scispace - formally typeset
Journal ArticleDOI

Real-time polymerase chain reaction quantification of specific butyrate-producing bacteria, Desulfovibrio and Enterococcus faecalis in the feces of patients with colorectal cancer.

Reads0
Chats0
TLDR
The present study quantitated Eubacterium rectale, Faecalibacterium prausnitzii, Desulfovibrio (sulfate‐reducing bacteria), and Enterococcus faecalis (that produces extracellular superoxide) in the feces of patients with colorectal cancer.
Abstract
Background and Aim: Bacterial metabolites produced in the bowel are potentially related to the genesis of colorectal cancer. Butyrate is protective against cancer, whereas hydrogen sulfide and oxygen free radicals can be toxic to the epithelium. The present study was designed to quantitate Eubacterium rectale, Faecalibacterium prausnitzii (both butyrate-producing bacteria), Desulfovibrio (sulfate-reducing bacteria), and Enterococcus faecalis (that produces extracellular superoxide) in the feces of patients with colorectal cancer. Methods: DNA was extracted from feces of 20 patients with colorectal cancer, nine patients with upper gastrointestinal cancer and 17 healthy volunteers. Real-time polymerase chain reaction using primers aimed at 16S rDNA was used to quantitate the above bacterial species or genus, and this was expressed relative to amplification of universal sequences conserved among all bacteria. Results: Levels of E. rectale and F. prausnitzii were decreased approximately fourfold (P = 0.0088 and 0.0028, respectively) in colorectal cancer patients compared to healthy control volunteers. Levels of Desulfovibrio were not significantly different between the three groups. E. faecalis populations were significantly higher in colorectal cancer patients compared to healthy volunteers (P = 0.0294). Conclusions: Butyrate producers were decreased and E. faecalis increased in the feces of colon cancer patients. These shifts in the colonic bacterial population could potentially lead to epithelial cell damage and increased turnover and may be a factor leading to colon cancer.

read more

Citations
More filters
Journal ArticleDOI

Structural segregation of gut microbiota between colorectal cancer patients and healthy volunteers

TL;DR: Reduction of butyrate-producing bacteria in the gut microbiota of CRC patients and increase of opportunistic pathogens may constitute a major structural imbalance of gut microbiota in CRC patients.
Journal ArticleDOI

The Warburg Effect Dictates the Mechanism of Butyrate-Mediated Histone Acetylation and Cell Proliferation

TL;DR: It is demonstrated that metabolic transformation plays an important role in the development of cancer cells and that butyrate stimulated the proliferation of normal colonocytes and cancerous colonocytes when the Warburg effect was prevented from occurring.
Journal ArticleDOI

Gut microbiota imbalance and colorectal cancer.

TL;DR: The possible links between the bacterial microbiota and colorectal carcinogenesis are discussed, focusing on dysbiosis and the potential pro-carcinogenic properties of bacteria, such as genotoxicity and other virulence factors, inflammation, host defenses modulation, bacterial-derived metabolism, oxidative stress and anti-oxidative defenses modulation.
Journal ArticleDOI

Faecalibacterium prausnitzii : from microbiology to diagnostics and prognostics

TL;DR: This species may be a useful potential biomarker to assist in ulcerative colitis and Crohn’s disease discrimination and its application as a biomarker for diagnostics and prognostics of gut diseases are discussed.
References
More filters
Journal ArticleDOI

Genetic alterations during colorectal-tumor development.

TL;DR: It is found that ras-gene mutations occurred in 58 percent of adenomas larger than 1 cm and in 47 percent of carcinomas, which are consistent with a model of colorectal tumorigenesis in which the steps required for the development of cancer often involve the mutational activation of an oncogene coupled with the loss of several genes that normally suppress tumors.
Journal ArticleDOI

The rdp (ribosomal database project)

TL;DR: The Ribosomal Database Project (RDP-II), previously described by Maidak et al. (2000), continued during the past year to add new rRNA sequences to the aligned data and to improve the analysis commands.
Journal ArticleDOI

Determination of bacterial load by real-time PCR using a broad-range (universal) probe and primers set.

TL;DR: The design and evaluation of a set of universal primers and probe for the amplification of 16S rDNA from the Domain Bacteria to estimate total bacterial load by real-time PCR is reported, and the number of anaerobic bacteria estimated by the universal probe and primers set in carious dentine was 40-fold greater than the totalacterial load detected by culture methods, demonstrating the utility of real- time PCR in the analysis of this environment.
Journal Article

Global burden of cancer.

TL;DR: The GLOBOCAN 2002 database was first made available in September 2005 and presented estimates for 2002, based on the most recent incidence, mortality, and survival data available at IARC, but more recent figures may be available directly from local sources.
Related Papers (5)