Biomedicines,
Journal Year:
2023,
Volume and Issue:
11(10), P. 2743 - 2743
Published: Oct. 10, 2023
One
of
the
major
goals
in
advancement
basic
cancer
research
focuses
on
development
new
anticancer
therapies.
To
understand
molecular
mechanisms
progression,
acquired
drug
resistance,
and
metastatic
process,
use
preclinical
vitro
models
that
faithfully
summarize
properties
tumor
patients
is
still
a
necessity.
The
represented
by
diverse
group
cell
clones,
recent
years,
to
reproduce
models,
monolayer
cultures
have
been
supplanted
patient-derived
xenograft
(PDX)
cultured
organoids
derived
from
patient
(PDO).
These
proved
indispensable
for
study
microenvironment
(TME)
its
interaction
with
cells.
Prostate
(PCa)
most
common
neoplasia
men
world.
It
characterized
genomic
instability
resistance
conventional
Despite
advances
diagnosis
treatment,
PCa
remains
leading
cause
death.
Here,
we
review
studies
last
10
years
as
number
papers
growing
very
fast
field.
We
also
discuss
discovered
limitations
challenges
using
organoid
culture
system
PDXs
studying
prostate
phenotype,
performing
testing,
developing
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(2), P. 1014 - 1014
Published: Jan. 13, 2024
Organoids
are
self-organized,
three-dimensional
structures
derived
from
stem
cells
that
can
mimic
the
structure
and
physiology
of
human
organs.
Patient-specific
induced
pluripotent
(iPSCs)
3D
organoid
model
systems
allow
to
be
analyzed
in
a
controlled
environment
simulate
characteristics
given
disease
by
modeling
underlying
pathophysiology.
The
recent
development
cell
models
has
offered
scientific
community
an
exceptionally
valuable
tool
study
rare
diseases,
overcoming
limited
availability
biological
samples
limitations
animal
models.
This
review
provides
overview
iPSC
genetic
engineering
techniques
used
develop
organoids.
In
particular,
some
applied
neuronal,
muscular
skeletal
diseases
described.
Furthermore,
potential
developing
new
therapeutic
approaches
discussed.
Biomolecules,
Journal Year:
2024,
Volume and Issue:
14(9), P. 1066 - 1066
Published: Aug. 26, 2024
Skin
aging
is
influenced
by
intrinsic
and
extrinsic
factors
that
progressively
impair
skin
functionality
over
time.
Investigating
the
process
requires
thorough
research
using
innovative
technologies.
This
review
explores
use
of
in
vitro
human
3D
culture
models,
serving
as
valuable
alternatives
to
animal
ones,
research.
The
aim
highlight
benefits
necessity
improving
methodology
analyzing
molecular
mechanisms
underlying
aging.
Traditional
2D
including
monolayers
keratinocytes,
fibroblasts,
or
melanocytes,
even
if
providing
cost-effective
straightforward
methods
study
critical
processes
such
extracellular
matrix
degradation,
pigmentation,
effects
secretome
on
cells,
fail
replicate
complex
tissue
architecture
with
its
intricated
interactions.
Advanced
models
(organoid
cultures,
“skin-on-chip”
technologies,
reconstructed
skin,
bioprinting)
considerably
enhance
physiological
relevance,
enabling
a
more
accurate
representation
peculiar
features.
By
reporting
advantages
limitations
this
highlights
importance
advanced
systems
develop
practical
anti-aging
preventive
reparative
approaches
improve
translational
field.
Further
exploration
these
technologies
will
provide
new
opportunities
for
previously
unexplored
knowledge
FEMS Microbiology Reviews,
Journal Year:
2024,
Volume and Issue:
48(2)
Published: Feb. 26, 2024
Abstract
Bacterial
pneumonia
greatly
contributes
to
the
disease
burden
and
mortality
of
lower
respiratory
tract
infections
among
all
age
groups
risk
profiles.
Therefore,
laboratory
modelling
bacterial
remains
important
for
elucidating
complex
host–pathogen
interactions
determine
drug
efficacy
toxicity.
In
vitro
cell
culture
enables
creation
high-throughput,
specific
models
in
a
tightly
controlled
environment.
Advanced
human
specifically,
can
bridge
research
gap
between
classical
two-dimensional
animal
models.
This
review
provides
an
overview
current
status
development
cellular
study
infections,
with
focus
on
air–liquid
interface
models,
spheroid,
organoid,
lung-on-a-chip
For
wide
scale,
comparative
literature
search,
we
selected
six
clinically
highly
relevant
bacteria
(Pseudomonas
aeruginosa,
Mycoplasma
pneumoniae,
Haemophilus
influenzae,
Mycobacterium
tuberculosis,
Streptococcus
Staphylococcus
aureus).
We
reviewed
lines
that
are
commonly
used,
as
well
trends
discrepancies
methodology,
ranging
from
infection
parameters
assay
read-outs.
also
highlighted
importance
model
validation
data
transparency
guiding
field
towards
more
Advances in Clinical Toxicology,
Journal Year:
2024,
Volume and Issue:
9(1), P. 1 - 14
Published: Jan. 1, 2024
Background:
Traditional
toxicity
testing
emphasizes
animal
models
with
growing
concerns
regarding
predictive
capacity,
throughput
and
ethics.
Rapid
innovation
surrounding
human
cell
platforms,
bioengineered
tissues,
omics
techniques
computational
tools
offers
more
modern
alternatives
aligned
expanding
knowledge
of
chemical
biological
pathways.
These
disruptive
approaches
promise
immense
potential
to
transform
next-generation
safety
assessment
drug
development
pipelines.
Purpose:
This
review
provides
clinical
researchers
an
updated,
comprehensive
perspective
across
evolving
areas
focus
in
new
methods
analysis
latest
advances
translational
context.
Main
Body:
We
survey
progress
two-
three-dimensional
cultures
recapitulating
tissue/organ
complexity
impossible
conventional
assays.
Complementing
this,
modeling
integrates
structure-activity
relationships,
physicochemical
properties
physiological
interactions
predict
pharmacokinetics
silico.
Expanding
model
organisms
add
further
dimensionality
demographic
relevance.
High-throughput
imaging
technologies
unravel
mechanisms
illuminate
biomarkers
undetectable
by
standard
measures.
Specialized
show
high
addressing
toxicodynamic
intricacies
within
disease
contexts
like
diabetes
NAFLD.
Evaluating
traditional
medicines
phytochemicals
likewise
represents
area
growth
well-suited
for
contemporary
platforms.
Future
outlook
weighs
remarkable
advantages
reducing
demands,
enabling
precision
toxicology
links
medicine
overhauling
core
risk
frameworks.
Conclusion:
intends
catalyze
discourse
on
strategic
optimization
priorities
roadmaps
towards
fully
unlocking
the
yet
still
emerging
public
health
these
poising
transformation
sciences
centered
human-focused
models.
Frontiers in Molecular Neuroscience,
Journal Year:
2023,
Volume and Issue:
16
Published: Aug. 3, 2023
Neurodegenerative
diseases
are
adult-onset
neurological
conditions
that
notoriously
difficult
to
model
for
drug
discovery
and
development
because
most
models
unable
accurately
recapitulate
pathology
in
disease-relevant
cells,
making
it
extremely
explore
the
potential
mechanisms
underlying
neurodegenerative
diseases.
Therefore,
alternative
of
human
or
animal
cells
have
been
developed
bridge
gap
allow
impact
new
therapeutic
strategies
be
anticipated
more
by
trying
mimic
neuronal
glial
cell
interactions
many
mechanisms.
In
tandem
with
emergence
human-induced
pluripotent
stem
which
were
first
generated
2007,
accessibility
(hiPSC)
derived
from
patients
can
differentiated
into
neurons,
providing
an
unrivaled
platform
Theranostics,
Journal Year:
2024,
Volume and Issue:
15(2), P. 682 - 706
Published: Dec. 2, 2024
Organoids,
self-organized
structures
derived
from
stem
cells
cultured
in
a
specific
three-dimensional
(3D)
vitro
microenvironment,
have
emerged
as
innovative
platforms
that
closely
mimic
vivo
cellular
behavior,
tissue
architecture,
and
organ
function.
Bone
organoids,
frontier
organoid
research,
can
replicate
the
complex
functional
characteristics
of
bone
tissue.
Recent
advancements
led
to
successful
development
including
models
callus,
woven
bone,
cartilage,
trabecular
marrow.
These
organoids
are
widely
utilized
establishing
bone-related
disease
models,
injury
repair,
drug
screening.
However,
significant
discrepancies
remain
between
current
human
skeletal
tissues
terms
morphology
functionality,
limiting
their
ability
accurately
model
physiology
pathology.
To
address
these
challenges
promote
standardization
construction,
evaluation,
application
we
convened
experts
research
teams
with
substantial
expertise
field.
By
integrating
existing
findings,
this
consortium
aims
establish
consensus
guide
future
organoids.
Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(1), P. 224 - 224
Published: Jan. 19, 2024
Biocompatibility
testing
of
materials
is
carried
out
in
2D
cell
cultures
or
animal
models
despite
serious
limitations.
3D
skin
equivalents
are
advanced
vitro
for
human
skin.
Silicone
has
been
shown
to
be
noncytotoxic
but
capable
eliciting
an
immune
response.
Our
aim
was
(1)
establish
a
equivalent
(2)
assess
the
proinflammatory
properties
silicone.
We
developed
coculture
keratinocytes
and
fibroblasts
resulting
with
implant
using
samples
from
breast
implant.
Samples
without
silicone
were
studied
histologically
immunohistochemically
comparison
native
samples.
Cytotoxicity
assessed
via
LDH-assay,
cytokine
response
ELISA.
Histologically,
our
had
four-layered
epidermal
dermal
component.
The
presence
tight
junctions
demonstrated
immunofluorescence.
only
difference
implants
thinning.
Implanting
did
not
cause
more
death,
however,
inflammatory
triggered.
able
organotypical
implant,
which
can
utilised
studies
on
biocompatibility
materials.
This
first
integration
into
confirmed
previous
findings
being
non-cell-toxic
exerting
effect.
Stem Cell Research & Therapy,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: June 21, 2024
Abstract
In
the
realm
of
studying
joint-related
diseases,
there
is
a
continuous
quest
for
more
accurate
and
representative
models.
Recently,
regenerative
medicine
tissue
engineering
have
seen
growing
interest
in
utilizing
organoids
as
powerful
tools
complex
biological
systems
vitro.
Organoids,
three-dimensional
structures
replicating
architecture
function
organs,
provide
unique
platform
investigating
disease
mechanisms,
drug
responses,
regeneration.
The
surge
organoid
research
fueled
by
need
physiologically
relevant
models
to
bridge
gap
between
traditional
cell
cultures
vivo
studies.
Osteochondral
emerged
promising
avenue
this
pursuit,
offering
better
mimic
intricate
interactions
within
bone
cartilage.
This
review
explores
significance
osteochondral
their
development
advancing
our
understanding
treatment
cartilage-related
diseases.
It
summarizes
organoids’
insights
progress,
focusing
on
composition,
materials,
sources,
cultivation
methods,
well
concept
chips
application
scenarios.
Additionally,
we
address
limitations
challenges
these
face,
emphasizing
necessity
further
overcome
obstacles
facilitate
orthopedic
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(2), P. 620 - 620
Published: Jan. 13, 2025
In
vitro
models
play
a
pivotal
role
in
advancing
our
understanding
of
neurodegenerative
diseases
(NDs)
such
as
Parkinson’s
and
Alzheimer’s
disease
(PD
AD).
Traditionally,
2D
cell
cultures
have
been
instrumental
elucidating
the
cellular
mechanisms
underlying
these
diseases.
Cultured
cells
derived
from
patients
or
animal
provide
valuable
insights
into
pathological
processes
at
level.
However,
they
often
lack
native
tissue
environment
complexity,
limiting
their
ability
to
fully
recapitulate
features.
contrast,
3D
offer
more
physiologically
relevant
platform
by
mimicking
brain
architecture.
These
can
incorporate
multiple
types,
including
neurons,
astrocytes,
microglia,
creating
microenvironment
that
closely
resembles
brain’s
complexity.
Bioengineering
approaches
allow
researchers
better
replicate
cell–cell
interactions,
neuronal
connectivity,
disease-related
phenotypes.
Both
advantages
limitations.
While
simplicity
scalability
for
high-throughput
screening
basic
processes,
enhanced
physiological
relevance
Integrating
findings
both
model
systems
NDs,
ultimately
aiding
development
novel
therapeutic
strategies.
Here,
we
review
existing
study
PD
AD.