Pharmacological network study on the effect of 6-gingerol on cervical cancer using computerized databases

Fernando Martínez-Esquivias1, Juan Manuel Guzmán-Flores1, Ismael Fernando Chávez-Díaz2

  • 1Instituto de Investigación en Biociencias, Centro Universitario de Los Altos, Universidad de Guadalajara, Tepatitlán de Morelos, México.

Insights

6-gingerol, a compound from ginger, shows anticancer potential against cervical cancer (CC) by targeting key genes involved in apoptosis and cell cycle regulation. Further experimental studies are recommended to validate these bioinformatics findings.

Area of Science:

  • Pharmacology
  • Bioinformatics
  • Oncology

Background:

  • Cervical cancer (CC) is a prevalent global health issue with limited treatment efficacy and significant adverse effects.
  • 6-gingerol, a bioactive compound in ginger, exhibits promising anticancer properties.
  • Understanding the molecular mechanisms of 6-gingerol in CC is crucial for developing novel therapeutic strategies.

Purpose of the Study:

  • To elucidate the anticancer mechanism of 6-gingerol against cervical cancer using a pharmacological network approach.
  • To identify potential therapeutic targets and pathways affected by 6-gingerol in CC.

Main Methods:

  • Utilized bioinformatics databases (MalaCard, Swiss Target Prediction, CTD, TCMPSP) to identify 6-gingerol and CC target genes.
  • Analyzed gene ontology and pathways using ShinyGO and DAVID.
  • Constructed a protein-protein interaction network with Cytoscape to identify hub genes.
  • Performed molecular docking and dynamics simulations to assess drug-target interactions.

Main Results:

  • Identified 26 overlapping genes and 12 hub genes.
  • Gene ontology analysis revealed involvement in apoptosis, cell cycle, and HPV infection pathways.
  • Molecular docking indicated strong binding affinity of 6-gingerol to target proteins.
  • Molecular dynamics confirmed stable interactions with AKT1, CCNB1, and CTNNB1.

Conclusions:

  • 6-gingerol demonstrates potential anticancer activity in cervical cancer through modulation of apoptosis and cell cycle pathways.
  • The identified hub genes and interactions provide a basis for experimental validation.
  • This study offers insights into the pharmacological action of 6-gingerol for CC treatment.