BioTech (Mar 2022)

Oxidative Stress- and Autophagy-Inducing Effects of PSI-LHCI from <em>Botryococcus braunii</em> in Breast Cancer Cells

  • Freisa M. Joaquín-Ovalle,
  • Grace Guihurt,
  • Vanessa Barcelo-Bovea,
  • Andraous Hani-Saba,
  • Nicole C. Fontanet-Gómez,
  • Josell Ramirez-Paz,
  • Yasuhiro Kashino,
  • Zally Torres-Martinez,
  • Katerina Doble-Cacho,
  • Louis J. Delinois,
  • Yamixa Delgado,
  • Kai Griebenow

DOI
https://doi.org/10.3390/biotech11020009
Journal volume & issue
Vol. 11, no. 2
p. 9

Abstract

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Botryococcus braunii (B. braunii) is a green microalga primarily found in freshwater, reservoirs, and ponds. Photosynthetic pigments from algae have shown many bioactive molecules with therapeutic potential. Herein, we report the purification, characterization, and anticancer properties of photosystem I light-harvesting complex I (PSI-LHCI) from the green microalga B. braunii UTEX2441. The pigment–protein complex was purified by sucrose density gradient and characterized by its distinctive peaks using absorption, low-temperature (77 K) fluorescence, and circular dichroism (CD) spectroscopic analyses. Protein complexes were resolved by blue native-PAGE and two-dimensional SDS-PAGE. Triple-negative breast cancer MDA-MB-231 cells were incubated with PSI-LHCI for all of our experiments. Cell viability was assessed, revealing a significant reduction in a time- and concentration-dependent manner. We confirmed the internalization of PSI-LHCI within the cytoplasm and nucleus after 12 h of incubation. Cell death mechanism by oxidative stress was confirmed by the production of reactive oxygen species (ROS) and specifically superoxide. Furthermore, we monitored autophagic flux, apoptotic and necrotic features after treatment with PSI-LHCI. Treated MDA-MB-231 cells showed positive autophagy signals in the cytoplasm and nucleus, and necrotic morphology by the permeabilization of the cell membrane. Our findings demonstrated for the first time the cytotoxic properties of B. braunii PSI-LHCI by the induction of ROS and autophagy in breast cancer cells.

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