SLAS TECHNOLOGY,
Journal Year:
2023,
Volume and Issue:
28(3), P. 152 - 164
Published: April 3, 2023
Cancer
treatment
development
is
a
complex
process,
with
tumor
heterogeneity
and
inter-patient
variations
limiting
the
success
of
therapeutic
intervention.
Traditional
two-dimensional
cell
culture
has
been
used
to
study
cancer
metabolism,
but
it
fails
capture
physiologically
relevant
cell-cell
cell-environment
interactions
required
mimic
tumor-specific
architecture.
Over
past
three
decades,
research
efforts
in
field
3D
model
fabrication
using
tissue
engineering
have
addressed
this
unmet
need.
The
self-organized
scaffold-based
shown
potential
microenvironment
eventually
bridge
gap
between
2D
animal
models.
Recently,
three-dimensional
(3D)
bioprinting
emerged
as
an
exciting
novel
biofabrication
strategy
aimed
at
developing
compartmentalized
hierarchical
organization
precise
positioning
biomolecules,
including
living
cells.
In
review,
we
discuss
advancements
techniques
for
models,
well
their
benefits
limitations.
We
also
highlight
future
directions
associated
technological
advances,
detailed
applicative
research,
patient
compliance,
regulatory
challenges
achieve
successful
bed-to-bench
transition.
Cell,
Journal Year:
2024,
Volume and Issue:
187(13), P. 3165 - 3186
Published: June 1, 2024
Patterned
morphologies,
such
as
segments,
spirals,
stripes,
and
spots,
frequently
emerge
during
embryogenesis
through
self-organized
coordination
between
cells.
Yet,
complex
patterns
also
in
adults,
suggesting
that
the
capacity
for
spontaneous
self-organization
is
a
ubiquitous
property
of
biological
tissues.
We
review
current
knowledge
on
principles
mechanisms
patterning
embryonic
tissues
explore
how
these
apply
to
adult
exhibit
features
patterning.
discuss
why
pattern
generation
integral
homeostasis
healing
tissues,
illustrating
it
with
examples
from
regenerative
biology.
examine
aberrant
underlies
diverse
pathological
states,
including
inflammatory
skin
disorders
tumors.
Lastly,
we
posit
based
blueprints,
targeted
engineering
pattern-driving
molecular
circuits
can
be
leveraged
synthetic
biology
organoids
intricate
patterns.
Journal of Translational Medicine,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: Nov. 8, 2024
The
complexity
of
tumors
and
the
challenges
associated
with
treatment
often
stem
from
limitations
existing
models
in
accurately
replicating
authentic
tumors.
Recently,
organoid
technology
has
emerged
as
an
innovative
platform
for
tumor
research.
This
bioengineering
approach
enables
researchers
to
simulate,
vitro,
interactions
between
their
microenvironment,
thereby
enhancing
intricate
interplay
cells
surroundings.
Organoids
also
integrate
multidimensional
data,
providing
a
novel
paradigm
understanding
development
progression
while
facilitating
precision
therapy.
Furthermore,
advancements
imaging
genetic
editing
techniques
have
significantly
augmented
potential
organoids
review
explores
application
more
precise
simulations
its
specific
contributions
cancer
research
advancements.
Additionally,
we
discuss
evolving
trends
developing
comprehensive
utilizing
technology.
Cancers,
Journal Year:
2022,
Volume and Issue:
14(15), P. 3703 - 3703
Published: July 29, 2022
Lung
cancer
is
the
leading
cause
of
death
worldwide.
Despite
significant
advances
in
research
and
therapy,
a
dismal
5-year
survival
rate
only
10–20%
urges
development
reliable
preclinical
models
effective
therapeutic
tools.
characterized
by
high
degree
heterogeneity
its
histology,
genomic
landscape,
response
to
therapies
that
has
been
traditionally
difficult
reproduce
models.
However,
advent
three-dimensional
culture
technologies
opened
new
perspectives
recapitulate
vitro
individualized
tumor
features
anticipate
treatment
efficacy.
The
generation
lung
organoids
(LCOs)
encountered
greater
challenges
as
compared
derived
from
other
tumors.
In
last
two
years,
many
efforts
have
dedicated
optimizing
LCO-based
platforms,
resulting
improved
rates
LCO
production,
purity,
timing,
long-term
expansion.
due
complexity
cancer,
further
are
required
order
meet
clinical
needs.
Here,
we
discuss
evolution
technology
use
LCOs
basic
translational
research.
Although
field
still
infancy,
prospective
will
likely
lead
strategies
for
drug
testing
biomarker
identification,
thus
allowing
more
personalized
approach
patients.
Molecular Cancer,
Journal Year:
2025,
Volume and Issue:
24(1)
Published: March 21, 2025
Tumor
drug
resistance
presents
a
growing
challenge
in
medical
practice,
particularly
during
anti-cancer
therapies,
where
the
emergence
of
drug-resistant
cancer
cells
significantly
complicates
clinical
treatment.
In
recent
years,
three-dimensional
(3D)
tumor
culture
technology,
which
more
effectively
simulates
vivo
physiological
environment,
has
gained
increasing
attention
research
and
applications.
By
mimicking
cellular
microenvironment,
3D
technology
not
only
recapitulates
cell-cell
interactions
but
also
faithfully
reproduces
biological
effects
therapeutic
agents.
Consequently,
is
emerging
as
crucial
tool
biomedical
research.
We
summarize
benefits
models
organoid
explore
their
application
realm
resistance,
screening,
personalized
therapy,
discuss
potential
prospects
challenges
transformation,
with
aim
providing
insights
for
optimizing
treatment
strategies
advancing
precision
therapy.
Advanced Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 28, 2025
Abstract
Heterogeneity
and
the
absence
of
a
tumor
microenvironment
(TME)
in
traditional
patient‐derived
organoid
(PDO)
cultures
limit
their
effectiveness
for
clinical
use.
Here,
Embedded
Bioprinting‐enabled
Arrayed
PDOs
(Eba‐PDOs)
featuring
uniformly
arrayed
colorectal
cancer
(CRC)
within
recreated
TME
is
presented.
This
model
faithfully
reproduces
critical
attributes,
including
elevated
matrix
stiffness
(≈7.5
kPa)
hypoxic
conditions
found
CRC.
Transcriptomic
immunofluorescence
microscopy
analysis
reveal
that
Eba‐PDOs
more
accurately
represent
actual
tissues
compared
to
PDOs.
Furthermore,
Eba‐PDO
effectively
capture
variability
CEACAM5
expression—a
CRC
marker—across
different
patients,
correlating
with
patient
classification
differential
responses
5‐fluorouracil
treatment.
method
achieves
an
uniform
size
shape
from
same
while
preserving
distinct
morphological
features
among
those
individuals.
These
enable
efficient
development
label‐free,
morphology‐based
predictive
using
supervised
learning,
enhancing
its
suitability
applications.
Thus,
this
approach
PDO
bioprinting
promising
tool
generating
personalized
models
advancing
precision
medicine.
BMC Research Notes,
Journal Year:
2025,
Volume and Issue:
18(1)
Published: March 31, 2025
One
of
the
most
important
and
devastating
side
effects
breast
cancer
is
brain
metastasis.
Our
understanding
heterogeneity
revolutionized
by
tumoral
organoids
seems
promising
for
personalized
medicine.
This
study
aimed
to
generate
a
hydrogel-based
metastasis
organoid.
Mouse
metastatic
tumor
cells
(4T1B)
were
isolated
cultured
from
lesions
mice
with
cancer.
Different
hydrogels,
including
alginate,
carboxymethylcellulose,
gelatin,
collagen,
matrigel,
prepared.
Pre-coated
hydrogels
in
96-well
plates
treated
4T1B
cells.
The
morphology
viability
analyzed
after
7
days.
According
our
results,
formed
semi-regular
cluster
structures
alginate
hydrogel.
In
this
group,
cell
survival
rate
formation
three-dimensional
significantly
higher
than
other
groups.
For
organoid
cultures,
there's
lot
research
on
natural
synthetic
scaffolds
that
are
chemically
or
mechanically
well-designed.
present
study,
we
used
highly
detected
hydrogel
best
choice
modeling.
Annual Review of Biomedical Engineering,
Journal Year:
2025,
Volume and Issue:
27(1), P. 307 - 333
Published: May 1, 2025
Despite
the
advances
in
detection,
diagnosis,
and
treatments,
cancer
remains
a
lethal
disease,
claiming
lives
of
more
than
600,000
people
United
States
alone
2024.
To
accelerate
development
new
therapeutic
strategies
with
improved
responses,
significant
efforts
have
been
made
to
develop
microfabricated
vitro
models
tumor
microenvironments
(TMEs)
that
address
limitations
animal-based
models.
These
incorporate
several
advanced
tissue
engineering
techniques
better
reflect
organ-
patient-specific
TMEs.
Additionally,
integrated
next-generation
single-cell
omics
technologies
provide
unprecedented
insights
into
patient's
cellular
molecular
heterogeneity
complexity.
This
review
provides
an
overview
recent
understanding
outlines
key
TME
elements
can
be
captured
enhance
their
physiological
relevance.
We
highlight
unique
characteristics
organs
origin
or
sites
dissemination.
Cancers,
Journal Year:
2022,
Volume and Issue:
14(9), P. 2144 - 2144
Published: April 25, 2022
The
cancer
burden
is
rapidly
increasing
in
most
countries,
and
thus,
new
anticancer
drugs
for
effective
therapy
must
be
developed.
Cancer
model
systems
that
recapitulate
the
biological
processes
of
human
cancers
are
one
cores
drug
development
process.
PDCO
has
emerged
as
a
unique
preserves
genetic,
physiological,
histologic
characteristics
original
cancer,
including
inter-
intratumoral
heterogeneities.
Due
to
these
advantages,
PCDO
increasingly
investigated
screening
efficacy
testing,
preclinical
patient
stratification,
precision
medicine
selecting
patients.
Here,
we
review
prospects
limitations
compared
conventional
models.
With
advances
culture
success
rates,
co-culture
with
tumor
microenvironment,
organoid-on-a-chip
technology,
automation
will
become
promising
develop
medicine.