Abstract
Amidst
the
escalating
cancer
cases
and
relentless
spread
of
multidrug‐resistant
microbes,
urgency
for
effective
medication
is
undeniable.
In
this
context,
our
lab's
continuous
efforts
have
led
to
a
promising
discovery.
We
conducted
an
extensive
study
on
series
new
heterocycles
with
indazolylthiazole
component,
which
holds
great
promise
as
antimicrobial
anticancer
drugs.
The
bioactivity
tests,
meticulous
methodology,
demonstrated
that
synthesized
compounds
possess
remarkable
antibacterial
activity
against
various
pathogenic
strains.
controlled
lab
setting,
we
observed
derivatives
9
,
11
12
effectively
induce
apoptosis
in
HCT‐166
Huh‐7
(liver
carcinoma)
cell
lines.
Among
these,
derivative
has
shown
highest
selectivity
(SI=14.54±1.2
16.51±1.4)
lowest
IC50
value.
These
also
exhibit
broad‐spectrum
activity.
been
computationally
confirmed
through
molecular
modeling
using
MOE
software
pharmacokinetic
studies.
Most
tested
significant
cytotoxic
tumor
lines,
high
safety
normal
human
cells,
thereby
paving
way
hopeful
future
drugs,
potential
applications
[specific_application_1]
[specific_application_2].
Nutrients,
Год журнала:
2025,
Номер
17(3), С. 529 - 529
Опубликована: Янв. 31, 2025
Fasting-feeding
timing
is
a
crucial
pattern
implicated
in
the
regulation
of
daily
circadian
rhythms.
The
interplay
between
sleep
and
meal
underscores
importance
maintaining
alignment
order
to
avoid
creating
metabolic
environment
conducive
carcinogenesis
following
molecular
systemic
disruption
performance
immune
function.
chronicity
such
condition
may
support
initiation
progression
cancer
through
variety
mechanisms,
including
increased
oxidative
stress,
suppression,
activation
proliferative
signaling
pathways.
This
review
aims
summarize
current
evidence
from
human
studies
provide
an
overview
potential
mechanisms
underscoring
role
chrononutrition
(including
time-restricted
eating)
on
risk.
Current
shows
that
morning
chronotype,
suggesting
physiological
rhythms
eating
timing,
associated
with
lower
risk
cancer.
Also,
early
prolonged
nighttime
fasting
were
also
suggests
chronotype
influences
cell
cycle
regulation,
modulation
pathways
inflammation,
gut
microbiota
fluctuations.
In
conclusion,
although
there
are
no
clear
guidelines
this
matter,
emerging
supports
hypothesis
time-related
(i.e.,
time/calorie-restricted
feeding
intermittent/periodic
fasting)
could
potentially
lead
reduced
Frontiers in Oncology,
Год журнала:
2025,
Номер
15
Опубликована: Янв. 30, 2025
Background
Glioblastoma
(GBM)
is
the
deadliest
form
of
brain
cancer,
impacting
both
adults
and
children,
marked
by
exceptionally
high
morbidity
mortality
rates,
even
with
current
standard
treatments
such
as
surgery,
radiation
therapy,
chemotherapy.
Therefore,
there
a
pressing
need
for
new
therapeutic
strategies
to
improve
survival
reduce
treatment
side
effects.
In
this
study,
we
investigated
effect
HSP90
inhibition
in
combination
radiotherapy
established
patient-derived
glioblastoma
cell
lines.
Methods
Potential
radiosensitizing
effects
inhibitor
Onalespib
were
studied
XTT
clonogenic
assays
well
tumor-mimicking
multicellular
spheroid
models.
Further,
migration
capacity
on
protein
expression
after
exposure
using
Proximity
Extension
Assay
analysis.
Results
synergistically
enhanced
radiosensitivity
cells
grown
2D
3D
models,
resulting
increased
death,
reduced
activation
apoptotic
signaling
pathway.
The
proteomic
analysis
treated
Onalespib,
radiation,
their
revealed
significant
alterations
profiles,
involved
growth
signaling,
immune
modulation
pathways
angiogenesis.
Moreover,
indicated
potential
enhancing
cycle
arrest
apoptosis,
suggesting
promising
anti-tumor
Conclusion
These
findings
demonstrate
that
may
be
strategy
enhance
efficacy
GBM,
potentially
leading
improved
outcomes
patients
battling
challenging
disease.
Current Issues in Molecular Biology,
Год журнала:
2025,
Номер
47(2), С. 105 - 105
Опубликована: Фев. 7, 2025
Previous
studies
have
demonstrated
corilagin's
inhibitory
effects
on
the
growth
of
various
cancer
cells.
Given
limited
research
impact
ovarian
cancer,
a
particularly
deadly
gynecological
malignancy,
this
study
aimed
to
investigate
influence
A2780
cell
apoptosis
and
its
underlying
mechanisms.
The
goal
was
evaluate
potential
as
therapeutic
agent
for
cancer.
results
CCK-8
assay
showed
that
corilagin
inhibited
proliferation
cells
while
exhibiting
lower
toxicity
normal
surface
epithelial
(IOSE-80).
We
found
significantly
altered
cycle,
decreasing
proportion
in
G0/G1
G2/M
phases
inducing
cycle
arrest
S
phase.
At
low
concentrations,
induced
cells,
accompanied
by
decline
mitochondrial
membrane
calcium
influx.
Transcriptome
sequencing
analysis
identified
differentially
expressed
apoptosis-related
genes
corilagin-treated
primarily
within
PI3K-AKT
pathway.
Furthermore,
qPCR
Western
blot
confirmed
upregulation
p53
Bax
downregulation
BCL-2.
Corilagin
also
increased
expression
apoptotic
factors
caspase-9,
caspase-3,
PUMA,
cytochrome
C,
indicating
ability
induce
apoptosis.
Overall,
effectively
proliferation,
arrest,
triggered
Its
anti-tumor
effect
vitro
suggests
A2780,
especially
through
PI3K/p53
Research Square (Research Square),
Год журнала:
2025,
Номер
unknown
Опубликована: Март 3, 2025
Abstract
Background
Renal
cell
carcinoma
(RCC)
is
a
prevalent
malignant
tumor
with
high
morbidity
and
mortality.
The
TGF-β/smad
signaling
pathway
plays
significant
role
in
the
development
progression
of
RCC.
Methods
This
study
explored
impact
lathyrol
on
proliferation
mice
RCC
renca
cells
by
inhibiting
arresting
cycle.
Bioinformatics
analysis,
culture
experiments,
animal
experiments
were
conducted
to
detect
effects
activity,
mRNA,
protein
expressions
xenograft
tumors,
as
well
cycle
proteins
regulatory
proteins.
Results
Lathyrol
treatment
showed
positive
correlation
inhibitory
effect
proliferation.
IC
values
786-O
comparable.
In
vitro,
decreased
mRNA
TGF-β1,
TGF-βR1,
smad2,
smad3,
smad4,
smad9,
while
increasing
smad4.
vivo,
suppressed
smad9
xenografts,
cyclinD1,
cyclinB1,
cyclinA1,
cyclinE1,
CDK6,
CDK4,
CDK1,
P16,
P21,
P27.
Conclusion
can
repress
expression
key
pathway,
impede
signal
transduction,
arrest
cells,
subsequently
inhibit
cells.
Future
studies
are
needed
further
explore
mechanism
treatment.
Genes,
Год журнала:
2024,
Номер
15(1), С. 100 - 100
Опубликована: Янв. 15, 2024
The
heterogeneity
and
intricate
cellular
architecture
of
complex
ecosystems
play
a
crucial
role
in
the
progression
therapeutic
response
cancer.
Understanding
regulatory
relationships
malignant
cells
at
invasive
front
tumor
microenvironment
(TME)
is
important
to
explore
TME
its
disease
progression.
In
this
study,
we
inferred
invasion
by
analyzing
single-cell
RNA
sequencing
(scRNA-seq)
spatial
transcriptomics
(ST)
data
ER-positive
(ER+)
breast
cancer
patients.
addition,
developed
software
pipeline
for
constructing
intercellular
gene
networks
(IGRNs),
which
help
reduce
errors
generated
communication
analysis
increase
confidence
selected
cell
signals.
Based
on
constructed
IGRN
between
immune
ER+
patients,
found
that
high
expression
transcription
factors
FOXA1
EZH2
played
key
driving
Meanwhile,
elevated
levels
their
downstream
target
genes
(ESR1
CDKN1A)
were
associated
with
poor
prognosis
This
study
demonstrates
bioinformatics
workflow
combining
scRNA-seq
ST
data;
provides
pipelines
IGRNs
automatically
(cIGRN).
strategy
will
decipher
revealing
bidirectional
signaling
frontline
cells,
molecules
network
may
serve
as
biomarkers
mechanism
studies
or
targets.
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(20), С. 11078 - 11078
Опубликована: Окт. 15, 2024
Environmental
exposure
to
a
mixture
of
chemical
xenobiotics
acts
as
double-edged
sword,
promoting
or
suppressing
tumorigenesis
and
the
development
breast
cancer
(BC).
Before
anything
else,
we
are
what
eat.
In
this
review,
highlight
both
“the
good”
bad”
sides
daily
human
diet
dietary
patterns
that
could
influence
BC
risk
(BCR)
incidence.
Thus,
regularly
eating
new,
diversified,
colorful,
clean,
nutrient-rich,
energy-boosting,
raw
food,
increases
apoptosis
autophagy,
antioxidation,
cell
cycle
arrest,
anti-inflammation,
immune
response
against
cells.
Moreover,
healthy
lead
reduction
in
inhibition
genomic
instability,
stemness,
growth,
proliferation,
invasion,
migration,
distant
metastasis.
We
also
emphasize
that,
addition
beneficial
compounds,
our
food
is
more
contaminated
by
chemicals
with
harmful
effects,
which
interact
each
other
endogenous
proteins
lipids,
resulting
synergistic
antagonistic
effects.
diverse
diet,
combined
appropriate
nutritional
behaviors,
can
exert
anti-carcinogenic
effects
improve
treatment
efficacy,
patient
outcomes,
overall
quality
life
patients.
Previous
studies
found
that
corilagin
inhibits
the
growth
of
many
cancer
cells.
Ovarian
is
deadliest
gynecological
malignancy,
but
research
on
effects
ovarian
limited.
This
experiment
aims
to
explore
impact
A2780
cell
apoptosis
and
its
mechanism
action
evaluate
prospects
in
treating
cancer.
Corilagin
significantly
affects
cycle,
reducing
proportion
G0/G1
G2/M
phase
cells
blocking
them
S
phase.
at
low
concentrations
can
cause
apoptosis,
mitochondrial
membrane
potential
decline,
calcium
influx.
After
were
stained
with
Acridine
Orange,
autophagosomes
observed
under
a
fluorescence
microscope
increased
increase
concentration.
The
results
transcriptome
sequencing
showed
effect
could
differential
expression
apoptosis-related
genes
concentrated
PI3K-AKT
pathway.
qPCR
P53
Bax
while
BCL-2
decreased.
expressions
apoptotic
factors
caspase-9,
caspase-3,
p53-upregulated
modulator
(PUMA),
cytochrome
C
after
corilagin,
indicating
induce
apoptosis.
effectively
inhibit
proliferation
cells,
cycle
arrest,
Moreover,
it
trigger
autophagy
has
vitro
antitumor
effects.
It
promising
drug
for
through
PI3K/P53