Biomedicine & Pharmacotherapy,
Journal Year:
2021,
Volume and Issue:
142, P. 112043 - 112043
Published: Aug. 16, 2021
Despite
its
adverse
effects,
chemotherapy
is
generally
used
for
the
treatment
of
colorectal
cancer
(CRC).
Development
supplement
preparations
targeting
stem
cells
(CSCs)
that
cause
distant
metastasis
and
drug
resistance
required.
Although
curcumin
known
to
have
anti-tumor,
hepatoprotective,
hypoglycemic-like
actions,
low
water
solubility,
oral
absorption,
bioavailability
impede
therapeutic
uses.
Patient-derived
organoid
cultures
can
recapitulate
heterogeneity,
epithelial
structures,
molecular
imprints
their
parental
tissues.
In
present
study,
anti-carcinogenic
properties
amorphous
(AC),
a
compound
with
improved
solubility
bioavailability,
were
evaluated
against
human
CRC
organoids.
Treatment
AC
inhibited
cell
viability
organoids
in
concentration-dependent
manner.
arrested
cycle
induced
apoptosis.
phosphorylation
ERK.
Expression
downstream
signals
ERK,
namely
c-MYC
cyclin-D1,
inhibited.
Expressions
CSC
markers,
CD44,
LGR5,
CD133,
declined
AC-treated
The
combinational
anti-cancer
drugs,
oxaliplatin,
5-FU,
or
irinotecan
showed
synergistic
activity.
vivo,
decreased
tumor
growth
mice
induction
necrotic
lesions.
conclusion,
diminished
through
inhibition
proliferation-related
marker
expression
addition
arresting
cycle.
Collectively,
these
data
suggest
value
as
promising
could
be
combination
drugs
prevent
recurrence
CRC.
International Journal of Molecular Sciences,
Journal Year:
2020,
Volume and Issue:
21(7), P. 2364 - 2364
Published: March 29, 2020
Curcumin
diffuses
through
cell
membranes
into
the
endoplasmic
reticulum,
mitochondria,
and
nucleus,
where
it
exerts
actions,
as
an
antioxidant
property.
Therefore,
its
use
has
been
advocated
for
chemopreventive,
antimetastatic,
anti-angiogenic
purposes.
We
conducted
a
literature
review
to
summarize
studies
investigating
relationship
between
curcumin
colorectal
cancer
(CRC).
In
vitro
studies,
performed
on
human
colon
lines,
showed
that
inhibited
cellular
growth
cycle
arrest
at
G2/M
G1
phases,
well
stimulated
apoptosis
by
interacting
with
multiple
molecular
targets.
vivo
have
in
inflammatory
genetic
CRC
animal
models
chemopreventive
effect.
To
improve
bioavailability,
associated
small
particles
increase
absorption
when
orally
administered
excellent
results
both
inflammation
carcinogenesis.
used,
moreover,
component
of
dietetic
formulations
chemoprevention.
These
combinations
anticarcinogenetic
properties
inflammation-related
CRC.
A
synergic
effect
was
suggested
using
individual
constituent
dosage,
which
lower
than
experimentally
used
“in
vivo”
single
components.
conclusion,
falls
within
category
plant
origin
substances
able
prevent
animals.
This
property
offers
promising
expectations
humans.
International Journal of Molecular Sciences,
Journal Year:
2022,
Volume and Issue:
23(3), P. 1532 - 1532
Published: Jan. 28, 2022
Cisplatin
and
other
platinum-based
drugs,
such
as
carboplatin,
ormaplatin,
oxaliplatin,
have
been
widely
used
to
treat
a
multitude
of
human
cancers.
However,
considerable
proportion
patients
often
relapse
due
drug
resistance
and/or
toxicity
multiple
organs
including
the
liver,
kidneys,
gastrointestinal
tract,
cardiovascular,
hematologic,
nervous
systems.
In
this
study,
we
sought
provide
comprehensive
review
current
state
science
highlighting
use
cisplatin
in
cancer
therapy,
with
special
emphasis
on
its
molecular
mechanisms
action,
treatment
modalities
combination
therapy
natural
products.
Hence,
searched
literature
using
various
scientific
databases.,
MEDLINE,
PubMed,
Google
Scholar,
relevant
sources,
collect
publications
cisplatin,
products,
uses
treatment,
modes
therapeutic
strategies.
Our
search
results
revealed
that
new
strategic
approaches
for
evaluated
some
degree
success.
Scientific
evidence
from
both
vitro
vivo
studies
demonstrates
many
medicinal
plants
contain
bioactive
compounds
are
promising
candidates
diseases,
therefore
represent
an
excellent
source
discovery.
preclinical
studies,
it
has
demonstrated
products
not
only
enhance
activity
but
also
attenuate
chemotherapy-induced
toxicity.
Many
experimental
reported
exert
their
action
by
triggering
apoptosis
through
modulation
mitogen-activated
protein
kinase
(MAPK)
p53
signal
transduction
pathways
enhancement
chemosensitivity.
Furthermore,
protect
against
cisplatin-induced
organ
modulating
several
gene
transcription
factors
inducing
cell
death
necrosis.
addition,
formulations
polymeric,
lipid,
inorganic,
carbon-based
nano-drug
delivery
systems
found
delay
release,
prolong
half-life,
reduce
systemic
while
formulations,
nanocapsules,
nanogels,
hydrogels,
penetration,
target
cells,
inhibit
tumor
progression.
Frontiers in Oncology,
Journal Year:
2022,
Volume and Issue:
12
Published: April 22, 2022
Colorectal
cancer
(CRC)
is
one
of
the
most
common
and
reoccurring
diseases,
as
well
world's
second
largest
cause
mortality.
Despite
existing
preventative,
diagnostic,
treatment
methods,
such
chemotherapy,
number
instances
rises
year
after
year.
As
a
result,
new
effective
medications
targeting
specific
checkpoints
should
be
developed
to
combat
CRC.
Natural
compounds,
curcumin,
have
shown
significant
anti-colorectal
characteristics
among
that
can
used
treat
These
chemicals
are
phenolic
compounds
belong
curcuminoids
category.
Curcumin
exerts
its
anti-proliferative
properties
against
CRC
cell
lines
in
vitro
vivo
via
variety
mechanisms,
including
suppression
intrinsic
extrinsic
apoptotic
signaling
pathways,
stoppage
cycle,
activation
autophagy.
also
has
anti-angiogenesis
properties.
Thus,
this
review
aimed
at
emphasizing
biological
effect
mode
action
curcumin
on
Furthermore,
critical
role
these
substances
chemoprevention
was
emphasized.
Advances in Cancer Biology - Metastasis,
Journal Year:
2024,
Volume and Issue:
10, P. 100114 - 100114
Published: Jan. 17, 2024
A
significant
obstacle
to
treating
cancer
is
multidrug
resistance
(MDR),
which
the
capacity
of
cancerous
cells
develop
both
traditional
and
cutting-edge
chemotherapeutic
treatments.
Following
initial
discovery
that
cellular
pumps
reliant
on
ATP
were
root
chemotherapy
resistance,
more
research
has
revealed
involvement
additional
mechanisms,
including
increased
drug
metabolism,
reduced
entry,
compromised
apoptotic
pathways.
Numerous
projects
have
focused
MDR,
innumerable
been
conducted
better
understand
MDR
methods
mitigate
its
consequences.
Multidrug
(MDR)
a
key
challenge
in
cancer.
90%
cancer-related
fatalities
are
brought
by
tumor
metastasis
recurrence,
possible
with
MDR.
Drug
influenced
diverse
internal
extrinsic
variables,
genetic
epigenetic
changes,
efflux
systems,
DNA
repair
apoptosis,
autophagy.
In
this
review
paper,
we
list
potential
hazards
associated
therapy
general,
primarily
developing
theory
for
colorectal
particular.
We
discussed
unique
instance
malignancies
generally
5-fluorouracil,
curcumin,
lipids
as
viable
options
condition.
The
use
nanotechnology
(mainly
nanoparticles)
facilitated
vitro
well
vivo
efficacy
during
preclinical
phases,
summarized
below,
allowing
thorough
investigation
cancers
pancreatic
carcinomas
their
translation
following
clinical
trials.
Molecular Cancer,
Journal Year:
2025,
Volume and Issue:
24(1)
Published: Feb. 24, 2025
As
one
part
of
the
innate
immune
response
to
external
stimuli,
chronic
inflammation
increases
risk
various
cancers,
and
tumor-promoting
is
considered
enabling
characteristics
cancer
development.
Recently,
there
has
been
growing
evidence
on
role
anti-inflammation
therapy
in
prevention
treatment.
And
researchers
have
already
achieved
several
noteworthy
outcomes.
In
review,
we
explored
underlying
mechanisms
by
which
affects
occurrence
development
cancer.
The
pro-
or
anti-tumor
effects
these
inflammatory
factors
such
as
interleukin,
interferon,
chemokine,
inflammasome,
extracellular
matrix
are
discussed.
Since
FDA-approved
drugs
like
aspirin
show
obvious
effects,
unique
advantages
due
their
relatively
fewer
side
with
long-term
use
compared
chemotherapy
drugs.
make
them
promising
candidates
for
chemoprevention.
Overall,
this
review
discusses
molecules
carcinogenesis
new
molecules-directed
therapeutic
opportunities,
ranging
from
cytokine
inhibitors/agonists,
inflammasome
inhibitors,
some
inhibitors
that
expected
be
applied
clinical
practice,
well
recent
discoveries
effect
non-steroidal
anti-inflammatory
steroidal
disadvantages
application
chemoprevention
also
Nutrients,
Journal Year:
2019,
Volume and Issue:
11(12), P. 2989 - 2989
Published: Dec. 6, 2019
Lung
cancer
is
among
the
most
common
cancers
with
a
high
mortality
rate
worldwide.
Despite
significant
advances
in
diagnostic
and
therapeutic
approaches,
lung
prognoses
survival
rates
remain
poor
due
to
late
diagnosis,
drug
resistance,
adverse
effects.
Therefore,
new
intervention
therapies,
such
as
use
of
natural
compounds
decreased
toxicities,
have
been
considered
therapy.
Curcumin,
occurring
polyphenol
derived
from
turmeric
(Curcuma
longa)
has
studied
extensively
recent
years
for
its
It
shown
that
curcumin
demonstrates
anti-cancer
effects
through
various
mechanisms,
including
inhibition
cell
proliferation,
invasion,
metastasis,
induction
apoptosis,
epigenetic
alterations,
regulation
microRNA
expression.
Several
vitro
vivo
studies
these
mechanisms
are
modulated
by
multiple
molecular
targets
STAT3,
EGFR,
FOXO3a,
TGF-β,
eIF2α,
COX-2,
Bcl-2,
PI3KAkt/mTOR,
ROS,
Fas/FasL,
Cdc42,
E-cadherin,
MMPs,
adiponectin.
In
addition,
limitations,
strategies
overcome
bioavailability,
potential
side
well
clinical
trials
were
also
reviewed.
Biomolecules,
Journal Year:
2020,
Volume and Issue:
10(1), P. 105 - 105
Published: Jan. 8, 2020
Gastrointestinal
(GI)
cancer
is
a
prevailing
global
health
disease
with
high
incidence
rate
which
varies
by
region.
It
huge
economic
burden
on
care
providers.
GI
affects
different
organs
in
the
body
such
as
gastric
organs,
colon,
esophagus,
intestine,
and
pancreas.
Internal
external
factors
like
smoking,
obesity,
urbanization,
genetic
mutations,
prevalence
of
Helicobacter
pylori
Hepatitis
B
C
viral
infections
could
increase
risk
cancer.
Phytochemicals
are
non-nutritive
bioactive
secondary
compounds
abundantly
found
fruits,
grains,
vegetables.
Consumption
phytochemicals
may
protect
against
chronic
diseases
cardiovascular
disease,
neurodegenerative
Multiple
studies
have
assessed
chemoprotective
effect
selected
cancer,
offering
support
to
their
potential
towards
reducing
pathogenesis
disease.
The
aim
this
review
was
summarize
current
knowledge
addressing
anti-cancerous
effects
dietary
molecular
activities
mechanisms,
i.e.,
nuclear
factor
kappa-light-chain-enhancer
activated
cells
(NF-κB),
detoxification
enzymes,
adenosine
monophosphate
protein
kinase
(AMPK),
wingless-related
integration
site/β-catenin
(wingless-related
site
(Wnt)
β-catenin,
cell
apoptosis,
phosphoinositide
3-kinases
(PI3K)/
AKT/
mammalian
target
rapamycin
(mTOR),
mitogen-activated
(MAPK).
In
were
classified
into
four
main
categories:
(i)
carotenoids,
including
lutein,
lycopene,
β-carotene;
(ii)
proanthocyanidins,
quercetin
ellagic
acid;
(iii)
organosulfur
compounds,
allicin,
allyl
propyl
disulphide,
asparagusic
acid,
sulforaphane;
(iv)
other
pectin,
curcumins,
p-coumaric
acid
ferulic
acid.
Overall,
improve
prognosis
through
downregulation
β-catenin
phosphorylation,
therefore
enhancing
upregulation
AMPK
pathway,
supports
cellular
homeostasis.
Nevertheless,
more
needed
provide
better
understanding
mechanism
treatment
using
possible
side
associated
approach.
Molecules,
Journal Year:
2020,
Volume and Issue:
25(22), P. 5319 - 5319
Published: Nov. 14, 2020
Cancer
is
one
of
the
main
causes
death
globally
and
considered
as
a
major
challenge
for
public
health
system.
The
high
toxicity
lack
selectivity
conventional
anticancer
therapies
make
search
alternative
treatments
priority.
In
this
review,
we
describe
plant-derived
natural
products
used
agents.
Natural
sources,
extraction
methods,
mechanisms,
clinical
studies,
pharmaceutical
formulation
are
discussed
in
review.
Studies
covered
by
review
should
provide
solid
foundation
researchers
physicians
to
enhance
basic
research
on
developing
therapies.
Scientific Reports,
Journal Year:
2022,
Volume and Issue:
12(1)
Published: Feb. 4, 2022
Abstract
Nowadays,
the
usage
of
nanoparticles
in
various
fields
such
as
drug
delivery,
attracts
attention
many
researchers
treatment
cancers.
Graphene
oxide
(GO)
is
one
novel
delivery
systems
which
used
broadly
owing
to
its
unique
features.
In
this
survey,
doxorubicin
(DOX)
was
accompanied
by
natural
medicine,
curcumin
(CUR),
diminish
side
effects
and
enhance
efficiency.
Cytotoxicity
assay
human
gastric
cancer
(AGS),
prostate
(PC3),
ovarian
(A2780),
evaluated.
Also,
uptake
DOX
CUR
into
cells,
assessed
using
a
fluorescence
microscope.
Moreover,
real-time
PCR
applied
for
evaluation
expression
RB1
CDK2
genes,
were
involved
cell
cycle.
both
separate
simultaneous
forms,
loaded
with
high
efficiency
release
behavior
drugs
pH-sensitive.
The
higher
rate
attained
at
pH
5.5
42
°C
(80.23%)
(13.06),
respectively.
intensity
free
form
drugs,
than
form.
same
concentration,
more
toxic
all
lines.
showed
impact
on
genes.
Co-delivery
mentioned
lines,
effective
due
lower
toxicity
normal
cells.
Molecules,
Journal Year:
2022,
Volume and Issue:
27(15), P. 4818 - 4818
Published: July 27, 2022
Cancer
is
the
second
leading
cause
of
death
after
cardiovascular
diseases.
Conventional
anticancer
therapies
are
associated
with
lack
selectivity
and
serious
side
effects.
hallmarks
biological
capabilities
acquired
by
cancer
cells
during
neoplastic
transformation.
Targeting
multiple
a
promising
strategy
to
treat
cancer.
The
diversity
in
chemical
structure
relatively
low
toxicity
make
plant-derived
natural
products
source
for
development
new
more
effective
that
have
capacity
target
In
this
review,
we
discussed
activities
ten
extracted
from
plants.
majority
these
inhibit
targeting
hallmarks,
many
chemicals
reached
clinical
applications.
Studies
review
provide
solid
ground
researchers
physicians
design
combination
using
products.