Medical Review,
Journal Year:
2024,
Volume and Issue:
4(1), P. 68 - 85
Published: Feb. 1, 2024
Cardiovascular
research
has
heavily
relied
on
studies
using
patient
samples
and
animal
models.
However,
often
miss
the
data
from
crucial
early
stage
of
cardiovascular
diseases,
as
obtaining
primary
tissues
at
this
is
impracticable.
Transgenic
models
can
offer
some
insights
into
disease
mechanisms,
although
they
usually
do
not
fully
recapitulate
phenotype
diseases
their
progression.
In
recent
years,
a
promising
breakthrough
emerged
in
form
Bioactive Materials,
Journal Year:
2023,
Volume and Issue:
31, P. 475 - 496
Published: Sept. 9, 2023
In
the
human
body,
almost
all
cells
interact
with
extracellular
matrices
(ECMs),
which
have
tissue
and
organ-specific
compositions
architectures.
These
ECMs
not
only
function
as
cellular
scaffolds,
providing
structural
support,
but
also
play
a
crucial
role
in
dynamically
regulating
various
functions.
This
comprehensive
review
delves
into
examination
of
biofabrication
strategies
used
to
develop
bioactive
materials
that
accurately
mimic
one
or
more
biophysical
biochemical
properties
ECMs.
We
discuss
potential
integration
these
ECM-mimics
range
physiological
pathological
vitro
models,
enhancing
our
understanding
behavior
organization.
Lastly,
we
propose
future
research
directions
for
context
engineering
organ-on-a-chip
applications,
offering
advancements
therapeutic
approaches
improved
patient
outcomes.
Advanced Healthcare Materials,
Journal Year:
2024,
Volume and Issue:
13(20)
Published: March 7, 2024
The
human
microbiome
significantly
influences
drug
metabolism
through
the
gut-liver
axis,
leading
to
modified
responses
and
potential
toxicity.
Due
complex
nature
of
gut
environment,
understanding
microbiome-driven
impacts
on
these
processes
is
limited.
To
address
this,
a
multiorgan-on-a-chip
(MOoC)
platform
that
combines
microbial-crosstalk
(HuMiX)
gut-on-chip
(GoC)
Dynamic42
liver-on-chip
(LoC),
mimicking
bidirectional
interconnection
between
liver
known
as
introduced.
This
supports
viability
functionality
intestinal
cells.
In
proof-of-concept
study,
irinotecan,
widely
used
colorectal
cancer
drug,
imitated
within
MOoC.
Utilizing
liquid
chromatography
coupled
tandem
mass
spectrometry
(LC-MS/MS),
irinotecan
metabolites
are
tracked,
confirming
platform's
ability
represent
along
axis.
Further,
using
authors'
platform,
it
shown
cancer-associated
bacterium,
Escherichia
coli,
modifies
transformation
its
inactive
metabolite
SN-38G
into
toxic
SN-38.
serves
robust
tool
for
investigating
intricate
interplay
microbes
pharmaceuticals,
offering
representative
alternative
animal
models
providing
novel
development
strategies.
Cell Biology and Toxicology,
Journal Year:
2024,
Volume and Issue:
40(1)
Published: July 29, 2024
Abstract
Advancements
in
the
CRISPR
technology,
a
game-changer
experimental
research,
have
revolutionized
various
fields
of
life
sciences
and
more
profoundly,
cancer
research.
Cell
death
pathways
are
among
most
deregulated
cells
considered
as
critical
aspects
development.
Through
decades,
our
knowledge
mechanisms
orchestrating
programmed
cellular
has
increased
substantially,
attributed
to
revolution
cutting-edge
technologies.
The
heroic
appearance
systems
expanded
available
screening
platform
genome
engineering
toolbox
detect
mutations
create
precise
edits.
In
that
context,
ability
this
system
for
identification
targeting
cell
signaling
result
development
therapy
resistance
is
an
auspicious
choice
transform
accelerate
individualized
therapy.
concept
personalized
stands
on
molecular
characterization
individual
tumor
its
microenvironment
order
provide
treatment
with
highest
possible
outcome
minimum
toxicity.
This
study
explored
potential
technology
precision
by
identifying
specific
pathways.
It
showed
promise
finding
key
components
involved
death,
making
it
tool
targeted
However,
also
highlighted
challenges
limitations
need
be
addressed
future
research
fully
realize
treatment.
Graphical
abstract
Current
application
through
glance.
A
choosing
appropriate
biological
model
vitro
(using
established
lines,
animal
derived
cells,
human
stem
or
T
cells),
vivo
models
which
can
harbor
tumor),
ex
(human/animal-derived
organoids).
B
preparation
gRNA
library.
C
design
screening,
desired
gRNAs
phenotypic
response.
D
CRISPR-Cas
identified
targets,
Cas9
gene
editing
(Knockout,
base
editing,
prime
editing),
RNA
modulation
(modulation
splicing,
interference),
epigenomic
edits
interference/activation
using
dead
(dCas9)
(Bock
et
al.
2022b)
Colloids and Surfaces B Biointerfaces,
Journal Year:
2025,
Volume and Issue:
249, P. 114507 - 114507
Published: Jan. 8, 2025
Organ-on-a-chip
systems,
also
referred
to
as
microphysiological
systems
(MPS),
represent
an
advance
in
bioengineering
microsystems
designed
mimic
key
aspects
of
human
organ
physiology
and
function.
Drawing
inspiration
from
the
intricate
hierarchical
architecture
body,
these
innovative
platforms
have
emerged
invaluable
vitro
tools
with
wide-ranging
applications
drug
discovery
development,
well
enhancing
our
understanding
disease
physiology.
The
facility
replicate
tissues
within
physiologically
relevant
three-dimensional
multicellular
environments
empowers
organ-on-a-chip
versatility
throughout
different
stages
development
process.
Moreover,
can
be
tailored
specific
states,
facilitating
investigation
progression,
responses,
potential
therapeutic
interventions.
In
particular,
they
demonstrate,
early-phase
pre-clinical
studies,
safety
toxicity
profiles
compounds.
Furthermore,
play
a
pivotal
role
evaluation
efficacy
modeling
diseases.
One
most
promising
prospects
technology
is
simulate
pathophysiology
subpopulations
even
individual
patients,
thereby
being
used
personalized
medicine.
By
mimicking
physiological
responses
diverse
patient
groups,
hold
promise
revolutionizing
strategies,
guiding
them
towards
intervention
unique
needs
each
patient.
This
review
presents
status
evolution
microfluidic
that
facilitated
transition
cells
organs
recreated
on
chips
some
opportunities
offered
by
technology.
Additionally,
current
future
perspectives
challenges
this
still
faces
are
discussed.
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
Stem Cell Research & Therapy,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: May 31, 2024
In
the
past
decade,
intestinal
organoid
technology
has
paved
way
for
reproducing
tissue
or
organ
morphogenesis
during
physiological
processes
in
vitro
and
studying
pathogenesis
of
various
diseases.
Intestinal
organoids
are
favored
drug
screening
due
to
their
ability
high-throughput
cultivation
closer
resemblance
patient
genetic
characteristics.
Furthermore,
as
disease
models,
find
wide
applications
diagnostic
markers,
identifying
therapeutic
targets,
exploring
epigenetic
mechanisms
Additionally,
a
transplantable
cellular
system,
have
played
significant
role
reconstruction
damaged
epithelium
conditions
such
ulcerative
colitis
short
bowel
syndrome,
well
material
exchange
metabolic
function
restoration.
The
rise
interdisciplinary
approaches,
including
organoid-on-chip
technology,
genome
editing
techniques,
microfluidics,
greatly
accelerated
development
organoids.
this
review,
VOSviewer
software
is
used
visualize
hot
co-cited
journal
keywords
trends
firstly.
Subsequently,
we
summarized
current
modeling,
screening,
regenerative
medicine.
This
will
deepen
our
understanding
further
explore
intestine
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: June 15, 2024
Organ
on
Chip
platforms
hold
significant
promise
as
alternatives
to
animal
models
or
traditional
cell
cultures,
both
of
which
poorly
recapitulate
human
pathophysiology
and
level
responses.
Within
the
last
15
years,
we
have
witnessed
seminal
scientific
developments
from
academic
laboratories,
a
flurry
startups
investments,
genuine
interest
pharmaceutical
industry
well
regulatory
authorities
translate
these
platforms.
This
Perspective
identifies
several
fundamental
design
process
features
that
may
act
roadblocks
prevent
widespread
dissemination
deployment
systems,
provides
roadmap
help
position
this
technology
in
mainstream
drug
discovery.
Nanoscale,
Journal Year:
2023,
Volume and Issue:
15(23), P. 9927 - 9940
Published: Jan. 1, 2023
Organ-on-chip
systems
recapitulate
the
form
and
function
of
biological
organs
in
highly
controlled
vitro
conditions
have
already
been
used
for
testing
a
variety
nanoparticles.
Can
they
unlock
translational
potential
nanomedicine?