Supplementation with Brazil nuts and green tea extract regulates targeted biomarkers related to colorectal cancer risk in humans

Se and green tea have been shown in epidemiological, observational and preclinical studies to be inversely related to the risk of developing colorectal cancer (CRC). However, there are limited studies to evaluate their regulatory effects on genes/proteins that relate to CRC oncogenesis in human subj...

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Published inBritish journal of nutrition Vol. 116; no. 11; pp. 1901 - 1911
Main Authors Hu, Ying, McIntosh, Graeme H., Le Leu, Richard K., Somashekar, Roshini, Meng, Xing Q., Gopalsamy, Geetha, Bambaca, Libby, McKinnon, Ross A., Young, Graeme P.
Format Journal Article
LanguageEnglish
Published Cambridge, UK Cambridge University Press 14.12.2016
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DNA
Tea
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Abstract Se and green tea have been shown in epidemiological, observational and preclinical studies to be inversely related to the risk of developing colorectal cancer (CRC). However, there are limited studies to evaluate their regulatory effects on genes/proteins that relate to CRC oncogenesis in human subjects, such as selenoproteins, WNT signalling pathway, inflammation and methylation. This study examined the effects of supplementation of Se using Brazil nuts and green tea extract (GTE) capsules, alone and in combination, on targeted biomarkers. In total, thirty-two volunteers (>50 years of age) with plasma Se≤1·36 µmol/l were randomised to one of three treatment groups: nine to Se (approximately 48 µg/d) as six Brazil nuts, eleven to four GTE capsules (800 mg (-)-epigallocatechin-3-gallate) and twelve to a combination of Brazil nuts and GTE. Blood and rectal biopsies were obtained before and after each intervention. Plasma Se levels, rectal selenoprotein P (SePP) and β-catenin mRNA increased significantly in subjects consuming Brazil nuts alone or in combination, whereas rectal DNA methyltransferase (DNMT1) and NF-κB mRNA were reduced significantly in subjects consuming GTE alone or in combination. None of the interventions significantly affected rectal acetylated histone H3 or Ki-67 expression at the protein level or plasma C-reactive protein. Effects of the combination of Brazil nuts and GTE did not differ from what would be expected from either agent alone. In conclusion, supplementation of Brazil nuts and/or GTE regulates targeted biomarkers related to CRC oncogenesis, specifically genes associated with selenoproteins (SePP), WNT signalling (β-catenin), inflammation (NF-κB) and methylation (DNMT1). Their combination does not appear to provide additional effects compared with either agent alone.
AbstractList Se and green tea have been shown in epidemiological, observational and preclinical studies to be inversely related to the risk of developing colorectal cancer (CRC). However, there are limited studies to evaluate their regulatory effects on genes/proteins that relate to CRC oncogenesis in human subjects, such as selenoproteins, WNT signalling pathway, inflammation and methylation. This study examined the effects of supplementation of Se using Brazil nuts and green tea extract (GTE) capsules, alone and in combination, on targeted biomarkers. In total, thirty-two volunteers (>50 years of age) with plasma Se≤1·36 µmol/l were randomised to one of three treatment groups: nine to Se (approximately 48 µg/d) as six Brazil nuts, eleven to four GTE capsules (800 mg (-)-epigallocatechin-3-gallate) and twelve to a combination of Brazil nuts and GTE. Blood and rectal biopsies were obtained before and after each intervention. Plasma Se levels, rectal selenoprotein P (SePP) and β-catenin mRNA increased significantly in subjects consuming Brazil nuts alone or in combination, whereas rectal DNA methyltransferase (DNMT1) and NF-κB mRNA were reduced significantly in subjects consuming GTE alone or in combination. None of the interventions significantly affected rectal acetylated histone H3 or Ki-67 expression at the protein level or plasma C-reactive protein. Effects of the combination of Brazil nuts and GTE did not differ from what would be expected from either agent alone. In conclusion, supplementation of Brazil nuts and/or GTE regulates targeted biomarkers related to CRC oncogenesis, specifically genes associated with selenoproteins (SePP), WNT signalling (β-catenin), inflammation (NF-κB) and methylation (DNMT1). Their combination does not appear to provide additional effects compared with either agent alone.
Se and green tea have been shown in epidemiological, observational and preclinical studies to be inversely related to the risk of developing colorectal cancer (CRC). However, there are limited studies to evaluate their regulatory effects on genes/proteins that relate to CRC oncogenesis in human subjects, such as selenoproteins, WNT signalling pathway, inflammation and methylation. This study examined the effects of supplementation of Se using Brazil nuts and green tea extract (GTE) capsules, alone and in combination, on targeted biomarkers. In total, thirty-two volunteers (>50 years of age) with plasma Se≤1·36 µmol/l were randomised to one of three treatment groups: nine to Se (approximately 48 µg/d) as six Brazil nuts, eleven to four GTE capsules (800 mg (-)-epigallocatechin-3-gallate) and twelve to a combination of Brazil nuts and GTE. Blood and rectal biopsies were obtained before and after each intervention. Plasma Se levels, rectal selenoprotein P (SePP) and β -catenin mRNA increased significantly in subjects consuming Brazil nuts alone or in combination, whereas rectal DNA methyltransferase (DNMT1) and NF- κ B mRNA were reduced significantly in subjects consuming GTE alone or in combination. None of the interventions significantly affected rectal acetylated histone H3 or Ki-67 expression at the protein level or plasma C-reactive protein. Effects of the combination of Brazil nuts and GTE did not differ from what would be expected from either agent alone. In conclusion, supplementation of Brazil nuts and/or GTE regulates targeted biomarkers related to CRC oncogenesis, specifically genes associated with selenoproteins (SePP), WNT signalling ( β -catenin), inflammation (NF- κ B) and methylation (DNMT1). Their combination does not appear to provide additional effects compared with either agent alone.
Se and green tea have been shown in epidemiological, observational and preclinical studies to be inversely related to the risk of developing colorectal cancer (CRC). However, there are limited studies to evaluate their regulatory effects on genes/proteins that relate to CRC oncogenesis in human subjects, such as selenoproteins, WNT signalling pathway, inflammation and methylation. This study examined the effects of supplementation of Se using Brazil nuts and green tea extract (GTE) capsules, alone and in combination, on targeted biomarkers. In total, thirty-two volunteers (>50 years of age) with plasma Se[LESS-THAN OR EQUAL TO]1·36 µmol/l were randomised to one of three treatment groups: nine to Se (approximately 48 µg/d) as six Brazil nuts, eleven to four GTE capsules (800 mg (-)-epigallocatechin-3-gallate) and twelve to a combination of Brazil nuts and GTE. Blood and rectal biopsies were obtained before and after each intervention. Plasma Se levels, rectal selenoprotein P (SePP) and [...]-catenin mRNA increased significantly in subjects consuming Brazil nuts alone or in combination, whereas rectal DNA methyltransferase (DNMT1) and NF-[...]B mRNA were reduced significantly in subjects consuming GTE alone or in combination. None of the interventions significantly affected rectal acetylated histone H3 or Ki-67 expression at the protein level or plasma C-reactive protein. Effects of the combination of Brazil nuts and GTE did not differ from what would be expected from either agent alone. In conclusion, supplementation of Brazil nuts and/or GTE regulates targeted biomarkers related to CRC oncogenesis, specifically genes associated with selenoproteins (SePP), WNT signalling ([...]-catenin), inflammation (NF-[...]B) and methylation (DNMT1). Their combination does not appear to provide additional effects compared with either agent alone.
Se and green tea have been shown in epidemiological, observational and preclinical studies to be inversely related to the risk of developing colorectal cancer (CRC). However, there are limited studies to evaluate their regulatory effects on genes/proteins that relate to CRC oncogenesis in human subjects, such as selenoproteins, WNT signalling pathway, inflammation and methylation. This study examined the effects of supplementation of Se using Brazil nuts and green tea extract (GTE) capsules, alone and in combination, on targeted biomarkers. In total, thirty-two volunteers (>50 years of age) with plasma Se less than or equal to 1.36 mu mol/l were randomised to one of three treatment groups: nine to Se (approximately 48 mu g/d) as six Brazil nuts, eleven to four GTE capsules (800 mg (-)-epigallocatechin-3-gallate) and twelve to a combination of Brazil nuts and GTE. Blood and rectal biopsies were obtained before and after each intervention. Plasma Se levels, rectal selenoprotein P (SePP) and beta -catenin mRNA increased significantly in subjects consuming Brazil nuts alone or in combination, whereas rectal DNA methyltransferase (DNMT1) and NF- Kappa B mRNA were reduced significantly in subjects consuming GTE alone or in combination. None of the interventions significantly affected rectal acetylated histone H3 or Ki-67 expression at the protein level or plasma C-reactive protein. Effects of the combination of Brazil nuts and GTE did not differ from what would be expected from either agent alone. In conclusion, supplementation of Brazil nuts and/or GTE regulates targeted biomarkers related to CRC oncogenesis, specifically genes associated with selenoproteins (SePP), WNT signalling ( beta -catenin), inflammation (NF- Kappa B) and methylation (DNMT1). Their combination does not appear to provide additional effects compared with either agent alone.
Author Bambaca, Libby
Somashekar, Roshini
Hu, Ying
Young, Graeme P.
McIntosh, Graeme H.
Le Leu, Richard K.
Gopalsamy, Geetha
Meng, Xing Q.
McKinnon, Ross A.
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  fullname: Le Leu, Richard K.
  organization: Flinders Centre for Innovation in Cancer, Flinders University, Adelaide, South Australia, Australia
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  surname: Somashekar
  fullname: Somashekar, Roshini
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  fullname: Young, Graeme P.
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/27923410$$D View this record in MEDLINE/PubMed
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DocumentTitleAlternate Effects of Se and green tea extract on biomarkers of colorectal cancer risk
Y. Hu et al.
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Issue 11
Keywords Biomarkers
Colorectal cancer risk
Green tea extract
Brazil nuts
Selenium
DNMT DNA methyltransferase
CRC colorectal cancer
Ac-H3 acetylated histone H3
EGCG (-)-epigallocatechin-3-gallate
SePP selenoprotein P
GTE green tea extract
Language English
License https://www.cambridge.org/core/terms
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PublicationDate 2016-12-14
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  year: 2016
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PublicationDecade 2010
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PublicationTitle British journal of nutrition
PublicationTitleAlternate Br J Nutr
PublicationYear 2016
Publisher Cambridge University Press
Publisher_xml – name: Cambridge University Press
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Snippet Se and green tea have been shown in epidemiological, observational and preclinical studies to be inversely related to the risk of developing colorectal cancer...
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pubmed
crossref
cambridge
SourceType Aggregation Database
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StartPage 1901
SubjectTerms Aged
Anticarcinogenic Agents - therapeutic use
Bertholletia - adverse effects
Bertholletia - chemistry
beta catenin
Biomarkers
Biomarkers, Tumor - blood
Biomarkers, Tumor - metabolism
biopsy
blood
Brazil nuts
C-reactive protein
Camellia sinensis - chemistry
carcinogenesis
Colorectal cancer
Colorectal carcinoma
colorectal neoplasms
Colorectal Neoplasms - epidemiology
Colorectal Neoplasms - metabolism
Colorectal Neoplasms - pathology
Colorectal Neoplasms - prevention & control
Dietary supplements
Dietary Supplements - adverse effects
DNA
Extraction processes
Feasibility Studies
Female
Food Handling
Functional Food - adverse effects
genes
Green tea
Health risks
histones
Human and Clinical Nutrition
Humans
inflammation
Intestinal Mucosa - metabolism
Intestinal Mucosa - pathology
Male
messenger RNA
Methylation
methyltransferases
Middle Aged
nutrition risk assessment
Nuts
Nuts - adverse effects
Nuts - chemistry
Plant Extracts - adverse effects
Plant Extracts - chemistry
Plant Extracts - therapeutic use
Plant Leaves - chemistry
protein content
Rectum - metabolism
Rectum - pathology
Risk
Selenium - administration & dosage
Selenium - adverse effects
Selenium - blood
Selenium - therapeutic use
selenoproteins
signal transduction
South Australia - epidemiology
Tea
transcription factor NF-kappa B
volunteers
Title Supplementation with Brazil nuts and green tea extract regulates targeted biomarkers related to colorectal cancer risk in humans
URI https://www.cambridge.org/core/product/identifier/S0007114516003937/type/journal_article
https://www.ncbi.nlm.nih.gov/pubmed/27923410
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https://www.proquest.com/docview/1868322678
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Volume 116
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