bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 23, 2024
Abstract
Understanding
the
phenotypic
transitions
of
cancer
cells
is
crucial
for
elucidating
tumor
progression
mechanisms,
particularly
transition
from
a
non-invasive
spheroid
phenotype
to
an
invasive
network
phenotype.
We
developed
agent-based
model
(ABM)
using
Compucell3D,
open-source
biological
simulation
software,
investigate
how
varying
biophysical
and
biochemical
parameters
influence
emerging
properties
cellular
communities,
including
cell
growth,
division,
migration.
Our
focus
was
on
cell-cell
contact
adhesion
matrix
remodeling
effects
simplified
enzymatic
extracellular
subsequent
enhancements
chemotaxis
or
durotaxis
as
combined
effect
localized
secretion
chemoattractant.
By
chemoattractant
rate
energy,
we
simulated
their
behavior
driving
The
serves
digital
twin
3D
culture,
simulating
invasion
over
1
week,
validated
against
published
data.
simulations
track
emergent
morphological
collective
changes
key
metrics
such
circularity
invasion.
findings
indicate
that
increased
enhances
invasiveness
cells,
promoting
Additionally,
changing
energy
strong
weak
affects
compactness
spheroids,
resulting
in
lower
work
advances
understanding
by
providing
insights
into
mechanisms
behind
transitions.
Frontiers in Applied Mathematics and Statistics,
Journal Year:
2025,
Volume and Issue:
11
Published: May 15, 2025
In
this
paper,
we
adapt
a
two-species
agent-based
cancer
model
that
describes
the
interaction
between
cells
and
healthy
on
uniform
grid
to
include
with
third
species—namely
immune
cells.
We
run
six
different
scenarios
explore
competition
initial
concentration
of
dynamics.
then
use
coupled
equation
learning
construct
population-based
reaction
for
each
scenario.
show
how
they
can
be
unified
into
single
surrogate
model,
whose
underlying
three
ordinary
differential
equations
are
much
easier
analyse
than
original
model.
As
an
example,
by
finding
steady
state
concentration,
able
find
linear
relationship
This
enables
us
estimate
suitable
values
reduce
substantially
without
performing
additional
complex
expensive
simulations
from
stochastic
Journal of Clinical Medicine,
Journal Year:
2025,
Volume and Issue:
14(10), P. 3574 - 3574
Published: May 20, 2025
Background:
Digital
twin
(DT)
technology,
integrated
with
artificial
intelligence
(AI)
and
machine
learning
(ML),
holds
significant
potential
to
transform
oncology
care.
By
creating
dynamic
virtual
replicas
of
patients,
DTs
allow
clinicians
simulate
disease
progression
treatment
responses,
offering
a
personalized
approach
cancer
treatment.
Aim:
This
narrative
review
aimed
synthesize
existing
studies
on
the
application
digital
twins
in
oncology,
focusing
their
benefits,
challenges,
ethical
considerations.
Methods:
The
reviews
(NRR)
followed
structured
selection
process
using
standardized
checklist.
Searches
were
conducted
PubMed
Scopus
predefined
query
oncology.
Reviews
prioritized
based
synthesis
prior
studies,
focus
Studies
evaluated
quality
parameters
(clear
rationale,
research
design,
methodology,
results,
conclusions,
conflict
disclosure).
Only
scores
above
prefixed
threshold
disclosed
conflicts
interest
included
final
synthesis;
seventeen
selected.
Results
Discussion:
offer
advantages
such
as
enhanced
decision-making,
optimized
regimens,
improved
clinical
trial
design.
Moreover,
economic
forecasts
suggest
that
integration
into
healthcare
systems
may
significantly
reduce
costs
drive
growth
precision
medicine
market.
However,
challenges
include
data
issues,
complexity
biological
modeling,
need
for
robust
computational
resources.
A
comparison
cutting-edge
contributes
this
direction
confirms
also
legal
considerations,
particularly
concerning
AI,
privacy,
accountability,
remain
barriers.
Conclusions:
great
promise,
but
requires
careful
attention
ethical,
legal,
operational
challenges.
Multidisciplinary
efforts,
supported
by
evolving
regulatory
frameworks
like
those
EU,
are
essential
ensuring
responsible
effective
implementation
improve
patient
outcomes.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 22, 2024
Abstract
Diffusion
and
migration
play
pivotal
roles
in
microbial
communities
-
shaping,
for
example,
colonization
new
environments
the
maintenance
of
spatial
structures
biodiversity.
While
previous
research
has
extensively
studied
free
diffusion,
such
as
range
expansion,
there
remains
a
gap
understanding
effects
biologically
or
physically
eleterious
confined
environments.
In
this
study,
we
examine
interplay
between
drug
heterogeneity
within
an
experimental
meta-community
E.
faecalis
,
Gram-positive
opportunistic
pathogen.
When
community
is
to
spatially-extended
habitats
(‘islands’)
bordered
by
deleterious
conditions,
find
that
population
level
response
depends
on
trade-off
growth
rate
island
transfer
into
regions
with
harsher
phenomenon
explore
modulating
antibiotic
concentration
island.
heterogeneous
islands,
composed
spatially
patterned
patches
support
varying
levels
growth,
population’s
fate
critically
specific
arrangement
these
same
averaged
leads
diverging
responses.
These
results
are
qualitatively
captured
simple
simulations,
analytical
expressions
which
derive
using
first-order
perturbation
approximations
reaction-diffusion
models
explicit
dependence.
Among
all
possible
arrangements,
our
theoretical
findings
reveal
highest
rates
at
center
most
effectively
mitigates
decline,
while
lowest
least
effective.
They
thus
serve
optimal
arrangements
bounding
mixed
phase,
where
outcomes
emerge
tuning
arrangements.
Extending
approach
more
complex
varied
structures,
ring-structured
community,
further
validates
impact
arrangement.
Our
suggest
approaches
interpreting
clinical
when
applying
identical
doses
inform
optimization
spatially-explicit
dosing
strategies.
Author
summary
develop
automated
platform
experimentally
investigate
short-term
dynamics
under
heterogeneity.
collective
can
vary
significantly,
even
dose,
due
different
By
constructing
model,
observed
simulated
closely
matches
data.
Furthermore,
aligns
well
long-term
rate,
defined
largest
eigenvalue,
system
quickly
enters
equilibrium
state.
Using
concepts
from
theory,
derived
relationship
boundary
diffusion
effect,
homogeneous
effect.
highlight
habitats,
emergent
property.
The
bacterial
near
equilibrium,
suggesting
measured
ecological
scale
may
be
used
predict
resistance
evolutionary
behavior.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 23, 2024
Abstract
Understanding
the
phenotypic
transitions
of
cancer
cells
is
crucial
for
elucidating
tumor
progression
mechanisms,
particularly
transition
from
a
non-invasive
spheroid
phenotype
to
an
invasive
network
phenotype.
We
developed
agent-based
model
(ABM)
using
Compucell3D,
open-source
biological
simulation
software,
investigate
how
varying
biophysical
and
biochemical
parameters
influence
emerging
properties
cellular
communities,
including
cell
growth,
division,
migration.
Our
focus
was
on
cell-cell
contact
adhesion
matrix
remodeling
effects
simplified
enzymatic
extracellular
subsequent
enhancements
chemotaxis
or
durotaxis
as
combined
effect
localized
secretion
chemoattractant.
By
chemoattractant
rate
energy,
we
simulated
their
behavior
driving
The
serves
digital
twin
3D
culture,
simulating
invasion
over
1
week,
validated
against
published
data.
simulations
track
emergent
morphological
collective
changes
key
metrics
such
circularity
invasion.
findings
indicate
that
increased
enhances
invasiveness
cells,
promoting
Additionally,
changing
energy
strong
weak
affects
compactness
spheroids,
resulting
in
lower
work
advances
understanding
by
providing
insights
into
mechanisms
behind
transitions.