Resveratrol 3‐O‐d‐glucuronide and resveratrol 4′‐O‐d‐glucuronide inhibit colon cancer cell growth: Evidence for a role of A3 adenosine receptors, cyclin D1 depletion, and G1 cell cycle arrest. Issue 10 (7th May 2013)
- Record Type:
- Journal Article
- Title:
- Resveratrol 3‐O‐d‐glucuronide and resveratrol 4′‐O‐d‐glucuronide inhibit colon cancer cell growth: Evidence for a role of A3 adenosine receptors, cyclin D1 depletion, and G1 cell cycle arrest. Issue 10 (7th May 2013)
- Main Title:
- Resveratrol 3‐O‐d‐glucuronide and resveratrol 4′‐O‐d‐glucuronide inhibit colon cancer cell growth: Evidence for a role of A3 adenosine receptors, cyclin D1 depletion, and G1 cell cycle arrest
- Authors:
- Polycarpou, Elena
Meira, Lisiane B.
Carrington, Simon
Tyrrell, Elizabeth
Modjtahedi, Helmout
Carew, Mark A. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="mnfr1972-sec-0010" sec-type="section"> <title>Scope</title> <p>Resveratrol is a plant‐derived polyphenol with chemotherapeutic properties in animal cancer models and many biochemical effects in vitro. Its bioavailability is low and raises the possibility that the metabolites of resveratrol have biological effects. Here we investigate the actions of resveratrol 3‐<italic>O</italic>‐<sc>d</sc>‐glucuronide, resveratrol 4′‐<italic>O</italic>‐<sc>d</sc>‐glucuronide, and resveratrol 3‐<italic>O</italic>‐<sc>d</sc>‐sulfate on the growth of colon cancer cells in vitro.</p> </sec> <sec id="mnfr1972-sec-0020" sec-type="section"> <title>Methods and results</title> <p>The growth of Caco‐2, HCT‐116, and CCL‐228 cells was measured using the neutral red and MTT assays. Resveratrol and each metabolite inhibited cell growth with IC50 values of 9.8–31 μM. Resveratrol caused S phase arrest in all three cell lines. Resveratrol 3‐<italic>O</italic>‐<sc>d</sc>‐glucuronide and resveratrol 4′‐<italic>O</italic>‐<sc>d</sc>‐glucuronide caused G1 arrest in CCL‐228 and Caco‐2 cells. Resveratrol 3‐<italic>O</italic>‐<sc>d</sc>‐sulfate had no effect on cell cycle. Growth inhibition was reversed by an inhibitor of AMP‐activated protein kinase (compound C) or an adenosine A3 receptor antagonist (MRS1191). The A3 receptor agonist 2Cl‐IB‐MECA inhibited growth and A3 receptors were detected in all cell lines. The<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="mnfr1972-sec-0010" sec-type="section"> <title>Scope</title> <p>Resveratrol is a plant‐derived polyphenol with chemotherapeutic properties in animal cancer models and many biochemical effects in vitro. Its bioavailability is low and raises the possibility that the metabolites of resveratrol have biological effects. Here we investigate the actions of resveratrol 3‐<italic>O</italic>‐<sc>d</sc>‐glucuronide, resveratrol 4′‐<italic>O</italic>‐<sc>d</sc>‐glucuronide, and resveratrol 3‐<italic>O</italic>‐<sc>d</sc>‐sulfate on the growth of colon cancer cells in vitro.</p> </sec> <sec id="mnfr1972-sec-0020" sec-type="section"> <title>Methods and results</title> <p>The growth of Caco‐2, HCT‐116, and CCL‐228 cells was measured using the neutral red and MTT assays. Resveratrol and each metabolite inhibited cell growth with IC50 values of 9.8–31 μM. Resveratrol caused S phase arrest in all three cell lines. Resveratrol 3‐<italic>O</italic>‐<sc>d</sc>‐glucuronide and resveratrol 4′‐<italic>O</italic>‐<sc>d</sc>‐glucuronide caused G1 arrest in CCL‐228 and Caco‐2 cells. Resveratrol 3‐<italic>O</italic>‐<sc>d</sc>‐sulfate had no effect on cell cycle. Growth inhibition was reversed by an inhibitor of AMP‐activated protein kinase (compound C) or an adenosine A3 receptor antagonist (MRS1191). The A3 receptor agonist 2Cl‐IB‐MECA inhibited growth and A3 receptors were detected in all cell lines. The resveratrol glucuronides also reduced cyclin D1 levels but at higher concentrations than in growth experiments and generally did not increase phosphorylated AMP‐activated protein kinase.</p> </sec> <sec id="mnfr1972-sec-0030" sec-type="section"> <title>Conclusion</title> <p>Resveratrol glucuronides inhibit cell growth by G1 arrest and cyclin D1 depletion, and our results strongly suggest a role for A3 adenosine receptors in this inhibition.</p> </sec> </abstract> … (more)
- Is Part Of:
- Molecular nutrition & food research. Volume 57:Issue 10(2013:Oct.)
- Journal:
- Molecular nutrition & food research
- Issue:
- Volume 57:Issue 10(2013:Oct.)
- Issue Display:
- Volume 57, Issue 10 (2013)
- Year:
- 2013
- Volume:
- 57
- Issue:
- 10
- Issue Sort Value:
- 2013-0057-0010-0000
- Page Start:
- 1708
- Page End:
- 1717
- Publication Date:
- 2013-05-07
- Subjects:
- Food -- Biotechnology -- Periodicals
Food -- Microbiology -- Periodicals
Nutrition -- Periodicals
Food -- Toxicology -- Periodicals
Nutrition -- Periodicals
Food Microbiology -- Periodicals
Food Technology -- Periodicals
Molecular Biology -- Periodicals
664.0705 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/mnfr.201200742 ↗
- Languages:
- English
- ISSNs:
- 1613-4125
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817992
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3804.xml