Journal of Biochemical and Molecular Toxicology,
Год журнала:
2025,
Номер
39(3)
Опубликована: Фев. 23, 2025
ABSTRACT
Radiotherapy
is
a
cornerstone
of
lung
cancer
management,
though
its
efficacy
frequently
undermined
by
intrinsic
and
acquired
radioresistance.
This
review
examines
the
complexity
tumors,
highlighting
their
potential
as
reservoir
novel
targets
for
radiosensitization.
Ionizing
radiation
(IR)
primarily
exerts
effects
through
oxidative
damage
DNA
double‐strand
breaks
(DSBs).
Lung
cells,
however,
develop
mutations
that
enhance
response
(DDR)
suppress
cell
death
pathways.
Additionally,
interactions
between
tumor
cells
microenvironment
(TME)
components—including
immune
stromal
molecular
mediators
such
cytokines,
chemokines,
growth
factors—contribute
to
resistance
against
IR.
Understanding
these
intricate
relationships
reveals
improve
radiotherapy
outcomes.
Promising
include
DDR
pathways,
immunosuppressive
molecules,
hypoxia,
proangiogenic
mediators,
other
key
signaling
discusses
emerging
strategies,
combining
with
immunomodulators,
hypoxia
inhibitors,
DDR‐targeting
agents,
innovative
approaches.
By
offering
comprehensive
analysis
TME,
this
underscores
opportunities
effectiveness
targeted
radiosensitization
strategies.
The
integration
of
small
interfering
RNA
(siRNA)
with
traditional
cancer
therapies
represents
a
promising
frontier
in
oncology
aimed
at
enhancing
treatment
effectiveness,
reducing
side
effects,
and
overcoming
drug
resistance.
This
review
highlights
the
potential
siRNA
to
selectively
silence
genes
that
are
overexpressed
or
uniquely
expressed
cells,
thereby
disrupting
critical
pathways
support
tumor
growth
survival.
Key
target
discussed
include
survivin,
VEGF,
EGFR,
c-MET,
HER2,
MUC1,
Bcl-2,
all
which
play
vital
roles
proliferation,
angiogenesis,
resistance
therapies.
Clinical
trials
investigating
various
candidates,
such
as
EZN-3042
ALN-VSP,
indicate
these
generally
well-tolerated;
however,
significant
challenges
persist,
including
effective
delivery
stability
siRNA.
Recent
advancements
nanoparticle-based
systems
have
shown
promise
addressing
issues.
Future
research
will
focus
on
optimizing
methods,
personalizing
based
individual
genetic
profiles,
establishing
clearer
regulatory
guidelines
for
approval.
As
field
evolves,
siRNA-based
combination
poised
become
an
integral
part
precision
oncology,
offering
new
therapeutic
options
hope
patients
difficult-to-treat
cancers.
Cancers,
Год журнала:
2025,
Номер
17(3), С. 472 - 472
Опубликована: Янв. 30, 2025
Background/Objectives:
Ovarian
cancer
is
a
leading
cause
of
gynecological
mortality
worldwide,
often
diagnosed
at
advanced
stages
due
to
vague
symptoms
and
the
lack
effective
early
detection
methods.
Long
non-coding
RNAs
(lncRNAs)
have
emerged
as
key
regulators
in
biology,
influencing
cellular
processes
such
proliferation,
apoptosis,
chemoresistance.
This
review
explores
multifaceted
roles
lncRNAs
ovarian
pathogenesis
their
potential
biomarkers
therapeutic
targets.
Methods:
A
comprehensive
literature
was
conducted
analyze
structural
functional
characteristics
contributions
biology.
includes
regulatory
mechanisms,
interactions
with
signaling
pathways,
implications
for
resistance.
Advanced
bioinformatics
omics
approaches
were
also
evaluated
lncRNA
research.
Results:
The
highlights
dual
role
oncogenes
tumor
suppressors,
modulating
cell
invasion,
angiogenesis.
Specific
lncRNAs,
HOTAIR
GAS5,
demonstrate
significant
diagnostic
Emerging
technologies,
single-cell
sequencing,
provide
valuable
insights
into
microenvironment
heterogeneity
expression.
Conclusions:
LncRNAs
hold
transformative
advancing
diagnosis,
prognosis,
treatment.
Targeting
or
associated
pathways
offers
promising
strategies
overcome
therapy
resistance
enhance
personalized
medicine.
Continued
research
integrating
will
be
essential
unlock
full
clinical
management.
Frontiers in Oncology,
Год журнала:
2025,
Номер
15
Опубликована: Фев. 7, 2025
Background
Glioma
is
the
most
aggressive
primary
malignant
tumor
of
central
nervous
system,
characterized
by
high
recurrence
rates
and
resistance
to
chemoradiotherapy,
making
therapeutic
a
major
challenge
in
neuro-oncology.
Recent
research
emphasizes
role
microenvironment
(TME)
immune
modulation
glioma
progression
resistance.
Despite
these
advances,
comprehensive
bibliometric
analysis
trends
chemoradiotherapy
over
past
two
decades
lacking.
This
study
aims
systematically
evaluate
landscape,
identify
emerging
hotspots,
provide
guidance
for
future
investigations.
Methods
Articles
on
published
between
2003
2023
were
retrieved
from
Web
Science
Core
Collection,
resulting
4,528
publications.
Bibliometric
tools,
including
VOSviewer,
CiteSpace,
R
packages
such
as
bibliometrix
ggplot2,
used
analyze
co-authorship
networks,
keyword
evolution,
citation
bursts
collaboration
patterns,
thematic
developments,
influential
contributions.
Results
Publication
output
increased
significantly
2013
2022,
peaking
at
650
articles
2022.
Over
1,000
institutions
88
countries
contributed
this
research.
The
United
States,
Switzerland,
Germany
showed
highest
impact,
while
China
led
publication
volume
but
demonstrated
relatively
lower
influence.
focus
has
shifted
traditional
topics
“MGMT
gene”
areas
“tumor
microenvironment,”
“immune
infiltration,”
“nanoparticles.”
androgen
receptor
was
identified
promising
underexplored
target.
Conclusions
Research
seen
substantial
growth,
with
increasing
emphasis
modulation,
microenvironment,
novel
targets
receptor.
represents
first
field,
providing
detailed
overview
potential
directions
studies.
findings
highlight
need
strengthened
international
multidisciplinary
approaches
address
challenges
glioma.
DNA
damage
is
a
common
event
in
cells,
resulting
from
both
internal
and
external
factors.
The
maintenance
of
genomic
integrity
vital
for
cellular
function
physiological
processes.
inadequate
repair
results
the
instability,
which
has
been
associated
with
development
progression
various
human
diseases.
Accumulation
can
lead
to
multiple
diseases,
such
as
neurodegenerative
disorders,
cancers,
immune
deficiencies,
infertility
aging.
This
comprehensive
review
delves
impact
alterations
response
genes
(DDR)
tries
elucidate
how
what
extent
same
traits
modulate
diverse
major
cancer,
immunological
disorders.
DDR
apparently
trait
connecting
important
complex
disorders
humans.
However,
pathogenesis
above
diseases
are
different
leading
divergent
consequences.
It
discover
switch(es)
that
direct
further
pathogenic
process
either
proliferative,
or
degenerative
Our
understanding
influence
on
may
enable
strategies
prevent,
diagnose,
treat
these
In
our
article,
we
analysed
publicly
available
GWAS
summary
statistics
NHGRI-EBI
Catalog
identified
12,009
single
nucleotide
polymorphisms
(SNPs)
cancer.
Among
these,
119
SNPs
were
found
pathways,
exhibiting
significant
p-values.
Additionally,
44
linked
cancer
types
(NDDs),
including
four
located
DDR-related
genes:
ATM,
CUX2,
WNT3.
Furthermore,
402
two
gene
RAD51B.
highlights
versatility
pathway
multifactorial
specific
mechanisms
regulate
initiate
distinct
processes
remain
be
elucidated.
Journal of Biochemical and Molecular Toxicology,
Год журнала:
2025,
Номер
39(3)
Опубликована: Фев. 23, 2025
ABSTRACT
Radiotherapy
is
a
cornerstone
of
lung
cancer
management,
though
its
efficacy
frequently
undermined
by
intrinsic
and
acquired
radioresistance.
This
review
examines
the
complexity
tumors,
highlighting
their
potential
as
reservoir
novel
targets
for
radiosensitization.
Ionizing
radiation
(IR)
primarily
exerts
effects
through
oxidative
damage
DNA
double‐strand
breaks
(DSBs).
Lung
cells,
however,
develop
mutations
that
enhance
response
(DDR)
suppress
cell
death
pathways.
Additionally,
interactions
between
tumor
cells
microenvironment
(TME)
components—including
immune
stromal
molecular
mediators
such
cytokines,
chemokines,
growth
factors—contribute
to
resistance
against
IR.
Understanding
these
intricate
relationships
reveals
improve
radiotherapy
outcomes.
Promising
include
DDR
pathways,
immunosuppressive
molecules,
hypoxia,
proangiogenic
mediators,
other
key
signaling
discusses
emerging
strategies,
combining
with
immunomodulators,
hypoxia
inhibitors,
DDR‐targeting
agents,
innovative
approaches.
By
offering
comprehensive
analysis
TME,
this
underscores
opportunities
effectiveness
targeted
radiosensitization
strategies.