Clinical Cancer Research,
Journal Year:
2024,
Volume and Issue:
30(10), P. 2193 - 2205
Published: April 9, 2024
TGFβ
signaling
is
implicated
in
the
progression
of
most
cancers,
including
esophageal
adenocarcinoma
(EAC).
Emerging
evidence
indicates
that
a
key
factor
development
resistance
toward
cancer
therapy.
Biomedicine & Pharmacotherapy,
Journal Year:
2024,
Volume and Issue:
175, P. 116663 - 116663
Published: April 30, 2024
Cancer
is
caused
by
a
complex
interaction
of
factors
that
interrupt
the
normal
growth
and
division
cells.
At
center
this
process
intricate
relationship
between
DNA
damage
cellular
mechanisms
responsible
for
maintaining
genomic
stability.
When
not
repaired,
it
can
cause
genetic
mutations
contribute
to
initiation
progression
cancer.
On
other
hand,
response
system,
which
involves
phosphorylation
histone
variant
H2AX
(γH2AX),
crucial
in
preserving
integrity
signaling
facilitating
repair
double-strand
breaks.
This
review
provides
an
explanation
molecular
dynamics
context
response.
It
emphasizes
role
recruiting
localizing
machinery
at
sites
chromatin
damage.
The
explains
how
phosphorylation,
facilitated
master
kinases
ATM
ATR,
acts
as
signal
damage,
triggering
downstream
pathways
govern
cell
cycle
checkpoints,
apoptosis,
fate
decision
death.
critical
regulatory
point,
ensuring
survival
promoting
or
steering
cells
towards
apoptosis
cases
catastrophic
Moreover,
we
explore
therapeutic
potential
targeting
cancer
treatment,
leveraging
its
dual
function
biomarker
target.
By
delineating
lead
roles
control,
highlight
significance
both
prognostic
tool
focal
point
intervention,
offering
insights
into
utility
enhancing
efficacy
treatments.
Molecular and Cellular Probes,
Journal Year:
2024,
Volume and Issue:
75, P. 101961 - 101961
Published: April 8, 2024
As
one
of
the
earliest
discovered
lncRNA
molecules,
H19
is
usually
expressed
in
large
quantities
during
embryonic
development
and
involved
cell
differentiation
tissue
formation.
In
recent
years,
role
tumors
has
been
gradually
recognized.
Increasing
evidence
suggests
that
its
aberrant
expression
closely
related
to
cancer
development.
LncRNA
as
an
oncogene
not
only
promotes
growth,
proliferation,
invasion
metastasis
many
tumors,
but
also
develops
resistance
treatment,
affecting
patients'
prognosis
survival.
Therefore,
this
review,
we
summarise
extensive
research
on
involvement
tumor
progression
discuss
how
H19,
a
key
target
gene,
affects
sensitivity
radiotherapy,
chemotherapy
immunotherapy
by
participating
multiple
cellular
processes
regulating
signaling
pathways,
which
provides
promising
prospect
for
further
into
treatment
cancer.
Biomarker Research,
Journal Year:
2024,
Volume and Issue:
12(1)
Published: Sept. 27, 2024
Abstract
DNA
damage
response
(DDR)
deficiency
has
been
one
of
the
emerging
targets
in
treating
breast
cancer
recent
years.
On
hand,
DDR
coordinates
cell
cycle
and
signal
transduction,
whose
dysfunction
may
lead
to
apoptosis,
genomic
instability,
tumor
development.
Conversely,
is
an
intrinsic
feature
tumors
that
underlies
their
treatments
inflict
damage.
In
this
review,
we
systematically
explore
various
mechanisms
DDR,
rationale
research
advances
DDR-targeted
drugs
cancer,
discuss
challenges
its
clinical
applications.
Notably,
poly
(ADP-ribose)
polymerase
(PARP)
inhibitors
have
demonstrated
favorable
efficacy
safety
with
high
homogenous
recombination
(HRD)
status
a
series
trials.
Moreover,
several
studies
on
novel
DDR-related
molecules
are
actively
exploring
target
become
resistant
PARP
inhibition.
Before
further
application
new
regimens
or
drugs,
standardized
biomarkers
needed
develop
for
accurately
characterizing
benefit
population
predicting
efficacy.
Despite
promising
treatments,
off-target
toxicity
drug
resistance
need
be
addressed.
Strategies
overcome
await
exploration
mechanisms,
combined
targeted
immunotherapy
will
hopefully
provide
more
precise
strategies
expand
potential
responsive
populations.
Animal Cells and Systems,
Journal Year:
2024,
Volume and Issue:
28(1), P. 75 - 83
Published: March 3, 2024
The
CRISPR-Cas
system
stands
out
as
a
promising
genome
editing
tool
due
to
its
cost-effectiveness
and
time
efficiency
compared
other
methods.
This
has
tremendous
potential
for
treating
various
diseases,
including
genetic
disorders
cancer,
promotes
therapeutic
research
wide
range
of
diseases.
Additionally,
the
simplifies
generation
animal
models,
offering
more
accessible
alternative
traditional
CRISPR-Cas9
can
be
used
cleave
target
DNA
strands
that
need
corrected,
causing
double-strand
breaks
(DSBs).
with
DSBs
then
recovered
by
repair
pathway
uses
edit
gene
sequences.
High
cleavage
is
thus
imperative
effective
editing.
Herein,
we
explore
several
factors
affecting
system.
These
include
GC
content
protospacer-adjacent
motif
(PAM)
proximal
distal
regions,
single-guide
RNA
(sgRNA)
properties,
chromatin
state.
considerations
contribute
Expert Opinion on Therapeutic Targets,
Journal Year:
2024,
Volume and Issue:
unknown, P. 1 - 13
Published: Dec. 4, 2024
Introduction
The
four
members
of
the
p90
ribosomal
S6
kinase
(RSK)
family
are
serine/threonine
protein
kinases,
which
phosphorylated
and
activated
by
ERK1/2.
RSK1/2/3
further
PDK1.
Receiving
inputs
from
two
major
signaling
pathways
places
RSK
as
a
key
node
in
numerous
pathologies.
A
plethora
RSK1/2
substrates
have
been
identified,
majority
cases
causative
roles
these
play
pathology
unknown.