p53 inhibition by MDM2 in human pterygium

Exp Eye Res. 2018 Oct:175:142-147. doi: 10.1016/j.exer.2018.06.021. Epub 2018 Jun 19.

Abstract

Aims: To confirm that mouse double minute 2 (MDM2) could inhibit p53 activity in human pterygium. And to show the disruption of MDM2-p53 interaction could reactive the functions of p53 in pterygium.

Method: Pterygium and corresponding conjunctiva tissues were collected for establishment of primary cell lines. Expression patterns of MDM2 and p53 were detected by immunofluorescence. Protein localization of p53 and MDM2, and transcriptional activity of p53 in both untreated and MDM2 antagonist (Nutlin) treated pterygium cells were quantified.

Results: In pterygium, p53 was highly expressed in cytoplasm and slightly expressed in the nuclei. MDM2 was localized in the nuclei. A p53 transcriptional regulated target gene, p21, was not expressed in pterygium tissues, suggesting the p53 transcriptional activity was not active in pterygium. After treatment with Nutlin, increased nuclear localization of p53 (4.05%-80.56%) was observed in pterygium cells along with increasing Nutlin dosages (from 0 to 50 μM, p < 0.001). The expression of p21 was increased after Nutlin treatments in pterygium cells (2.49 folds in 20 μM Nutlin treated cells compared to control treated cells, p = 0.012).

Conclusion: We discovered a novel mechanism in pterygium whereby MDM2 suppresses p53 transcriptional activity despite abundant p53 in pterygium. Disruption of MDM2-p53 interaction by Nutlin could be a potential treatment for pterygium.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Cell Line
  • Conjunctiva / metabolism
  • Female
  • Fluorescent Antibody Technique, Indirect
  • Humans
  • Imidazoles / pharmacology
  • Immunoblotting
  • Male
  • Middle Aged
  • Piperazines / pharmacology
  • Proto-Oncogene Proteins c-mdm2 / antagonists & inhibitors
  • Proto-Oncogene Proteins c-mdm2 / physiology*
  • Pterygium / metabolism*
  • Tumor Suppressor Protein p53 / antagonists & inhibitors*
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • Imidazoles
  • Piperazines
  • Tumor Suppressor Protein p53
  • nutlin 1
  • Proto-Oncogene Proteins c-mdm2