MOLECULAR DOCKING OF BREAST CANCER RECEPTORS AGAINST  ANTI-CANCER DRUG SOLASODINE

Authors

  • B Gopal Samy Department of Biotechnology, VSB Engineering College (Autonomous), Karur-639111, Tamil Nadu (India)
  • S Karthika Devi Department of Biotechnology, VSB Engineering College (Autonomous), Karur-639111, Tamil Nadu (India)
  • J Priya Dharshini Department of Biotechnology, VSB Engineering College (Autonomous), Karur-639111, Tamil Nadu (India)

DOI:

https://doi.org/10.48165/abr.2024.26.01.8

Keywords:

Autodock, breast cancer, discovery studio, Farnesoid x receptor, molecular docking, solasodine

Abstract

Cancer is a deadly disease that occurs in skin, pancreas, breast, and other body  

parts. Breast cancer is nowadays more common and can develop from various  

cell lines like MCF-7, MDA-MB-231, BT-20, etc. Early diagnosis and treatment  

can reduce the frequency of fatalities due to breast cancer, but early cancer  

screenings are often postponed due to erroneous information, fear, and  

ignorance. In the present work, we used molecular docking to find out the  

effect of solasodine binding on different cancer receptors. Solasodine was  

extracted from black nightshade (Solanum nigrum), a weed that was long used  

against stomach ache in Ayurveda. The isolated solasodine was even used in  

ointments against skin cancer. Docking such a medicinally potent compound  

resulted in positive response against a few receptors like Farnesoid X,  

epidermal growth factor receptor and progesterone receptor. MCF-7 breast  

cancer cell line was chosen for further ex-vivo studies and the results of MTT  

assay showed significant anti-cancer effects at solasodine concentrations of 500  

and 1000 µg mL-1. These findings indicated that Solasodine was a vital  

candidate as drug against breast cancer.  

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Published

2024-03-23

How to Cite

MOLECULAR DOCKING OF BREAST CANCER RECEPTORS AGAINST  ANTI-CANCER DRUG SOLASODINE. (2024). Applied Biological Research, 26(1), 58–65. https://doi.org/10.48165/abr.2024.26.01.8