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Gut microbiota composition in colorectal cancer patients is genetically regulated
by
Minnai, Francesca
, Noci, Sara
, Pintarelli, Giulia
, Vannelli, Alberto
, Sorrentino, Luca
, Colombo, Francesca
, Pettinicchio, Angela
, Cosimelli, Maurizio
, Dragani, Tommaso A.
, Illescas, Oscar
, Battaglia, Luigi
, Gariboldi, Manuela
in
631/208/69
/ 631/326/2565/2134
/ 692/4028/67/1504
/ Apoptosis
/ Bacteria
/ Bacteroides
/ Cancer
/ Cell adhesion
/ Colorectal cancer
/ Environmental factors
/ Faecalibacterium
/ Genetic factors
/ Genetics
/ Genomes
/ Genotyping
/ Gut microbiota
/ Humanities and Social Sciences
/ Inflammation
/ Intestinal microflora
/ Microbiota
/ Microenvironments
/ multidisciplinary
/ rRNA 16S
/ Science
/ Science (multidisciplinary)
2022
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Gut microbiota composition in colorectal cancer patients is genetically regulated
by
Minnai, Francesca
, Noci, Sara
, Pintarelli, Giulia
, Vannelli, Alberto
, Sorrentino, Luca
, Colombo, Francesca
, Pettinicchio, Angela
, Cosimelli, Maurizio
, Dragani, Tommaso A.
, Illescas, Oscar
, Battaglia, Luigi
, Gariboldi, Manuela
in
631/208/69
/ 631/326/2565/2134
/ 692/4028/67/1504
/ Apoptosis
/ Bacteria
/ Bacteroides
/ Cancer
/ Cell adhesion
/ Colorectal cancer
/ Environmental factors
/ Faecalibacterium
/ Genetic factors
/ Genetics
/ Genomes
/ Genotyping
/ Gut microbiota
/ Humanities and Social Sciences
/ Inflammation
/ Intestinal microflora
/ Microbiota
/ Microenvironments
/ multidisciplinary
/ rRNA 16S
/ Science
/ Science (multidisciplinary)
2022
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Gut microbiota composition in colorectal cancer patients is genetically regulated
by
Minnai, Francesca
, Noci, Sara
, Pintarelli, Giulia
, Vannelli, Alberto
, Sorrentino, Luca
, Colombo, Francesca
, Pettinicchio, Angela
, Cosimelli, Maurizio
, Dragani, Tommaso A.
, Illescas, Oscar
, Battaglia, Luigi
, Gariboldi, Manuela
in
631/208/69
/ 631/326/2565/2134
/ 692/4028/67/1504
/ Apoptosis
/ Bacteria
/ Bacteroides
/ Cancer
/ Cell adhesion
/ Colorectal cancer
/ Environmental factors
/ Faecalibacterium
/ Genetic factors
/ Genetics
/ Genomes
/ Genotyping
/ Gut microbiota
/ Humanities and Social Sciences
/ Inflammation
/ Intestinal microflora
/ Microbiota
/ Microenvironments
/ multidisciplinary
/ rRNA 16S
/ Science
/ Science (multidisciplinary)
2022
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Gut microbiota composition in colorectal cancer patients is genetically regulated
Journal Article
Gut microbiota composition in colorectal cancer patients is genetically regulated
2022
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Overview
The risk of colorectal cancer (CRC) depends on environmental and genetic factors. Among environmental factors, an imbalance in the gut microbiota can increase CRC risk. Also, microbiota is influenced by host genetics. However, it is not known if germline variants influence CRC development by modulating microbiota composition. We investigated germline variants associated with the abundance of bacterial populations in the normal (non-involved) colorectal mucosa of 93 CRC patients and evaluated their possible role in disease. Using a multivariable linear regression, we assessed the association between germline variants identified by genome wide genotyping and bacteria abundances determined by 16S rRNA gene sequencing. We identified 37 germline variants associated with the abundance of the genera
Bacteroides, Ruminococcus, Akkermansia, Faecalibacterium
and
Gemmiger
and with alpha diversity. These variants are correlated with the expression of 58 genes involved in inflammatory responses, cell adhesion, apoptosis and barrier integrity. Genes and bacteria appear to be involved in the same processes. In fact, expression of the pro-inflammatory genes
GAL
,
GSDMD
and
LY6H
was correlated with the abundance of
Bacteroides
, which has pro-inflammatory properties; abundance of the anti-inflammatory genus
Faecalibacterium
correlated with expression of KAZN, with barrier-enhancing functions. Both the microbiota composition and local inflammation are regulated, at least partially, by the same germline variants. These variants may regulate the microenvironment in which bacteria grow and predispose to the development of cancer. Identification of these variants is the first step to identifying higher-risk individuals and proposing tailored preventive treatments that increase beneficial bacterial populations.
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