Arabian Journal of Chemistry,
Год журнала:
2023,
Номер
16(7), С. 104834 - 104834
Опубликована: Март 23, 2023
There
has
been
growing
interest
in
the
biological
and
pharmacological
potential
of
C.
odorata
recent
times.
While
a
number
reports
had
highlighted
beneficial
attributes
various
extracts
prepared
from
odorata,
properties
lipophilic
extract
remained
unexplored.
This
work
aimed
at
examining
anticancer,
antimicrobial
antioxidant
aerial
part
(COLE).
The
results
revealed
that
COLE
possessed
potent
selective
anticancer
against
human
breast
colon
cancer
cells.
presented
strong
cytotoxic
activity
MCF-7
cells
(IC50
9.18
µg/mL),
MDA-MB-231
12.19
HT-29
19.48
HCT-116
14.12
µg/mL).
Meanwhile,
was
found
to
be
non-toxic
concentrations
tested
normal
(HEK-293
CCD-841
CoN)
In
addition,
demonstrated
significant
antibacterial
B.
cereus
(MIC
value
0.157
mg/mL),
moderate
L.
monocytogenes
0.63
mg/mL)
E.
coli
1.06
mg/mL).
Furthermore,
effectively
scavenged
free
radical
species,
including
ABTṠ+
46.80
DPPḢ
27.78
superoxide
anion
64.07
likely
due
high
phenolic
(262.48
mg
gallic
acid
equivalent/g)
flavonoid
content
(70.20
quercetin
equivalent/g).
UPLC-MS
analysis
putative
identities
85
secondary
metabolites
whereas
GC–MS
detected
36
volatile
constituents
COLE.
Also,
it
terpenes
compounds
were
predominant
specialized
present
COLE,
putatively
responsible
for
remarkable
properties.
Taken
together,
these
richness
terms
its
metabolite
profile
activities.
conclusion,
is
worthy
further
investigation
take
advantage
good
antioxidative
or
nutraceutical
application.
Cell Biochemistry and Function,
Год журнала:
2024,
Номер
42(1)
Опубликована: Янв. 1, 2024
Abstract
Curcumin
is
a
natural
compound
derived
from
turmeric
and
can
target
malignant
tumor
molecules
involved
in
cancer
propagation.
It
has
potent
antioxidant
activity,
but
its
effectiveness
limited
due
to
poor
absorption
rapid
elimination
the
body.
Various
curcumin
derivatives
have
also
shown
anticancer
potential
in‐vitro
in‐vivo
models.
multiple
signaling
pathways
development/progression
or
induce
cell
death
through
apoptosis.
In
addition,
could
enhance
of
conventional
chemotherapy,
radiation
therapy
reduce
their
associated
side
effects.
Lately,
nanoparticle‐based
delivery
systems
are
being
developed/explored
overcome
challenges
with
curcumin's
delivery,
increasing
overall
efficacy.
The
use
an
imaging
system
track
these
formulations
give
beneficial
information
about
bioavailability
distribution
nano‐curcumin
complex.
conclusion,
holds
significant
promise
fight
against
cancer,
especially
nanoform,
provide
precise
cells
without
affecting
normal
healthy
cells.
Frontiers in Pharmacology,
Год журнала:
2025,
Номер
15
Опубликована: Янв. 6, 2025
Nuclear
factor-κB
(NF-κB)
cell
signaling
pathway
is
essential
for
the
progression
and
development
of
numerous
human
disorders,
including
cancer.
NF-κB
regulates
a
wide
range
physiological
processes,
such
as
survival,
growth,
migration.
Deregulated
NF-kB
resulted
in
unregulated
proliferation,
viability,
movement,
invasion,
thus
promoting
tumor
development.
Recent
findings
have
increasingly
shown
that
plant
derived
phytochemicals
inhibit
potential
to
be
employed
cancer
therapeutics.
Flavonoids
are
group
polyphenolic
natural
compounds
present
various
plants
their
fruits,
vegetables,
leaves.
These
medicinal
properties
owing
antioxidant,
anti-inflammatory,
antiviral,
antitumor
characteristics.
The
main
mechanism
by
which
these
flavonoids
exhibit
anticancer
via
potent
antioxidative
immunomodulatory
actions.
Current
research
reports
demonstrated
exhibited
effects
suppressing
signaling.
Based
on
facts,
we
comprehensively
outlined
role
processes
progression,
drug
resistance,
angiogenesis
metastasis.
In
addition
these,
also
summarize
specifically
targeting
types
cancers.
Cells,
Год журнала:
2022,
Номер
11(14), С. 2209 - 2209
Опубликована: Июль 15, 2022
Natural
products
play
a
critical
role
in
the
discovery
and
development
of
numerous
drugs
for
treatment
various
types
cancer.
These
phytochemicals
have
demonstrated
anti-carcinogenic
properties
by
interfering
with
initiation,
development,
progression
cancer
through
altering
mechanisms
such
as
cellular
proliferation,
differentiation,
apoptosis,
angiogenesis,
metastasis.
Treating
multifactorial
diseases,
agents
targeting
single
target,
might
lead
to
limited
success
and,
many
cases,
unsatisfactory
outcomes.
Various
epidemiological
studies
shown
that
steady
consumption
fruits
vegetables
is
intensely
associated
reduced
risk
Since
ancient
period,
plants,
herbs,
other
natural
been
used
healing
agents.
Likewise,
most
medicinal
ingredients
accessible
today
are
originated
from
resources.
Regardless
achievements,
developing
bioactive
compounds
has
remained
challenging,
part
because
problem
large-scale
sequestration
mechanistic
understanding.
With
significant
progress
landscape
therapy
rising
use
cutting-edge
technologies,
we
may
come
crossroads
review
approaches
identify
potential
investigate
their
therapeutic
efficacy.
In
present
review,
summarize
recent
developments
products-based
research
its
application
generating
novel
systemic
strategies
focus
on
underlying
molecular
solid
Molecules,
Год журнала:
2022,
Номер
27(13), С. 4304 - 4304
Опубликована: Июль 4, 2022
Plant
bioactive
compounds,
particularly
apigenin,
have
therapeutic
potential
and
functional
activities
that
aid
in
the
prevention
of
infectious
diseases
many
mammalian
bodies
promote
tumor
growth
inhibition.
Apigenin
is
a
flavonoid
with
low
toxicities
numerous
properties
due
to
which
it
has
been
considered
as
traditional
medicine
for
decades.
shows
synergistic
effects
combined
treatment
sorafenib
HepG2
human
cell
line
(HCC)
less
time
statistically
reduces
viability
cells,
migration,
gene
expression
apoptosis.
The
combination
anti-cancerous
drugs
apigenin
shown
health
promoting
against
various
cancers.
It
can
prevent
mobility,
maintain
cycle
stimulate
immune
system.
also
suppresses
mTOR
activity
raises
UVB-induced
phagocytosis
cancerous
proliferation
growth.
high
safety
threshold,
active
(anti-cancer)
doses
be
gained
by
consuming
vegetable
rich
diet.
boosted
autophagosome
formation,
decreased
activated
autophagy
preventing
PI3K
pathway,
specifically
cells.
This
paper
provides
an
updated
overview
apigenin's
beneficial
anti-inflammatory,
antibacterial,
antiviral,
anticancer
effects,
making
step
right
direction
therapeutics.
study
critically
analyzed
effect
on
cancer
signaling
pathways
including
PI3K/AKT/MTOR,
JAK/STAT,
NF-κB
ERK/MAPK
pathways.
Antioxidants,
Год журнала:
2023,
Номер
12(3), С. 586 - 586
Опубликована: Фев. 27, 2023
Citrus
(genus
L.)
fruits
are
essential
sources
of
bioactive
compounds
with
antioxidant
properties,
such
as
flavonoids.
These
polyphenolic
divided
into
subclasses,
in
which
flavanones
the
most
prominent.
Among
them,
naringenin
and
hesperidin
emerging
anticancer
potential,
especially
for
breast
cancer
(BC).
Several
mechanisms
have
been
proposed,
including
modulation
epigenetics,
estrogen
signaling,
induction
cell
death
via
regulation
apoptotic
signaling
pathways,
inhibition
tumor
invasion
metastasis.
However,
this
information
is
sparse
literature
needs
to
be
brought
together
provide
an
overview
how
can
serve
therapeutic
tools
drug
development
a
successful
co-adjuvant
strategy
against
BC.
This
review
detailed
context
highlighted
could
interfere
BC
carcinogenesis
helpful
potential
alternative
treatment.
Chemistry & Biodiversity,
Год журнала:
2023,
Номер
20(9)
Опубликована: Авг. 7, 2023
With
the
increasing
prevalence
of
cancer
and
toxic
side
effects
synthetic
drugs,
natural
products
are
being
developed
as
promising
therapeutic
approaches.
Gracillin
is
a
naturally
occurring
triterpenoid
steroidal
saponin
with
several
activities.
It
obtained
major
compound
from
different
Dioscorea
species.
This
review
was
designated
to
summarize
research
progress
on
anti-cancer
activities
gracillin
focusing
underlying
cellular
molecular
mechanisms,
well
its
pharmacokinetic
features.
The
data
were
collected
(up
date
May
1,
2023)
various
reliable
authentic
literatures
comprising
PubMed,
Springer
Link,
Scopus,
Wiley
Online,
Web
Science,
ScienceDirect,
Google
Scholar.
findings
demonstrated
that
displays
anticancer
through
including
anti-inflammatory
effects,
apoptotic
cell
death,
induction
oxidative
stress,
cytotoxicity,
genotoxicity,
cycle
arrest,
anti-proliferative
effect,
autophagy,
inhibition
glycolysis,
blocking
migration.
Additionally,
this
highlighted
features
gracillin,
indicating
lower
oral
bioavailability.
As
conclusion,
it
can
be
proposed
could
serve
hopeful
chemotherapeutic
agent.
However,
further
extensive
clinical
recommended
establish
safety,
efficacy,
potential
in
treatment.
Journal of Functional Foods,
Год журнала:
2023,
Номер
104, С. 105502 - 105502
Опубликована: Март 21, 2023
Cancer
is
identified
as
second
leading
causes
of
death
and
imposes
a
significant
psychological
economic
burden
on
societies.
Due
to
its
high
prevalence,
main
cause
worldwide,
there
continuing
need
discover
new
potential
anticancer
compounds.
Plant-derived
compounds
have
recently
attracted
more
attention
among
researchers
for
their
potent
anti-cancer
properties.
A
numerous
research,
including
in-vitro,
in-vivo,
preclinical,
clinical,
epidemiological
studies,
has
indicated
that
the
flavonoid
silymarin
comprehensive
preventive
therapeutic
effects
array
inflammation-driven
diseases,
cancer.
Silymarin
clear
activities
through
distinctive
mechanisms
modulation
apoptosis
in-vitro
survival
in-vivo.
The
chemoprotection
constituent
suggest
they
could
be
promising
agents
in
various
cancer
types.
This
review
focus
vivo
vitro
variety
cancers,
explores
signaling
pathways
modulated
by
this
compound.
Cells,
Год журнала:
2023,
Номер
12(3), С. 458 - 458
Опубликована: Янв. 31, 2023
Recent
evidence
suggests
that
autophagy
is
a
governed
catabolic
framework
enabling
the
recycling
of
nutrients
from
injured
organelles
and
other
cellular
constituents
via
lysosomal
breakdown.
This
mechanism
has
been
associated
with
development
various
pathologic
conditions,
including
cancer
neurological
disorders;
however,
recently
updated
studies
have
indicated
plays
dual
role
in
cancer,
acting
as
cytoprotective
or
cytotoxic
mechanism.
Numerous
preclinical
clinical
investigations
shown
inhibiting
enhances
an
anticancer
medicine’s
effectiveness
malignancies.
Autophagy
antagonists,
chloroquine
hydroxychloroquine,
previously
authorized
trials,
encouraging
medication-combination
therapies
targeting
autophagic
processes
for
cancer.
In
this
review,
we
provide
update
on
recent
research
examining
efficacy
combining
drugs
activate
inhibitors.
Additionally,
highlight
difficulties
progress
toward
using
treatment
strategy.
Importantly,
must
enable
use
suitable
inhibitors
coadministration
delivery
systems
conjunction
agents.
Therefore,
review
briefly
summarizes
general
molecular
process
behind
its
bifunctional
important
suppression
tumor
growth
resistance
to
chemotherapy
metastasis
regulation.
We
then
emphasize
how
cells
interacting
one
another
promising
therapeutic
target
treatment.
Frontiers in Endocrinology,
Год журнала:
2023,
Номер
14
Опубликована: Июль 25, 2023
Colorectal
cancer
(CRC)
is
one
of
the
most
deaths
causing
diseases
worldwide.
Several
risk
factors
including
hormones
like
insulin
and
growth
(e.g.,
IGF-1)
have
been
considered
responsible
for
progression
colon
cancer.
Though
there
a
huge
advancement
in
available
screening
as
well
treatment
techniques
CRC.
There
no
significant
decrease
mortality
patients.
Moreover,
current
approaches
CRC
are
associated
with
serious
challenges
drug
resistance
re-growth.
Given
severity
disease,
an
urgent
need
novel
therapeutic
agents
ideal
characteristics.
pieces
evidence
suggested
that
natural
products,
specifically
medicinal
plants,
derived
phytochemicals
may
serve
potential
sources
discovery
various
On
other
hand,
cells
require
high
basal
level
reactive
oxygen
species
(ROS)
to
maintain
its
own
cellular
functions.
However,
excess
production
intracellular
ROS
leads
cell
death
via
disturbing
redox
homeostasis.
Therefore,
plants
phytocompounds
can
enhance
induce
apoptotic
modulating
molecular
targets
IGF-1
could
be
agents.
Alkaloids
form
major
class
such
phytoconstituents
play
key
role
prevention.
several
preclinical
clinical
studies
also
evidenced
these
compounds
show
potent
anti-colon
effects
exhibit
negligible
toxicity
towards
normal
cells.
Hence,
present
evidence-based
study
aimed
provide
update
on
alkaloids
reported
ROS-mediated
apoptosis
targeting
components
factors,
which
metastasis,
angiogenesis,
proliferation,
invasion.
This
provides
individual
account
each
alkaloid
underwent
trials
either
alone
or
combination
drugs.
In
addition,
classes
different
kinds
cancers
discussed.
Frontiers in Pharmacology,
Год журнала:
2023,
Номер
14
Опубликована: Сен. 25, 2023
Leonurine
refers
to
the
desiccated
aerial
portion
of
a
plant
in
Labiatae
family.
The
primary
bioactive
constituent
is
an
alkaloid,
alkaloid
(Leo),
renowned
for
its
substantial
therapeutic
efficacy
treatment
gynecological
disorders,
addition
broad-spectrum
antineoplastic
capabilities.
Over
recent
years,
pharmacodynamic
mechanisms
Leo
have
garnered
escalating
scholarly
interest.
exhibits
anticancer
potential
by
means
array
mechanisms,
encompassing
inhibition
neoplastic
cell
proliferation,
induction
both
apoptosis
and
autophagy,
containment
oncogenic
invasion
migration.
key
signal
transduction
pathways
implicated
these
processes
include
Tumor
Necrosis
Factor-Related
Apoptosis-Inducing
Ligand
(TRAIL),
Phosphoinositide3-Kinase/Serine/Threonine
Protein
Kinase
(PI3K/AKT),
Signal
Transducer
Activator
Transcription
3
(STAT3),
Mitogen-Activated
Protein/Extracellular
Signal-Regulated
(MAP/ERK).
This
paper
commences
with
exploration
principal
cellular
behaviors
influenced
associated
pathways,
thereby
scrutinizing
sequence
events.
intention
offer
theoretical
reinforcement
elucidation
more
profound
underpinning
Leo's
correlating
pharmaceutical
development.