International Journal of Biological Sciences,
Год журнала:
2023,
Номер
19(2), С. 691 - 704
Опубликована: Янв. 1, 2023
Cervical
cancer
(CC)
is
one
of
the
most
common
gynecological
malignancies
with
poor
prognosis
for
advanced
CC
patients.
LRRC8A
a
volume-regulated
anion
channel
protein
involved
in
cellular
homeostasis,
but
its
role
remains
largely
unknown.
In
this
study,
we
found
that
elevated
and
associated
prognosis.
maintains
cell
survivals
under
hypotonic
condition,
promotes
tumorigenesis
through
apoptosis
suppression
vitro
vivo.
Notably,
upregulated
by
NSUN2-mediated
m5C
modification.
modified-LRRC8A
mRNA
bound
RNA
binding
YBX1
followed
increased
stability.
Moreover,
loss
NSUN2
suppresses
proliferation
metastasis
cells,
expression
positively
correlated
CC.
Altogether,
our
study
demonstrates
NSUN2-m5C-LRRC8A
axis
crucial
would
be
potential
therapeutic
target
Chemical Reviews,
Год журнала:
2022,
Номер
122(6), С. 5977 - 6039
Опубликована: Фев. 2, 2022
The
stimulator
of
interferon
genes
(STING)
cellular
signaling
pathway
is
a
promising
target
for
cancer
immunotherapy.
Activation
the
intracellular
STING
protein
triggers
production
multifaceted
array
immunostimulatory
molecules,
which,
in
proper
context,
can
drive
dendritic
cell
maturation,
antitumor
macrophage
polarization,
T
priming
and
activation,
natural
killer
vascular
reprogramming,
and/or
death,
resulting
immune-mediated
tumor
elimination
generation
immune
memory.
Accordingly,
there
significant
amount
ongoing
preclinical
clinical
research
toward
further
understanding
role
surveillance
as
well
development
modulators
strategy
to
stimulate
immunity.
Yet,
efficacy
agonists
limited
by
many
drug
delivery
pharmacological
challenges.
Depending
on
class
agonist
desired
administration
route,
these
may
include
poor
stability,
immunocellular
toxicity,
immune-related
adverse
events,
or
lymph
node
targeting
retention,
low
uptake
delivery,
complex
dependence
magnitude
kinetics
signaling.
This
review
provides
concise
summary
pathway,
highlighting
recent
biological
developments,
immunological
consequences,
implications
delivery.
also
offers
critical
analysis
an
expanding
arsenal
chemical
strategies
that
are
being
employed
enhance
efficacy,
safety,
utility
lastly
draws
attention
several
opportunities
therapeutic
advancements.
Signal Transduction and Targeted Therapy,
Год журнала:
2021,
Номер
6(1)
Опубликована: Июнь 2, 2021
Cell
death
and
immune
response
are
at
the
core
of
life.
In
past
decades,
endoplasmic
reticulum
(ER)
protein
STING1
(also
known
as
STING
or
TMEM173)
was
found
to
play
a
fundamental
role
in
production
type
I
interferons
(IFNs)
pro-inflammatory
cytokines
DNA
derived
from
invading
microbial
pathogens
damaged
hosts
by
activating
multiple
transcription
factors.
addition
this
well-known
function
infection,
inflammation,
immunity,
emerging
evidence
suggests
that
STING1-dependent
signaling
network
is
implicated
health
disease
regulating
autophagic
degradation
various
cell
modalities
(e.g.,
apoptosis,
necroptosis,
pyroptosis,
ferroptosis,
mitotic
death,
immunogenic
[ICD]).
Here,
we
outline
latest
advances
our
understanding
mechanisms
pathways
autophagy
which
may
shed
light
on
new
targets
for
therapeutic
interventions.
Signal Transduction and Targeted Therapy,
Год журнала:
2021,
Номер
6(1)
Опубликована: Апрель 30, 2021
Abstract
Sensing
invasive
cytosolic
DNA
is
an
integral
component
of
innate
immunity.
cGAS
was
identified
in
2013
as
the
major
sensor
that
binds
dsDNA
to
catalyze
synthesis
a
special
asymmetric
cyclic-dinucleotide,
2′3′-cGAMP,
secondary
messenger
bind
and
activate
STING
for
subsequent
production
type
I
interferons
other
immune-modulatory
genes.
Hyperactivation
signaling
contributes
autoimmune
diseases
but
serves
adjuvant
anticancer
immune
therapy.
On
hand,
inactivation
causes
deficiency
sense
clear
viral
bacterial
infection
creates
tumor-prone
microenvironment
facilitate
tumor
evasion
surveillance.
Thus,
activation
tightly
controlled.
In
this
review,
we
summarize
up-to-date
multilayers
regulatory
mechanisms
governing
activation,
including
pre-
post-translational
regulations,
cGAS-binding
proteins,
additional
regulators
such
ions
small
molecules.
We
will
also
reveal
pathophysiological
function
its
product
cGAMP
human
diseases.
hope
provide
review
recent
research
advances
biology
cGAS-targeted
therapies
Signal Transduction and Targeted Therapy,
Год журнала:
2022,
Номер
7(1)
Опубликована: Дек. 23, 2022
Since
the
discovery
of
Stimulator
Interferon
Genes
(STING)
as
an
important
pivot
for
cytosolic
DNA
sensation
and
interferon
(IFN)
induction,
intensive
efforts
have
been
endeavored
to
clarify
molecular
mechanism
its
activation,
physiological
function
a
ubiquitously
expressed
protein,
explore
potential
therapeutic
target
in
wide
range
immune-related
diseases.
With
orthodox
ligand
2'3'-cyclic
GMP-AMP
(2'3'-cGAMP)
upstream
sensor
2'3'-cGAMP
synthase
(cGAS)
be
found,
STING
acquires
central
functionality
best-studied
signaling
cascade,
namely
cGAS-STING-IFN
pathway.
However,
recently
updated
research
through
structural
research,
genetic
screening,
biochemical
assay
greatly
extends
current
knowledge
biology.
A
second
pocket
was
discovered
transmembrane
domain
synthetic
agonist.
On
downstream
outputs,
accumulating
studies
sketch
primordial
multifaceted
roles
beyond
cytokine-inducing
function,
such
autophagy,
cell
death,
metabolic
modulation,
endoplasmic
reticulum
(ER)
stress,
RNA
virus
restriction.
Furthermore,
with
expansion
interactome,
details
trafficking
also
get
clearer.
After
retrospecting
brief
history
viral
interference
milestone
events
since
STING,
we
present
vivid
panorama
biology
taking
into
account
information,
especially
versatile
outputs
functions
IFN
induction.
We
summarize
pathogenesis
various
diseases
highlight
development
small-molecular
compounds
targeting
disease
treatment
combination
latest
research.
Finally,
discuss
open
questions
imperative
answer.
Annual Review of Biochemistry,
Год журнала:
2022,
Номер
91(1), С. 599 - 628
Опубликована: Март 15, 2022
In
the
decade
since
discovery
of
innate
immune
cyclic
GMP-AMP
synthase
(cGAS)-2'3'-cyclic
(cGAMP)-stimulator
interferon
genes
(STING)
pathway,
its
proper
activation
and
dysregulation
have
been
rapidly
implicated
in
many
aspects
human
disease.
Understanding
biochemical,
cellular,
regulatory
mechanisms
this
pathway
is
critical
to
developing
therapeutic
strategies
that
either
harness
it
boost
defense
or
inhibit
prevent
unwanted
inflammation.
review,
we
first
discuss
how
second
messenger
cGAMP
synthesized
by
cGAS
response
double-stranded
DNA
cGAMP's
subsequent
cell-type-dependent
STING
signaling
cascades
with
differential
physiological
consequences.
We
then
review
as
an
immunotransmitter
mediates
tightly
controlled
cell-cell
communication
being
exported
from
producing
cells
imported
into
responding
via
cell-type-specific
transporters.
Finally,
which
thecGAS-cGAMP-STING
responds
different
sources
mislocalized
pathogen
defense,
cancer,
autoimmune
diseases.