PI3K/AKT/mTOR pathway.Nature reviews. Drug discovery · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. 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
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Involvement of Akt/mTOR in the Neurotoxicity of Rotenone-Induced Parkinson's Disease Models.International journal of environmental research and public health · 2019
    Article
  17. Article
  18. Article
  19. Protective Effects the Akt Activator SC79 in Hepatic Ischemia-Reperfusion Injury.Medical science monitor : international medical journal of experimental and clinical research · 2018
    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

7 authors at 2 institutions in 1 country.

Yi-Qing GongThe Affiliated Eye Hospital of Nanjing Medical University, Nanjing, China.
Wei HuangThe Affiliated Eye Hospital of Nanjing Medical University, Nanjing, China.
Ke-Ran LiThe Affiliated Eye Hospital of Nanjing Medical University, Nanjing, China.
Yuan-Yuan LiuInstitute of Neuroscience, Soochow University, Suzhou, Jiangsu, China.
Guo-Fan CaoThe Affiliated Eye Hospital of Nanjing Medical University, Nanjing, China.
Cong CaoInstitute of Neuroscience, Soochow University, Suzhou, Jiangsu, China.
Qin JiangThe Affiliated Eye Hospital of Nanjing Medical University, Nanjing, China.
Second Affiliated Hospital of Nanjing Medical University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Excessive Ultra-violet (UV) radiation causes oxidative damages and apoptosis in retinal pigment epithelium (RPE) cells. Here we tested the potential activity of SC79, a novel small molecule activator of Akt, against the process. We showed that SC79 activated Akt in primary and established (ARPE-19 line) RPE cells. It protected RPE cells from UV damages possibly via inhibiting cell apoptosis. Akt inhibition, via an Akt specific inhibitor (MK-2206) or Akt1 shRNA silence, almost abolished SC79-induced RPE cytoprotection. Further studies showed that SC79 activated Akt-dependent NF-E2-related factor 2 (Nrf2) signaling and inhibited UV-induced oxidative stress in RPE cells. Reversely, Nrf2 shRNA knockdown or S40T mutation attenuated SC79-induced anti-UV activity. For the in vivo studies, we showed that intravitreal injection of SC79 significantly protected mouse retina from light damages. Based on these results, we suggest that SC79 protects RPE cells from UV damages possibly via activating Akt-Nrf2 signaling axis.

Indexed as

AcetatesAnimalsApoptosisBenzopyransCell LineCells, CulturedHeterocyclic Compounds, 3-RingHumansMaleMice, Inbred BALB CMolecular StructureMutationNF-E2-Related Factor 2Oxidative StressProto-Oncogene Proteins c-aktRetinal Pigment EpitheliumAcetatesAKT activator SC79BenzopyransHeterocyclic Compounds, 3-RingMK 2206NFE2L2 protein, humanNF-E2-Related Factor 2Proto-Oncogene Proteins c-aktAktretinal pigment epitheliumSC79UV

Identifiers

PMID27517753
PMCPMC5312373
OpenAlexW2508684321

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.