Discover Oncology,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: April 17, 2025
Abstract
Triple-negative
breast
cancer
(TNBC)
is
an
aggressive
malignancy
characterized
by
limited
therapeutic
options
and
poor
prognosis.
Despite
advancements
in
precision
oncology,
conventional
chemotherapy
remains
the
cornerstone
of
TNBC
treatment,
often
accompanied
debilitating
side
effects
suboptimal
outcomes.
This
review
presents
a
comprehensive
analysis
clinical
trials
on
targeted
therapies,
aiming
to
establish
novel,
evidence-based
treatment
strategy
exclusively
leveraging
molecularly
agents.
By
integrating
patient-specific
genetic
profiles
with
responses
observed
across
various
trial
phases,
this
approach
seeks
optimize
efficacy
while
minimizing
toxicity.
The
proposed
therapy
combinations
hold
significant
potential
revolutionize
offering
paradigm
shift
toward
medicine
improved
patient
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: March 6, 2025
Triple-negative
breast
cancer
(TNBC)
has
the
highest
mortality
rate
of
all
subtypes
and
currently
lacks
effective
targeted
therapies.
LARP6
is
an
RNA-binding
protein
associated
with
promotion,
but
its
mechanism
action
in
TNBC
remains
unclear.
We
conducted
RNA
sequencing
(RNA-seq)
improved
immunoprecipitation
(iRIP-seq)
to
identify
differentially
expressed
genes
(DEGs)
alternative
splice
sites
bound
regulated
by
MDA-MB-231
cells.
Finally,
both
RT-qPCR
RIP-qPCR
were
employed
for
verification.
Our
study
revealed
that
overexpression
altered
expression
levels
171
number
splicing
events
(RASEs)
exceeded
1000.
The
(RASGs)
corresponding
RASEs
enriched
biological
processes
such
as
DNA
repair,
cell
cycle,
cellular
response
damage
stimulus.
In
addition,
we
found
tends
bind
CGACGAG
motif.
intersection
peak-related
RASGs
suggested
can
16
regulate
their
(AS),
thus
playing
important
role
progression.
research
indicated
may
promote
proliferation
invasion
cells
directly
regulating
AS
related
genes,
providing
new
clues
therapy
TNBC.
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 12, 2025
Background
Neoadjuvant
chemotherapy
has
become
a
common
and
effective
treatment
modality
for
triple-negative
breast
cancer
(TNBC).
The
primary
goal
is
to
reduce
the
size
of
tumor,
enabling
breast-conserving
surgery,
axillary
preservation,
transition
operability,
thereby
providing
patients
with
more
therapeutic
options.
Although
neoadjuvant
(NAC)
demonstrated
favorable
outcomes
in
clinical
practice,
predicting
its
efficacy
prognostic
value
TNBC
remains
key
challenge
current
research.
Methods
This
study
included
248
who
received
NAC
at
two
centers.
By
employing
modeling
validation
approach,
we
aim
explore
predictors
potential
biomarkers
associated
NAC.
Results
In
multivariable
analysis
training
set,
factors
pathological
complete
response
(pCR)
include
high
biopsy-sTILs
expression,
biopsy-Ki67
>
20%,
positive
expression
biopsy-androgen
receptor
(AR).
disease-free
survival
(DFS)
are
ypN3,
postoperative
sTIL
receipt
radiotherapy,
overall
(OS)
ypN2,
Ki67
C-indices
sets
prediction
pCR
using
nomogram
were
0.729
0.816,
respectively.
DFS
0.895
0.865,
OS
0.899
0.860,
Conclusion
established
validated
model
pCR,
DFS,
undergoing
demonstrates
good
discrimination
accuracy.
Cancer Biology & Therapy,
Journal Year:
2025,
Volume and Issue:
26(1)
Published: April 2, 2025
Triple-negative
breast
cancer
(TNBC)
is
a
common
malignant
disease
among
females
and
severely
threatens
the
health
of
women
worldwide.
Nowadays,
circular
RNAs
(circRNAs)
aroused
our
interest
for
their
functions
in
human
cancers,
including
TNBC.
However,
mechanism
most
circRNAs
progression
TNBC
remains
unclear.
We
found
novel
circRNA
named
circATP5C1,
whose
function
uncovered.
Tissue
microarray
was
used
to
analyze
association
between
expression
circATP5C1
prognoses
patients.
Gain-and
loss-of-function
experiments
were
performed
validate
biological
different
cell
lines.
RNA-seq
analyses
conducted
find
out
target
genes
regulated
by
circATP5C1.
RNA
pull-down
assay
mass
spectrometry
select
proteins
associated
with
FISH-immunofluorescence
immunoprecipitation
(RIP)
complemented
interaction
its
binding
protein.
CircATP5C1
identified
have
predictive
prognosis
advanced
cells.
Mechanistically,
Colony
stimulating
factor
1
(CSF-1)
vital
downstream
gene
The
alteration
CSF-1
level
validated
due
insulin-like
growth
2
mRNA
protein
(IGF2BP2).
Rescue
demonstrated
that
accelerates
partly
via
IGF2BP2
increase
secretion
CSF-1.
This
study
uncovers
circATP5C1/IGF2BP2/CSF-1
pathway
regulating
Discover Oncology,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: April 17, 2025
Abstract
Triple-negative
breast
cancer
(TNBC)
is
an
aggressive
malignancy
characterized
by
limited
therapeutic
options
and
poor
prognosis.
Despite
advancements
in
precision
oncology,
conventional
chemotherapy
remains
the
cornerstone
of
TNBC
treatment,
often
accompanied
debilitating
side
effects
suboptimal
outcomes.
This
review
presents
a
comprehensive
analysis
clinical
trials
on
targeted
therapies,
aiming
to
establish
novel,
evidence-based
treatment
strategy
exclusively
leveraging
molecularly
agents.
By
integrating
patient-specific
genetic
profiles
with
responses
observed
across
various
trial
phases,
this
approach
seeks
optimize
efficacy
while
minimizing
toxicity.
The
proposed
therapy
combinations
hold
significant
potential
revolutionize
offering
paradigm
shift
toward
medicine
improved
patient