Frontiers in Pharmacology,
Journal Year:
2022,
Volume and Issue:
12
Published: Jan. 28, 2022
Gastric
cancer
(GC),
second
most
leading
cause
of
cancer-associated
mortality
globally,
is
the
gastrointestinal
tract
in
which
malignant
cells
form
lining
stomach,
resulting
indigestion,
pain,
and
stomach
discomfort.
Autophagy
an
intracellular
system
misfolded,
aggregated,
damaged
proteins,
as
well
organelles,
are
degraded
by
lysosomal
pathway,
avoiding
abnormal
accumulation
huge
quantities
harmful
cellular
constituents.
However,
exact
molecular
mechanism
autophagy-mediated
GC
management
has
not
been
clearly
elucidated.
Here,
we
emphasized
role
autophagy
modulation
development
transformation
addition
to
underlying
mechanisms
regulation
GC.
Accumulating
evidences
have
revealed
that
targeting
small
molecule
activators
or
inhibitors
become
one
greatest
auspicious
approaches
for
managements.
Particularly,
it
verified
phytochemicals
play
important
treatment
prevention
use
combination
therapies
modulators
order
overcome
drug
resistance
through
will
provide
novel
opportunities
develop
promising
therapeutic
approaches.
In
addition,
investigations
pathophysiological
with
potential
challenges
urgently
needed,
limitations
strategies.
Therefore,
this
review,
would
like
deliver
existing
standard
strategy
focusing
on
relationship
between
chemotherapeutic
drugs
autophagy,
help
improve
current
treatments
patients.
Drug Delivery and Translational Research,
Journal Year:
2024,
Volume and Issue:
14(10), P. 2845 - 2916
Published: July 13, 2024
Abstract
Several
efforts
have
been
extensively
accomplished
for
the
amelioration
of
cancer
treatments
using
different
types
new
drugs
and
less
invasives
therapies
in
comparison
with
traditional
therapeutic
modalities,
which
are
widely
associated
numerous
drawbacks,
such
as
drug
resistance,
non-selectivity
high
costs,
restraining
their
clinical
response.
The
application
natural
compounds
prevention
treatment
cells
has
attracted
significant
attention
from
pharmaceuticals
scientific
communities
over
past
decades.
Although
use
nanotechnology
therapy
is
still
preliminary
stages,
nanotherapeutics
demonstrated
to
decrease
various
limitations
related
compounds,
physical/chemical
instability,
poor
aqueous
solubility,
low
bioavailability.
Despite
emerged
a
promise
improve
bioavailability
there
limited
trials
performed
challenges
required
pre-clinical
trials,
production
at
an
industrial
level,
assurance
long-term
stability,
physiological
barriers
safety
regulatory
issues.
This
review
highlights
most
recent
advances
nanocarriers
secreted
plants,
bacteria,
fungi,
marine
organisms,
well
role
on
cell
signaling
pathways
anticancer
treatments.
Additionally,
status
main
regarding
loaded
applications
were
also
discussed.
Graphical
abstract
Pharmaceuticals,
Journal Year:
2021,
Volume and Issue:
14(11), P. 1069 - 1069
Published: Oct. 22, 2021
Cancer
is
a
complex
ailment
orchestrated
by
numerous
intrinsic
and
extrinsic
pathways.
Recent
research
has
displayed
deep
interest
in
developing
plant-based
cancer
therapeutics
for
better
management
of
the
disease
limited
side
effects.
A
wide
range
plant-derived
compounds
have
been
reported
their
anticancer
potential
quest
finding
an
effective
therapeutic
approach.
Rutin
(vitamin
P)
low-molecular
weight
flavonoid
glycoside
(polyphenolic
compound),
abundantly
present
various
vegetables,
fruits
(especially
berries
citrus
fruits),
medicinal
herbs.
Numerous
studies
delineated
several
pharmacological
properties
rutin
such
as
its
antiprotozoal,
antibacterial,
anti-inflammatory,
antitumor,
antiviral,
antiallergic,
vasoactive,
cytoprotective,
antispasmodic,
hypolipidemic,
antihypertensive,
antiplatelet
properties.
Specifically,
rutin-mediated
anticancerous
activities
cancerous
cell
lines,
but
most
common
scientific
evidence,
encompassing
molecular
processes
interactions,
including
apoptosis
pathway
regulation,
aberrant
signaling
pathways,
oncogenic
genes,
not
thoroughly
studied.
In
this
direction,
we
attempted
to
project
regulation
carcinomas.
Additionally,
also
incorporated
advanced
that
uncovered
notable
modulation
key
cellular
functions
via
interaction
with
mRNAs,
major
emphasis
on
elucidating
direct
miRNA
targets
well
process
needed
transform
these
approaches
novel
interventions
treatment
cancers.
International Journal of Molecular Sciences,
Journal Year:
2022,
Volume and Issue:
23(18), P. 10479 - 10479
Published: Sept. 9, 2022
In
recent
years,
interest
in
natural
products
such
as
alternative
sources
of
pharmaceuticals
for
numerous
chronic
diseases,
including
tumors,
has
been
renewed.
Propolis,
a
product
collected
by
honeybees,
and
polyphenolic/flavonoid
propolis-related
components
modulate
all
steps
the
cancer
progression
process.
Anticancer
activity
propolis
its
compounds
relies
on
various
mechanisms:
cell-cycle
arrest
attenuation
cells
proliferation,
reduction
number
stem
cells,
induction
apoptosis,
modulation
oncogene
signaling
pathways,
inhibition
matrix
metalloproteinases,
prevention
metastasis,
anti-angiogenesis,
anti-inflammatory
effects
accompanied
tumor
microenvironment
(by
modifying
macrophage
activation
polarization),
epigenetic
regulation,
antiviral
bactericidal
activities,
gut
microbiota,
chemotherapy-induced
deleterious
side
effects.
Ingredients
from
also
”sensitize“
to
chemotherapeutic
agents,
likely
blocking
transcription
factor
nuclear
kappa-light-chain-enhancer
activated
B
(NF-κB).
this
review,
we
summarize
current
knowledge
related
flavonoids
other
polyphenolic
growth
metastasizing
ability,
discuss
possible
molecular
cellular
mechanisms
involved
inflammatory
pathways
processes
that
affect
survival,
invasion,
angiogenesis,
metastasis
tumor.
Biomedicine & Pharmacotherapy,
Journal Year:
2022,
Volume and Issue:
157, P. 114032 - 114032
Published: Dec. 6, 2022
Pinocembrin
(5,7-dihydroxyflavone)
is
a
major
flavonoid
found
in
many
plants,
fungi
and
hive
products,
mainly
honey
propolis.
Several
vitro
preclinical
studies
revealed
numerous
pharmacological
activities
of
pinocembrin
including
antioxidant,
anti-inflammatory,
antimicrobial,
neuroprotective,
cardioprotective
anticancer
activities.
Here,
we
comprehensively
review
critically
analyze
the
carried
out
on
pinocembrin.
We
also
discuss
its
potential
mechanisms
action,
bioavailability,
toxicity,
clinical
investigations.
The
wide
therapeutic
window
makes
it
promising
drug
candidate
for
applications.
recommend
some
future
perspectives
to
improve
pharmacokinetic
pharmacodynamic
properties
better
delivery
that
may
lead
new
advances.
Nutrients,
Journal Year:
2023,
Volume and Issue:
15(4), P. 797 - 797
Published: Feb. 4, 2023
High-grade
adult-type
diffuse
gliomas
are
the
most
common
and
deadliest
malignant
adult
tumors
of
central
nervous
system.
Despite
advancements
in
multimodality
treatment
high-grade
gliomas,
five-year
survival
rates
still
remain
poor.
The
biggest
challenge
treating
is
intra-tumor
heterogeneity
feature
glioma
tumors.
Introducing
dietary
flavonoids
to
current
strategies
crucial
overcome
this
challenge,
as
can
target
several
molecular
targets.
This
review
discusses
anticancer
mechanism
(quercetin,
rutin,
chrysin,
apigenin,
naringenin,
silibinin,
EGCG,
genistein,
biochanin
A
C3G)
through
targeting
molecules
associated
with
cell
proliferation,
apoptosis,
oxidative
stress,
cycle
arrest,
migration,
invasion,
autophagy
DNA
repair.
In
addition,
targeted
by
such
Bax,
Bcl-2,
MMP-2,
MMP-9,
caspase-8,
caspase-3,
p53,
p38,
Erk,
JNK,
beclin-1
LC3B
were
also
discussed.
Moreover,
clinical
relevance
flavonoid
targets
discussed
comparison
small
inhibitors:
ralimetinib,
AMG232,
marimastat,
hydroxychloroquine
chloroquine.
positive
pre-clinical
results,
further
investigations
studies
warranted
substantiate
efficacy
safety
use
on
patients.
Cancers,
Journal Year:
2024,
Volume and Issue:
16(12), P. 2171 - 2171
Published: June 7, 2024
Cancer
cells
show
altered
antioxidant
defense
systems,
dysregulated
redox
signaling,
and
increased
generation
of
reactive
oxygen
species
(ROS).
Targeting
cancer
through
ROS-mediated
mechanisms
has
emerged
as
a
significant
therapeutic
strategy
due
to
its
implications
in
progression,
survival,
resistance.
Extensive
research
focused
on
selective
H2O2
for
cell
killing
by
employing
various
strategies
such
metal-based
prodrugs,
photodynamic
therapy,
enzyme-based
nano-particle
mediated
approaches,
chemical
modulators,
combination
therapies.
Many
these
H2O2-amplifying
approaches
have
demonstrated
promising
anticancer
effects
selectivity
preclinical
investigations.
They
selectively
induce
cytotoxicity
while
sparing
normal
cells,
sensitize
resistant
modulate
the
tumor
microenvironment.
However,
challenges
remain
achieving
selectivity,
addressing
heterogeneity,
ensuring
efficient
delivery,
managing
safety
toxicity.
To
address
those
issues,
H2O2-generating
agents
been
combined
with
other
treatments
leading
optimized
This
review
focuses
agents/approaches
that
kill
via
H2O2-mediated
mechanisms.
Different
categories
compounds
generate
are
summarized,
their
underlying
function
elucidated,
clinical
studies
well
recent
advancements
discussed,
prospects
targeted
utility
explored.
By
understanding
potential
compounds,
researchers
can
pave
way
development
effective
personalized
treatments.
Cancer
cells
show
altered
antioxidant
defense
systems,
dysregulated
redox
signaling,
and
increased
generation
of
reactive
oxygen
species
(ROS).
Targeting
cancer
through
ROS-mediated
mechanisms
has
emerged
as
a
significant
therapeutic
strategy
due
to
its
implications
in
progression,
survival,
resistance.
Extensive
research
focused
on
selective
H2O2
for
cell
killing
by
employing
various
strategies
such
metal-based
prodrugs,
photodynamic
therapy,
enzyme-based
nano-particle
mediated
approaches,
chemical
modulators,
combination
therapies.
Many
these
H2O2-amplifying
approaches
have
demonstrated
promising
anticancer
effects
selectivity
preclinical
investigations.
They
selectively
induce
cytotoxicity
while
sparing
normal
cells,
sensitize
resistant
modulate
the
tumor
microenvironment.
However,
challenges
remain
achieving
selectivity,
addressing
heterogeneity,
ensuring
efficient
delivery,
managing
safety
toxicity.
To
address
those
issues,
H2O2-generating
agents
been
combined
with
other
treatments
leading
optimized
This
review
focuses
agents/approaches
that
kill
via
H2O2-mediated
mechanisms.
Different
categories
compounds
generate
are
summarized,
their
underlying
function
elucidated,
clinical
studies
well
recent
advancements
discussed,
prospects
targeted
utility
explored.
By
understanding
potential
compounds,
researchers
can
pave
way
development
effective
personalized
treatments.
Oxidative Medicine and Cellular Longevity,
Journal Year:
2022,
Volume and Issue:
2022, P. 1 - 15
Published: June 8, 2022
Stroke
is
one
of
the
leading
causes
death
and
disability
worldwide.
Autophagy
a
conserved
cellular
catabolic
pathway
that
maintains
homeostasis
by
removal
damaged
proteins
organelles,
which
critical
for
maintenance
energy
function
cells.
Accumulating
evidence
demonstrates
autophagy
plays
important
roles
in
pathophysiological
mechanisms
under
ischemic
stroke.
Previous
investigations
show
serves
as
"double-edged
sword"
stroke
it
can
either
promote
survival
neuronal
cells
or
induce
cell
special
conditions.
Following
stroke,
activated
inhibited
several
types
brain,
including
neurons,
astrocytes,
microglia,
well
microvascular
endothelial
cells,
involves
inflammatory
activation,
modulation
microglial
phenotypes,
blood-brain
barrier
permeability.
However,
exact
underlying
role
are
not
fully
understood.
This
review
focuses
on
recent
advances
regarding
potential
molecular
different
types.
The
focus
also
discussing
effect
its
possible
mechanisms.
In
addition,
therapeutic
strategies
targeting
reviewed.
Frontiers in Pharmacology,
Journal Year:
2023,
Volume and Issue:
14
Published: June 30, 2023
Glioblastoma
(GBM)
is
the
most
common
malignant
tumor
of
central
nervous
system
(CNS).
It
a
leading
cause
death
among
patients
with
intracranial
tumors.
GBM
exhibits
intra-
and
inter-tumor
heterogeneity,
to
drug
resistance
eventual
recurrence.
Conventional
treatments
for
include
maximum
surgical
resection
glioma
tissue,
temozolomide
administration,
radiotherapy,
but
these
methods
do
not
effectively
halt
cancer
progression.
Therefore,
development
novel
treatment
identification
new
therapeutic
targets
are
urgently
required.
In
recent
years,
studies
have
shown
that
drugs
related
mitophagy
mitochondrial
apoptosis
pathways
can
promote
glioblastoma
cells
by
inducing
damage,
impairing
adenosine
triphosphate
(ATP)
synthesis,
depleting
large
amounts
ATP.
Some
also
modern
nano-drug
delivery
technology
targeting
mitochondria
achieve
better
release
deeper
tissue
penetration,
suggesting
could
be
target
intervention
therapy.
The
combination
autophagy
nanotechnology
promising
approach
treating
GBM.This
article
reviews
current
status
therapy
GBM,
pathways,
potential
as
treatment,
latest
developments
pertaining
directions
future
research.