4.5 Article

Nisin ZP, an Antimicrobial Peptide, Induces Cell Death and Inhibits Non-Small Cell Lung Cancer (NSCLC) Progression in vitro in 2D and 3D Cell Culture

期刊

PHARMACEUTICAL RESEARCH
卷 39, 期 11, 页码 2859-2870

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11095-022-03220-2

关键词

Apoptosis; Mitochondrial membrane depolarization; Nisin ZP; Non-small cell lung cancer; Reactive oxygen species

资金

  1. Office of Grants and Sponsored Research, St. John's University
  2. New Investigator Award, American Association of Colleges of Pharmacy (AACP)
  3. Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences (CPHS), St. John's University

向作者/读者索取更多资源

This study evaluated the anticancer potential of the antimicrobial peptide Nisin ZP in non-small cell lung cancer (NSCLC) cells. The results showed that Nisin ZP selectively targeted cancer cells, induced apoptosis and cell cycle arrest, and inhibited cancer cell growth and migration through non-membranolytic pathways.
Lung cancer is the leading cause of cancer deaths globally with most of the reported cases (> 85%) associated with non-small cell lung cancer (NSCLC). Current therapies have enhanced the overall survival rate of patients but treatment-related adverse effects and increase in drug-resistance limit the success of these treatment options. Antimicrobial peptides (AMPs) have gained interest as anticancer agents as they selectively target cancer cells and decrease the possibility of resistance. Nisin ZP is a polycyclic antimicrobial peptide produced by the Gram-positive bacterium, Lactococcus lactis and is commonly used as a food preservative. Nisin ZP has recently demonstrated anticancer activity in melanoma, head and neck squamous cell carcinoma, hepatic, colon, and blood cancer. In this study, we evaluated the anticancer potential of nisin ZP and assessed the underlying mechanisms in NSCLC cells. The results revealed that nisin ZP induced selective toxicity in cancer (A549 and H1299) cells compared to healthy (HEK293) cells after 48 h of treatment. Nisin ZP exposure induced apoptosis and cell cycle arrest (G0/G1 phase) in NSCLC cells irrespective of tumor protein p53 expression. The cancer cell proliferation was inhibited via non-membranolytic pathways by mitochondrial membrane depolarization and elevation in reactive oxygen species (ROS) generation. Furthermore, nisin ZP decreased cancer cells' clonal expansion and migration, demonstrating potential use against highly metastatic NSCLC. The 3D spheroid growth and cell viability of the A549 cells were significantly inhibited by nisin ZP compared to control. Overall, the results suggest an excellent antitumor potential in vitro and, thus, can further be developed as a novel therapeutic for NSCLC.

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