Clinical and Translational Medicine,
Journal Year:
2020,
Volume and Issue:
11(1)
Published: Dec. 31, 2020
Abstract
Background
Neuroinflammation‐induced
secondary
injury
is
an
important
cause
of
sustained
progression
spinal
cord
injury.
Inflammatory
programmed
cell
death
pyroptosis
executed
by
the
pore‐forming
protein
gasdermin
D
(GSDMD)
essential
step
neuroinflammation.
However,
it
unclear
whether
CD73,
a
widely
accepted
immunosuppressive
molecule,
can
inhibit
via
mediating
GSDMD.
Methods
C57BL/6J
CD73
deficient
mice
and
wild‐type
mice,
Lipopolysaccharide
(LPS)‐induced
primary
microglia
BV2
cells
were
respectively
used
to
illustrate
effect
on
in
vivo
vitro.
A
combination
molecular
histological
methods
was
performed
assess
explore
mechanism
both
Results
We
have
shown
evidence
for
suppresses
activation
NLRP3
inflammasome
complexes
reduce
maturation
GSDMD,
leading
decreased
microglia.
Further
analysis
reveals
that
adenosine‐A
2B
adenosine
receptor‐PI3K‐AKT‐Foxo1
cascade
possible
regulation.
Importantly,
we
determine
inhibits
expression
GSDMD
at
transcriptional
level
through
Foxo1.
What's
more,
confirm
accumulation
HIF‐1α
promotes
overexpression
after
(SCI),
increased
turn
upregulates
HIF‐1α,
eventually
forming
positive
feedback
regulatory
loop.
Conclusion
Our
data
reveal
novel
function
pyroptosis,
suggesting
unique
therapeutic
opportunity
mitigating
disease
process
SCI.
Signal Transduction and Targeted Therapy,
Journal Year:
2021,
Volume and Issue:
6(1)
Published: March 29, 2021
Abstract
Currently,
pyroptosis
has
received
more
and
attention
because
of
its
association
with
innate
immunity
disease.
The
research
scope
expanded
the
discovery
gasdermin
family.
A
great
deal
evidence
shows
that
can
affect
development
tumors.
relationship
between
tumors
is
diverse
in
different
tissues
genetic
backgrounds.
In
this
review,
we
provide
basic
knowledge
pyroptosis,
explain
tumors,
focus
on
significance
tumor
treatment.
addition,
further
summarize
possibility
as
a
potential
treatment
strategy
describe
side
effects
radiotherapy
chemotherapy
caused
by
pyroptosis.
brief,
double-edged
sword
for
rational
use
dual
effect
will
help
us
explore
formation
ideas
patients
to
develop
new
drugs
based
International Journal of Environmental Research and Public Health,
Journal Year:
2020,
Volume and Issue:
17(3), P. 679 - 679
Published: Jan. 21, 2020
Nickel
is
a
transition
element
extensively
distributed
in
the
environment,
air,
water,
and
soil.
It
may
derive
from
natural
sources
anthropogenic
activity.
Although
nickel
ubiquitous
its
functional
role
as
trace
for
animals
human
beings
has
not
been
yet
recognized.
Environmental
pollution
be
due
to
industry,
use
of
liquid
solid
fuels,
well
municipal
industrial
waste.
contact
can
cause
variety
side
effects
on
health,
such
allergy,
cardiovascular
kidney
diseases,
lung
fibrosis,
nasal
cancer.
molecular
mechanisms
nickel-induced
toxicity
are
clear,
mitochondrial
dysfunctions
oxidative
stress
thought
have
primary
crucial
this
metal.
Recently,
researchers,
trying
characterize
capability
induce
cancer,
found
out
that
epigenetic
alterations
induced
by
exposure
perturb
genome.
The
purpose
review
describe
chemical
features
toxicity.
Furthermore,
attention
focused
strategies
remove
phytoremediation
phytomining.
European Journal of Immunology,
Journal Year:
2019,
Volume and Issue:
49(10), P. 1457 - 1973
Published: Oct. 1, 2019
These
guidelines
are
a
consensus
work
of
considerable
number
members
the
immunology
and
flow
cytometry
community.
They
provide
theory
key
practical
aspects
enabling
immunologists
to
avoid
common
errors
that
often
undermine
immunological
data.
Notably,
there
comprehensive
sections
all
major
immune
cell
types
with
helpful
Tables
detailing
phenotypes
in
murine
human
cells.
The
latest
techniques
applications
also
described,
featuring
examples
data
can
be
generated
and,
importantly,
how
analysed.
Furthermore,
tips,
tricks
pitfalls
avoid,
written
peer-reviewed
by
leading
experts
field,
making
this
an
essential
research
companion.
Signal Transduction and Targeted Therapy,
Journal Year:
2022,
Volume and Issue:
7(1)
Published: Aug. 13, 2022
Regulated
cell
death
(RCD),
also
well-known
as
programmed
(PCD),
refers
to
the
form
of
that
can
be
regulated
by
a
variety
biomacromolecules,
which
is
distinctive
from
accidental
(ACD).
Accumulating
evidence
has
revealed
RCD
subroutines
are
key
features
tumorigenesis,
may
ultimately
lead
establishment
different
potential
therapeutic
strategies.
Hitherto,
targeting
with
pharmacological
small-molecule
compounds
been
emerging
promising
avenue,
rapidly
progressed
in
many
types
human
cancers.
Thus,
this
review,
we
focus
on
summarizing
not
only
apoptotic
and
autophagy-dependent
signaling
pathways,
but
crucial
pathways
other
subroutines,
including
necroptosis,
pyroptosis,
ferroptosis,
parthanatos,
entosis,
NETosis
lysosome-dependent
(LCD)
cancer.
Moreover,
further
discuss
current
situation
several
improve
cancer
treatment,
such
single-target,
dual
or
multiple-target
compounds,
drug
combinations,
some
new
strategies
would
together
shed
light
future
directions
attack
vulnerabilities
drugs
for
purposes.
Cell Death Discovery,
Journal Year:
2020,
Volume and Issue:
6(1)
Published: Oct. 28, 2020
Abstract
Apoptosis
has
long
been
recognized
as
a
mechanism
that
kills
the
cancer
cells
by
cytotoxic
drugs.
In
recent
years,
studies
have
proved
pyroptosis
can
also
shrink
tumors
and
inhibit
proliferation.
Both
apoptosis
are
caspase-dependent
programmed
cell
death
pathways.
Cysteinyl
aspartate
specific
proteinase-3
(Caspase-3)
is
common
key
protein
in
pathways,
when
activated,
expression
level
of
tumor
suppressor
gene
Gasdermin
E
(GSDME)
determines
death.
When
GSDME
highly
expressed,
active
caspase-3
cuts
it
releases
N-terminal
domain
to
punch
holes
membrane,
resulting
swelling,
rupture,
low,
will
lead
classical
death,
which
apoptosis.
More
interestingly,
researchers
found
be
located
upstream
caspase-3,
connecting
extrinsic,
intrinsic
apoptotic
Then,
promoting
activation,
forming
self-amplifying
feed-forward
loop.
GSDME-mediated
correlated
with
side
effects
chemotherapy
anti-tumor
immunity.
This
article
mainly
reviews
caspase-3/GSDME
signal
pathway
switch
between
cancer,
provide
new
strategies
targets
for
treatment.
Advanced Materials,
Journal Year:
2018,
Volume and Issue:
31(5)
Published: Dec. 9, 2018
Abstract
The
tumor
microenvironment
(TME)
has
been
increasingly
recognized
as
a
crucial
contributor
to
tumorigenesis.
Based
on
the
unique
TME
for
achieving
tumor‐specific
therapy,
here
novel
concept
of
photothermal‐enhanced
sequential
nanocatalytic
therapy
in
both
NIR‐I
and
NIR‐II
biowindows
is
proposed,
which
innovatively
changes
condition
Fenton
reaction
production
highly
efficient
hydroxyl
radicals
(•OH)
consequently
suppressing
growth.
Evidence
suggests
that
glucose
plays
vital
role
powering
cancer
progression.
Encouraged
by
oxidation
gluconic
acid
H
2
O
oxidase
(GOD),
an
Fe
3
4
/GOD‐functionalized
polypyrrole
(PPy)‐based
composite
nanocatalyst
constructed
achieve
diagnostic
imaging‐guided,
photothermal‐enhanced,
TME‐specific
therapy.
consumption
intratumoral
GOD
leads
situ
elevation
level,
integrated
component
then
catalyzes
into
toxic
•OH
efficiently
induce
cancer‐cell
death.
Importantly,
high
photothermal‐conversion
efficiency
(66.4%
biowindow)
PPy
elevates
local
temperature
substaintially
accelerate
improve
disproportionation
degree
enhancing
nanocatalytic‐therapeutic
efficacy,
successfully
achieves
remarkable
synergistic
anticancer
outcome
with
minimal
side
effects.
Cell Death Discovery,
Journal Year:
2021,
Volume and Issue:
7(1)
Published: April 7, 2021
Abstract
Ovarian
cancer
(OC)
is
a
highly
malignant
gynaecological
tumour
that
has
very
poor
prognosis.
Pyroptosis
been
demonstrated
in
recent
years
to
be
an
inflammatory
form
of
programmed
cell
death.
However,
the
expression
pyroptosis-related
genes
OC
and
their
correlations
with
prognosis
remain
unclear.
In
this
study,
we
identified
31
pyroptosis
regulators
were
differentially
expressed
between
normal
ovarian
tissues.
Based
on
these
(DEGs),
all
cases
could
divided
into
two
subtypes.
The
prognostic
value
each
gene
for
survival
was
evaluated
construct
multigene
signature
using
Cancer
Genome
Atlas
(TCGA)
cohort.
By
applying
least
absolute
shrinkage
selection
operator
(LASSO)
Cox
regression
method,
7-gene
built
classified
patients
TCGA
cohort
low-
or
high-risk
group.
low-risk
group
showed
significantly
higher
possibilities
than
those
(
P
<
0.001).
Utilizing
median
risk
score
from
cohort,
Gene
Expression
Omnibus
(GEO)
subgroups,
had
increased
overall
(OS)
time
=
0.014).
Combined
clinical
characteristics,
found
independent
factor
predicting
OS
patients.
ontology
(GO)
Kyoto
Encylopedia
Genes
Genomes
(KEGG)
analyses
indicated
immune-related
enriched
immune
status
decreased
conclusion,
play
important
roles
immunity
can
used
predict
OCs.
International Journal of Molecular Sciences,
Journal Year:
2018,
Volume and Issue:
19(10), P. 3082 - 3082
Published: Oct. 9, 2018
Neuronal
cell
death
in
the
central
nervous
system
has
always
been
a
challenging
process
to
decipher.
In
normal
physiological
conditions,
neuronal
is
restricted
adult
brain,
even
aged
individuals.
However,
pathological
conditions
of
various
neurodegenerative
diseases,
and
shrinkage
specific
region
brain
represent
fundamental
feature
across
different
diseases.
this
review,
we
will
briefly
go
through
general
pathways
describe
evidence
for
context
individual
common
discussing
our
current
understanding
by
connecting
with
renowned
pathogenic
proteins,
including
Tau,
amyloid-beta,
alpha-synuclein,
huntingtin
TDP-43.