ACS Nano,
Journal Year:
2023,
Volume and Issue:
17(12), P. 11466 - 11480
Published: May 18, 2023
Intratumoral
pathogens
can
contribute
to
cancer
progression
and
affect
therapeutic
response.
Fusobacterium
nucleatum,
a
core
pathogen
of
colorectal
(CRC),
is
an
important
cause
low
efficacy
metastasis.
Thus,
the
modulation
intratumoral
may
provide
target
for
therapy
metastasis
inhibition.
Herein,
we
propose
F.
nucleatum-modulating
strategy
enhancing
CRC
inhibiting
lung
by
designing
antibacterial
nanoplatform
(Au@BSA-CuPpIX),
which
produced
reactive
oxygen
species
(ROS)
under
ultrasound
exhibited
strong
activity.
Importantly,
Au@BSA-CuPpIX
reduced
levels
apoptosis-inhibiting
proteins
thereby
ROS-induced
apoptosis.
In
vivo
results
demonstrated
that
effectively
eliminated
nucleatum
enhance
sonodynamic
(SDT)
orthotopic
inhibit
Notably,
entrapped
gold
nanoparticles
phototoxicity
metalloporphyrin
accumulated
in
skin
during
tumor
treatment,
preventing
severe
inflammation
damage
skin.
Therefore,
this
study
proposes
elimination
effect
SDT,
thus
providing
promising
paradigm
improving
treatment
with
fewer
toxic
side
effects
promoting
clinical
translational
potential
SDT.
Advanced Science,
Journal Year:
2023,
Volume and Issue:
10(23)
Published: June 1, 2023
Colorectal
cancer
(CRC)
is
the
most
common
of
digestive
system
with
high
mortality
and
morbidity
rates.
Gut
microbiota
found
in
intestines,
especially
colorectum,
has
structured
crosstalk
interactions
host
that
affect
several
physiological
processes.
The
gut
include
CRC-promoting
bacterial
species,
such
as
Fusobacterium
nucleatum,
Escherichia
coli,
Bacteroides
fragilis,
CRC-protecting
Clostridium
butyricum,
Streptococcus
thermophilus,
Lacticaseibacillus
paracasei,
which
along
other
microorganisms,
viruses
fungi,
play
critical
roles
development
CRC.
Different
features
are
identified
patients
early-onset
CRC,
combined
different
patterns
between
fecal
intratumoral
microbiota.
may
be
beneficial
diagnosis
treatment
CRC;
some
bacteria
serve
biomarkers
while
others
regulators
chemotherapy
immunotherapy.
Furthermore,
metabolites
produced
by
essential
CRC
cells.
Harmful
primary
bile
acids
short-chain
fatty
acids,
whereas
others,
including
ursodeoxycholic
acid
butyrate,
impede
tumor
progression.
This
review
focuses
on
its
metabolites,
their
potential
development,
diagnosis,
Advanced Science,
Journal Year:
2023,
Volume and Issue:
10(15)
Published: March 23, 2023
Abstract
Gut
microbiota‐derived
metabolites
are
key
hubs
connecting
the
gut
microbiome
and
cancer
progression,
primarily
by
remodeling
tumor
microenvironment
regulating
signaling
pathways
in
cells
multiple
immune
cells.
The
use
of
microbial
radiotherapy
chemotherapy
mitigates
severe
side
effects
from
treatment
improves
efficacy
treatment.
Immunotherapy
combined
with
effectively
activates
system
to
kill
tumors
overcomes
drug
resistance.
Consequently,
various
novel
strategies
have
been
developed
modulate
metabolites.
Manipulation
genes
involved
metabolism
using
synthetic
biology
approaches
directly
affects
levels
metabolites,
while
fecal
transplantation
phage
affect
altering
composition
microbiome.
However,
some
harbor
paradoxical
functions
depending
on
context
(e.g.,
type
cancer).
Furthermore,
metabolic
microorganisms
certain
anticancer
drugs
such
as
irinotecan
gemcitabine,
render
ineffective
or
exacerbate
their
adverse
effects.
Therefore,
a
personalized
comprehensive
consideration
patient's
condition
is
required
when
employing
treat
cancer.
purpose
this
review
summarize
correlation
between
cancer,
provide
fresh
ideas
for
future
scientific
research.
Annual Review of Pathology Mechanisms of Disease,
Journal Year:
2022,
Volume and Issue:
18(1), P. 467 - 492
Published: Nov. 2, 2022
Reprogrammed
metabolism
is
a
hallmark
of
colorectal
cancer
(CRC).
CRC
cells
are
geared
toward
rapid
proliferation,
requiring
nutrients
and
the
removal
cellular
waste
in
nutrient-poor
environments.
Intestinal
stem
(ISCs),
primary
cell
origin
for
CRCs,
must
adapt
their
along
adenoma-carcinoma
sequence
to
unique
features
complex
microenvironment
that
include
interactions
with
intestinal
epithelial
cells,
immune
stromal
commensal
microbes,
dietary
components.
Emerging
evidence
implicates
modifiable
risk
factors
related
environment,
such
as
diet,
important
pathogenesis.
Here,
we
focus
on
describing
ISCs,
diets
influence
initiation,
genetics
metabolism,
tumor
microenvironment.
The
mechanistic
links
between
environmental
factors,
metabolic
adaptations,
enhancing
or
supporting
tumorigenesis
becoming
better
understood.
Thus,
greater
knowledge
holds
promise
improved
prevention
treatment.
Nature Microbiology,
Journal Year:
2023,
Volume and Issue:
8(5), P. 919 - 933
Published: April 17, 2023
Epidemiological
studies
have
indicated
an
association
between
statin
use
and
reduced
incidence
of
colorectal
cancer
(CRC),
work
in
preclinical
models
has
demonstrated
a
potential
chemopreventive
effect.
Statins
are
also
associated
with
dysbiosis
the
gut
microbiome,
yet
role
microbiome
protective
effect
statins
CRC
is
unclear.
Here
we
validated
by
retrospectively
analysing
cohort
patients
who
underwent
colonoscopies.
This
was
confirmed
patient
cohorts,
found
that
tumour
burden
partly
due
to
modulation
microbiota.
Specifically,
commensal
Lactobacillus
reuteri
increased
as
result
microbial
tryptophan
availability
after
atorvastatin
treatment.
Our
vivo
further
revealed
L.
administration
suppressed
tumorigenesis
via
catabolite,
indole-3-lactic
acid
(ILA).
ILA
exerted
anti-tumorigenic
effects
downregulating
IL-17
signalling
pathway.
metabolite
inhibited
T
helper
17
cell
differentiation
targeting
nuclear
receptor,
RAR-related
orphan
receptor
γt
(RORγt).
Together,
our
study
provides
insights
into
anti-cancer
mechanism
driven
suggests
interventions
or
could
complement
chemoprevention
strategies
for
CRC.
Probiotics and Antimicrobial Proteins,
Journal Year:
2023,
Volume and Issue:
15(6), P. 1626 - 1643
Published: Feb. 10, 2023
With
the
emphasis
on
intestinal
health,
probiotics
have
exploded
into
a
vast
market
potential.
However,
new
scientific
evidence
points
out
that
beneficial
health
benefits
of
are
not
necessarily
directly
related
to
viable
bacteria.
metabolites
or
bacterial
components
live
bacteria
driving
force
behind
promotion.
Therefore,
scientists
gradually
noticed
effects
based
itself,
metabolites,
cell
lysates,
and
these
factors
officially
named
"postbiotics"
by
ISAPP.
Postbiotic
diverse
outperform
in
terms
technology,
safety,
cost
due
their
good
absorption,
metabolism,
organismal
distribution.
Postbiotics
been
shown
bioactivities
such
as
antimicrobial,
antioxidant,
anti-inflammatory,
anti-proliferative,
immunomodulation.
Moreover,
numerous
studies
revealed
significant
potential
postbiotics
for
disease
treatment.
This
paper
first
presents
production
classification
with
examples
from
lactic
acid
(LAB),
followed
mechanisms
action
most
recent
pre-clinical
clinical
wide
range
non-clinical
applications
postbiotics.
Furthermore,
current
future
prospects
postbiotic
commercial
available
products
discussed.
Finally,
we
comment
knowledge
gaps
several
examples.
Biomedicines,
Journal Year:
2023,
Volume and Issue:
11(5), P. 1388 - 1388
Published: May 8, 2023
The
human
gastrointestinal
tract
is
home
to
a
complex
microbial
community
that
plays
an
important
role
in
the
general
well-being
of
entire
organism.
gut
microbiota
generates
variety
metabolites
and
thereby
regulates
many
biological
processes,
such
as
regulation
immune
system.
In
gut,
bacteria
are
direct
contact
with
host.
major
challenge
here
prevent
unwanted
inflammatory
reactions
on
one
hand
other
ensure
system
can
be
activated
when
pathogens
invade.
Here
REDOX
equilibrium
utmost
importance.
This
controlled
by
either
directly
or
indirectly
via
bacterial-derived
metabolites.
A
balanced
microbiome
sorts
for
stable
balance,
whereas
dysbiosis
destabilizes
this
equilibrium.
An
imbalanced
status
affects
disrupting
intracellular
signaling
promoting
responses.
we
(i)
focus
most
common
reactive
oxygen
species
(ROS)
(ii)
define
transition
from
state
oxidative
stress.
Further,
(iii)
describe
ROS
regulating
Thereafter,
(iv)
examine
influence
homeostasis
how
shifts
pro-
anti-oxidative
cellular
conditions
suppress
promote
responses
inflammation.
Cancers,
Journal Year:
2023,
Volume and Issue:
15(3), P. 866 - 866
Published: Jan. 30, 2023
Colorectal
cancer
(CRC)
is
the
second-leading
cause
of
cancer-related
deaths
worldwide.
While
CRC
thought
to
be
an
interplay
between
genetic
and
environmental
factors,
several
lines
evidence
suggest
involvement
gut
microbiota
in
promoting
inflammation
tumor
progression.
Gut
refer
~40
trillion
microorganisms
that
inhabit
human
gut.
Advances
next-generation
sequencing
technologies
metagenomics
have
provided
new
insights
into
microbial
ecology
helped
linking
CRC.
Many
studies
carried
out
humans
animal
models
emphasized
role
certain
bacteria,
such
as
Fusobacterium
nucleatum,
enterotoxigenic
Bacteroides
fragilis,
colibactin-producing
Escherichia
coli,
onset
progression
Metagenomic
opened
up
avenues
for
application
diagnosis,
prevention,
treatment
This
review
article
summarizes
development
its
use
a
biomarker
predict
disease
potential
therapeutic
applications.
BMEMat,
Journal Year:
2023,
Volume and Issue:
1(1)
Published: Feb. 16, 2023
Abstract
Chemodynamic
therapy
(CDT)
utilizes
Fenton
and/or
Fenton‐like
reactions
in
the
tumor
microenvironment
(TME)
to
produce
cytotoxic
reactive
oxygen
species
(ROS,
mainly
hydroxyl
radicals,
•OH)
for
inducing
cancer
cell
death.
Since
CDT
exhibits
minimal
invasiveness
and
high
specificity
by
responding
TME
(overexpressed
hydrogen
peroxide
(H
2
O
)
glutathione
(GSH)
generation),
a
lot
of
related
research
has
been
conducted
recently.
Photo‐facilitated
can
further
enhance
catalytic
activity
controllability
treatment.
In
addition,
other
photo‐induced
therapies,
including
photodynamic
photothermal
(PDT,
PTT),
may
synergize
with
obtain
boosting
treatment
efficacy
avoid
multidrug
resistance.
this
minireview,
we
summarize
recent
advances
photo‐assisted
CDT,
PTT‐facilitated
PDT‐facilitated
CDT.
More
importantly,
challenges
encountered
process
are
discussed
potential
development
directions
suggested
facilitate
clinical
translation
future.