Abstract
The
gut
microbiota
is
pivotal
in
maintaining
health,
with
most
microorganisms
being
beneficial,
except
for
a
few
pathogens.
Emerging
evidence
suggests
link
between
the
microbiome
and
aging,
hinting
at
its
potential
role
longevity.
However,
understanding
relationship
challenging
due
to
microbiota's
complexity.
This
perspective
summarizes
mechanisms
by
which
microbes
regulate
host
lifespan
explores
genetic
manipulation
strategies
promote
healthy
aging
elderly.
Abstract
Consumption
of
dietary
fiber
and
anthocyanin
has
been
linked
to
a
lower
incidence
colorectal
cancer
(CRC).
This
study
scrutinizes
the
potential
antitumorigenic
attributes
black
rice
diet
(BRD),
abundantly
rich
in
anthocyanin.
Our
results
demonstrate
notable
effects
mice
on
BRD,
indicated
by
reduction
both
size
number
intestinal
tumors
consequent
extension
life
span,
compared
control
diet‐fed
counterparts.
Furthermore,
fecal
transplants
from
BRD‐fed
germ‐free
led
decrease
colonic
cell
proliferation,
coupled
with
maintained
integrity
barrier.
The
BRD
was
associated
significant
shifts
gut
microbiota
composition,
specifically
an
augmentation
probiotic
strains
Bacteroides
uniformis
Lactobacillus
.
Noteworthy
changes
metabolites
were
also
documented,
including
upregulation
indole‐3‐lactic
acid
indole.
These
have
identified
stimulate
aryl
hydrocarbon
receptor
pathway,
inhibiting
CRC
proliferation
tumorigenesis.
In
summary,
these
findings
propose
that
may
modulate
progression
fostering
protective
metabolite
profiles.
accentuates
health
advantages
whole‐grain
foods,
emphasizing
utility
promoting
health.
The
gut
microbiota
can
produce
a
variety
of
microbial-derived
metabolites
to
influence
tumor
development.
Tryptophan,
an
essential
amino
acid
in
the
human
body,
be
converted
by
microorganisms
via
indole
pathway
such
as
Indole-3-Lactic
Acid
(ILA),
Indole-3-Propionic
(IPA),
Indole
Acetic
(IAA)
and
Indole-3-Aldehyde
(IAld).
Recent
studies
have
shown
that
play
key
roles
progression,
they
used
adjuvant
regimens
for
immunotherapy
or
chemotherapy.
Here,
we
summarize
recent
findings
on
common
microbial
provide
review
mechanisms
different
microenvironment.
We
further
discuss
limitations
current
metabolite
research
future
possibilities.
It
is
expected
will
new
strategies
clinical
therapy.
First
introduced
in
2021,
MetOrigin
has
quickly
established
itself
as
a
powerful
web
server
to
distinguish
microbial
metabolites
and
identify
the
bacteria
responsible
for
specific
metabolic
processes.
Building
on
growing
understanding
of
interplay
between
microbiome
metabolome,
response
user
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2.0.
This
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incorporates
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Orthology
analysis
links
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genes
their
corresponding
bacteria;
(3)
Mediation
investigates
potential
causal
relationships
among
bacteria,
metabolites,
phenotypes,
highlighting
mediating
role
metabolites.
Additionally,
backend
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been
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(KEGG,
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210,732
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at
http://metorigin.met-bioinformatics.cn.
Research Square (Research Square),
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 7, 2025
Abstract
Background
Colorectal
cancer
(CRC)
is
the
third
most
prevalent
malignant
tumor
and
second
leading
cause
of
cancer-related
deaths
globally.
The
genus
Parabacteroides
an
important
component
gut
microbiota.
P.
distasonis
goldsteinii
are
reported
probiotics,
their
roles
in
CRC
have
been
investigated
related
studies.
However,
association
between
johnsonii
remains
unknown.
Methods
(10–42)
Lactococcus
formosensis
(22–2)
were
isolated
from
healthy
human
feces.
25
mice
that
demonstrated
normal
feeding
activity
randomly
assigned
to
four
groups
:
control
(NC
group),
model
(IC
(PJ
L.
(LO
group).
Colonic
tissues
IC,
PJ,
LO
colon
NC
group
then
collected
for
HE
staining
immunohistochemical
staining.
Fecal
samples
during
hyperproliferative
adenoma
phases
Metagenomic
sequencing
metabolite
analysis.
Results
intervention
reduced
number
slowed
growth
colonic
tumors,
improved
histological
scores,
decreased
microenvironmental
inflammation
levels.
composition
intestinal
flora
with
cancer,
increased
microbial
species
diversity,
maintained
microbiota
stability.
Furthermore,
abundance
Bifidobacterium
pseudolongum
Lactobacillus,
which
play
a
role
ameliorating
AOM/DSS-induced
dysbiosis.
affected
metabolic
pathways,
including
amino
sugar
degradation
galactose
metabolism,
sphingolipid
synthesis,
acid
polyphenol
synthesis
tryptophan
metabolism
pathway
as
primary
being
affected.
Conclusion
Our
study
profiled
administration
reduces
tumors
lower
staging
by
modulating
its
metabolites
at
early
stages.
Foods,
Год журнала:
2025,
Номер
14(10), С. 1816 - 1816
Опубликована: Май 20, 2025
Atopic
Dermatitis
(AD)
is
a
common
inflammatory
skin
disease
characterized
primarily
by
its
chronic
and
recurrent
nature.
This
has
significant
impact
on
productivity
human
longevity.
Dysbiosis
of
gut
flora
been
demonstrated
to
be
significantly
associated
with
the
progression
AD.
In
our
previous
research,
it
was
shown
that
Lactobacillus
rhamnosus
RL5-H3-005
(RL)
Pediococcus
acidilactici
RP-H3-006
(RP)
have
ability
reduce
risk
in
AD
mice
through
gut–mammary
axis.
Based
work,
this
study
aims
further
investigate
effects
kynurenine
(KYN),
metabolite
RL
RP,
induced
2,
4-dinitrofluorobenzene
(DNFB).
study,
we
found
supplementing
KYN
effectively
alleviates
pathological
symptoms
atopic
dermatitis
improves
levels
SCFAs
their
intestines.
Further
research
indicates
KYN’s
therapeutic
are
manifested
reduction
secretory
immunoglobulin
A
(sIgA),
E
(IgE),
interleukin-4
(IL-4),
IL-5,
IL-13,
thymic
stromal
lymphopoietin
(TSLP)
mice,
while
also
repairing
intestinal
barrier
function
mice.
Overall,
metabolites
probiotics
RP
can
regulate
potentially
improving
gut–skin
Research
indicates
that
abnormal
gut
microbiota
metabolism
is
linked
to
colorectal
cancer
(CRC)
progression,
but
the
role
of
microbiota-related
tryptophan
disruption
remains
unclear.
Using
metagenomic
sequencing
and
targeted
Trp
metabolomics,
our
research
identified
CRC
patients
had
indole-3-lactic
acid
(ILA)
levels,
which
were
related
tumor
malignancy.
Exogenous
ILA
administration
suppressed
development
in
AOM/DSS
induced
xenograft
mice
models.
Furthermore,
vitro
experiments
demonstrated
inhibits
cell
proliferation,
migration,
anti-apoptotic
capabilities.
Mechanistically,
appears
directly
occupy
phosphorylation
sites
STAT3,
leading
a
reduction
intracellular
phosphorylated
STAT3
(p-STAT3)
levels
inhibition
HK2
pathway,
thereby
downregulating
glucose
cells.
Notably,
this
independent
aryl
hydrocarbon
receptor
(AHR).
In
conclusion,
findings
demonstrate
alterations
among
can
influence
progression
reveal
novel
mechanism
through
exerts
its
inhibitory
effects
on
CRC.
These
offer
new
insights
into
identify
potential
clinical
therapeutic
targets.
Frontiers in Microbiology,
Год журнала:
2025,
Номер
16
Опубликована: Май 29, 2025
Background
and
objectives
Intermittent
fasting
is
an
emerging
dietary
approach,
but
its
specific
role
in
colorectal
cancer
(CRC)
not
yet
clear.
In
this
study,
we
investigated
the
relationship
between
intermittent
development
mice.
Methods
First,
APC
Min
/+
mouse
models
(a
spontaneous
model
of
cancer)
were
subjected
to
intervention
(2
days/week)
with
regular
monitoring
body
weight
changes.
Subsequently,
16S
rRNA
sequencing
untargeted
metabolomics
employed
analyze
alterations
fecal
microbial
community
structure
metabolic
profiles
following
intervention.
Tumor
was
quantitatively
assessed
by
enumerating
CRC
lesions
using
HE
staining,
while
histopathological
evaluation
performed
determine
degree
neoplastic
progression.
Concurrently,
western
blotting
conducted
examine
expression
levels
intestinal
barrier
function-related
proteins.
Finally,
vitro
validation
experiments,
including
colony
formation
assay
transwell
invasion
assay,
investigate
effects
key
metabolite
isovaleric
acid
on
proliferative
invasive
capacities
cells.
Results
significantly
reduced
tumor
incidence
approximately
50%
compared
control
group
(1.25
±
0.38
vs
2.50
tumors/mouse,
P
=
0.017)
markedly
attenuated
analysis
revealed
significant
enrichment
two
bacterial
genera,
Alistipes
(P
0.030)
Odoribacter
(
0.030),
along
a
reduction
<
0.05)
group.
Furthermore,
effectively
controlled
gain
improved
function
0.05).
experiments
further
demonstrated
that
directly
promoted
cell
proliferation
enhanced
their
capacity
Conclusion
suppresses
mice
through
gut
microbiota
related
metabolites.