Frontiers in Oncology,
Journal Year:
2024,
Volume and Issue:
14
Published: March 13, 2024
Animal
models
have
been
commonly
used
in
immunotherapy
research
to
study
the
cell
response
external
agents
and
assess
effectiveness
safety
of
new
therapies.
Over
past
few
decades,
immunocompromised
(also
called
immunodeficient)
mice
allowed
researchers
grow
human
tumor
cells
without
impact
host’s
immune
system.
However,
while
this
model
is
very
valuable
understand
biology
underlying
mechanism
immunotherapy,
results
may
not
always
directly
translate
humans.
The
microenvironment
has
significant
implications
for
engraftment,
growth,
invasion,
etc.,
system
plays
a
critical
role
shaping
microenvironment.
Human
immunocompetent
mice,
also
named
humanized
are
engineered
that
possess
functional
cells.
This
vivo
can
be
effectively
effect
implanted
tumor.
Moreover,
mimic
treatment.
section
an
overview
current
understanding
different
could
utilized
chordoma.
Cancer Cell International,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: March 18, 2025
Intratumoral
heterogeneity
is
the
main
cause
of
tumor
treatment
failure,
varying
across
disease
sites
(spatial
heterogeneity)
and
polyclonal
properties
tumors
that
evolve
over
time
(temporal
heterogeneity).
As
our
understanding
intratumoral
heterogeneity,
formation
which
mainly
related
to
genomic
instability,
epigenetic
modifications,
plastic
gene
expression,
different
microenvironments,
plays
a
substantial
role
in
drug-resistant
as
far
metastasis
recurrence.
Understanding
it
becomes
clear
single
therapeutic
agent
or
regimen
may
only
be
effective
for
subsets
cells
with
certain
features,
but
not
others.
This
necessitates
shift
from
current,
unchanging
approach
one
tailored
against
killing
patterns
cancer
clones.
In
this
review,
we
discuss
recent
evidence
concerning
global
perturbations
associations
specific
lung
cancer,
underlying
mechanisms
potentially
leading
formation,
how
drives
drug
resistance.
Our
findings
highlight
most
up-to-date
progress
its
mediating
resistance,
could
support
development
future
strategies.
Expert Review of Molecular Diagnostics,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 7, 2025
Breast
cancer
remains
a
major
global
health
challenge.
While
advances
in
precision
oncology
have
contributed
to
improvements
patient
outcomes
and
provided
deeper
understanding
of
the
biological
mechanisms
that
drive
disease,
historically,
research
patients'
allocation
treatment
heavily
relied
on
single-omic
approaches,
analyzing
individual
molecular
dimensions
such
as
genomics,
transcriptomics,
or
proteomics.
these
deep
insights
into
breast
biology,
they
often
fail
offer
complete
disease's
complex
landscape.
In
this
review,
authors
explore
recent
advancements
multi-omic
realm
using
clinical
data
show
how
integration
can
more
holistic
alterations
their
functional
consequences
underlying
cancer.
The
overall
developments
AI
are
expected
complement
diagnostics
through
potentially
refining
prognostic
models,
selection.
Overcoming
challenges
cost,
complexity,
lack
standardization
is
crucial
for
unlocking
full
potential
multi-omics
care
enable
advancement
personalized
treatments
improve
outcomes.
Frontiers in Oncology,
Journal Year:
2025,
Volume and Issue:
15
Published: April 16, 2025
The
aim
of
this
study
was
to
explore
the
application
value
dynamic
contrast-enhanced
magnetic
resonance
imaging
(DCE-MRI)
radiomics
and
heterogeneity
analysis
in
differentiation
molecular
subtypes
luminal
non-luminal
breast
cancer.
In
retrospective
study,
388
female
cancer
patients
(48.37
±
9.41
years)
with
(n
=
190)
198)
who
received
surgical
treatment
at
Jilin
Cancer
Hospital
were
recruited
from
January
2019
June
2023.
All
underwent
MRI
scan
DCE
before
surgery.
then
divided
into
a
training
set
272)
validation
116)
7:3
ratio.
three-dimensional
texture
feature
parameters
lesion
areas
extracted.
Four
tumor
parameters,
including
type
I
curve
proportion,
II
III
proportion
values
calculated
normalized.
Five
machine
learning
(ML)
models,
logistic
regression,
naive
Bayes
algorithm
(NB),
k-nearest
neighbor
(KNN),
decision
tree
(DT)
extreme
gradient
boosting
(XGBoost)
model
used
process
data
further
validated.
best
ML
selected
according
performance
set.
subtype
lesions,
index
significantly
lower
than
corresponding
lesions
both
Eight
features
together
four
heterogeneity-related
significant
differences
between
groups
retained
as
signatures
for
constructing
prediction
model.
regression
achieved
highest
area
under
(0.93),
accuracy
(86.94%),
sensitivity
(87.55%)
specificity
(86.25%).
based
on
DCE-MRI
exhibit
good
discriminating
demonstrates
predictive
among
various
models.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: March 27, 2024
Introduction
In
vivo
studies
of
cancer
biology
and
assessment
therapeutic
efficacy
are
critical
to
advancing
research
ultimately
improving
patient
outcomes.
Murine
models
have
proven
be
an
invaluable
tool
in
pre-clinical
studies.
this
context,
multi-parameter
flow
cytometry
is
a
powerful
method
for
elucidating
the
profile
immune
cells
within
tumor
microenvironment
and/or
play
role
hematological
diseases.
However,
designing
appropriate
panel
comprehensively
increasing
diversity
across
different
murine
tissues
can
extremely
challenging.
Methods
To
address
issue,
we
designed
with
13
fixed
markers
that
define
major
populations
–referred
as
backbone
panel–
profiled
but
option
incorporate
up
seven
additional
fluorochromes,
including
any
marker
specific
study
question.
Results
This
maintains
its
resolution
spectral
cytometers
organs,
both
hematopoietic
non-hematopoietic,
well
tumors
complex
microenvironments.
Discussion
Having
robust
easily
customized
pre-validated
drop-in
fluorochromes
saves
time
resources
brings
consistency
standardization,
making
it
versatile
solution
immuno-oncology
researchers.
addition,
approach
presented
here
serve
guide
develop
similar
types
customizable
panels
questions
requiring
high-parameter
panels.