Cancers,
Journal Year:
2024,
Volume and Issue:
16(11), P. 1984 - 1984
Published: May 23, 2024
The
impact
of
tyrosine
kinase
inhibitors
(TKIs)
on
multidrug
resistance
(MDR)
in
non-small
cell
lung
carcinoma
(NSCLC)
is
a
critical
aspect
cancer
therapy.
While
TKIs
effectively
target
specific
signaling
pathways
cells,
they
can
also
act
as
substrates
for
ABC
transporters,
potentially
triggering
MDR.
aim
our
study
was
to
evaluate
the
response
17
patient-derived
NSCLC
cultures
10
commonly
prescribed
and
correlate
these
responses
with
patient
mutational
profiles.
Using
an
ex
vivo
immunofluorescence
assay,
we
analyzed
expression
MDR
markers
ABCB1,
ABCC1,
ABCG2,
correlated
data
genetic
profiles
patients
functional
diagnostic
approach.
responded
differently
TKIs,
erlotinib
showing
good
efficacy
regardless
mutation
burden
or
EGFR
status.
However,
modulation
mechanisms
by
erlotinib,
such
increased
ABCG2
expression,
highlights
challenges
associated
treatment.
Other
showed
limited
efficacy,
highlighting
variability
NSCLC.
Genetic
alterations
drug
sensitivity,
including
TP53
mutations,
likely
contributed
variable
TKIs.
relationships
between
transporter
gene
alterations,
did
not
show
consistent
patterns.
Our
results
suggest
that
addition
status,
performing
sensitivity
screening
identifying
appropriate
treatment
strategies
These
underscore
importance
considering
off-target
effects,
risks,
patient-specific
when
optimizing
highlight
potential
personalized
approaches,
especially
early
stages.
Frontiers in Oncology,
Journal Year:
2022,
Volume and Issue:
12
Published: Aug. 17, 2022
Cancer
is
one
of
the
most
frequently
diagnosed
malignant
diseases
worldwide,
posing
a
serious,
long-term
threat
to
patients’
health
and
life.
Systemic
chemotherapy
remains
first-line
therapeutic
approach
for
recurrent
or
metastatic
cancer
patients
after
surgery,
with
potential
effectively
extend
patient
survival.
However,
development
drug
resistance
seriously
limits
clinical
efficiency
ultimately
results
in
treatment
failure
death.
A
large
number
studies
have
shown
that
non-coding
RNAs
(ncRNAs),
particularly
microRNAs,
long
RNAs,
circular
are
widely
involved
regulation
resistance.
Their
dysregulation
contributes
by
modulating
expression
specific
target
genes
cellular
apoptosis,
autophagy,
efflux,
epithelial-to-mesenchymal
transition
(EMT),
stem
cells
(CSCs).
Moreover,
some
ncRNAs
also
possess
great
as
efficient,
biomarkers
diagnosis
prognosis
well
targets
patients.
In
this
review,
we
summarize
recent
findings
on
emerging
role
underlying
mechanisms
focus
their
applications
treatment.
This
information
will
be
benefit
early
prognostic
assessments
ncRNA-based
strategies
Cancers,
Journal Year:
2024,
Volume and Issue:
16(13), P. 2478 - 2478
Published: July 7, 2024
The
rise
of
drug
resistance
in
cancer
cells
presents
a
formidable
challenge
modern
oncology,
necessitating
the
exploration
innovative
therapeutic
strategies.
This
review
investigates
latest
advancements
overcoming
mechanisms
employed
by
cells,
focusing
on
emerging
modalities.
intricate
molecular
insights
into
resistance,
including
genetic
mutations,
efflux
pumps,
altered
signaling
pathways,
and
microenvironmental
influences,
are
discussed.
Furthermore,
promising
avenues
offered
targeted
therapies,
combination
treatments,
immunotherapies,
precision
medicine
approaches
highlighted.
Specifically,
synergistic
effects
combining
traditional
cytotoxic
agents
with
molecularly
inhibitors
to
circumvent
pathways
examined.
Additionally,
evolving
landscape
immunotherapeutic
interventions,
immune
checkpoint
adoptive
cell
is
explored
terms
bolstering
anti-tumor
responses
evasion
mechanisms.
Moreover,
significance
biomarker-driven
strategies
for
predicting
monitoring
treatment
underscored,
thereby
optimizing
outcomes.
For
future
direction
paradigms,
current
focused
prevailing
challenges
improving
patient
outcomes,
through
an
integrative
analysis
these
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(19), P. 14964 - 14964
Published: Oct. 6, 2023
Epigenetics
play
a
crucial
role
in
gene
regulation
and
cellular
processes.
Most
importantly,
its
dysregulation
can
contribute
to
the
development
of
tumors.
Epigenetic
modifications,
such
as
DNA
methylation
histone
acetylation,
are
reversible
processes
that
be
utilized
targets
for
therapeutic
intervention.
inhibitors
disrupt
patterns
by
inhibiting
methyltransferases.
Such
restore
normal
expression
patterns,
they
effective
against
various
forms
cancer.
Histone
deacetylase
increase
acetylation
levels,
leading
altered
expressions.
Like
inhibitors,
methyltransferase
target
molecules
involved
methylation.
Bromodomain
extra-terminal
domain
proteins
expression.
They
oncogene
inducing
anti-proliferative
effects
seen
Understanding
epigenetic
modifications
utilizing
will
offer
new
possibilities
cancer
research.
Molecular Cancer,
Journal Year:
2024,
Volume and Issue:
23(1)
Published: Aug. 27, 2024
Abstract
The
development
of
drug
resistance
remains
a
major
challenge
in
cancer
treatment.
Ferroptosis,
unique
type
regulated
cell
death,
plays
pivotal
role
inhibiting
tumour
growth,
presenting
new
opportunities
treating
chemotherapeutic
resistance.
Accumulating
studies
indicate
that
epigenetic
modifications
by
non-coding
RNAs
(ncRNA)
can
determine
vulnerability
to
ferroptosis.
In
this
review,
we
first
summarize
the
growth/development.
Then,
core
molecular
mechanisms
ferroptosis,
its
upstream
regulation,
and
downstream
effects
on
Finally,
review
recent
advances
understanding
how
ncRNAs
regulate
ferroptosis
from
such
modulate
This
aims
enhance
general
ncRNA-mediated
regulatory
which
highlighting
ncRNA-ferroptosis
axis
as
key
druggable
target
overcoming
Oncogene,
Journal Year:
2024,
Volume and Issue:
43(23), P. 1727 - 1741
Published: May 8, 2024
Abstract
Epigenetic
regulation
established
during
development
to
maintain
patterns
of
transcriptional
expression
and
silencing
for
metabolism
other
fundamental
cell
processes
can
be
reprogrammed
in
cancer,
providing
a
molecular
mechanism
persistent
alterations
phenotype.
Metabolic
deregulation
reprogramming
are
thus
an
emerging
hallmark
cancer
with
opportunities
classification
as
critical
preliminary
step
precision
therapeutic
intervention.
Yet,
acquisition
therapy
resistance
against
most
conventional
treatment
regimens
coupled
tumor
relapse,
continue
pose
unsolved
problems
healthcare,
exemplified
breast
where
existing
data
informs
both
genotype
Furthermore,
epigenetic
reprograming
the
metabolic
milieu
cells
is
among
crucial
determinants
relapse.
Importantly,
subtype-specific
epigenetic-metabolic
interplay
profoundly
affects
malignant
transformation,
chemotherapy,
response
targeted
therapies.
In
this
review,
we
therefore
prismatically
dissect
interconnected
regulatory
pathways
then
integrate
them
into
observable
metabolism-therapy-resistance
axis
that
may
inform
clinical
Optimally
coupling
genome-wide
analysis
understanding
elements,
reprogramming,
their
integration
by
profiling
decode
missing
mechanisms
at
level
individual
tumors.
The
proposed
approach
linking
biochemistry
back
genotype,
epigenetics,
phenotype
specific
tumors
microenvironment
enable
successful
mechanistic
targeting
modifiers
oncometabolites
despite
heterogeneity.
Frontiers in Cell and Developmental Biology,
Journal Year:
2025,
Volume and Issue:
13
Published: Jan. 24, 2025
Exosomes,
as
key
mediators
of
intercellular
communication,
have
been
increasingly
recognized
for
their
role
in
the
oncogenic
processes,
particularly
facilitating
drug
resistance.
This
article
delves
into
emerging
evidence
linking
exosomal
lncRNAs
to
modulation
resistance
mechanisms
cancers
such
ovarian,
cervical,
and
endometrial
cancer.
It
synthesizes
current
research
findings
on
how
these
influence
cancer
cell
survival,
tumor
microenvironment,
chemotherapy
efficacy.
Additionally,
review
highlights
potential
therapeutic
strategies
targeting
lncRNAs,
proposing
a
new
frontier
overcoming
By
mapping
interface
resistance,
this
aims
provide
comprehensive
understanding
that
could
pave
way
innovative
treatments
improved
patient
outcomes
female
reproductive
system
cancers.
Immunological Reviews,
Journal Year:
2023,
Volume and Issue:
321(1), P. 228 - 245
Published: Oct. 30, 2023
Summary
Ferroptosis
is
a
novel
form
of
programmed
cell
death
morphologically,
genetically,
and
biochemically
distinct
from
other
pathways
characterized
by
the
accumulation
iron‐dependent
lipid
peroxides
oxidative
damage.
It
now
understood
that
ferroptosis
plays
an
essential
role
in
various
biological
processes,
especially
metabolism
iron,
lipids,
amino
acids.
Gastric
cancer
(GC)
prevalent
malignant
tumor
worldwide
with
low
early
diagnosis
rates
high
metastasis
rates,
accounting
for
its
relatively
poor
prognosis.
Although
chemotherapy
commonly
used
to
treat
GC,
drug
resistance
often
leads
therapeutic
outcomes.
In
last
several
years,
extensive
research
on
has
highlighted
significant
potential
GC
therapy,
providing
promising
strategy
address
associated
standard
therapies.
this
review,
we
offer
summary
key
regulatory
factors
related
mechanisms
underlying
ferroptosis.
Various
inducers
inhibitors
specifically
targeting
are
uncovered.
Additionally,
explore
prospective
applications
outcomes
these
agents
field
emphasizing
their
capacity
improve
patient
population.
Pharmaceutics,
Journal Year:
2022,
Volume and Issue:
14(8), P. 1606 - 1606
Published: Aug. 1, 2022
Clinically,
cancer
drug
resistance
to
chemotherapy,
targeted
therapy
or
immunotherapy
remains
the
main
impediment
towards
curative
therapy,
which
leads
directly
treatment
failure
along
with
extended
hospital
stays,
increased
medical
costs
and
high
mortality.
Therefore,
increasing
attention
has
been
paid
nanotechnology-based
delivery
systems
for
overcoming
in
cancer.
In
this
respect,
novel
tumor-targeting
nanomedicines
offer
fairly
effective
therapeutic
strategies
surmounting
various
limitations
of
immunotherapy,
enabling
more
precise
treatment,
convenient
monitoring
agents,
as
well
resistance,
including
multidrug
(MDR).
Nanotechnology-based
systems,
liposomes,
polymer
micelles,
nanoparticles
(NPs),
DNA
nanostructures,
enable
a
large
number
properly
designed
nanomedicines.
paper,
we
review
different
mechanisms
discuss
latest
developments
resistance.