International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(20), С. 11300 - 11300
Опубликована: Окт. 21, 2024
Osteosarcoma
(OS)
is
the
most
severe
bone
tumor
in
children.
A
chemotherapy
regimen
includes
a
combination
of
high-dose
Methotrexate
(MTX),
doxorubicin,
and
cisplatin.
These
drugs
cause
acute
chronic
side
effects,
such
as
infections,
thrombocytopenia,
neutropenia,
DNA
damage,
inflammation.
Therefore,
to
identify
new
therapeutic
strategies,
effective
with
safety
profile,
necessary.
The
Hedgehog
(Hh)
signaling
pathway
involved
tumorigenesis
active
OS.
Hh
components
Patched
receptor
1
(PTCH1),
Smoothened
(SMO),
glioma-associated
oncogene
homolog
transcription
factors
(GLI1
GLI2)
are
overexpressed
OS
cell
lines
patient
samples.
Curcumin
(CUR)-with
antioxidant
anti-cancer
properties-downregulates
cancer,
inhibiting
progression.
This
study
investigates
CUR
effects
on
MG-63
line,
alone
combined
MTX,
propose
novel
approach.
Our
suggests
agent
OS,
particularly
when
MTX.
Targeting
pathway,
MTX
showed
significant
pro-apoptotic
increasing
BAX/Bcl-2
ratio
total
apoptotic
percentage.
They
reduced
expression
(PTCH1,
SMO,
GLI1,
GLI2),
proliferation,
survival,
invasion.
determined
β-Catenin
decrease
trend
toward
reducing
NF-kB
matrix
metalloproteinases
(MMP-2
MMP-9).
findings
suggest
support
treatment,
improving
outcomes
adverse
current
therapies.
Scientific Reports,
Год журнала:
2025,
Номер
15(1)
Опубликована: Янв. 31, 2025
Despite
the
diverse
applications
of
γ
radiation
in
radiotherapy,
industrial
processes,
and
sterilization,
it
causes
hazardous
effects
on
living
organisms,
such
as
cellular
senescence,
persistent
cell
cycle
arrest,
mitochondrial
dysfunction.
This
study
evaluated
efficacy
curcumin
nanoparticles
(CNPs)
mitigating
dysfunction
senescence
induced
by
rat
brain
tissues.
Four
groups
male
Wistar
albino
rats
(n
=
8
per
group)
were
included:
(Gr1)
control
group;
(Gr2)
CNPs
group
(healthy
receiving
oral
administration
at
a
dose
10
mg/kg/day,
three
times
week
for
eight
weeks);
(Gr3)
irradiated
(rats
exposed
to
single
Gy
head
irradiation);
(Gr4)
+
(irradiated
treated
with
CNPs).
The
data
obtained
demonstrated
that
weeks
attenuated
oxidative
stress
γ-irradiated
lowering
brain's
lipid
peroxidation
level
[malondialdehyde
(MDA)]
enhancing
antioxidant
markers
[superoxide
dismutase
(SOD),
reduced
glutathione
(GSH),
total
capacity
(TAC)]
(P
<
0.05).
In
addition,
significantly
increased
function
improving
complex
I,
II,
ATP
production
levels
compared
group.
rats,
also
showed
anti-neuroinflammatory
reducing
interleukin
6
(IL-6),
tumor
necrosis
factor-alpha
(TNF-α),
nuclear
factor-kappa
B
(NF-ĸB)
Moreover,
administered
β-galactosidase
activity
expression
p53,
p21,
p16
genes
0.05)
while
concurrently
inducing
significant
increase
AMPK
mRNA
conclusion,
ameliorated
neurotoxicity
hold
promise
novel
agent
delay
via
their
combined
antioxidant,
anti-inflammatory,
mitochondrial-enhancing
properties.
Current Issues in Molecular Biology,
Год журнала:
2025,
Номер
47(1), С. 30 - 30
Опубликована: Янв. 6, 2025
Extensive
investigation
has
been
conducted
on
plant-based
resources
for
their
pharmacological
usefulness,
including
various
cancer
types.
The
scope
of
this
review
is
wider
than
several
studies
with
a
particular
focus
breast
cancer,
which
an
international
health
concern
while
studying
sources
flavonoids,
carotenoids,
polyphenols,
saponins,
phenolic
compounds,
terpenoids,
and
glycosides
apart
from
focusing
nursing.
Important
findings
prior
are
synthesized
to
explore
these
compounds'
sources,
mechanisms
action,
complementary
synergistic
effects,
associated
side
effects.
It
was
reviewed
that
the
exposure
certain
doses
catechins,
piperlongumine,
lycopene,
isoflavones
cucurbitacinfor
sufficient
period
can
provide
profound
anticancer
benefits
through
biological
events
such
as
cell
cycle
arrest,
cells
undergoing
apoptosis
disruption
signaling
pathways
including,
but
not
limited
JAK-STAT3,
HER2-integrin,
MAPK.
Besides,
study
also
covers
potential
adverse
effects
phytochemicals.
Regarding
mechanisms,
widest
attention
paid
Complementary
strategies
discussed
indicate
it
would
be
realistic
alter
dosage
delivery
systems
liposomes,
nanoparticles,
nanoemulsions,
films
enhance
efficacy.
Future
research
directions
include
refining
approaches,
further
elucidating
molecular
conducting
clinical
trials
validate
findings.
These
efforts
could
significantly
advance
role
phytocompounds
in
management.
Pharmaceutics,
Год журнала:
2025,
Номер
17(1), С. 114 - 114
Опубликована: Янв. 15, 2025
Curcumin,
a
bioactive
compound
derived
from
the
rhizome
of
Curcuma
longa
L.,
has
garnered
significant
attention
for
its
potent
anticancer
properties.
Despite
promising
therapeutic
potential,
poor
bioavailability,
rapid
metabolism,
and
low
water
solubility
hinder
curcumin’s
clinical
application.
Nanotechnology
offers
viable
solution
to
these
challenges
by
enabling
development
curcumin-based
nanoparticles
(CNPs)
that
enhance
bioavailability
efficacy.
This
review
provides
comprehensive
overview
recent
advancements
in
design
synthesis
CNPs
cancer
therapy.
We
discuss
various
NP
formulations,
including
polymeric,
lipid-based,
inorganic
nanoparticles,
highlighting
their
role
improving
pharmacokinetic
pharmacodynamic
profiles.
The
mechanisms
which
exert
effects,
such
as
inducing
apoptosis,
inhibiting
cell
proliferation,
modulating
signaling
pathways,
are
explored
details.
Furthermore,
we
examine
preclinical
studies
have
demonstrated
efficacy
treating
different
types
tumors,
breast,
colorectal,
pancreatic
cancers.
Finally,
addresses
current
future
perspectives
translation
CNPs,
emphasizing
need
further
research
optimize
targeted
delivery
outcomes.
By
synthesizing
latest
research,
this
underscores
potential
avenue
advancing
Pharmaceutics,
Год журнала:
2025,
Номер
17(2), С. 263 - 263
Опубликована: Фев. 17, 2025
Background:
Thyroid
cancer
(TC)
is
the
most
prevalent
endocrine
malignancy,
and
categorized
into
well-differentiated
aggressive
anaplastic
types.
Novel
therapeutic
modalities
are
needed
for
TC.
Nanomedicine
a
promising
strategy
development
of
precision
medicine.
In
this
context,
we
investigated
use
nanogels
(NGs)
to
deliver
agents
with
different
physicochemical
properties,
specifically
hydrophilic
agent
doxorubicin
(DOX)
hydrophobic
compound
curcumin
(CUR),
in
TC
cell
lines.
Methods:
Nα-9-fluorenylmethoxycarbonyl-diphenylalanine
(Fmoc-FF)
peptide-based
NGs
loaded
DOX
CUR
were
formulated
using
solvent-switch
method.
DOX-loaded
previously
characterized.
CUR-loaded
characterized
through
rheology,
scanning
electron
microscopy
(SEM),
dynamic
light
scattering
(DLS),
nanoparticle
tracking
analysis
(NTA),
Fourier
transform
infrared
(FT-IR)
spectroscopy.
Confocal
microscopy,
q-RT-PCR,
ATP
lite
assays
performed
evaluate
uptake
delivery
DOX-
on
Results:
exhibited
mean
diameter
approximately
204.3
nm
zeta
potential
-34.6
mV,
indicative
good
stability.
vitro
release
studies
revealed
sustained
profile
over
72
h.
Functional
analyses
demonstrated
that
Fmoc-FF-loaded
internalized
They
primarily
localized
cytoplasm
rather
than
early
endosomes,
thereby
ensuring
intracellular
Furthermore,
Fmoc-FF
reduced
nuclear
kinetics
cells,
suggesting
reduction
dose-limiting
toxicity.
Comparative
similar
internalization
delayed
uptake,
highlighting
efficacy
delivering
agents.
Conclusions:
Overall,
data
suggest
represent
diverse
properties
TC,
enhancing
their
safety
warranting
further
investigation.
Cancers,
Год журнала:
2024,
Номер
16(14), С. 2580 - 2580
Опубликована: Июль 18, 2024
Curcumin,
a
polyphenolic
compound
derived
from
Curcuma
longa,
exhibits
significant
therapeutic
potential
in
cancer
management.
This
review
explores
curcumin’s
mechanisms
of
action,
the
challenges
related
to
its
bioavailability,
and
enhancement
through
modern
technology
approaches.
Curcumin
demonstrates
strong
antioxidant
anti-inflammatory
properties,
contributing
ability
neutralize
free
radicals
inhibit
inflammatory
mediators.
Its
anticancer
effects
are
mediated
by
inducing
apoptosis,
inhibiting
cell
proliferation,
interfering
with
tumor
growth
pathways
various
colon,
pancreatic,
breast
cancers.
However,
clinical
application
is
limited
poor
bioavailability
due
rapid
metabolism
low
absorption.
Novel
delivery
systems,
such
as
curcumin-loaded
hydrogels
nanoparticles,
have
shown
promise
improving
curcumin
efficacy.
Additionally,
photodynamic
therapy
has
emerged
complementary
approach,
where
light
exposure
enhances
modulating
molecular
crucial
for
survival.
Studies
highlight
that
combining
concentrations
visible
irradiation
significantly
boosts
antitumor
efficacy
compared
alone.
The
interaction
cytochromes
or
drug
transporters
may
play
role
altering
pharmacokinetics
conventional
medications,
which
necessitates
careful
consideration
settings.
Future
research
should
focus
on
optimizing
understanding
fully
harness
treatment.
Drug Development and Industrial Pharmacy,
Год журнала:
2025,
Номер
unknown, С. 1 - 31
Опубликована: Март 21, 2025
This
review
examines
recent
advancements
in
nanoparticle-based
delivery
systems
for
phytochemicals,
focusing
on
their
role
overcoming
multidrug
resistance,
improving
therapeutic
efficacy,
and
facilitating
clinical
translation.
highlights
advances
nanoparticle-enabled
phytochemical
to
enhance
bioavailability,
improve
outcomes,
enable
targeted
applications.
By
comparing
various
nanoparticle
systems,
formulation
methods,
efficacy
data,
it
identifies
gaps
current
research
guides
the
development
of
more
effective,
next-generation
phytochemical-loaded
nanocarriers.
A
systematic
literature
published
between
2000
2024
was
conducted
using
PubMed,
Scopus,
Web
Science.
Articles
cancer
therapy
were
included.
Compounds
such
as
curcumin,
resveratrol,
quercetin,
epigallocatechin
gallate
demonstrate
enhanced
anti-cancer
when
encapsulated
nanoparticles,
leading
improved
increased
tumor
cell
targeting,
reduced
toxicity.
Clinical
trials
indicate
regression
fewer
adverse
effects.
Emerging
approaches-such
nanogels,
hybrid
combination
therapies
with
immune
checkpoint
inhibitors-further
refine
treatment
efficacy.
Nanoparticle-based
significantly
potential
making
them
promising
candidates
safer,
effective
treatments.
However,
challenges
related
regulatory
guidelines,
scalability,
long-term
safety
must
be
addressed
fully
realize
potential.
International Journal of Molecular Sciences,
Год журнала:
2025,
Номер
26(8), С. 3565 - 3565
Опубликована: Апрель 10, 2025
Head
and
neck
squamous
cell
carcinoma
(HNSCC)
remains
a
major
health
burden,
with
abnormal
activation
of
phosphatidylinositol
3-kinase
alpha
(PI3Kα)
strongly
implicated
in
its
pathogenesis.
Targeting
PI3Kα
represents
promising
therapeutic
strategy.
In
this
study,
we
employed
structure-based
virtual
screening
to
identify
natural
small-molecule
inhibitors
PI3Kα.
A
total
12,800
molecules
were
screened,
five
compounds
selected
for
further
evaluation
based
on
binding
affinity
interaction
patterns.
Pharmacokinetic
properties
assessed
using
ADMET
predictions,
molecular
dynamics
(MD)
simulations
conducted
validate
the
stability.
Among
candidates,
Apigetrin
demonstrated
favorable
properties,
high
safety
profile,
stable
within
ATP-binding
pocket
These
findings
suggest
that
is
inhibitor
potential
relevance
HNSCC.