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Traditional use of Cissampelos pareira L. for hormone disorder and fever provides molecular links of ESR1 modulation to viral inhibition
Madiha Haider; Dhwani Dholakia; Aleksha Panwar; Parth Garg; Atish Prabhakar Gheware; Khushboo Singhal; Dayanidhi Singh; Shaunak A Burse; Surekha Kumari; Anmol Kumar; Arjun Ray; Guruprasad R Medigeshi; Upendra Sharma; Bhavana Prasher; Mitali Mukerji.
Afiliación
  • Madiha Haider; Institute of Genomics and Integrative Biology
  • Dhwani Dholakia; Institute of Genomics and Integrative Biology
  • Aleksha Panwar; Translational Health Science and Technology Institute
  • Parth Garg; Indraprastha Institute of Information Technology
  • Atish Prabhakar Gheware; Institute of Genomics and Integrative Biology
  • Khushboo Singhal; Institute of Genomics and Integrative Biology
  • Dayanidhi Singh; Institute of Genomics and Integrative Biology
  • Shaunak A Burse; Institute of Genomics and Integrative Biology
  • Surekha Kumari; Institute of Himalayan Bioresource Technology
  • Anmol Kumar; Institute of Himalayan Bioresource Technology
  • Arjun Ray; Indraprastha Institute of Information Technology
  • Guruprasad R Medigeshi; Translational Health Science and Technology Institute
  • Upendra Sharma; Institute of Himalayan Bioresource Technology
  • Bhavana Prasher; Institute of Genomics and Integrative Biology
  • Mitali Mukerji; Institute of Genomics and Integrative Biology
Preprint en En | PREPRINT-BIORXIV | ID: ppbiorxiv-431579
ABSTRACT
Bioactive fractions or compounds obtained from medicinal plants have been used for the treatment of multiple diseases. This effect could be due to common pathways underlying these conditions that are targeted by such medicines. In this study, we explored the molecular basis of action of one such herbal formulation Cissampelos pareira, used for the treatment of female hormone disorders and fever. Genome-wide expression studies on MCF7 cell lines treated with Cipa extract were carried out using Affymetrix arrays. Transcriptome analysis revealed a downregulation of signatures of estrogen response governed by estrogen receptor (ER). Molecular docking analysis identified 38 constituent molecules in Cipa that potentially bind ({Delta}G< -7.5) with ER at the same site as estrogen. Cipa transcriptome signatures show high positive connectivity (https//clue.io/) scores with protein translation inhibitors such as emetine (score 99.61) and knockdown signatures of genes linked to the antiviral response such as ribosomal protein RPL7 (score 99.92), which is also an ER coactivator. Cipa exhibits antiviral activity in dengue infected MCF7 cells that is decreased upon ESR1 (estrogen receptor 1) gene knockdown. This approach reveals a novel pathway involving ESR1-RPL7 axis that could be a potential target in dengue viral infection.
Licencia
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Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-BIORXIV Tipo de estudio: Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-BIORXIV Tipo de estudio: Prognostic_studies Idioma: En Año: 2021 Tipo del documento: Preprint