Molecules,
Год журнала:
2024,
Номер
29(13), С. 3073 - 3073
Опубликована: Июнь 27, 2024
The
microbiome
is
capable
of
modulating
the
bioavailability
chemotherapy
drugs,
mainly
due
to
metabolizing
these
agents.
Multiple
cytostatic
bacterial
metabolites
were
recently
identified
that
have
effects
on
cancer
cells.
In
this
study,
we
addressed
question
whether
a
set
(cadaverine,
indolepropionic
acid
and
indoxylsulfate)
can
interfere
with
agents
used
in
management
breast
(doxorubicin,
gemcitabine,
irinotecan,
methotrexate,
rucaparib,
5-fluorouracil
paclitaxel).
drugs
applied
wide
concentration
range
which
metabolite
was
added
within
its
serum
reference
range,
cell
proliferation
assessed.
There
no
interference
between
methotrexate
or
rucaparib
metabolites.
Nevertheless,
cadaverine
modulated
Hill
coefficient
inhibitory
curve
doxorubicin
5-fluorouracil.
Changes
implicate
alterations
kinetics
binding
their
targets.
These
an
unpredictable
significance
from
clinical
pharmacological
perspective.
Importantly,
decreased
IC50
value
paclitaxel,
potentially
advantageous
combination.
Cellular and Molecular Life Sciences,
Год журнала:
2022,
Номер
79(5)
Опубликована: Апрель 16, 2022
Abstract
Bile
acids
are
soluble
derivatives
of
cholesterol
produced
in
the
liver
that
subsequently
undergo
bacterial
transformation
yielding
a
diverse
array
metabolites.
The
bulk
bile
acid
synthesis
takes
place
primary
acids;
however,
other
tissues
have
also
capacity
to
generate
(e.g.
ovaries).
Hepatic
then
transported
and
released
into
intestines.
In
large
intestine,
fraction
is
converted
secondary
by
gut
bacteria.
majority
intestinal
reuptake
return
liver.
A
small
remains
circulation
exert
receptor-mediated
pure
chemical
effects
acidic
oesophageal
cancer)
on
cancer
cells.
this
review,
we
assess
how
changes
biosynthesis,
flux
local
concentration
modulate
behavior
different
cancers.
Here,
present
in-depth
involvement
oesophageal,
gastric,
hepatocellular,
pancreatic,
colorectal,
breast,
prostate,
ovarian
cancer.
Previous
studies
often
used
supraphysiological
concentration,
sometimes
concentrations
1000
times
higher
than
highest
reported
tissue
or
serum
likely
eliciting
unspecific
effects,
practice
advocate
against
review.
Furthermore,
show
that,
although
were
classically
considered
as
pro-carcinogenic
agents
cancer),
dogma
switch,
lower
correspond
their
reference
possess
anticancer
activity
subset
Differences
response
cancers
lie
differential
expression
receptors
between
FXR
vs.
TGR5).
UDCA,
sold
generic
medication
cholestasis
biliary
surge,
its
conjugates
identified
with
almost
purely
features
suggesting
possibility
for
drug
repurposing.
Taken
together,
tumor
inducers
promoter
molecules;
nevertheless,
certain
cancers,
like
breast
cancer,
may
act
suppressors
Janus-faced
nature
carcinogenesis.
Regardless
of
the
global
progress
in
early
diagnosis
and
novel
therapeutic
regimens,
breast
carcinoma
poses
a
devastating
threat,
advances
are
somewhat
marred
by
high
mortality
rates.
Breast
cancer
risk
prediction
models
based
on
known
factors
extremely
useful,
but
large
number
cancers
develop
women
with
no/low
risk.
The
gut
microbiome
exerts
profound
impact
host
health
physiology
has
emerged
as
pivotal
frontier
pathogenesis.
Progress
metagenomic
analysis
enabled
identification
specific
changes
microbial
signature.
In
this
review,
we
discuss
metabolomic
associated
initiation
metastatic
progression.
We
summarize
bidirectional
various
cancer-related
therapies
microbiota
vice-versa.
Finally,
strategies
to
modulate
toward
more
favorable
state
that
confers
anticancer
effects.
Polish Journal of Microbiology,
Год журнала:
2022,
Номер
71(2), С. 217 - 226
Опубликована: Май 31, 2022
Breast
cancer
(BC)
and
benign
breast
lesions
(BBLs)
are
common
diseases
in
women
worldwide.
The
gut
microbiota
plays
a
vital
role
regulating
diseases'
formation,
progression,
therapy
response.
Hence,
we
explored
the
structure
function
of
microflora
patients
with
BC
BBLs.
A
cohort
66
subjects
was
enrolled
study.
Twenty-six
had
BC,
20
BBLs,
matched
healthy
controls.
High
throughput
16S
ribosomal
RNA
(16S
rRNA)
gene
sequencing
technology
used
to
determine
microbial
community
structure.
Compared
individuals,
significantly
lower
alpha
diversity
indices
(Sobs
index,
p
=
0.019;
Chao1
0.033).
Sobs
were
also
BBLs
than
without
statistical
significance
(p
0.279,
0.314,
respectively).
Both
unweighted
weighted
UniFrac
analysis
showed
that
beta
differed
among
three
groups
3.376e-14,
<
0.001,
levels
Porphyromonas
Peptoniphilus
higher
0.004,
0.007,
respectively),
whereas
Escherichia
Lactobacillus
more
enriched
lesion
group
0.011,
Our
study
indicates
may
undergo
significant
changes
intestinal
microbiota.
These
findings
can
help
elucidate
flora
patients.
Abstract
Breast
cancer
is
a
significant
and
deadly
threat
to
women
globally.
Moreover,
metastasis
complicated
process
involving
multiple
biological
stages,
which
considered
substantial
cause
of
death,
where
cells
spread
from
the
original
tumor
other
organs
in
body—representing
primary
mortality
factor.
Circulating
(CTCs)
are
detached
or
metastatic
enter
bloodstream,
allowing
them
establish
new
sites.
CTCs
can
travel
alone
groups
called
CTC
clusters.
Studies
have
shown
that
clusters
more
potential
for
poorer
prognosis
than
individual
breast
patients.
However,
our
understanding
clusters'
formation,
structure,
function,
detection
still
limited.
This
review
summarizes
current
knowledge
properties,
isolation,
prognostic
significance
cancer.
It
also
highlights
challenges
future
directions
research
clinical
application
Frontiers in Immunology,
Год журнала:
2022,
Номер
13
Опубликована: Ноя. 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.
Cell Reports,
Год журнала:
2025,
Номер
44(3), С. 115358 - 115358
Опубликована: Март 1, 2025
SummaryThe
human
microbiome,
an
intricate
ecosystem
of
trillions
microbes
residing
across
various
body
sites,
significantly
influences
cancer,
a
leading
cause
morbidity
and
mortality
worldwide.
Recent
studies
have
illuminated
the
microbiome's
pivotal
role
in
cancer
development,
either
through
direct
cellular
interactions
or
by
secreting
bioactive
compounds
such
as
metabolites.
Microbial
metabolites
contribute
to
initiation
mechanisms
DNA
damage,
epithelial
barrier
dysfunction,
chronic
inflammation.
Furthermore,
microbial
exert
dual
roles
on
progression
response
therapy
modulating
metabolism,
gene
expression,
signaling
pathways.
Understanding
these
complex
is
vital
for
devising
new
therapeutic
strategies.
This
review
highlights
promising
targets
prevention
treatment,
emphasizing
their
impact
responses
underscoring
need
further
research
into
metastasis
resistance.
Frontiers in Microbiology,
Год журнала:
2023,
Номер
14
Опубликована: Авг. 23, 2023
Observational
epidemiological
studies
suggested
an
association
between
the
gut
microbiota
and
breast
cancer,
but
it
remains
unclear
whether
causally
influences
risk
of
cancer.
We
employed
two-sample
Mendelian
randomization
(MR)
analysis
to
investigate
this
association.We
used
summary
statistics
microbiome
from
a
genome-wide
study
(GWAS)
18,340
individuals
in
MiBioGen
study.
GWAS
for
overall
cancer
hormone
receptor
subtype-specific
analyses
were
obtained
UK
Biobank
FinnGen
databases,
totaling
400,000
individuals.
The
inverse
variance-weighted
(IVW)
MR
method
was
examine
causal
relationship
its
subtypes.
Sensitivity
conducted
using
maximum
likelihood,
MR-Egger,
pleiotropic
residual
sums
outliers
methods.The
IVW
estimates
indicated
that
increased
abundance
Genus_Sellimonas
is
associated
with
ER+
[odds
ratio
(OR)
=
1.09,
p
1.72E-04,
false
discovery
rate
(FDR)
0.02],
whereas
Genus_Adlercreutzia
protective
against
(OR
0.88,
6.62E-04,
FDR
0.04).
For
Her2+
Genus_Ruminococcus2
decreased
0.77,
4.91E-04,
0.04),
Genus_Erysipelatoclostridium
1.25,
6.58E-04,
No
evidence
heterogeneity
or
horizontal
pleiotropy
found.Our
revealed
microbiota-mammary
axis,
providing
important
data
supporting
potential
use
as
candidate
target
prevention,
diagnosis,
treatment.
International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(24), С. 17199 - 17199
Опубликована: Дек. 6, 2023
Cancer
cell
dissemination
involves
invasion,
migration,
resistance
to
stressors
in
the
circulation,
extravasation,
colonization,
and
other
functions
responsible
for
macroscopic
metastases.
By
enhancing
invasiveness,
motility,
intravasation,
epithelial-to-mesenchymal
transition
(EMT)
process
promotes
generation
of
circulating
tumor
cells
their
collective
migration.
Preclinical
clinical
studies
have
documented
intensive
crosstalk
between
gut
microbiome,
host
organism,
immune
system.
According
findings,
polymorphic
microbes
might
play
diverse
roles
tumorigenesis,
cancer
progression,
therapy
response.
Microbial
imbalances
changes
levels
bacterial
metabolites
toxins
promote
progression
via
EMT
angiogenesis.
In
contrast,
a
favorable
microbial
composition,
together
with
microbiota-derived
metabolites,
such
as
short-chain
fatty
acids
(SCFAs),
can
attenuate
processes
initiation,
disease
formation
distant
this
review,
we
highlight
role
intratumoral
microbiomes
metastatic
ability
outline
potential
options
microbiota
modulation.
As
shown
murine
models,
probiotics
inhibited
development,
reduced
volume,
suppressed
angiogenesis
metastasis.
Moreover,
modulation
an
unfavorable
microbiome
improve
efficacy
reduce
treatment-related
toxicities,
bringing
benefit
patients
cancer.
GeroScience,
Год журнала:
2024,
Номер
46(5), С. 4037 - 4057
Опубликована: Июнь 26, 2024
Oncobiosis
has
emerged
as
a
key
contributor
to
the
development,
and
modulator
of
treatment
efficacy
cancer.
Hereby,
we
review
modalities
through
which
oncobiome
can
support
progression
tumors,
emerging
therapeutic
opportunities
they
present.
The
highlights
inherent
challenges
limitations
faced
in
sampling
accurately
characterizing
oncobiome.
Additionally,
underscores
critical
need
for
standardization
microbial
analysis
techniques
consistent
reporting
microbiome
data.
We
provide
suggested
metadata
set
that
should
accompany
datasets
from
oncological
settings
so
studies
remain
comparable
decipherable.