The Oncolytic Effect of an Iraqi Newcastle Disease Virus Attenuated Strain (AMHA1) Against Colorectal Cancer Cells.

Authors

  • Farah essa mustansiryah university college of medicine
  • Ahmed Al-Shammari
  • Ali Al-Saffar
  • Marwa Salman

DOI:

https://doi.org/10.24126/jobrc.2023.17.2.658

Keywords:

oncolytic virotherapy, Newcastle Disease Virus, colorectal cancer cell line.

Abstract

Objective: The most recent World Health Organization statistics show that colorectal cancer is the third foremost cause of death by cancer among Iraqis. It has become necessary to search and develop novel and unconventional treatment methods. Oncolytic virotherapy is one of the innovative cancer therapeutics that showed to be safe and selective and there is increased efforts in the recent years to move them to clinic. For the reason we were developing our Iraqi strain of oncolytic NDV to fight colorectal cancer. Materials and Methods: This study tested the killing rate of Iraqi strain of Newcastle disease virus (AMHA1) on colorectal cancer cells and testing the safety on normal cells. The virus tittered using vero cells, and then the cytotoxic effect of the virus on both types of cells was determined using the crystal violet assay. Finally, we performed a morphological analysis using hematoxylin and eosin staining. Results: Newcastle disease virus 0.3 MOI causes significant cytotoxicity with prominent cytopathic effect in the colorectal cancer cell line HRT-18G with 50% percentage of growth inhibition, but not in the normal human fibroblast (NHF) percentage of growth inhibition where it was less than 20%.    Conclusion oncolytic NDV AMHA1 strain effective against colorectal cancer cells because it has selectivity in replication and safety profile.

Downloads

Published

2023-07-26

How to Cite

essa, F., Al-Shammari, A., Al-Saffar, A. . . . . . ., & Salman, M. (2023). The Oncolytic Effect of an Iraqi Newcastle Disease Virus Attenuated Strain (AMHA1) Against Colorectal Cancer Cells. Journal of Biotechnology Research Center (JOBRC), 17(2), 5–15. https://doi.org/10.24126/jobrc.2023.17.2.658

Issue

Section

Research articles