Olive oil's bitter principle reverses acquired autoresistance to trastuzumab (Herceptin™) in HER2-overexpressing breast cancer cells

<p>Abstract</p> <p>Background</p> <p>A low incidence of breast cancer in the Mediterranean basin suggests that a high consumption of Extra Virgin Olive Oil (EVOO) might confer this benefit. While the anti-HER2 oncogene effects of the main ω-9 fatty acid present in EVOO...

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Main Authors: Brunet Joan, Colomer Ramon, Vazquez-Martin Alejandro, Menendez Javier A, Carrasco-Pancorbo Alegria, Garcia-Villalba Rocio, Fernandez-Gutierrez Alberto, Segura-Carretero Antonio
Format: Article
Language:English
Published: BMC 2007-05-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/7/80
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author Brunet Joan
Colomer Ramon
Vazquez-Martin Alejandro
Menendez Javier A
Carrasco-Pancorbo Alegria
Garcia-Villalba Rocio
Fernandez-Gutierrez Alberto
Segura-Carretero Antonio
author_facet Brunet Joan
Colomer Ramon
Vazquez-Martin Alejandro
Menendez Javier A
Carrasco-Pancorbo Alegria
Garcia-Villalba Rocio
Fernandez-Gutierrez Alberto
Segura-Carretero Antonio
author_sort Brunet Joan
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>A low incidence of breast cancer in the Mediterranean basin suggests that a high consumption of Extra Virgin Olive Oil (EVOO) might confer this benefit. While the anti-HER2 oncogene effects of the main ω-9 fatty acid present in EVOO triacylglycerols (<it>i.e</it>., oleic acid) have been recently described, the anti-breast cancer activities of EVOO non-glyceridic constituents -which consist of at least 30 phenolic compounds-, remained to be evaluated.</p> <p>Methods</p> <p>Semi-preparative HPLC was used to isolate EVOO polyphenols (<it>i.e</it>., tyrosol, hydroxytyrosol, oleuropein). Both the anti-proliferative and the pro-apoptotic effects of EVOO phenolics were evaluated by using MTT-based quantification of metabolically viable cells and ELISA-based detection of histone-associated DNA fragments, respectively. The nature of the interaction between oleuropein aglycone and the anti-HER2 monoclonal antibody trastuzumab (Herceptin™) was mathematically evaluated by the dose-oriented isobologram technique. HER2-specific ELISAs were employed to quantitatively assess both the basal cleavage of the HER2 extracellular domain (ECD) and the expression level of total HER2. The activation status of HER2 was evaluated by immunoblotting procedures using a monoclonal antibody specifically recognizing the tyrosine phosphorylated (Phosphor-Tyr1248) form of HER2.</p> <p>Results</p> <p>Among EVOO polyphenols tested, oleuropein aglycone was the most potent EVOO phenolic in decreasing breast cancer cell viability. HER2 gene-amplified SKBR3 cells were ~5-times more sensitive to oleuropein aglycone than HER2-negative MCF-7 cells. Retroviral infection of the HER2 oncogene in MCF-7 cells resulted in a "SKBR3-assimilated" phenotype of hypersensitivity to oleuropein aglycone. An up to 50-fold increase in the efficacy of trastuzumab occurred in the presence of oleuropein aglycone. A preclinical model of acquired autoresistance to trastuzumab (SKBR3/Tzb100 cells) completely recovered trastuzumab sensitivity (> 1,000-fold sensitization) when co-cultured in the presence of oleuropein aglycone. Indeed, the nature of the interaction between oleuropein aglycone and trastuzumab was found to be strongly synergistic in Tzb-resistant SKBR3/Tzb100 cells. Mechanistically, oleuropein aglycone treatment significantly reduced HER2 ECD cleavage and subsequent HER2 auto-phosphorylation, while it dramatically enhanced Tzb-induced down-regulation of HER2 expression.</p> <p>Conclusion</p> <p>Olive oil's bitter principle (<it>i.e</it>., oleuropein aglycone) is among the first examples of how selected nutrients from an EVOO-rich "Mediterranean diet" directly regulate HER2-driven breast cancer disease.</p>
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spelling doaj.art-f94038d333094461b4e40688045a75d52022-12-21T22:02:48ZengBMCBMC Cancer1471-24072007-05-01718010.1186/1471-2407-7-80Olive oil's bitter principle reverses acquired autoresistance to trastuzumab (Herceptin™) in HER2-overexpressing breast cancer cellsBrunet JoanColomer RamonVazquez-Martin AlejandroMenendez Javier ACarrasco-Pancorbo AlegriaGarcia-Villalba RocioFernandez-Gutierrez AlbertoSegura-Carretero Antonio<p>Abstract</p> <p>Background</p> <p>A low incidence of breast cancer in the Mediterranean basin suggests that a high consumption of Extra Virgin Olive Oil (EVOO) might confer this benefit. While the anti-HER2 oncogene effects of the main ω-9 fatty acid present in EVOO triacylglycerols (<it>i.e</it>., oleic acid) have been recently described, the anti-breast cancer activities of EVOO non-glyceridic constituents -which consist of at least 30 phenolic compounds-, remained to be evaluated.</p> <p>Methods</p> <p>Semi-preparative HPLC was used to isolate EVOO polyphenols (<it>i.e</it>., tyrosol, hydroxytyrosol, oleuropein). Both the anti-proliferative and the pro-apoptotic effects of EVOO phenolics were evaluated by using MTT-based quantification of metabolically viable cells and ELISA-based detection of histone-associated DNA fragments, respectively. The nature of the interaction between oleuropein aglycone and the anti-HER2 monoclonal antibody trastuzumab (Herceptin™) was mathematically evaluated by the dose-oriented isobologram technique. HER2-specific ELISAs were employed to quantitatively assess both the basal cleavage of the HER2 extracellular domain (ECD) and the expression level of total HER2. The activation status of HER2 was evaluated by immunoblotting procedures using a monoclonal antibody specifically recognizing the tyrosine phosphorylated (Phosphor-Tyr1248) form of HER2.</p> <p>Results</p> <p>Among EVOO polyphenols tested, oleuropein aglycone was the most potent EVOO phenolic in decreasing breast cancer cell viability. HER2 gene-amplified SKBR3 cells were ~5-times more sensitive to oleuropein aglycone than HER2-negative MCF-7 cells. Retroviral infection of the HER2 oncogene in MCF-7 cells resulted in a "SKBR3-assimilated" phenotype of hypersensitivity to oleuropein aglycone. An up to 50-fold increase in the efficacy of trastuzumab occurred in the presence of oleuropein aglycone. A preclinical model of acquired autoresistance to trastuzumab (SKBR3/Tzb100 cells) completely recovered trastuzumab sensitivity (> 1,000-fold sensitization) when co-cultured in the presence of oleuropein aglycone. Indeed, the nature of the interaction between oleuropein aglycone and trastuzumab was found to be strongly synergistic in Tzb-resistant SKBR3/Tzb100 cells. Mechanistically, oleuropein aglycone treatment significantly reduced HER2 ECD cleavage and subsequent HER2 auto-phosphorylation, while it dramatically enhanced Tzb-induced down-regulation of HER2 expression.</p> <p>Conclusion</p> <p>Olive oil's bitter principle (<it>i.e</it>., oleuropein aglycone) is among the first examples of how selected nutrients from an EVOO-rich "Mediterranean diet" directly regulate HER2-driven breast cancer disease.</p>http://www.biomedcentral.com/1471-2407/7/80
spellingShingle Brunet Joan
Colomer Ramon
Vazquez-Martin Alejandro
Menendez Javier A
Carrasco-Pancorbo Alegria
Garcia-Villalba Rocio
Fernandez-Gutierrez Alberto
Segura-Carretero Antonio
Olive oil's bitter principle reverses acquired autoresistance to trastuzumab (Herceptin™) in HER2-overexpressing breast cancer cells
BMC Cancer
title Olive oil's bitter principle reverses acquired autoresistance to trastuzumab (Herceptin™) in HER2-overexpressing breast cancer cells
title_full Olive oil's bitter principle reverses acquired autoresistance to trastuzumab (Herceptin™) in HER2-overexpressing breast cancer cells
title_fullStr Olive oil's bitter principle reverses acquired autoresistance to trastuzumab (Herceptin™) in HER2-overexpressing breast cancer cells
title_full_unstemmed Olive oil's bitter principle reverses acquired autoresistance to trastuzumab (Herceptin™) in HER2-overexpressing breast cancer cells
title_short Olive oil's bitter principle reverses acquired autoresistance to trastuzumab (Herceptin™) in HER2-overexpressing breast cancer cells
title_sort olive oil s bitter principle reverses acquired autoresistance to trastuzumab herceptin™ in her2 overexpressing breast cancer cells
url http://www.biomedcentral.com/1471-2407/7/80
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