MD-Onco,
Journal Year:
2024,
Volume and Issue:
4(2), P. 87 - 92
Published: June 14, 2024
To
date,
the
etiological
causes
of
adverse
outcomes
associated
with
cardiovascular
diseases
and
concomitant
colorectal
cancer
in
one
patient,
especially
over
60
years
age,
are
multifactorial:
from
undiagnosed
timely
above-mentioned
pathological
conditions
to
poor
adherence
treatment.
It
is
a
multi-level
approach
that
future
guarantee
reducing
burden
on
public
health
as
result
these
most
common
nosologies.
The
aim
work
evaluate
discussions
between
different
experts
an
analysis
fundamental
clinical
studies
based
world
literature
search
for
new
prospects
treatment
patients
pathology
comorbid
composition
function
intestinal
microbiota.
A
was
conducted
PubMed
electronic
database
using
keywords:
microbiota,
cardio-oncology,
oncosurgery,
cancer,
diseases.
Additional
sources
were
identified
through
cross-referencing.
Search
period:
2023.
gut
microbiome
potential
marker
better
risk
stratification
diseases,
prediction
shortand
long-term
major
events.
develop
clear
recommendations
conclusions,
additional
research
required.
World Journal of Gastroenterology,
Journal Year:
2022,
Volume and Issue:
28(30), P. 4053 - 4060
Published: Aug. 9, 2022
The
gut
microbiota
is
a
complex
community
of
microorganisms
that
inhabit
the
digestive
tracts
humans,
living
in
symbiosis
with
host.
Dysbiosis,
characterized
by
an
imbalance
between
beneficial
and
opportunistic
microbiota,
associated
several
gastrointestinal
disorders,
such
as
irritable
bowel
syndrome
(IBS);
inflammatory
disease
(IBD),
represented
ulcerative
colitis
Crohn's
disease;
colorectal
cancer
(CRC).
Dysbiosis
can
disrupt
mucosal
barrier,
resulting
perpetuation
inflammation
carcinogenesis.
increase
some
specific
groups
harmful
bacteria,
Escherichia
coli
(E.
coli)
enterotoxigenic
Bacteroides
fragilis
(ETBF),
has
been
chronic
tissue
release
pro-inflammatory
carcinogenic
mediators,
increasing
chance
developing
CRC,
following
inflammation-dysplasia-cancer
sequence
IBD
patients.
Therefore,
aim
present
review
was
to
analyze
correlation
changes
development
maintenance
IBD,
IBD-associated
CRC.
Patients
CRC
have
shown
reduced
bacterial
diversity
abundance
compared
healthy
individuals,
enrichment
Firmicute
sand
Bacteroidetes.
Specific
bacteria
are
also
onset
progression
Fusobacterium
nucleatum,
E.
coli,
Enterococcus
faecalis,
Streptococcus
gallolyticus,
ETBF.
Future
research
evaluate
advantages
modulating
preventive
measures
high-risk
patients,
directly
affecting
prognosis
quality
life
Trends in Microbiology,
Journal Year:
2024,
Volume and Issue:
32(8), P. 807 - 822
Published: Feb. 3, 2024
The
microbiota
of
solid
tumors
was
identified
>100
years
ago;
however,
heterogeneous
composition
and
diversity
have
been
revealed
only
recently.
Growing
evidence
has
suggested
that
several
functional
mechanisms
the
intratumoral
affect
tumorigenesis
progression,
suggesting
is
a
promising
biomarker
for
multiple
cancers.
low
biomass
poses
major
challenge
to
related
research,
thus
necessitating
use
multiple-modality
integrated
framework
resolve
this
dilemma.
Advanced
techniques
such
as
single-cell
sequencing
provide
significant
clues,
gradual
optimization
experiments
culture-based
methods
enables
deeper
investigation
underlying
involved.
In
review,
we
outline
current
state
research
on
describe
challenges
comprehensive
strategies
future
research.
Journal of Biomedical Science,
Journal Year:
2022,
Volume and Issue:
29(1)
Published: Oct. 27, 2022
Abstract
Background
Owing
to
the
heterogeneity
of
microbiota
among
individuals
and
populations,
only
Fusobacterium
nucleatum
Bacteroides
fragilis
have
been
reported
be
enriched
in
colorectal
cancer
(CRC)
multiple
studies.
Thus,
discovery
additional
bacteria
contributing
CRC
development
various
populations
can
expected.
We
aimed
identify
associated
with
progression
adenoma
carcinoma
determine
contribution
these
malignant
transformation
patients
Han
Chinese
origin.
Methods
Microbiota
composition
was
determined
through
16S
rRNA
V3–V4
amplicon
sequencing
autologous
adenocarcinomas,
adenomatous
polyps,
non-neoplastic
colon
tissue
samples
(referred
as
“tri-part
samples”)
CRC.
Enriched
taxa
adenocarcinoma
tissues
were
identified
pairwise
comparison.
The
abundance
candidate
quantified
genomic
quantitative
polymerase
chain
reaction
(qPCR)
from
116
patients.
Associations
clinicopathological
features
genetic
alterations
evaluated
odds
ratio
tests.
Additionally,
effects
on
cell
proliferation,
migration,
invasion
co-culture
cells
bacterial
or
conditioned
media
bacteria.
Results
Prevotella
intermedia
overrepresented
adenocarcinomas
compared
paired
polyps.
Furthermore,
co-abundance
P.
F.
observed
tumor
tissues.
More
notably,
coexistence
two
lymph
node
involvement
distant
metastasis.
These
also
exerted
additive
enhancement
migration
abilities
cells.
Finally,
promoted
Conclusion
This
report
is
first
demonstrate
that
enhances
Moreover,
exert
adenomas
into
carcinomas.
findings
used
at
a
high
risk
metastasis
CRC,
they
accordingly
provided
optimal
clinical
management.
Biology,
Journal Year:
2025,
Volume and Issue:
14(3), P. 243 - 243
Published: Feb. 27, 2025
Growing
evidence
reveals
that
the
tumor
microbiome—comprising
distinct
microbial
communities
within
neoplastic
tissues—exerts
a
profound
influence
on
cancer
initiation,
progression,
and
therapeutic
response.
These
microbes
actively
reshape
microenvironment
(TME)
through
metabolite
secretion,
modulation
of
immune
pathways,
direct
interactions
with
host
cells,
thereby
affecting
biology
outcomes.
Despite
substantial
heterogeneity
among
types,
recent
insights
underscore
microbiome’s
potential
as
both
diagnostic/prognostic
biomarker
targetable
component
for
innovative
treatments.
In
this
review,
we
synthesize
emerging
knowledge
mechanistic
roles
tumor-associated
microbiota
in
shaping
TME,
focus
how
these
discoveries
can
guide
novel
strategies.
We
further
explore
interdisciplinary
advances,
including
convergence
microbiomics
nanotechnology,
to
enhance
drug
delivery,
circumvent
resistance,
foster
TME
remodeling.
By
highlighting
cutting-edge
developments,
our
review
underscores
transformative
integrating
microbiome
research
into
precision
oncology
advancing
more
personalized
therapies.
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: Nov. 18, 2022
In
the
past
few
decades,
great
progress
has
been
achieved
in
understanding
of
microbiome-cancer
interactions.
However,
most
studies
have
focused
on
gut
microbiome,
ignoring
how
other
microbiomes
interact
with
tumors.
Emerging
evidence
suggests
that
many
types
cancers,
such
as
lung
cancer,
pancreatic
and
colorectal
intratumoral
microbiome
plays
a
significant
role.
addition,
accumulating
microbes
multiple
effects
biological
behavior
tumors,
for
example,
regulating
tumor
initiation
progression
altering
response
to
chemotherapy
immunotherapy.
fully
understand
role
further
investigation
mechanisms
is
still
needed.
This
review
discusses
bacteria
tumorigenesis
progression,
recurrence
metastasis,
well
their
effect
cancer
prognosis
treatment
outcome,
summarizes
relevant
mechanisms.
Frontiers in Microbiology,
Journal Year:
2023,
Volume and Issue:
14
Published: March 21, 2023
As
the
second
leading
cause
of
cancer
worldwide,
colorectal
(CRC)
is
associated
with
a
poor
prognosis.
Although
recent
studies
have
explored
prognostic
markers
in
patients
CRC,
whether
tissue
microbes
carry
information
remains
unknown.
Here,
by
assessing
533
CRC
patients,
we
found
that
Proteobacteria
(43.5%),
Firmicutes
(25.3%),
and
Actinobacteria
(23.0%)
dominated
microbiota,
which
was
different
from
gut
microbiota.
Moreover,
two
clear
clusters
were
obtained
clustering
based
on
across
all
samples.
By
comparison,
relative
abundances
Bacteroidetes
cluster
1
significantly
higher
than
those
2;
while
compared
1,
more
abundant
2.
In
addition,
Firmicutes/Bacteroidetes
ratios
lower
Further,
2,
had
relatively
survival
(Log-rank
test,
p
=
0.0067).
correlating
patient
survival,
abundance
dominant
phyla,
including
Proteobacteria,
Firmicutes,
Bacteroidetes,
patients.
Besides,
co-occurrence
network
at
phylum
level
2
complicated
1.
Lastly,
detected
some
pathogenic
bacteria
enriched
promote
development
thus
to
survival.
contrast,
showed
significant
increases
probiotics
genera
resist
development.
Altogether,
this
study
provides
first
evidence
microbiome
carries
can
help
design
approaches
for
clinically
evaluating
Journal of Clinical Laboratory Analysis,
Journal Year:
2022,
Volume and Issue:
36(5)
Published: March 21, 2022
Certain
"star
intestinal
bacteria"
have
been
found
to
act
as
a
contributor
the
development
of
colorectal
cancer
(CRC).
Besides,
given
that
gut
microbiome
can
be
detected
in
diverse
range
samples
(stool,
tissue,
blood,
etc),
it
is
categorized
into
fecal
microbiome,
blood
and
tissue
microbiome.To
provide
an
overview
recent
research
progress,
this
review
summarizes
characteristics
different
at
each
stage
CRC
their
screening
efficiency.The
models
constructed
from
sample
microbiomes
(healthy/colorectal
adenoma,
healthy/CRC,
adenoma/CRC)
both
strengths
constraints
terms
biomarker
reproducibility
area
under
receiver-operating
characteristic
curve
(AUC)
models.
Many
bacteria,
such
Bifidobacteria,
Fusobacterium
nucleatum
(F.
n),
Geotrichum
candidum,
Porphyromonas
asaccharolytica,
Escherichia
coli,
Rhodococcus,
Anaerostipes
caccae,
Enhydrobacter,
Lachnoclostridiumsp.
m3,
Bacteroides
clarus,
Clostridium
hathewayi,
Ruminococcaceae,
thetaiotaomicron,
Culinariside,
enterotoxigenic
fragilis
(ETBF),
show
favorable
diagnostic
efficacy
early
cancer.This
highlights
stool,
bowel
fluid
are
main
sources
for
biomarkers,
with
its
own
advantages
limitations.
Moreover,
other
extracellular
vesicles
biofilms
also
should
deserved
further
attention.
Frontiers in Cellular and Infection Microbiology,
Journal Year:
2022,
Volume and Issue:
11
Published: Jan. 17, 2022
Colorectal
cancer
(CRC)
is
one
of
the
most
prevalent
and
deadly
forms
in
Western
countries.
Inflammation
a
well-known
driver
colonic
carcinogenesis;
however,
its
role
CRC
extends
beyond
colitis-associated
cancer.
Over
last
decades,
numerous
associations
between
intestinal
dysbiosis
have
been
identified,
with
more
recent
studies
providing
mechanistic
evidence
causative
relationship.
Nonetheless,
much
remains
to
be
discovered
regarding
precise
implications
microbiome
alterations
pathogenesis
CRC.
Research
confirms
importance
bidirectional
crosstalk
gut
mucosal
immune
system
which
inflammasomes,
multiprotein
complexes
that
can
sense
"danger
signals,"
serve
as
conduits
by
detecting
microbial
signals
activating
innate
responses,
including
induction
microbicidal
activities
alter
composition.
Current
strongly
supports
an
active
for
this
"inflammasome-microbiome
axis"
initiation
development
Furthermore,
gasdermin
(GSDM)
family
proteins,
are
downstream
effectors
inflammasome
primarily
known
their
pyroptosis,
recently
linked
pathogenesis.
These
findings,
do
not
come
without
controversy,
pyroptosis
reported
exert
both
anti-
protumorigenic
functions.
multi-faceted
interactions
GSDMs
microbiome,
well
CRC,
only
superficially
investigated.
In
review,
we
summarize
existing
literature
supporting
inflammasome-microbiota
axis,
activation
function
GSDMs,
gain
better
understanding