Study2016

In vitro chemo-preventive activities of hydroxytyrosol: the main phenolic compound present in extra-virgin olive oil

Rosignoli P, Fuccelli R, Sepporta MV, Fabiani R

Food & function · 47 citations

Review labels

Funding not disclosedMechanisms only

Neutral facts our review recorded about how this study was done. They describe method, never whether we like the result.

How it was studied

Design
In vitro/mechanistic study (classified by our AI screen)
Studied in
Cells or lab samples
Main outcome
Mechanisms only

Who paid for it

Funding
Funding not disclosed

Publication

Published
2015-10-05 · Food Funct · vol. 7 · issue 1 · pp. 301–307
Publisher
Royal Society of Chemistry
Cited
65 citations · more than 91% of similar papers · 3.2× the field average
Impact
Top 10% most cited in its field
References
34 works
Access
Paywalled
Research areas
Edible Oils Quality and Analysis · Essential Oils and Antimicrobial Activity · Potato Plant Research
Keywords
Hydroxytyrosol, Peripheral blood mononuclear cell, Olive oil, Chemistry, In vitro, Ethanol, Incubation, Food science, Biochemistry, Antioxidant, Polyphenol
MeSH
cell line, tumor, humans, dna damage, hydrogen peroxide, phenylethyl alcohol, phenols, antioxidants, comet assay, olive oil

4 authors

From IT

  • Patrizia Rosignoli · correspondingUniversity of Perugia
  • Raffaela FuccelliUniversity of Perugia
  • Maria Vittoria SepportaUniversity of Perugia
  • Roberto FabianiUniversity of Perugia

Abstract

The co-incubation in the culture medium with hydroxytyrosol [3,4-dihydroxyphenyl ethanol (3,4-DHPEA)], the main phenolic compound present in extra-virgin olive oil, and H2O2 reduces the oxidative DNA damage in peripheral blood mononuclear cells (PBMC). In this study we investigate, by the comet assay, the ability of 3,4-DHPEA to inhibit the H2O2 induced DNA damage when pre-incubated with PBMC and then removed before the exposure of cells to H2O2. Low doses of 3,4-DHPEA (10-100 μM) pre-incubated for 30 min with PBMC reduced the DNA damage induced by the treatment with H2O2 200 μM for 5 min at 4 °C. Prolonging the exposure time up to 6 h completely prevented the DNA damage. Furthermore we extensively analysed, by the MTT assay, the anti-proliferative activities of 3,4-DHPEA on breast (MDA and MCF-7), prostate (LNCap and PC3) and colon (SW480 and HCT116) cancer cell lines and correlated these effects with the H2O2 accumulation. The concentration of H2O2 in the culture medium was measured by the ferrous ion oxidation-xylenol orange method. The proliferation of all the cell lines was inhibited but at different levels: the prostate cancer cells were more resistant to the growth inhibition with respect to breast and colon cancer cells. The ability of the different cell lines to remove H2O2 from the culture medium was inversely correlated with their sensitivity to the anti-proliferative effect of 3,4-DHPEA. Therefore, 3,4-DHPEA may act as a chemopreventive agent acting on both initiation and promotion/progression phases of carcinogenesis.

Abstract via Europe PMC. Copyright remains with the authors or publisher.

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