Scimex: A US study has looked into the bellies of patients with colon cancer and
have found that certain forms of gut bacteria may be helping the
disease along. The researchers were able to narrow it down to three main
culprits, suggesting that clinicians could use this as a means to
discover what bacterial changes in the gut means for a patient's health.
Changes in the gut bacteria of colon cancer patients indicate that
some virulent bacteria could be linked to the progression of the
disease, according to research published in the open access journal Genome Medicine.
The findings could eventually be used to identify a virulence signature
in these cancers and help doctors predict how bacterial changes in
patients' guts could affect their prognosis.
The human gut
microbiome, the collection of microorganisms, their genomes and habitat
that contributes to maintaining a healthy intestine, is thought to play
an active role in colon cancer progression. Previous studies have shown
that changes in the bacterial community occur in the gut microbiome of
colon cancer patients, with tumors harboring increased bacterial
diversity and an abundance of pathogenic bacteria compared to
surrounding healthy tissue.
Although researchers have uncovered a
variety of potentially pathogenic bacteria associated with colon cancer,
little work has been done to determine if there is a single signature
that might unify their findings.
Lead author Michael Burns from
The University of Minnesota, USA, said: "It was surprising that the
results were so clear. We were able to clearly identify the presence of
two virulent strains of bacteria, including the discovery of a new
potential culprit, Providencia. This has obvious implications
for colon cancer patients and by analyzing the similarities among these
pathogens, we have uncovered a single signature of colon cancer when
analyzing the gut microbiome that might help researchers identify these
cancers in the future."
This was the first study to focus on the
pathogenic potential of the bacterial genes present in the colon cancer
'tumor microenvironment', the environment of surrounding blood vessels,
immune cells and other cells. The genes of the gut microbiomes were
predicted in 44 primary tumor and 44 patient-matched normal colon
tissues to analyze the general microbial function.
The team in Ran Blekhman's lab noted changes in the abundances of helpful, harmless, and pathogenic bacteria, including Fusobacterium and Providencia. Fusobacterium has previously been implicated as a cancer-causing group of bacteria, but this is the first time that Providencia has been linked to colon cancer.
Analyzing
the major changes that take place in the gut microbiome could help
researchers categorize the role particular bacteria play and identify
the key players.
Additionally, by showing that the microbial genes
predicted to be present in colon cancer tissue are enriched for
virulence functions, clinicians could use this signature to uncover what
bacterial changes in the gut mean for a patient's health.
At this stage, the research cannot determine a definite causal link between Providencia
species and colon cancer. While the study's methods are robust for
analyzing human gut samples, more research will be needed to assess the
interactions between gut bacteria and the progression and development of
colon cancer.