Nanomedicine,
Journal Year:
2024,
Volume and Issue:
20(3), P. 305 - 318
Published: Dec. 30, 2024
Colorectal
cancer
(CRC)
is
a
significant
threat
to
human
health.
The
dynamic
equilibrium
between
probiotics
and
pathogenic
bacteria
within
the
gut
microbiota
crucial
in
mitigating
risk
of
CRC.
An
overgrowth
harmful
microorganisms
gastrointestinal
tract
can
result
an
excessive
accumulation
bacterial
toxins
carcinogenic
metabolites,
thereby
disrupting
delicate
balance
microbiota.
This
disruption
may
lead
alterations
microbial
composition,
impairment
mucosal
barrier
function,
potential
promotion
abnormal
cell
proliferation,
ultimately
contribute
progression
Recently,
research
has
indicated
that
intestinal
presence
Fusobacterium
nucleatum
(Fn)
significantly
influences
onset,
progression,
metastasis
Consequently,
interaction
CRC
cells
Fn
presents
promising
strategy
against
Nanomaterials
have
been
extensively
utilized
therapy
infection
control,
demonstrating
substantial
treating
bacteria-associated
tumors.
review
begins
by
elucidating
mechanisms
occurrence
CRC,
with
particular
emphasis
on
clarifying
intricate
relationship
Subsequently,
we
highlight
strategies
utilize
nanomaterials
disrupt
association
Overall,
this
offers
valuable
insight
guidance
for
leveraging
therapy.
Journal of Hematology & Oncology,
Journal Year:
2025,
Volume and Issue:
18(1)
Published: Jan. 13, 2025
The
tumor
microenvironment
(TME)
is
integral
to
cancer
progression,
impacting
metastasis
and
treatment
response.
It
consists
of
diverse
cell
types,
extracellular
matrix
components,
signaling
molecules
that
interact
promote
growth
therapeutic
resistance.
Elucidating
the
intricate
interactions
between
cells
TME
crucial
in
understanding
progression
challenges.
A
critical
process
induced
by
epithelial-mesenchymal
transition
(EMT),
wherein
epithelial
acquire
mesenchymal
traits,
which
enhance
their
motility
invasiveness
progression.
By
targeting
various
components
TME,
novel
investigational
strategies
aim
disrupt
TME's
contribution
EMT,
thereby
improving
efficacy,
addressing
resistance,
offering
a
nuanced
approach
therapy.
This
review
scrutinizes
key
players
emphasizing
avenues
therapeutically
components.
Moreover,
article
discusses
implications
for
resistance
mechanisms
highlights
current
toward
modulation
along
with
potential
caveats.
Biomedicines,
Journal Year:
2025,
Volume and Issue:
13(2), P. 422 - 422
Published: Feb. 10, 2025
The
intricate
relationship
between
anticancer
drugs
and
the
gut
microbiome
influences
cancer
treatment
outcomes.
This
review
paper
focuses
on
role
of
integrity
in
enhancing
efficacy
safety
drug
therapy,
emphasizing
pharmacokinetic
interactions
microbiota.
It
explores
how
disruptions
to
composition,
or
dysbiosis,
can
alter
metabolism,
immune
responses,
side
effects.
By
examining
mechanisms
disruption
caused
by
drugs,
this
highlights
specific
case
studies
like
cyclophosphamide,
5-fluorouracil,
irinotecan,
their
impact
microbial
diversity
clinical
also
discusses
microbiome-targeted
strategies,
including
prebiotics,
probiotics,
postbiotics,
fecal
microbiota
transplantation
(FMT),
as
promising
interventions
enhance
treatment.
Furthermore,
potential
profiling
personalizing
therapy
integrating
these
into
practice
is
explored.
Finally,
proposes
future
research
directions,
developing
novel
biomarkers
a
deeper
comprehension
drug-microbiome
interactions,
respond
current
gaps
knowledge
improve
patient
outcomes
care.
Abstract
Gliomas
are
the
most
common
primary
tumors
of
central
nervous
system,
with
glioblastoma
multiforme
(GBM)
having
highest
incidence,
and
their
therapeutic
efficacy
depends
primarily
on
extent
surgical
resection
postoperative
chemotherapy.
The
role
intracranial
blood–brain
barrier
occurrence
drug‐resistant
gene
O6‐methylguanine‐DNA
methyltransferase
have
greatly
limited
chemotherapeutic
agents
in
patients
GBM
made
it
difficult
to
achieve
expected
clinical
response.
In
recent
years,
rapid
development
nanotechnology
has
brought
new
hope
for
treatment
tumors.
Nanoparticles
(NPs)
shown
great
potential
tumor
therapy
due
unique
properties
such
as
light,
heat,
electromagnetic
effects,
passive
targeting.
Furthermore,
NPs
can
effectively
load
drugs,
significantly
reduce
side
effects
improve
efficacy,
showing
chemotherapy
glioma.
this
article,
we
reviewed
mechanisms
glioma
drug
resistance,
physicochemical
NPs,
advances
resistance.
We
aimed
provide
perspectives
Biomedicines,
Journal Year:
2025,
Volume and Issue:
13(1), P. 100 - 100
Published: Jan. 3, 2025
The
gut
microbiota,
a
dynamic
ecosystem
of
trillions
microorganisms,
produces
secondary
metabolites
that
profoundly
influence
host
health.
Recent
research
has
highlighted
the
significant
role
these
metabolites,
particularly
short-chain
fatty
acids,
indoles,
and
bile
in
modulating
immune
responses,
impacting
epigenetic
mechanisms,
contributing
to
disease
processes.
In
gastrointestinal
(GI)
cancers
such
as
colorectal,
liver,
gastric
cancer,
microbial
can
drive
tumorigenesis
by
promoting
inflammation,
DNA
damage,
evasion.
Conversely,
same
hold
therapeutic
promise,
potentially
enhancing
responses
chemotherapy
immunotherapy
even
directly
suppressing
tumor
growth.
addition,
play
crucial
roles
infectious
susceptibility
resilience,
mediating
pathways
impact
pathogen
resistance.
By
consolidating
recent
insights
into
microbiota's
shaping
health,
this
review
underscores
potential
targeting
microbiome-derived
for
treating
GI
diseases
calls
further
microbiome-based
interventions.
Pharmacological Research,
Journal Year:
2024,
Volume and Issue:
206, P. 107278 - 107278
Published: June 20, 2024
Accumulating
evidence
has
proved
the
close
association
between
alterations
in
gut
microbiota
and
resistance
to
chemotherapeutic
drugs.
However,
potential
roles
of
regulating
oxaliplatin
sensitivity
gastric
cancer
(GC)
have
not
been
investigated
before.
We
first
found
that
antibiotic
treatment
diminished
therapeutic
efficacy
a
GC
mouse
model.
Importantly,
this
effect
could
be
transmitted
germ-free
mice
via
fecal
transplantation,
indicating
role
modulation
efficacy.
Further,
metagenomics
data
showed
Akkermansia
muciniphila
(A.
muciniphila)
ranked
among
bacterial
species
with
decreased
relative
abundances
after
treatment.
Metabolically
active
A.
promotes
As
shown
by
metabolomics
analysis,
metabolic
pattern
was
disrupted
significantly
downregulated
levels
pentadecanoic
acid
(PEA),
use
PEA
promoted
Mechanistically,
FUBP1
positively
regulated
aerobic
glycolysis
cells
hinder
oxaliplatin.
muciniphila-derived
functioned
as
an
inhibitory
factor
directly
antagonizing
activity
FUBP1,
which
potentiated
responses
Our
research
suggested
key
for
intestinal
its
metabolite
promoting
efficacy,
thus
providing
new
perspective
probiotic
prebiotic
intervention
patients
during
chemotherapy.
EMBO Molecular Medicine,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 16, 2025
Abstract
The
gut
microbiome,
or
the
community
of
microorganisms
residing
in
gastrointestinal
tract,
has
emerged
as
an
important
factor
breast
cancer
etiology
and
treatment.
Specifically,
impact
bacterial
populations
on
therapeutic
outcomes
is
emerging
area
research.
microbiota’s
role
modifying
pharmacokinetics
chemotherapy
endocrine-targeting
therapies
can
alter
drug
efficacy
toxicity
profiles.
In
addition,
microbiome’s
capacity
to
regulate
systemic
inflammation
immune
responses
may
influence
effectiveness
both
conventional
immunotherapeutic
strategies
for
treatment
cancer.
Overall,
while
bidirectional
interactions
between
microbiome
are
still
being
studied,
its
increasingly
recognized.
Future
research
provide
more
definitive
insights
help
develop
personalized
harness
improve
outcomes.
World Journal of Experimental Medicine,
Journal Year:
2025,
Volume and Issue:
15(2)
Published: April 11, 2025
The
gut
microbiome,
a
complex
ecosystem
of
microorganisms,
has
significant
role
in
modulating
pain,
particularly
within
orthopaedic
conditions.
Its
impact
on
immune
and
neurological
functions
is
underscored
by
the
gut-brain
axis,
which
influences
inflammation,
pain
perception,
systemic
responses.
This
integrative
review
examines
current
research
how
dysbiosis
associated
with
various
pathways,
notably
nociceptive
neuroinflammatory
mechanisms
linked
to
central
sensitization.
We
highlight
advancements
meta-omics
technologies,
such
as
metagenomics
metaproteomics,
deepen
our
understanding
microbiome-host
interactions
their
implications
pain.
Recent
studies
emphasize
that
gut-derived
short-chain
fatty
acids
microbial
metabolites
play
roles
neuroinflammation
nociception,
contributing
management.
Probiotics,
prebiotics,
synbiotics,
faecal
microbiome
transplants
are
explored
potential
therapeutic
strategies
alleviate
through
modulation,
offering
an
adjunct
or
alternative
opioids.
However,
variability
individual
microbiomes
poses
challenges
standardizing
these
treatments,
necessitating
further
rigorous
clinical
trials.
A
multidisciplinary
approach
combining
microbiology,
immunology,
neurology,
orthopaedics
essential
develop
innovative,
personalized
management
rooted
health,
transform
care.
Discover Oncology,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Feb. 26, 2025
A
growing
body
of
research
indicates
that
a
wide
range
cancer
types
may
correlate
with
human
microbiome
components.
On
the
other
hand,
little
is
known
about
potential
contribution
oral
microbiota
to
cancer.
However,
some
components
can
stimulate
different
tumorigenic
processes
associated
development
In
this
line,
two
prevalent
infections,
Porphyromonas
gingivalis,
and
Fusobacterium
nucleatum
increase
tumor
growth.
The
impact
course
illness
through
direct
interactions
major
modifications
toxicity
responsiveness
kinds
therapy.
Recent
has
demonstrated
relationship
between
specific
phylogenetic
groupings
results
immunotherapy
treatment
for
particular
types.
Conversely,
there
been
recent
upsurge
in
interest
possibility
using
microbes
treat
At
moment,
species,
such
as
Salmonella
typhimurium
Clostridium
spp.,
are
being
explored
possible
vectors.
Thus,
understanding
these
microbial
highlights
importance
maintaining
healthy
preventing
cancers.
From
perspective,
review
will
discuss
role
on
cancers
their
application
treatment/improvement.