Molecular signatures associated with prostate cancer cell line (PC-3) exposure to inactivated Zika virus

Jeany Delafiori1, Estela de Oliveira Lima2, Mohamed Ziad Dabaja1

  • 1Innovare Biomarkers Laboratory, School of Pharmaceutical Sciences, University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.

Scientific Reports
|October 27, 2019
PubMed

Insights

Zika virus (ZIKV) shows potential as an anti-cancer agent, inhibiting prostate cancer cell growth. Metabolomic analysis revealed key metabolic pathways altered by an inactivated ZIKV prototype (ZVp), offering insights into its antiproliferative effects.

Area of Science:

  • Virology
  • Oncology
  • Metabolomics

Background:

  • Zika virus (ZIKV) infection has been linked to microcephaly, prompting research into ZIKV-host interactions.
  • ZIKV's ability to impair cell growth suggests potential oncolytic properties against cancer cells.
  • Previous studies confirmed ZIKV's growth inhibition in glioblastoma and demonstrated antiproliferative activity of an inactivated ZIKV prototype (ZVp) in other cancer cell lines, including PC-3 prostate cancer cells.

Purpose of the Study:

  • To investigate the metabolic pathways involved in the antiproliferative effect of Zika virus against prostate cancer cells.
  • To identify molecular signatures associated with ZVp treatment in PC-3 cells.

Main Methods:

  • Utilized a metabolomic approach employing high-resolution mass spectrometry.
  • Analyzed PC-3 prostate cancer cells treated with an inactivated ZIKV prototype (ZVp).

Main Results:

  • Identified 21 statistically significant metabolic markers in ZVp-treated PC-3 cells.
  • Observed metabolic alterations including lipid remodeling, endoplasmic reticulum stress, inflammatory mediator changes, and disrupted porphyrin and folate metabolism.
  • These markers represent molecular signatures of the ZVp-induced cellular response.

Conclusions:

  • This study provides the first metabolomic assessment of ZIKV's effect on prostate cancer cells.
  • The findings highlight specific metabolic pathways potentially mediating ZVp's antiproliferative action.
  • Further research into ZIKV as a therapeutic agent for prostate cancer is warranted.

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