Advanced Science,
Journal Year:
2022,
Volume and Issue:
9(23)
Published: June 16, 2022
In
the
field
of
nanomedicine,
there
is
a
tendency
matching
designed
nanomaterials
with
suitable
type
orthotopic
cancer
model,
not
just
casual
subcutaneous
one.
Under
this
condition,
knowing
specific
features
chosen
model
priority,
then
introducing
proper
therapy
strategy
using
nanomaterials.
Here,
Fenton
chemistry
combined
zinc
peroxide
nanoparticles
in
treatment
liver
which
has
"chemical
factory"
including
that
main
place
for
iron
storage,
metabolism,
and
also
metabolic
sites
majority
ingested
substances,
guaranteeing
customized
enhanced
chemodynamic
normal
cells
protection
as
well.
The
good
results
vitro
vivo
can
set
an
inspiring
example
exploring
utilizing
corresponding
models,
ensuring
well-fitness
disease
satisfactory
therapeutic
effect.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(5), P. 4491 - 4491
Published: Feb. 24, 2023
The
life
expectancy
of
the
global
population
has
increased.
Aging
is
a
natural
physiological
process
that
poses
major
challenges
in
an
increasingly
long-lived
and
frail
population.
Several
molecular
mechanisms
are
involved
aging.
Likewise,
gut
microbiota,
which
influenced
by
environmental
factors
such
as
diet,
plays
crucial
role
modulation
these
mechanisms.
Mediterranean
well
components
present
it,
offer
some
proof
this.
Achieving
healthy
aging
should
be
focused
on
promotion
lifestyle
habits
reduce
development
pathologies
associated
with
aging,
order
to
increase
quality
In
this
review
we
analyze
influence
diet
pathways
microbiota
more
favorable
patterns,
its
possible
anti-aging
treatment.
Cell Death and Disease,
Journal Year:
2024,
Volume and Issue:
15(4)
Published: April 18, 2024
The
Unfolded
Protein
Response
(UPR)
is
an
essential
cellular
process
activated
by
the
accumulation
of
unfolded
proteins
within
Endoplasmic
Reticulum
(ER),
a
condition
referred
to
as
ER
stress.
Three
anchored
receptors,
IRE1,
PERK
and
ATF6
act
stress
sensors
monitoring
health
ER.
Upon
detection
stress,
initiate
downstream
signaling
pathways
collectively
UPR.
overarching
aim
UPR
restore
homeostasis
reducing
however
if
that
not
possible,
transitions
from
pro-survival
pro-death
response.
While
our
understanding
key
central
well
defined,
same
true
subtle
events
help
fine
tune
UPR,
supporting
its
ability
adapt
varying
amplitudes
or
durations
In
this
study,
we
demonstrate
cross
talk
between
IRE1
branches
wherein
via
XBP1s
helps
sustain
expression
during
prolonged
Our
findings
suggest
aids
adaptiveness
thereby
helping
support
plasticity
responses.
Medicines,
Journal Year:
2019,
Volume and Issue:
6(3), P. 82 - 82
Published: July 30, 2019
Prostate
cancer
is
the
most
frequent
nonskin
and
second
common
cause
of
cancer-related
deaths
in
man.
a
clinically
heterogeneous
disease
with
many
patients
exhibiting
an
aggressive
progression,
metastasis,
other
showing
indolent
low
tendency
to
progression.
Three
stages
development
human
prostate
tumors
have
been
identified:
intraepithelial
neoplasia,
adenocarcinoma
androgen-dependent,
androgen-independent
or
castration-resistant.
Advances
molecular
technologies
provided
very
rapid
progress
our
understanding
genomic
events
responsible
for
initial
progression
cancer.
These
studies
shown
that
genome
displays
relatively
mutation
rate
compared
cancers
few
chromosomal
loss
gains.
The
ensemble
these
has
led
suggest
existence
two
main
groups
cancers:
one
characterized
by
presence
ERG
rearrangements
(~50%
harbor
recurrent
gene
fusions
involving
ETS
transcription
factors,
fusing
5′
untranslated
region
androgen-regulated
TMPRSS2
nearly
coding
sequence
family
factor
ERG)
features
chemoplexy
(complex
developing
from
coordinated
simultaneous
event),
absence
mutations
E3
ubiquitin
ligase
adapter
SPOP
and/or
deletion
CDH1,
chromatin
remodeling
factor,
interchromosomal
are
early
during
development.
During
epigenomic
abnormalities
accrued
converged
on
pathways,
leading
highly
transcriptomic
landscape,
hyperactive
androgen
receptor
signaling
axis.
Frontiers in Immunology,
Journal Year:
2019,
Volume and Issue:
10
Published: Dec. 4, 2019
An
imbalance
in
the
correct
protein
folding
milieu
of
endoplasmic
reticulum
(ER)
can
cause
ER
stress,
which
leads
to
activation
unfolded
response
(UPR).
The
UPR
constitutes
a
highly
conserved
and
intricately
regulated
group
pathways
that
serve
restore
homeostasis
through
adaptation
or
apoptosis.
Numerous
studies
over
last
decade
have
shown
plays
critical
role
shaping
immunity
inflammation,
resulting
recognition
as
key
player
pathological
processes
including
complex
inflammatory,
autoimmune
neoplastic
diseases.
intestinal
epithelium,
with
its
many
secretory
cells,
forms
an
important
barrier
messenger
between
luminal
environment
host
immune
system.
It
is
not
surprising,
numerous
associated
stress
diseases
such
inflammatory
bowel
disease
(IBD)
colorectal
cancer
(CRC).
In
this
review,
we
discuss
our
current
understanding
roles
responses
maintaining
tissue
homeostasis.
Furthermore,
played
by
disease,
particularly
emphasis
ion
inflammation
cancerIBD
CRC,
described
here.
As
has
been
increasingly
recognized
pharmacological
target
development
therapeutic
strategies
for
immune-mediated
pathologies.
We
summarize
available
targeting
their
implications.
Understanding
balance
pathophysiology,
well
means
manipulating
balance,
provides
avenue
future
research.
Science,
Journal Year:
2019,
Volume and Issue:
365(6450)
Published: July 18, 2019
A
“sUPR”
target
for
pain
management?
The
unfolded
protein
response
(UPR)
is
initiated
when
or
misfolded
proteins
accumulate
in
the
endoplasmic
reticulum.
One
highly
conserved
arm
of
UPR,
IRE1α–XBP1
signaling
pathway,
also
plays
a
role
various
other
UPR-independent
processes,
including
hypoxia,
angiogenesis,
and
inflammation.
Chopra
et
al.
report
that
this
pathway
additionally
regulates
production
two
molecules,
cyclooxygenase
2
microsomal
prostaglandin
E
synthase
1,
help
mediate
inflammation-induced
(see
Perspective
by
Avril
Chevet).
When
elements
were
knocked
out,
behaviors
reduced
different
mouse
models
pain.
Targeting
may
result
improved
management
therapies.
Science
,
issue
p.
eaau6499
;
see
224
Biomedicine & Pharmacotherapy,
Journal Year:
2020,
Volume and Issue:
127, P. 110069 - 110069
Published: April 12, 2020
X-box
binding
protein
1
(XBP1)
is
a
unique
basic-region
leucine
zipper
(bZIP)
transcription
factor
whose
dynamic
form
controlled
by
an
alternative
splicing
response
upon
disturbance
of
homeostasis
in
the
endoplasmic
reticulum
(ER)
and
activation
unfolded
(UPR).
XBP1
was
first
distinguished
as
key
regulator
major
histocompatibility
complex
(MHC)
class
II
gene
expression
B
cells.
communicates
with
foremost
conserved
signalling
component
UPR
essential
for
cell
fate
determination
to
ER
stress
(ERS).
Here,
we
review
recent
advances
our
understanding
this
multifaceted
translation
cancer.
In
review,
briefly
discuss
role
mediators
transcriptional
function
XBP1.
addition,
describe
how
operates
tumour
progression
metastasis.
We
mainly
XBP1's
expression,
prognostic
value
research
on
solid
tumours.
Finally,
multiple
approaches,
especially
those
involving
XBP1,
that
overcome
immunosuppressive
effect
cancer
could
potentially
be
useful
antitumour
therapies.
Antioxidants,
Journal Year:
2021,
Volume and Issue:
10(9), P. 1419 - 1419
Published: Sept. 5, 2021
Reactive
oxygen
species
(ROS)
are
noxious
to
cells
because
their
increased
level
interacts
with
the
body’s
defense
mechanism.
These
also
cause
mutations
and
uncontrolled
cell
division,
resulting
in
oxidative
stress
(OS).
Prolonged
is
responsible
for
incorrect
protein
folding
endoplasmic
reticulum
(ER),
causing
a
stressful
condition,
ER
stress.
cellular
stresses
(oxidative
stress)
well-recognized
biological
factors
that
play
prominent
role
progression
of
hepatocellular
carcinoma
(HCC).
HCC
critical
global
health
problem
third
leading
cancer-related
mortality.
The
application
anti-oxidants
from
herbal
sources
significantly
reduces
Kaempferol
(KP)
naturally
occurring,
aglycone
dietary
flavonoid
present
various
plants
(Crocus
sativus,
Coccinia
grandis,
Euphorbia
pekinensis,
varieties
Aloe
vera,
etc.)
It
capable
interacting
pleiotropic
proteins
human
body.
Efforts
progress
develop
KP
as
potential
candidate
prevent
no
adverse
effects.
This
review
emphasizes
molecular
mechanism
treating
HCC,
targeting