Evidence map›Paper›PMID 28487964›Full record

ArticleMolecular medicine reports2017

Effects of the cyclophilin-type peptidylprolyl cis-trans isomerase from Pyropia yezoensis against hydrogen peroxide-induced oxidative stress in HepG2 cells.

Eun-Young Kim, Youn Hee Choi, Chang Geun Choi, Taek-Jeong Nam

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Therapeutic Potential ofMarine drugs · 2025
    Review
  2. Article
  3. Article
  4. Article
  5. Effect of Cyclophilin fromMarine drugs · 2019
    Article
  6. Article
  7. Marine drugs · 2018
    Article
  8. Article
  9. Microbial cyclophilins: specialized functions in virulence and beyond.World journal of microbiology & biotechnology · 2017
    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

4 authors at 1 institution in 1 country.

Eun-Young KimInstitute of Fisheries Sciences, Pukyong National University, Ilgwang‑myeon, Gijang‑gun, Busan 46041, Republic of Korea.
Youn Hee ChoiInstitute of Fisheries Sciences, Pukyong National University, Ilgwang‑myeon, Gijang‑gun, Busan 46041, Republic of Korea.
Chang Geun ChoiDepartment of Ecological Engineering, Pukyong National University, Nam‑Gu, Busan 48513, Republic of Korea.
Taek-Jeong NamInstitute of Fisheries Sciences, Pukyong National University, Ilgwang‑myeon, Gijang‑gun, Busan 46041, Republic of Korea.
Pukyong National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study aimed to describe the expression and purification of cyclophilin-type peptidylprolyl cis-trans isomerase (PPI) from the red alga Pyropia yezoensis. The antioxidant activity of the purified protein was also demonstrated, based on its ability to act against oxidative stress in HepG2 human hepatocellular carcinoma cells. HepG2 cells that were treated with recombinant PPI protein exhibited a reduction in the formation of hydrogen peroxide (H2O2)‑mediated reactive oxygen species (ROS). In HepG2 cells, treatment of recombinant PPI protein expression diminished H2O2‑mediated oxidative stress and restored both the expression and the activity of certain antioxidant enzymes, including superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx) and thioredoxin reductase (TRR). CAT, SOD and TRR activities were upregulated by treatment with the purified protein. CAT mRNA expression was significantly increased in HepG2 cells treated with recombinant PPI protein. These enzymes are the first line of antioxidant defense against ROS generated in times of oxidative stress. Accordingly, data from the present study indicate that the recombinant PPI protein is able to regulate the expression of antioxidant enzymes. Recombinant PPI has antioxidant properties that prevent oxidative stress‑induced toxicity, enhance cell viability, decrease ROS production and inhibit oxidative damage and mitochondrial dysfunction in HepG2 cells. Therefore, the present study hypothesizes that the recombinant PPI protein has the potential to protect the liver against oxidative stress‑induced cell damage and should be considered as an antioxidant.

Indexed as

AntioxidantsCatalaseCells, CulturedCell SurvivalCyclophilinsGlutathione PeroxidaseHep G2 CellsHumansHydrogen PeroxideOxidative StressPlant ExtractsReactive Oxygen SpeciesRecombinant ProteinsRhodophytaSuperoxide DismutaseAntioxidantsCatalaseCyclophilinsGlutathione PeroxidaseHydrogen PeroxidePlant ExtractsReactive Oxygen SpeciesRecombinant ProteinsSuperoxide Dismutase

Identifiers

PMID28487964
PMCPMC5436269
OpenAlexW2607570555

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.