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G-protein Coupled Receptors (GPCRs): A Potential Target of Apigenin as a Novel hACE2 Receptor Specific Therapeutic for Impeding Lung Cancer Considering a Group of Missense and Nonsense Mutations in COVID-19 Patients

Author

Listed:
  • Rasel Ahmed
  • Sharmin Akter
  • Fnu Nurunnahar
  • Sabiha Sultana
  • Sabbir Hasan
  • Sharmin Ahmed
  • Md. Al Hasibuzzaman
  • Syed Nafis Shadman Ali
  • Ramisha Tahsin
  • Nasiha Tahsin
  • Niloy Das
  • Mohammad Habibur Rahman

Abstract

This research investigates the role of mutation cascades in enhancing COVID-19-related lung cancer fatalities, specifically through analyzing mutations in the ACE2 gene associated with SARS-CoV-2 infections. Notably, a natural flavonoid, apigenin, has been identified as a promising hACE2-specific therapeutic. The study involved detailed examinations of 27 mutations (23 missense and four nonsense) and the molecular interactions between apigenin and hACE2, revealing a binding energy of -8.1 Kcal/mol. Various molecular dynamics parameters suggested stable interactions, while the drug-gene interaction analysis demonstrated that 18 GPCR genes could metabolize apigenin, effectively blocking hACE2 and thereby inhibiting S-protein attachment. The findings propose that apigenin could serve as a targeted therapy for COVID-19-induced lung cancer.

Suggested Citation

  • Rasel Ahmed & Sharmin Akter & Fnu Nurunnahar & Sabiha Sultana & Sabbir Hasan & Sharmin Ahmed & Md. Al Hasibuzzaman & Syed Nafis Shadman Ali & Ramisha Tahsin & Nasiha Tahsin & Niloy Das & Mohammad Habi, 2025. "G-protein Coupled Receptors (GPCRs): A Potential Target of Apigenin as a Novel hACE2 Receptor Specific Therapeutic for Impeding Lung Cancer Considering a Group of Missense and Nonsense Mutations in COVID-19 Patients," European Journal of Pharmaceutical Research, European Open Science Publishing, vol. 5(1), pages 6-15, January.
  • Handle: RePEc:epw:pharma:v:5:y:2025:i:1:id:785
    DOI: 10.24018/ejpharma.2025.5.1.85
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