Precise
prognostication
is
vital
for
guiding
treatment
decisions
in
people
diagnosed
with
pancreatic
cancer.
Existing
models
depend
on
predetermined
variables,
constraining
their
effectiveness.
Our
objective
was
to
explore
a
novel
machine
learning
approach
enhance
prognostic
model
predicting
cancer-specific
mortality
and,
subsequently,
assess
its
performance
against
Cox
regression
models.
Datasets
were
retrospectively
collected
and
analyzed
9,752
patients
cancer
surgery
performed.
The
primary
outcomes
the
of
carcinoma
at
one
year,
three
years,
five
years.
Model
discrimination
assessed
using
concordance
index
(C-index),
calibration
Brier
scores.
Survival
Quilts
compared
clinical
use,
decision
curve
analysis
done.
demonstrated
robust
one-year
(C-index
0.729),
three-year
0.693),
five-year
0.672)
mortality.
In
comparison
models,
exhibited
higher
C-index
up
32
months
but
displayed
inferior
after
33
months.
A
subgroup
conducted,
revealing
that
within
subset
individuals
without
metastasis,
showcased
significant
advantage
over
cohort
metastatic
cancer,
outperformed
before
24
weaker
25
This
study
has
developed
validated
learning-based
predict
outperforms
model.
Molecular Therapy — Nucleic Acids,
Год журнала:
2023,
Номер
33, С. 110 - 126
Опубликована: Июнь 5, 2023
Muscle-invasive
urothelial
cancer
(MUC),
characterized
by
high
aggressiveness
and
significant
heterogeneity,
is
currently
lacking
highly
precise
individualized
treatment
options.
We
used
a
computational
pipeline
to
synthesize
multiomics
data
from
MUC
patients
using
10
clustering
algorithms,
which
were
then
combined
with
machine
learning
algorithms
identify
molecular
subgroups
of
resolution
develop
robust
consensus
learning-driven
signature
(CMLS).
Through
clustering,
we
identified
three
subtypes
(CSs)
that
are
related
prognosis,
CS2
exhibiting
the
most
favorable
prognostic
outcome.
Subsequent
screening
enabled
identification
12
hub
genes
constitute
CMLS
predictive
power
for
prognosis.
The
low-CMLS
group
exhibited
more
prognosis
greater
responsiveness
immunotherapy
was
likely
exhibit
"hot
tumor"
phenotype.
high-CMLS
had
poor
lower
likelihood
benefitting
immunotherapy,
but
dasatinib
romidepsin
may
serve
as
promising
treatments
them.
Comprehensive
analysis
can
offer
important
insights
further
refine
classification
MUC.
Identification
represents
valuable
tool
early
prediction
patient
potential
candidates
benefit
broad
implications
clinical
practice.
Clinical and Translational Medicine,
Год журнала:
2024,
Номер
14(2)
Опубликована: Фев. 1, 2024
Osteosarcoma
(OSA)
presents
a
clinical
challenge
and
has
low
5-year
survival
rate.
Currently,
the
lack
of
advanced
stratification
models
makes
personalized
therapy
difficult.
This
study
aims
to
identify
novel
biomarkers
stratify
high-risk
OSA
patients
guide
treatment.
Cancer Cell International,
Год журнала:
2024,
Номер
24(1)
Опубликована: Янв. 31, 2024
A
minute
fraction
of
patients
stands
to
derive
substantial
benefits
from
immunotherapy,
primarily
attributable
immune
evasion.
Our
objective
was
formulate
a
predictive
signature
rooted
in
genes
associated
with
cytotoxic
T
lymphocyte
evasion
(CERGs),
the
aim
predicting
outcomes
and
discerning
immunotherapeutic
response
colorectal
cancer
(CRC).
Cancer Immunology Immunotherapy,
Год журнала:
2024,
Номер
73(3)
Опубликована: Фев. 13, 2024
Abstract
Background
The
tumor
microenvironment
(TME)
encompasses
a
variety
of
cells
that
influence
immune
responses
and
growth,
with
tumor-associated
macrophages
(TAM)
being
crucial
component
the
TME.
TAM
can
guide
prostate
cancer
in
different
directions
response
to
various
external
stimuli.
Methods
First,
we
downloaded
single-cell
sequencing
data
second-generation
from
multiple
public
databases.
From
these
data,
identified
characteristic
genes
associated
clusters.
We
then
employed
machine
learning
techniques
select
most
accurate
gene
set
developed
TAM-related
risk
label
for
cancer.
analyzed
tumor-relatedness
groups
within
population.
Finally,
validated
accuracy
prognostic
using
qPCR,
WB
assays,
among
other
methods.
Results
In
this
study,
TAM_2
cell
cluster
has
been
as
promoting
progression
cancer,
possibly
representing
M2
macrophages.
9
feature
selected
through
ten
methods
demonstrated
their
effectiveness
predicting
patients.
Additionally,
have
linked
clinical
pathological
characteristics,
allowing
us
construct
nomogram.
This
nomogram
provides
practitioners
quantitative
tool
assessing
prognosis
Conclusion
study
potential
relationship
between
PCa
established
model.
It
holds
promise
valuable
management
treatment
Frontiers in Immunology,
Год журнала:
2024,
Номер
15
Опубликована: Март 5, 2024
Background
Despite
advancements,
breast
cancer
outcomes
remain
stagnant,
highlighting
the
need
for
precise
biomarkers
in
precision
medicine.
Traditional
TNM
staging
is
insufficient
identifying
patients
who
will
respond
well
to
treatment.
Methods
Our
study
involved
over
6,900
from
14
datasets,
including
in-house
clinical
data
and
single-cell
8
(37,451
cells).
We
integrated
10
machine
learning
algorithms
55
combinations
analyzed
100
existing
signatures.
IHC
assays
were
conducted
validation,
potential
immunotherapies
chemotherapies
explored.
Results
pinpointed
six
stable
Panoptosis-related
genes
multi-center
cohorts,
leading
a
robust
Panoptosis-model.
This
model
outperformed
molecular
features
predicting
recurrence
mortality
risks,
with
high-risk
showing
worse
outcomes.
validation
30
confirmed
our
findings,
indicating
model’s
broader
applicability.
Additionally,
suggested
that
low-risk
benefit
more
immunotherapy,
while
are
sensitive
specific
like
BI-2536
ispinesib.
Conclusion
The
Panoptosis-model
represents
major
advancement
prognosis
treatment
personalization,
offering
significant
insights
effectively
managing
wide
range
of
patients.
Biomedicines,
Год журнала:
2024,
Номер
12(7), С. 1626 - 1626
Опубликована: Июль 22, 2024
Recent
studies
have
demonstrated
that
the
migrasome,
a
newly
functional
extracellular
vesicle,
is
potentially
significant
in
occurrence,
progression,
and
diagnosis
of
cardiovascular
diseases.
Nonetheless,
its
diagnostic
significance
biological
mechanism
acute
myocardial
infarction
(AMI)
yet
to
be
fully
explored.
Frontiers in Immunology,
Год журнала:
2025,
Номер
15
Опубликована: Янв. 14, 2025
Background
The
rising
incidence
of
breast
cancer
and
its
heterogeneity
necessitate
precise
tools
for
predicting
patient
prognosis
tailoring
personalized
treatments.
Epigenetic
changes
play
a
critical
role
in
progression
therapy
responses,
providing
foundation
prognostic
model
development.
Methods
We
developed
the
Machine
Learning-derived
Model
(MLEM)
to
identify
epigenetic
gene
patterns
cancer.
Using
multi-cohort
transcriptomic
datasets,
MLEM
was
constructed
with
rigorous
machine
learning
techniques
validated
across
independent
datasets.
model’s
performance
further
corroborated
through
immunohistochemical
validation
on
clinical
samples.
Results
effectively
stratified
patients
into
high-
low-risk
groups.
Low-MLEM
exhibited
improved
prognosis,
characterized
by
enhanced
immune
cell
infiltration
higher
responsiveness
immunotherapy.
High-MLEM
showed
poorer
but
were
more
responsive
chemotherapy,
vincristine
identified
as
promising
therapeutic
option.
demonstrated
robust
Conclusion
is
powerful
tool
outcomes
By
integrating
insights
learning,
this
has
potential
improve
decision-making
optimize
strategies
patients.
Cancer Cell International,
Год журнала:
2025,
Номер
25(1)
Опубликована: Фев. 13, 2025
Breast
cancer,
a
highly
heterogeneous
and
complex
disease,
remains
the
leading
cause
of
cancer-related
death
among
women
worldwide.
Despite
advances
in
treatment
modalities,
effective
prognostic
models
therapeutic
strategies
are
still
urgently
needed.
We
retrospectively
analyzed
15
independent
breast
cancer
cohorts
to
explore
role
RNA
modifications
prognosis
patients
with
cancer.
By
integrating
nine
types
modifications,
we
developed
comprehensive
machine
learning-based
modification
signature
(CMRS).
Furthermore,
single-cell
sequencing
data
were
understand
biological
mechanisms
underlying
CMRS.
In
addition,
immune
infiltration
levels
evaluated
via
six
different
algorithms,
checkpoint
inhibitor
responsiveness
was
predicted.
Moreover,
response
high-CMIS
chemotherapy
predicted
multiple
datasets.
Finally,
immunohistochemistry
performed
on
tissue
samples
from
validate
protein
expression
levels.
Our
analysis
revealed
five
key
modification-related
genes
(ENO1,
ARAF,
WT1,
GADD45A,
BIRC3)
associated
prognosis.
The
CMRS
model
demonstrated
high
predictive
accuracy
across
significantly
correlated
patient
survival
outcomes.
Multiomics
that
increased
tumor
mutational
burden
distinct
signatures,
particularly
pathways
related
TP53,
MYC,
cell
proliferation.
Single-cell
highlighted
involvement
epithelial
cells
MYC
signaling
activity.
Cell‒cell
communication
reduced
interaction
strength
hig
patients,
indicating
poor
low
presented
improved
inhibitors,
whereas
identified
as
potential
candidates
for
panobinostat
vincristine.
study
elucidates
significant
treatment.
serves
sensitive
biomarker
predicting
responsiveness,
offering
new
avenue
personalized
therapy