Antiausterity Activity of Secondary Metabolites from the Roots of Ferula hezarlalehzarica against the PANC-1 Human Pancreatic Cancer Cell Line
Author(s) -
Mostafa Alilou,
Dya Fita Dibwe,
Stefan Schwaiger,
Mojtaba Khodami,
Jakob Troppmair,
Suresh Awale,
Hermann Stuppner
Publication year - 2020
Publication title -
journal of natural products
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.976
H-Index - 139
eISSN - 1520-6025
pISSN - 0163-3864
DOI - 10.1021/acs.jnatprod.9b01109
Subject(s) - pancreatic cancer , phytochemical , dichloromethane , cell culture , cytotoxicity , cancer cell , chemistry , cytotoxic t cell , cancer , biological activity , terpenoid , biochemistry , bioactive compound , biology , in vitro , genetics , solvent
Human pancreatic cancer is one of the most aggressive types of cancer, with a high mortality rate. Due to the high tolerance of such cancer cells to nutrient starvation conditions, they can survive in a hypovascular tumor microenvironment. In this study, the dichloromethane extract of the roots of Ferula hezarlalehzarica showed potent preferential cytotoxic activity with a PC 50 value of 0.78 μg/mL. Phytochemical investigation of this extract led to the isolation of 18 compounds, including one new sesquiterpenoid ( 6 ) and one new monoterpenoid ( 18 ). All isolated compounds were evaluated for their preferential cytotoxicity against PANC-1 human pancreatic cancer cells by employing an antiausterity strategy. Among them, ferutinin ( 2 ) was identified as the most active compound, with a PC 50 value of 0.72 μM. In addition, the real-time effect of ferutinin ( 2 ) and compound 6 against PANC-1 cells, exposed to a nutrient-deprived medium (NDM), showed cell shrinkage, leading to cancer cell death within a short period of exposure. Compounds 2 and 6 also inhibited colony formation of PANC-1 cells. The present study indicates that the dichloromethane extract of the roots of F. hezarlalehzarica is a rich source of bioactive compounds for targeting PANC-1 cells.
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