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Network pharmacology of apigeniflavan: a novel bioactive compound of Trema orientalis Linn. in the treatment of pancreatic cancer through bioinformatics approaches.
Das, Richa; Agrawal, Shreni; Kumar, Pradeep; Singh, Amit Kumar; Shukla, Praveen Kumar; Bhattacharya, Indrani; Tiwari, Kavindra Nath; Mishra, Sunil Kumar; Tripathi, Amit Kumar.
Affiliation
  • Das R; Department of Biotechnology, Parul Institute of Applied Science, Parul University, Vadodara, 391760 Gujarat India.
  • Agrawal S; Department of Biotechnology, Parul Institute of Applied Science, Parul University, Vadodara, 391760 Gujarat India.
  • Kumar P; Department of Botany, MMV, Banaras Hindu University, Varanasi, 221005 UP India.
  • Singh AK; Department of Pharmaceutical Engineering and Technology, Indian Institute of Technology, Banaras Hindu University, Varanasi, 221005 UP India.
  • Shukla PK; Department of Botany, MMV, Banaras Hindu University, Varanasi, 221005 UP India.
  • Bhattacharya I; Department of Biotechnology, Parul Institute of Applied Science, Parul University, Vadodara, 391760 Gujarat India.
  • Tiwari KN; Department of Botany, MMV, Banaras Hindu University, Varanasi, 221005 UP India.
  • Mishra SK; Department of Pharmaceutical Engineering and Technology, Indian Institute of Technology, Banaras Hindu University, Varanasi, 221005 UP India.
  • Tripathi AK; School of Basic and Applied Science, Galgotias University, Gautam Buddha Nagar, Noida, 203201 UP India.
3 Biotech ; 13(5): 160, 2023 May.
Article in En | MEDLINE | ID: mdl-37151998
ABSTRACT
Pancreatic cancer is the seventh most prevalent cause of mortality globally. Since time immemorial, plant-derived products have been in use as therapeutic agents due to the existence of biologically active molecules called secondary metabolites. Flavonoids obtained from plants participate in cell cycle arrest, induce autophagy and apoptosis, and decrease oxidative stress in pancreatic cancer. The present study involves network pharmacology-based study of the methanolic leaf extract of Trema orientalis (MLETO) Linn. From the high-resolution mass spectrometry (HRMS) analysis, 21 nucleated flavonoids were screened out, of which only apigeniflavan was selected for further studies because it followed Lipinski's rule and showed no toxicity. The pharmacokinetics and physiochemical characteristics of apigeniflavan were performed using the online web servers pkCSM, Swiss ADME, and ProTox-II. This is the first in silico study to report the efficiency of apigeniflavan in pancreatic cancer treatment. The targets of apigeniflavan were fetched from SwissTargetPrediction database. The targets of pancreatic cancer were retrieved from DisGeNET and GeneCards. The protein-protein interaction of the common genes using Cytoscape yielded the top five hub genes KDR, VEGFA, AKT1, SRC, and ESR1. Upon molecular docking, the lowest binding energies corresponded to best docking score which indicated the highest protein-ligand affinity. Kyoto Encyclopaedia of Genes and Genomes (KEGG) database was employed to see the involvement of hub genes in pathways related to pancreatic cancer. The following, pancreatic cancer pathway, MAPK, VEGF, PI3K-Akt, and ErbB signaling pathways, were found to be significant. Our results indicate the involvement of the hub genes in tumor growth, invasion and proliferation in the above-mentioned pathways, and therefore necessitating their downregulation. Moreover, apigeniflavan can flourish as a promising drug for the treatment of pancreatic cancer in future.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: 3 Biotech Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: 3 Biotech Year: 2023 Document type: Article