Anacardic Acid, Salicylic Acid, and Oleic Acid Differentially Alter Cellular Bioenergetic Function in Breast Cancer Cells. Issue 11 (14th April 2016)

• Record Type: Journal Article
• Authors: Radde, Brandie N.; Alizadeh‐Rad, Negin; Price, Stephanie M.; Schultz, David J.; Klinge, Carolyn M.
• Is Part Of: Journal of cellular biochemistry. Volume 117:Issue 11(2016:Nov.)
• Page Start: 2521
• Page End: 2532
• Publication Date: 2016-04-14
• Subjects: ANACARDIC ACID -- BREAST CANCER -- OLEIC ACID -- SALICYLIC ACID -- MITOCHONDRIAL BIOENERGETICS -- ENDOCRINE RESISTANCE -- OXYGEN CONSUMPTION RATE; Cytochemistry -- Periodicals; 572
• DOI: 10.1002/jcb.25544
• Languages: English
• ISSNs: 0730-2312

Abstract

ABSTRACT: Anacardic acid is a dietary and medicinal phytochemical that inhibits breast cancer cell proliferation and uncouples oxidative phosphorylation (OXPHOS) in isolated rat liver mitochondria. Since mitochondrial‐targeted anticancer therapy (mitocans) may be useful in breast cancer, we examined the effect of anacardic acid on cellular bioenergetics and OXPHOS pathway proteins in breast cancer cells modeling progression to endocrine‐independence: MCF‐7 estrogen receptor α (ERα)+ endocrine‐sensitive; LCC9 and LY2 ERα+, endocrine‐resistant, and MDA‐MB‐231 triple negative breast cancer (TNBC) cells. At concentrations similar to cell proliferation IC50 s, anacardic acid reduced ATP‐linked oxygen consumption rate (OCR), mitochondrial reserve capacity, and coupling efficiency while increasing proton leak, reflecting mitochondrial toxicity which was greater in MCF‐7 compared to endocrine‐resistant and TNBC cells. These results suggest tolerance in endocrine‐resistant and TNBC cells to mitochondrial stress induced by anacardic acid. Since anacardic acid is an alkylated 2‐hydroxybenzoic acid, the effects of salicylic acid (SA, 2‐hydroxybenzoic acid moiety) and oleic acid (OA, monounsaturated alkyl moiety) were tested. SA inhibited whereas OA stimulated cell viability. In contrast to stimulation of basal OCR by anacardic acid (uncoupling effect), neither SA nor OA altered basal OCR‐ except OA inhibited basal and ATP‐linked OCR, and increased ECAR, in MDA‐MB‐231 cells. Changes in OXPHOS proteins correlated with changes in OCR. Overall, neither the 2‐hydroxybenzoic acid moiety nor the monounsaturated alky moiety of anacardic acid is solely responsible for the observed mitochondria‐targeted anticancer activity in breast cancer cells and hence both moieties are required in the same molecule for the observed effects. J. Cell. Biochem. 117: 2521–2532, 2016. © 2016 Wiley Periodicals, Inc. Abstract : Anacardic acid increases basal O2 consumption and proton leak, inhibits ATP‐linked O2 consumption, and decreases mitochondrial reserve in breast cancer cells, suggesting that it acts as an uncoupler of OXPHOS in breast cancer cells. Neither oleic acid nor salicylic acid, structural moieties of anacardic acid, acted as uncouplers, although oleic acid selectively inhibited O2 consumption in MDA‐MB‐231 triple negative breast cancer cells.