Potential Strategies for Overcoming Drug Resistance Pathways Using Propolis and Its Polyphenolic/Flavonoid Compounds in Combination with Chemotherapy and Radiotherapy
Nutrients,
Journal Year:
2024,
Volume and Issue:
16(21), P. 3741 - 3741
Published: Oct. 31, 2024
Conventional
cancer
treatments
include
surgical
resection,
chemotherapy,
hyperthermia,
immunotherapy,
hormone
therapy,
and
locally
targeted
therapies
such
as
radiation
therapy.
Standard
often
require
the
use
of
multiple
agents,
which
can
activate
nuclear
factor
kappa
B
(NF-κB)
in
tumor
cells,
leading
to
reduced
cell
death
increased
drug
resistance.
Moreover,
agents
also
contributes
added
toxicity,
resulting
poor
treatment
outcomes.
Cancer
cells
gradually
develop
resistance
almost
all
chemotherapeutics
through
various
mechanisms,
efflux,
alterations
metabolism
transport,
changes
signal
transduction
pathways,
enhanced
DNA
repair
capacity,
evasion
apoptosis,
mutations,
reactivation
targets,
interaction
with
microenvironment,
cell-stroma
interactions,
epithelial–mesenchymal
transition
(EMT)-mediated
chemoresistance,
epigenetic
modifications,
metabolic
alterations,
effect
stem
(CSCs).
Developing
new
strategies
improve
chemotherapy
sensitivity
while
minimizing
side
effects
is
essential
for
achieving
better
therapeutic
outcomes
enhancing
patients’
quality
life.
One
promising
approach
involves
combining
conventional
propolis
its
flavonoids.
These
natural
compounds
may
enhance
response
reducing
toxicity.
Propolis
components
sensitize
chemotherapeutic
likely
by
inhibiting
NF-κB
activation,
reprogramming
tumor-associated
macrophages
(TAMs;
an
M2-like
phenotype),
thereby
release
matrix
metalloproteinase
(MMP)-9,
cytokines,
chemokines,
vascular
endothelial
growth
(VEGF).
By
TAMs,
overcome
EMT-mediated
disrupt
crosstalk
between
CSCs,
inhibit
maintenance
stemness,
reverse
acquired
immunosuppression,
thus
promoting
antitumor
mediated
cytotoxic
T-cells.
This
review
highlights
potential
flavonoids
modulate
responsiveness
modalities.
The
evidence
suggests
that
novel
incorporating
could
be
developed
positive
cytotoxicity
peripheral
blood
leukocytes,
liver,
kidney
cells.
Therefore,
polyphenolic/flavonoid
hold
combination
clinical
types
cancers.
Language: Английский
The antioxidant property of CAPE depends on TRPV1 channel activation in microvascular endothelial cells.
Miltha Hidalgo,
No information about this author
Bárbara Railef,
No information about this author
Vania Rodríguez
No information about this author
et al.
Redox Biology,
Journal Year:
2025,
Volume and Issue:
80, P. 103507 - 103507
Published: Jan. 20, 2025
Caffeic
acid
phenethyl
ester
(CAPE)
is
a
hydrophobic
phytochemical
typically
found
in
propolis
that
acts
as
an
antioxidant,
anti-inflammatory
and
cardiovascular
protector,
among
several
other
properties.
However,
the
molecular
entity
responsible
for
recognising
CAPE
unknown,
whether
interaction
involved
developing
antioxidant
response
target
cells
remains
unanswered
question.
Herein,
we
hypothesized
subfamily
of
TRP
ion
channels
works
recognizes
at
plasma
membrane
allows
fast
shift
capacity
intact
endothelial
(EC).
By
monitoring
cytoplasmic
Ca2+
microvascular
EC
model,
compared
calcium
responses
evoked
by
three
structurally
related
compounds:
caffeic
ester,
neochlorogenic
acid.
Only
induced
rapid
transient
nanomolar
concentrations
together
with
gradual
increase
sodium
levels,
suggesting
activation
non-selective
cationic
permeation
membrane.
Electrophysiological
well
pharmacological,
RNA
silencing
assays
confirmed
involvement
TRPV1
recognition
ECs.
Finally,
demonstrated
influx
was
necessary
recording
CAPE-induced
redox
changes,
phenomenon
captured
real-time
ECs
expressing
HyPer
biosensor.
Our
data
depict
mechanism
behind
effect
cells,
connecting
channels,
increase,
reduction
disulfide
bonds
on
This
occurs
within
seconds
to
minutes
contributes
better
understanding
mechanisms
underlying
vasodilatory
compounds
interact
vascular
bed.
Language: Английский
Exploring Mechanism of Electroacupuncture in Modulating Neuroinflammation Based on Intestinal Flora and Its Metabolites
Hai-min Ye,
No information about this author
Z.-L. Li,
No information about this author
Peng Zhang
No information about this author
et al.
Chinese Journal of Integrative Medicine,
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 23, 2024
Language: Английский
The double-layer emulsions loaded with bitter melon (Momordica charantia L.) seed oil protect against dextran sulfate sodium-induced ulcerative colitis in mice
Yan Ma,
No information about this author
Wangting Zhou,
No information about this author
Huiling Wang
No information about this author
et al.
International Journal of Biological Macromolecules,
Journal Year:
2024,
Volume and Issue:
278, P. 134279 - 134279
Published: July 30, 2024
Language: Английский
Caffeic Acid Phenethyl Ester Administration Reduces Enterotoxigenic Bacteroides fragilis-Induced Colitis and Tumorigenesis
Toxins,
Journal Year:
2024,
Volume and Issue:
16(9), P. 403 - 403
Published: Sept. 18, 2024
The
human
colonic
commensal
enterotoxigenic
Bacteroides
fragilis
(ETBF)
is
associated
with
chronic
colitis
and
colon
cancer.
ETBF
colonization
induces
via
the
toxin
(BFT).
BFT
secreted
by
cause
inflammation
E-cadherin
cleavage/NF-κB
signaling.
promotes
tumorigenesis
interleukin
17A
(IL-17A)/CXCL-dependent
inflammation,
but
its
bioactive
therapeutics
in
ETBF-promoted
remain
unexplored.
In
current
study,
we
investigated
caffeic
acid
phenethyl
ester
(CAPE)
murine
model
of
tumorigenesis.
this
observed
that
CAPE
treatment
mitigated
induced
mice.
Additionally,
our
findings
indicate
offers
protective
effects
against
ETBF-enhanced
a
mouse
colitis-associated
cancer
azoxymethane
(AOM)
dextran
sulfate
sodium.
Notably,
decrease
following
administration
correlates
reduction
expression
IL-17A
CXCL1
gastrointestinal
tract.
molecular
mechanism
for
CAPE-induced
protection
ETBF-mediated
mediated
IL-17A/CXCL1,
NF-κB
activity
intestinal
epithelial
cells.
Our
may
serve
as
preventive
agent
development
ETBF-induced
colorectal
(CRC).
Language: Английский
Effects of Propolis Supplementation on Gut Microbiota and Uremic Toxin Profiles of Patients Undergoing Hemodialysis
Toxins,
Journal Year:
2024,
Volume and Issue:
16(10), P. 416 - 416
Published: Sept. 25, 2024
Background:
Propolis
possesses
many
bioactive
compounds
that
could
modulate
the
gut
microbiota
and
reduce
production
of
uremic
toxins
in
patients
with
chronic
kidney
disease
(CKD)
undergoing
hemodialysis
(HD).
This
clinical
trial
aimed
to
evaluate
effects
propolis
on
profile
toxin
plasma
levels
HD
patients.
These
are
secondary
analyses
from
a
previous
double-blind,
randomized
study,
42
divided
into
two
groups:
placebo
group
received
400
mg
green
extract/day
for
eight
weeks.
Indole-3
acetic
acid
(IAA),
indoxyl
sulfate
(IS),
p-cresyl
(p-CS)
were
evaluated
by
reversed-phase
liquid
chromatography,
cytokines
investigated
using
multiplex
assay
(Bio-Plex
Magpix®).
The
fecal
composition
was
analyzed
subgroup
(n
=
6)
commercial
kit
DNA
extraction.
V4
region
16S
rRNA
gene
then
amplified
polymerase
chain
reaction
(PCR)
short-read
sequencing
Illumina
NovaSeq
PE250
platform
subgroup.
Forty-one
completed
20
21
group.
There
positive
correlation
between
IAA
TNF-α
(r
0.53,
p
0.01),
IL-2
0.66,
0.002),
pCS
IL-7
0.46,
0.04)
at
baseline.
No
significant
changes
observed
values
after
intervention.
Despite
not
being
significant,
microbial
evenness
richness
increased
following
Counts
Fusobacteria
species
showed
IS,
while
counts
Firmicutes,
Lentisphaerae,
Proteobacteria
phyla
negatively
correlated
IS.
Two
months
supplementation
did
(IAA,
p-CS)
or
change
microbiota.
Language: Английский