Effects of a Grapevine Shoot Extract Containing Resveratrol and Resveratrol Oligomers on Intestinal Adenoma Development in Mice: In Vitro and In Vivo Studies

Research output: Contribution to journalArticleResearchpeer review

Authors

  • Michael T. Empl
  • Hong Cai
  • Shan Wang
  • Johannes ´ Junginger
  • T Kostka
  • Marion Hewicker-Trautwein
  • Karen Brown
  • Andreas J. Gescher
  • Pablo Steinberg

External Research Organisations

  • University of Veterinary Medicine of Hannover, Foundation
  • University of Leicester
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Details

Original languageEnglish
Article number1700450
JournalMolecular nutrition & food research
Volume62
Issue number2
Early online date10 Nov 2017
Publication statusPublished - 22 Jan 2018

Abstract

Scope: Evidence suggests that the dietary consumption of plant extracts containing polyphenols might help prevent the onset of cancers of the gastrointestinal tract. In the present study, the chemopreventive and antiproliferative efficacy of a grapevine shoot extract (Vineatrol®30) containing resveratrol and resveratrol oligomers is investigated in vivo and in vitro. 

Methods and results: The in vivo study is performed using Apc Min mice on a high-fat diet, which represents a model of human adenomatous polyposis, while the potential of the extract as well as some of its isolated constituents to inhibit intestinal adenoma cell proliferation in vitro is investigated using APC10.1 cells derived from an Apc Min mouse. Vineatrol®30 at a low (2.3 mg kg –1 diet) or high dose (476 mg kg –1 diet) reduces the adenoma number in male and adenoma volume in female animals. Furthermore, Vineatrol®30 as well as resveratrol and two resveratrol tetramers compromise the expansion of APC10.1 cells by reducing cell number, inducing cell cycle arrest, cellular senescence, and apoptosis. However, except for the extract, none of the isolated resveratrol oligomers is more efficacious than resveratrol in these cells. 

Conclusion: Vineatrol®30 may merit further investigation as a potential dietary gastrointestinal cancer chemopreventive agent in humans.

Keywords

    Apc mouse, chemoprevention, grapevine shoot extract, resveratrol, resveratrol oligomers, Intestinal Neoplasms/metabolism, Male, Adenoma/metabolism, Anticarcinogenic Agents/chemistry, Caspases/metabolism, Animals, Mice, Mutant Strains, Antineoplastic Agents, Phytogenic/chemistry, Female, Phenols/chemistry, Resveratrol/chemistry, Stilbenes/pharmacology, Cell Proliferation/drug effects

ASJC Scopus subject areas

Sustainable Development Goals

Cite this

Effects of a Grapevine Shoot Extract Containing Resveratrol and Resveratrol Oligomers on Intestinal Adenoma Development in Mice: In Vitro and In Vivo Studies. / Empl, Michael T.; Cai, Hong; Wang, Shan et al.
In: Molecular nutrition & food research, Vol. 62, No. 2, 1700450, 22.01.2018.

Research output: Contribution to journalArticleResearchpeer review

Empl, M. T., Cai, H., Wang, S., Junginger, J. ., Kostka, T., Hewicker-Trautwein, M., Brown, K., Gescher, A. J., & Steinberg, P. (2018). Effects of a Grapevine Shoot Extract Containing Resveratrol and Resveratrol Oligomers on Intestinal Adenoma Development in Mice: In Vitro and In Vivo Studies. Molecular nutrition & food research, 62(2), Article 1700450. https://doi.org/10.1002/mnfr.201700450
Empl MT, Cai H, Wang S, Junginger J, Kostka T, Hewicker-Trautwein M et al. Effects of a Grapevine Shoot Extract Containing Resveratrol and Resveratrol Oligomers on Intestinal Adenoma Development in Mice: In Vitro and In Vivo Studies. Molecular nutrition & food research. 2018 Jan 22;62(2):1700450. Epub 2017 Nov 10. doi: 10.1002/mnfr.201700450
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title = "Effects of a Grapevine Shoot Extract Containing Resveratrol and Resveratrol Oligomers on Intestinal Adenoma Development in Mice: In Vitro and In Vivo Studies",
abstract = "Scope: Evidence suggests that the dietary consumption of plant extracts containing polyphenols might help prevent the onset of cancers of the gastrointestinal tract. In the present study, the chemopreventive and antiproliferative efficacy of a grapevine shoot extract (Vineatrol{\textregistered}30) containing resveratrol and resveratrol oligomers is investigated in vivo and in vitro. Methods and results: The in vivo study is performed using Apc Min mice on a high-fat diet, which represents a model of human adenomatous polyposis, while the potential of the extract as well as some of its isolated constituents to inhibit intestinal adenoma cell proliferation in vitro is investigated using APC10.1 cells derived from an Apc Min mouse. Vineatrol{\textregistered}30 at a low (2.3 mg kg –1 diet) or high dose (476 mg kg –1 diet) reduces the adenoma number in male and adenoma volume in female animals. Furthermore, Vineatrol{\textregistered}30 as well as resveratrol and two resveratrol tetramers compromise the expansion of APC10.1 cells by reducing cell number, inducing cell cycle arrest, cellular senescence, and apoptosis. However, except for the extract, none of the isolated resveratrol oligomers is more efficacious than resveratrol in these cells. Conclusion: Vineatrol{\textregistered}30 may merit further investigation as a potential dietary gastrointestinal cancer chemopreventive agent in humans. ",
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author = "Empl, {Michael T.} and Hong Cai and Shan Wang and Junginger, {Johannes ´} and T Kostka and Marion Hewicker-Trautwein and Karen Brown and Gescher, {Andreas J.} and Pablo Steinberg",
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Download

TY - JOUR

T1 - Effects of a Grapevine Shoot Extract Containing Resveratrol and Resveratrol Oligomers on Intestinal Adenoma Development in Mice

T2 - In Vitro and In Vivo Studies

AU - Empl, Michael T.

AU - Cai, Hong

AU - Wang, Shan

AU - Junginger, Johannes ´

AU - Kostka, T

AU - Hewicker-Trautwein, Marion

AU - Brown, Karen

AU - Gescher, Andreas J.

AU - Steinberg, Pablo

N1 - © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

PY - 2018/1/22

Y1 - 2018/1/22

N2 - Scope: Evidence suggests that the dietary consumption of plant extracts containing polyphenols might help prevent the onset of cancers of the gastrointestinal tract. In the present study, the chemopreventive and antiproliferative efficacy of a grapevine shoot extract (Vineatrol®30) containing resveratrol and resveratrol oligomers is investigated in vivo and in vitro. Methods and results: The in vivo study is performed using Apc Min mice on a high-fat diet, which represents a model of human adenomatous polyposis, while the potential of the extract as well as some of its isolated constituents to inhibit intestinal adenoma cell proliferation in vitro is investigated using APC10.1 cells derived from an Apc Min mouse. Vineatrol®30 at a low (2.3 mg kg –1 diet) or high dose (476 mg kg –1 diet) reduces the adenoma number in male and adenoma volume in female animals. Furthermore, Vineatrol®30 as well as resveratrol and two resveratrol tetramers compromise the expansion of APC10.1 cells by reducing cell number, inducing cell cycle arrest, cellular senescence, and apoptosis. However, except for the extract, none of the isolated resveratrol oligomers is more efficacious than resveratrol in these cells. Conclusion: Vineatrol®30 may merit further investigation as a potential dietary gastrointestinal cancer chemopreventive agent in humans.

AB - Scope: Evidence suggests that the dietary consumption of plant extracts containing polyphenols might help prevent the onset of cancers of the gastrointestinal tract. In the present study, the chemopreventive and antiproliferative efficacy of a grapevine shoot extract (Vineatrol®30) containing resveratrol and resveratrol oligomers is investigated in vivo and in vitro. Methods and results: The in vivo study is performed using Apc Min mice on a high-fat diet, which represents a model of human adenomatous polyposis, while the potential of the extract as well as some of its isolated constituents to inhibit intestinal adenoma cell proliferation in vitro is investigated using APC10.1 cells derived from an Apc Min mouse. Vineatrol®30 at a low (2.3 mg kg –1 diet) or high dose (476 mg kg –1 diet) reduces the adenoma number in male and adenoma volume in female animals. Furthermore, Vineatrol®30 as well as resveratrol and two resveratrol tetramers compromise the expansion of APC10.1 cells by reducing cell number, inducing cell cycle arrest, cellular senescence, and apoptosis. However, except for the extract, none of the isolated resveratrol oligomers is more efficacious than resveratrol in these cells. Conclusion: Vineatrol®30 may merit further investigation as a potential dietary gastrointestinal cancer chemopreventive agent in humans.

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KW - Antineoplastic Agents, Phytogenic/chemistry

KW - Female

KW - Phenols/chemistry

KW - Resveratrol/chemistry

KW - Stilbenes/pharmacology

KW - Cell Proliferation/drug effects

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