Unraveling the multi-targeted curative potential of bioactive molecules against cervical cancer through integrated

Murali Aarthy1, Pandiyan Muthuramalingam2, Manikandan Ramesh2

  • 1Computer Aided Drug Design and Molecular Modeling Lab, Department of Bioinformatics, Alagappa University, Karaikudi, Tamil Nadu, 630003, India.

Scientific Reports
|August 21, 2022
PubMed

Insights

Understanding viral infections in cervical cancer is key for new treatments. This study identifies immune genes and plant compounds that target these mechanisms, offering potential anti-HPV therapies.

Area of Science:

  • Oncology
  • Virology
  • Pharmacology

Background:

  • Viral infections, particularly HPV, are a major cause of cervical cancer.
  • Developing targeted therapies requires understanding molecular mechanisms at the systems level.
  • Multi-omics and systems pharmacology approaches are crucial for identifying novel therapeutic strategies.

Purpose of the Study:

  • To elucidate the molecular mechanisms of viral infections in cervical cancer.
  • To identify key immune genes and potential therapeutic targets.
  • To discover plant-derived compounds effective against cervical cancer.

Main Methods:

  • Utilized systems pharmacology and a multi-omics approach.
  • Analyzed immuno-transcriptomic data from cervical cancer patients.
  • Employed Network Analyst 3.0 to identify differentially expressed immune genes.
  • Collected phytocompounds from medicinal plants described in literature.

Main Results:

  • Identified 384 differentially expressed immune genes critical for cervical cancer.
  • Found 79 plant-derived compounds targeting these identified immune genes.
  • Pinpointed virogenomic signatures associated with E7 oncoproteins as potential therapeutic targets.

Conclusions:

  • The study identified significant immune genes driving cervical cancer progression.
  • Discovered plant-derived compounds with potential as anti-HPV drug candidates.
  • The findings provide a rationale for optimizing small molecules as viable drug candidates for cervical cancer therapy.

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