International Journal of Molecular Sciences,
Год журнала:
2022,
Номер
23(13), С. 7292 - 7292
Опубликована: Июнь 30, 2022
Differential
evolution
of
apoptosis,
programmed
necrosis,
and
autophagy,
parthanatos
is
a
form
cell
death
mediated
by
poly(ADP-ribose)
polymerase
1
(PARP1),
which
caused
DNA
damage.
PARP1
hyper-activation
stimulates
apoptosis-inducing
factor
(AIF)
nucleus
translocation,
accelerates
nicotinamide
adenine
dinucleotide
(NAD+)
adenosine
triphosphate
(ATP)
depletion,
leading
to
fragmentation.
The
mechanisms
mainly
include
damage,
hyper-activation,
PAR
accumulation,
NAD+
ATP
AIF
translocation.
Now,
it
reported
that
widely
exists
in
different
diseases
(tumors,
retinal
diseases,
neurological
diabetes,
renal
cardiovascular
ischemia-reperfusion
injury...).
Excessive
or
defective
contributes
pathological
damage;
therefore,
critical
the
therapy
prevention
many
diseases.
In
this
work,
hallmarks
molecular
its
related
disorders
are
summarized.
questions
raised
recent
findings
also
presented.
Further
understanding
will
provide
new
treatment
option
for
associated
conditions.
International Journal of Molecular Sciences,
Год журнала:
2019,
Номер
20(14), С. 3423 - 3423
Опубликована: Июль 12, 2019
Microbial
biofilms
are
communities
of
aggregated
microbial
cells
embedded
in
a
self-produced
matrix
extracellular
polymeric
substances
(EPS).
Biofilms
recalcitrant
to
extreme
environments,
and
can
protect
microorganisms
from
ultraviolet
(UV)
radiation,
temperature,
pH,
high
salinity,
pressure,
poor
nutrients,
antibiotics,
etc.,
by
acting
as
“protective
clothing”.
In
recent
years,
research
works
on
have
been
mainly
focused
biofilm-associated
infections
strategies
for
combating
biofilms.
this
review,
we
focus
instead
the
contemporary
perspectives
biofilm
formation
describe
fundamental
roles
protecting
exposure
environmental
stresses
regulatory
factors
involved
formation.
Understanding
mechanisms
environments
is
essential
employment
beneficial
prevention
harmful
microorganisms.
Signal Transduction and Targeted Therapy,
Год журнала:
2021,
Номер
6(1)
Опубликована: Июль 9, 2021
Abstract
Genomic
instability
is
the
hallmark
of
various
cancers
with
increasing
accumulation
DNA
damage.
The
application
radiotherapy
and
chemotherapy
in
cancer
treatment
typically
based
on
this
property
cancers.
However,
adverse
effects
including
normal
tissues
injury
are
also
accompanied
by
chemotherapy.
Targeted
therapy
has
potential
to
suppress
cells’
damage
response
through
tailoring
patients
lacking
specific
functions.
Obviously,
understanding
broader
role
repair
became
a
basic
attractive
strategy
for
targeted
therapy,
particular,
raising
novel
hypothesis
or
theory
field
basis
previous
scientists’
findings
would
be
important
future
promising
druggable
emerging
targets.
In
review,
we
first
illustrate
timeline
steps
roles
promotion
developed,
then
summarize
mechanisms
regarding
associated
highlighting
proteins
behind
targeting
that
initiate
functioning
abnormally
duo
extrinsic
harm
environmental
factors,
also,
baseline
drift
leads
harmful
intrinsic
therapy.
addition,
clinical
therapeutic
drugs
effects,
as
well
scheme
relative
trials
were
intensive
discussed.
Based
background,
suggest
two
hypotheses,
namely
“environmental
gear
selection”
describe
pathway
evolution,
“DNA
drift”,
which
may
play
magnified
mediating
during
treatment.
This
new
shed
light
provide
much
better
more
comprehensive
holistic
view
promote
development
research
direction
overcoming
strategies
patients.
Abstract
Due
to
the
DNA
repair
defect,
BRCA1/2
deficient
tumor
cells
are
more
sensitive
PARP
inhibitors
(PARPi)
through
mechanism
of
synthetic
lethality.
At
present,
several
PAPRi
targeting
poly
(ADP-ribose)
polymerase
(PARP)
have
been
approved
for
ovarian
cancer
and
breast
indications.
However,
PARPi
resistance
is
ubiquitous
in
clinic.
More
than
40%
BRCA1/2-deficient
patients
fail
respond
PARPi.
In
addition,
lots
acquire
with
prolonged
oral
administration
Homologous
recombination
(HRD),
as
an
essential
prerequisite
lethality,
plays
a
vital
role
killing
cells.
Therefore,
restoration
(HRR)
becomes
predominant
reason
resistance.
Recently,
it
was
reported
that
replication
fork
protection
also
contributed
patients.
Moreover,
various
factors,
such
reversion
mutations,
epigenetic
modification,
ADP-ribosylation
(PARylation)
pharmacological
alteration
lead
well.
this
review,
we
reviewed
underlying
mechanisms
inhibitor
detail
summarized
potential
strategies
overcome
increase
sensitivity.
Cold Spring Harbor Perspectives in Biology,
Год журнала:
2019,
Номер
11(9), С. a033886 - a033886
Опубликована: Янв. 22, 2019
Most
of
the
secreted
and
plasma
membrane
proteins
are
synthesized
on
membrane-bound
ribosomes
endoplasmic
reticulum
(ER).
They
require
engagement
ER-resident
chaperones
foldases
that
assist
in
their
folding
maturation.
Since
protein
homeostasis
ER
is
crucial
for
cellular
function,
protein-folding
status
organelle's
lumen
continually
surveyed
by
a
network
signaling
pathways,
collectively
called
unfolded
response
(UPR).
Protein-folding
imbalances,
or
"ER
stress,"
detected
highly
conserved
sensors
adjust
ER's
capacity
according
to
physiological
needs
cell.
We
review
recent
developments
field
have
provided
new
insights
into
stress-sensing
mechanisms
used
UPR
which
they
integrate
various
inputs
organelle
accommodate
fluctuations
demands.
Endocrine Reviews,
Год журнала:
2021,
Номер
43(4), С. 678 - 719
Опубликована: Ноя. 6, 2021
Abstract
Uterine
fibroids
are
benign
monoclonal
neoplasms
of
the
myometrium,
representing
most
common
tumors
in
women
worldwide.
To
date,
no
long-term
or
noninvasive
treatment
option
exists
for
hormone-dependent
uterine
fibroids,
due
to
limited
knowledge
about
molecular
mechanisms
underlying
initiation
and
development
fibroids.
This
paper
comprehensively
summarizes
recent
research
advances
on
focusing
risk
factors,
origin,
pathogenetic
mechanisms,
options.
Additionally,
we
describe
current
interventions
Finally,
future
perspectives
studies
summarized.
Deeper
mechanistic
insights
into
tumor
etiology
complexity
can
contribute
progress
newer
targeted
therapies.
Oxidative Medicine and Cellular Longevity,
Год журнала:
2020,
Номер
2020, С. 1 - 16
Опубликована: Июль 24, 2020
Oxidative
stress
(OS)
has
the
ability
to
damage
different
molecules
and
cellular
structures,
altering
correct
function
of
organs
systems.
OS
accumulates
in
body
by
endogenous
exogenous
mechanisms.
Increasing
evidence
points
involvement
physiopathology
various
chronic
diseases
that
require
prolonged
periods
pharmacological
treatment.
Long-term
treatments
may
contribute
changes
systemic
OS.
In
this
review,
we
discuss
pathological
mechanisms
some
diseases,
pro-
or
antioxidant
effects
their
treatments,
possible
adjuvant
alternatives.
Diseases
such
as
high
blood
pressure,
arteriosclerosis,
diabetes
mellitus
increased
risk
cardiovascular
disease.
Antihypertensive,
lipid-lowering,
hypoglycemic
help
reduce
with
an
additional
benefit.
Treatment
methotrexate
autoimmune
inflammatory
rheumatoid
arthritis,
a
dual
role
stimulating
production
producing
mitochondrial
dysfunction.
However,
it
can
also
indirectly
decrease
induced
inflammation.
Medicaments
used
treat
neurodegenerative
tend
related
reactive
oxygen
species
(ROS)
balance
On
other
hand,
immunosuppressive
cancer
human
immunodeficiency
virus
infection
increase
ROS,
causing
significant
oxidative
systems
without
widely
documented
administration
Molecular Cell,
Год журнала:
2019,
Номер
77(3), С. 461 - 474.e9
Опубликована: Окт. 30, 2019
Acute
treatment
with
replication-stalling
chemotherapeutics
causes
reversal
of
replication
forks.
BRCA
proteins
protect
reversed
forks
from
nucleolytic
degradation,
and
their
loss
leads
to
chemosensitivity.
Here,
we
show
that
fork
degradation
is
no
longer
detectable
in
BRCA1-deficient
cancer
cells
exposed
multiple
cisplatin
doses,
mimicking
a
clinical
regimen.
This
effect
depends
on
increased
expression
chromatin
loading
PRIMPOL
regulated
by
ATR
activity.
Electron
microscopy
single-molecule
DNA
fiber
analyses
reveal
rescues
reinitiating
synthesis
past
lesions.
repriming
accumulation
ssDNA
gaps
while
suppressing
reversal.
We
propose
adapt
repeated
doses
activating
under
conditions
would
otherwise
promote
pathological
degradation.
generalizable
other
impaired
(e.g.,
SMARCAL1
or
PARP
inhibition)
suggests
new
strategy
modulate
chemosensitivity
targeting
the
pathway.