Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: April 4, 2023
Augmenting
adaptive
immunity
is
a
critical
goal
for
developing
next-generation
cancer
therapies.
T
and
B
cells
infiltrating
the
tumor
dramatically
influence
progression
through
complex
interactions
with
local
microenvironment.
Cancer
evade
limit
these
immune
responses
by
hijacking
normal
immunologic
pathways.
Current
experimental
models
using
conventional
primary
cells,
cell
lines,
or
animals
have
limitations
studying
cancer-immune
directly
relevant
to
human
biology
clinical
translation.
Therefore,
engineering
methods
emulate
such
interplay
at
systemic
levels
are
crucial
expedite
development
of
better
therapies
diagnostic
tools.
In
this
review,
we
discuss
challenges,
recent
advances,
future
directions
toward
tumor-immune
microenvironment
(TME),
including
key
elements
immunity.
We
first
offer
an
overview
research
that
has
advanced
our
understanding
role
system
in
Next,
developments
3D
Biomedical Physics & Engineering Express,
Journal Year:
2024,
Volume and Issue:
10(5), P. 052002 - 052002
Published: Aug. 14, 2024
Abstract
Purpose
.
This
review
aims
to
highlight
current
improvements
in
microfluidic
devices
designed
for
digestive
cancer
simulation.
The
emphasizes
the
use
of
multicellular
3D
tissue
engineering
models
understand
complicated
biology
tumor
microenvironment
(TME)
and
progression.
purpose
is
develop
oncology
research
improve
patients’
lives.
Methods
analyzes
recent
on
mimicking
cancer.
It
uses
tissue-engineered
devices,
notably
organs
a
chip
(OOC),
simulate
human
organ
function
lab.
Cell
cultivation
modern
three-dimensional
hydrogel
platforms
allows
precise
geometry,
biological
components,
physiological
qualities.
novel
methodologies,
key
findings,
technical
progress
explain
this
field’s
advances.
Results
study
discusses
advances
Micro
systems
with
are
emphasized.
These
capture
complex
biochemical
gradients,
niche
variables,
dynamic
cell–cell
interactions
(TME).
reveal
stomach
progression
by
duplicating
TME.
Recent
discoveries
technology
have
improved
our
understanding
gut
biology,
as
shown
review.
Conclusion
Microfluidic
play
crucial
role
modeling
furthering
research.
could
transform
drug
development
treatment
revealing
provides
complete
summary
suggests
future
field
professionals.
review’s
major
goal
further
medical
Frontiers in Bioengineering and Biotechnology,
Journal Year:
2024,
Volume and Issue:
12
Published: Jan. 23, 2024
Lack
of
adequate
models
significantly
hinders
advances
in
prostate
cancer
treatment,
where
resistance
to
androgen-deprivation
therapies
and
bone
metastasis
remain
as
major
challenges.
Current
vitro
fail
faithfully
mimic
the
complex
physiology.
In
vivo
animal
can
shed
light
on
oncogenes
involved
development
progression;
however,
gland
is
fundamentally
different
from
that
human,
underlying
genetic
mechanisms
are
different.
To
address
this
problem,
we
developed
first
microfluidic
human
Prostate-Cancer-on-Chip
(PCoC)
model,
stromal
fibroblast
cells
were
co-cultivated
two
channels
separated
by
a
porous
membrane
under
culture
medium
flow.
The
established
microenvironment
enables
soluble
signaling
factors
secreted
each
locally
diffuse
through
pores
affecting
neighboring
culture.
We
particularly
explored
conversion
fibroblasts
into
cancer-associated
(CAFs)
due
interaction
between
2
cell
types.
Immunofluorescence
microscopy
revealed
tumor
induced
CAF
biomarkers,
αSMA
COL1A1,
fibroblasts.
level
was
observed
increase
along
flow
direction
response
diffusion
agents,
consistent
with
simulations
solute
concentration
gradients.
also
downregulated
androgen
receptor
(AR)
expression
fibroblasts,
while
an
AR
maintained
normal
homeostasis.
further
investigated
invasion
stroma,
early
step
metastatic
cascade,
devices
featuring
serpentine
channel
orthogonal
segments
overlaying
straight
8
µm-pore
membrane.
Both
CAFs
cross
over
their
channel,
stroma’s
role
seemed
be
proactive
promoting
invasion.
As
control,
epithelial
neither
nor
promoted
summary,
PCoC
model
allows
spatiotemporal
analysis
tumor-stroma
dynamic
interactions,
bi-directional
physical
contact,
recapitulating
tissue-level
multicellular
responses
associated
.
Hence,
it
serve
dissect
seek
advanced
therapeutic
strategies.
Frontiers in Medicine,
Journal Year:
2025,
Volume and Issue:
11
Published: Jan. 24, 2025
The
liver
is
a
vital
organ
responsible
for
numerous
metabolic
processes
in
the
human
body,
including
metabolism
of
drugs
and
nutrients.
After
damage,
can
rapidly
return
to
its
original
size
if
causative
factor
promptly
eliminated.
However,
when
harmful
stimulus
persists,
liver’s
regenerative
capacity
becomes
compromised.
Substantial
theoretical
feasibility
has
been
demonstrated
at
levels
gene
expression,
molecular
interactions,
intercellular
dynamics,
complemented
by
successful
animal
studies.
robust
model
carrier
that
closely
resemble
physiology
are
still
lacking
translating
these
theories
into
practice.
potential
regeneration
central
focus
ongoing
research.
Over
past
decade,
advent
organoid
technology
provided
improved
models
materials
advancing
research
efforts.
Liver
represents
novel
vitro
culture
system.
several
years
refinement,
organoids
now
accurately
replicate
morphological
structure,
nutrient
drug
metabolism,
secretory
functions,
providing
disease
Regenerative
medicine
aims
or
tissue
functions
repair
replace
damaged
tissues,
restore
their
structure
function,
stimulate
tissues
organs
within
body.
possess
same
function
as
tissue,
offering
serve
viable
replacement
liver,
aligning
with
goals
medicine.
This
review
examines
role
Engineered Regeneration,
Journal Year:
2024,
Volume and Issue:
5(2), P. 153 - 169
Published: March 7, 2024
Microfluidic
is
a
technology
that
allows
the
precise
control
of
fluid
in
micro-channel.
With
its
advantages
high
throughput
and
low
cost,
microfluidic
has
achieved
good
performance
various
fields
recent
years.
Arthritis
general
term
for
variety
joint
diseases,
which
can
be
clinically
manifested
as
pain
swelling,
seriously
affecting
people's
physical
mental
health.
At
present,
causes
arthritis
disease
are
still
unknown,
existing
models
treatment
methods
limited,
so
more
treatments
need
to
developed.
organ
chip
cutting-edge
build
bionic
human
model,
reflect
structure
function
characteristics
organs
by
simulating
physiological
environment
tissues
cells
vitro.
This
paper
reviews
application
modeling
arthritis,
hoping
open
up
new
vision
study
arthritis.
Frontiers in Cell and Developmental Biology,
Journal Year:
2024,
Volume and Issue:
12
Published: April 22, 2024
The
tumor
microenvironment
(TME)
is
a
diverse
milieu
of
cells
including
cancerous
and
non-cancerous
such
as
fibroblasts,
pericytes,
endothelial
immune
cells.
intricate
cellular
interactions
within
the
TME
hold
central
role
in
shaping
dynamics
cancer
progression,
influencing
pivotal
aspects
initiation,
growth,
invasion,
response
to
therapeutic
interventions,
emergence
drug
resistance.
In
immunologically
'cold'
tumors,
marked
by
scarcity
infiltrating
cells,
limited
antigen
presentation
absence
potent
immune-stimulating
signals,
an
abundance
immunosuppressive
factors.
While
strategies
targeting
avenue
tumors
have
emerged,
there
pressing
need
for
novel
approaches
that
faithfully
replicate
complex
non-cellular
order
develop
targeted
therapies
can
effectively
stimulate
responses
improve
outcomes
patients.
Microfluidic
devices
offer
distinct
advantages
over
traditional
vitro
3D
co-culture
models
vivo
animal
models,
they
better
recapitulate
key
characteristics
allow
precise,
controlled
insights
into
dynamic
interplay
between
various
immune,
stromal
cell
types
at
any
timepoint.
This
review
aims
underscore
microfluidic
systems
advancing
our
understanding
presents
current
model
aim
dissect
tumor-stromal,
tumor-immune
immune-stromal
tumors.
Understanding
intricacies
crucial
devising
effective
reinvigorate
overcome
challenges
immunotherapy
approaches.
MGM Journal of Medical Sciences,
Journal Year:
2024,
Volume and Issue:
11(2), P. 331 - 339
Published: April 1, 2024
Abstract
Bioprinting
technology
aims
to
create
3D
structures
with
living
cells
mimic
real
tissue
and
organ
functions.
The
process
involves
various
additive
technologies,
including
bioprinters
bioinks.
Bioinks
comprise
hydrogels,
scaffolds,
additives,
growth
factors,
cells.
While
much
of
the
is
still
in
exploratory
stages,
it
has
successfully
produced
tissue,
blood
vessels,
bones.
Research
suggests
potential
for
bioprinting
whole
organs
revolutionize
medical
procedures.
Current
major
business
components
include
types
advanced
Advancements
technologies
such
as
cellular
reprogramming
hold
enhance
development
superior
bioinks,
thereby
enabling
fabrication
bioprinted
tissues.
offers
significant
benefits
across
research,
personalized
medicine,
other
applications.
This
review
provides
a
flavor
using
areas
usage,
Development
(R&D),
its
applications
on
wide
spectrum,
medicine.
Soft Matter,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
In
recent
years,
nano
and
micro
drug
delivery
systems
targeting
the
colon
have
gained
more
attention
due
to
increasing
interest
in
treating
diseases
such
as
colorectal
cancer
inflammatory
bowel
disease,
Frontiers in Molecular Biosciences,
Journal Year:
2025,
Volume and Issue:
11
Published: Jan. 13, 2025
Introduction
Current
in
vitro
intestinal
models
lack
the
mechanical
forces
present
physiological
environment,
limiting
their
reliability
for
nanotoxicology
studies.
Here,
we
developed
an
enhanced
Caco-2/HT29-MTX-E12
co-culture
model
incorporating
orbital
stimulation
to
better
replicate
conditions
and
investigate
nanoparticle
interactions.
Methods
We
established
co-cultures
under
static
dynamic
conditions,
evaluating
development
through
multiple
approaches
including
barrier
integrity
measurements,
gene
expression
analysis,
confocal
microscopy.
introduced
novel
quantitative
analysis
of
dome
formation
as
a
differentiation
marker
demonstrated
application
by
investigating
cellular
responses
titanium
dioxide
(TiO₂)
nanoparticles
digested
food
matrix.
Results
Dynamic
accelerated
epithelial
differentiation,
achieving
functional
properties
day
14
rather
than
21,
with
mucin
production
more
organized
three-dimensional
structure.
Mechanical
selectively
promoted
goblet
cell
without
affecting
general
markers.
The
optimized
successfully
detected
concentration-dependent
oxidative
stress
TiO₂
exposure,
revealing
dysfunction
preceding
membrane
damage.
Discussion
This
improved
system
provides
platform
By
forces,
each
type
exhibits
representative
behavior,
creating
realistic
experimental
setup.
bridges
gap
between
simple
monocultures
complex
3D
systems,
offering
practical
approach
nanoparticle-epithelium
interactions
food-relevant
context.