Evidence map›Paper›PMID 28791345›Full record

ArticleInternational journal of molecular medicine2017

Nova1 mediates resistance of rat pheochromocytoma cells to hypoxia-induced apoptosis via the Bax/Bcl-2/caspase-3 pathway.

Hualing Li, Bei Lv, Ling Kong, Jing Xia, Ming Zhu, Lijuan Hu, Danyang Zhen, Yifan Wu, Xiaoqin Jia, Sujuan Zhu and 1 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2017. 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
1.5field-weighted citation impact, top 19% 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, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Self-Healing and Injectable Hydrogel for Matching Skin Flap Regeneration.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2019
    Article
  14. Article
  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

11 authors at 2 institutions in 1 country.

Hualing LiDepartment of Biochemistry, Medical College of Yangzhou University, Yangzhou, Jiangsu 225001, P.R. China.
Bei LvDepartment of Biochemistry, Medical College of Yangzhou University, Yangzhou, Jiangsu 225001, P.R. China.
Ling KongDepartment of Biochemistry, Medical College of Yangzhou University, Yangzhou, Jiangsu 225001, P.R. China.
Jing XiaDepartment of Biochemistry, Medical College of Yangzhou University, Yangzhou, Jiangsu 225001, P.R. China.
Ming ZhuDepartment of Biochemistry, Medical College of Yangzhou University, Yangzhou, Jiangsu 225001, P.R. China.
Lijuan HuDepartment of Biochemistry, Medical College of Yangzhou University, Yangzhou, Jiangsu 225001, P.R. China.
Danyang ZhenDepartment of Biochemistry, Medical College of Yangzhou University, Yangzhou, Jiangsu 225001, P.R. China.
Yifan WuDepartment of Biochemistry, Medical College of Yangzhou University, Yangzhou, Jiangsu 225001, P.R. China.
Xiaoqin JiaDepartment of Biochemistry, Medical College of Yangzhou University, Yangzhou, Jiangsu 225001, P.R. China.
Sujuan ZhuDepartment of Biochemistry, Biosciences and Biotechnology College of Yangzhou University, Yangzhou, Jiangsu 225009, P.R. China.
Hengmi CuiJiangsu Key Laboratory of Integrated Traditional Chinese and Western Medicine for Prevention and Treatment of Senile Diseases, Yangzhou, Jiangsu 225001, P.R. China.
Yangzhou University · CNIntegrated Chinese Medicine (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuro-oncological ventral antigen 1 (Nova1) is a well known brain-specific splicing factor. Several studies have identified Nova1 as a regulatory protein at the top of a hierarchical network. However, the function of Nova1 during hypoxia remains poorly understood. This study aimed to investigate the protective effect of Nova1 against cell hypoxia and to further explore the Bax/Bcl-2/caspase-3 pathway as a potential mechanism. During hypoxia, the survival rate of pheochromocytoma PC12 cells was gradually decreased and the apoptosis rate was gradually increased, peaking at 48 h of hypoxia. At 48 h after transfection of PC12 cells with pCMV-Myc-Nova1, the expression of Nova1 was significantly increased, with wide distribution in the cytoplasm and nucleus. Moreover, the survival rate was significantly increased and the apoptosis rate was significantly decreased. Additionally, the mRNA and protein expression levels of Bax and caspase-3 were significantly increased in the pCMV-Myc group and significantly decreased in the pCMV‑Myc-Nova1 group, whereas that of Bcl-2 was significantly decreased in the pCMV-Myc group and significantly increased in the pCMV-Myc-Nova1 group. This study indicated that Nova1 could be linked to resistance to the hypoxia-induced apoptosis of PC12 cells via the Bax/Bcl-2/caspase-3 pathway, and this finding may be of significance for exploring novel mechanisms of hypoxia and the treatment of hypoxia-associated diseases.

Indexed as

AnimalsApoptosisbcl-2-Associated X ProteinCaspase 3Cell HypoxiaCell NucleusCell SurvivalCytoplasmGene Expression RegulationNeuro-Oncological Ventral AntigenOxygenPC12 CellsPlasmidsProto-Oncogene Proteins c-bcl-2RatsRNA-Binding ProteinsBax protein, ratbcl-2-Associated X ProteinBcl2 protein, ratCasp3 protein, ratCaspase 3Neuro-Oncological Ventral AntigenNova1 protein, ratOxygenProto-Oncogene Proteins c-bcl-2RNA-Binding Proteins

Identifiers

PMID28791345
PMCPMC5593465
OpenAlexW2744640215

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.