posted on 2018-09-06, 00:00authored byVishak Raman, Uma K. Aryal, Victoria Hedrick, Rodrigo Mohallem Ferreira, Jorge Luis Fuentes Lorenzo, Elena E. Stashenko, Morris Levy, Maria M. Levy, Ignacio G. Camarillo
Triple-negative breast cancer is
an aggressive subtype of breast
cancer with low 5-year survival rates, high 3-year recurrence rates,
and no known therapeutic targets. Recent studies have indicated
that triple-negative breast cancers possess an altered metabolic state
with higher rates of glycolysis, mitochondrial oxidative phosphorylation,
and increased generation and utilization of tricarboxylic acid cycle
intermediates. Here, we utilized label-free quantitative proteomics
to gain insight into the anticancer mechanisms of a methanolic extract
from the Central American plant Lippia origanoides on MDA-MB-231 triple-negative breast cancer cells. The L.
origanoides extract dysregulated mitochondrial oxidative
phosphorylation by suppressing the expression of several subunits
of Complex I of the electron transport chain, and inhibited cellular
metabolism by down-regulating key tricarboxylic acid cycle enzymes
and mitochondrial lipid and amino-acid metabolic pathways. Our study
also revealed that treatment with the extract activated the stress
response and pathways related to cell-cycle progression and DNA repair.
Overall, our results reveal compelling new evidence that
the extract from L. origanodes triggers rapid irreversible
apoptosis in MDA-MB-231 cells by effectively ‘starving’
the cells of metabolites and ATP. We continue to study the specific
bioactive components of the extract in the search for novel, highly
effective mitochondrial inhibitors to selectively target triple-negative
breast cancer.