Assembloid models of cell-cell interaction to study tissue and disease biology
Cell stem cell,
Journal Year:
2024,
Volume and Issue:
31(11), P. 1563 - 1573
Published: Oct. 24, 2024
Language: Английский
Anoikis in cell fate, physiopathology, and therapeutic interventions
Jie Mei,
No information about this author
Xue‐Yao Jiang,
No information about this author
Huixiang Tian
No information about this author
et al.
MedComm,
Journal Year:
2024,
Volume and Issue:
5(10)
Published: Sept. 15, 2024
The
extracellular
matrix
(ECM)
governs
a
wide
spectrum
of
cellular
fate
processes,
with
particular
emphasis
on
anoikis,
an
integrin-dependent
form
cell
death.
Currently,
anoikis
is
defined
as
intrinsic
apoptosis.
In
contrast
to
traditional
apoptosis
and
necroptosis,
integrin
correlates
ECM
signaling
intracellular
cascades,
describing
the
full
process
anoikis.
However,
frequently
overlooked
in
physiological
pathological
processes
well
vitro
research
models.
this
review,
we
summarized
role
spanning
embryonic
development,
organ
tissue
repair,
inflammatory
responses,
cardiovascular
diseases,
tumor
metastasis,
so
on.
Similarly,
realm
stem
focused
functional
evolution
cells,
offers
potential
solution
various
challenges,
including
culture
models,
therapy,
transplantation,
engineering
applications,
which
are
largely
based
regulation
by
More
importantly,
regulatory
mechanisms
molecular
will
provide
new
strategies
for
therapeutic
interventions
(drug
therapy
cell-based
therapy)
disease.
summary,
review
provides
systematic
elaboration
thus
shedding
light
its
future
research.
Language: Английский
Tumour organoids and assembloids: Patient‐derived cancer avatars for immunotherapy
Clinical and Translational Medicine,
Journal Year:
2024,
Volume and Issue:
14(4)
Published: April 1, 2024
Abstract
Background
Organoid
technology
is
an
emerging
and
rapidly
growing
field
that
shows
promise
in
studying
organ
development
screening
therapeutic
regimens.
Although
organoids
have
been
proposed
for
a
decade,
concerns
exist,
including
batch‐to‐batch
variations,
lack
of
the
native
microenvironment
clinical
applicability.
Main
body
The
concept
has
derived
patient‐derived
tumour
(PDTOs)
personalized
drug
new
discovery,
mitigating
risks
medication
misuse.
greater
similarity
between
PDTOs
primary
tumours,
more
influential
model
will
be.
Recently,
‘tumour
assembloids’
inspired
by
cell‐coculture
attracted
attention
to
complement
current
PDTO
technology.
High‐quality
must
reassemble
critical
components,
multiple
cell
types,
matrix,
paracrine
factors,
angiogenesis
microorganisms.
This
review
begins
with
brief
overview
history
PDTOs,
followed
approaches
generating
assembloids.
Personalized
practised;
however,
it
remains
unclear
whether
can
predict
immunotherapies,
immune
drugs
(e.g.
checkpoint
inhibitors)
cells
tumour‐infiltrating
lymphocyte,
T
receptor‐engineered
chimeric
antigen
receptor‐T
cell).
as
cancer
avatars
patients,
be
expanded
stored
form
biobank.
Conclusion
Fundamental
research
trials
are
ongoing,
intention
use
these
models
replace
animals.
Pre‐clinical
immunotherapy
using
beneficial
patients.
Key
Points
not
yet
constructed
key
cellular
non‐cellular
components.
should
expandable
editable.
promising
preclinical
unless
mature
established.
biobanks
consensual
standards
urgently
needed.
Language: Английский
Patient-Derived Organoid Models for NKT Cell-Based Cancer Immunotherapy
Pablo A. Palacios,
No information about this author
Iván Flores,
No information about this author
Lucas Cereceda
No information about this author
et al.
Cancers,
Journal Year:
2025,
Volume and Issue:
17(3), P. 406 - 406
Published: Jan. 26, 2025
Invariant
Natural
Killer
T
(iNKT)
cells
are
a
unique
subset
of
that
bridge
innate
and
adaptive
immunity,
displaying
potent
anti-tumor
properties
through
cytokine
secretion,
direct
cytotoxicity,
recruitment
immune
effector
such
as
CD8+
NK
cells.
Despite
their
therapeutic
potential,
the
immunosuppressive
tumor
microenvironment
(TME),
characterized
by
regulatory
cells,
myeloid-derived
suppressor
(MDSCs),
tumor-associated
macrophages
(TAMs),
limits
iNKT
cell
efficacy.
Patient-derived
organoid
(PDO)
platforms
provide
an
innovative
model
for
dissecting
these
complex
interactions
evaluating
strategies
to
reinvigorate
functionality
within
TME.
PDOs
closely
mimic
genetic,
phenotypic,
structural
characteristics
primary
tumors,
enabling
study
tumor–immune
dynamics.
Integrating
into
offers
robust
platform
investigating
CD1d-mediated
interactions,
Th1-biased
responses
driven
glycolipid
analogs
like
α-GalCer,
combination
therapies
checkpoint
inhibitors.
Additionally,
PDO
systems
can
assess
effects
metabolic
modulation,
including
reducing
lactic
acid
accumulation
or
targeting
glutamine
pathways,
on
enhancing
activity.
Emerging
innovations,
organoid-on-a-chip
systems,
CRISPR-Cas9
gene
editing,
multi-omics
approaches,
further
expand
potential
PDO–iNKT
personalized
immunotherapy
research.
Although
application
in
is
still
undeveloped,
hold
immense
promise
bridging
preclinical
studies
clinical
translation.
By
addressing
challenges
TME
optimizing
strategies,
offer
transformative
avenue
advancing
cancer
medicine.
Language: Английский
Bronchoalveolar lavage fluid (BALF): Clinical applications for present and future
The Innovation Medicine,
Journal Year:
2025,
Volume and Issue:
unknown, P. 100115 - 100115
Published: Jan. 1, 2025
<p>Lungs
are
exposed
to
a
wide
range
of
complex
internal
and
external
environmental
factors,
creating
pulmonary
microenvironment
that
remains
challenging
detect
interpret.
Bronchoalveolar
lavage
fluid
(BALF)
contains
an
abundance
cells,
microorganisms,
active
substances,
thus
is
considered
be
clinically
promising
body
detection
substance
representative
the
microenvironment.
The
combination
experimental
strategies
with
emerging
omics
technologies
has
advanced
identification
interpretation
microscopic
components
in
BALF,
underscoring
its
applications
clinical
detection.
In
summary,
this
review
provides
systematic
overview
development
understanding
discusses
possible
diagnosis,
prediction,
intervention,
highlights
role
deciphering
BALF.</p>
Language: Английский
Evolving from organoid to assembloid with enhanced cellular interactions
Cell organoid (Print),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 1, 2025
Language: Английский
TIL Therapy in Lung Cancer: Current Progress and Perspectives
Weilei Hu,
No information about this author
Y. Bian,
No information about this author
Hongbin Ji
No information about this author
et al.
Advanced Science,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Oct. 18, 2024
Lung
cancer
remains
the
most
prevalent
malignant
tumor
worldwide
and
is
leading
cause
of
cancer-related
mortality.
Although
immune
checkpoint
blockade
has
revolutionized
treatment
advanced
lung
cancer,
many
patients
still
do
not
respond
well,
often
due
to
lack
functional
T
cell
infiltration.
Adoptive
therapy
(ACT)
using
expanded
cells
emerged
as
an
important
therapeutic
modality.
Tumor-infiltrating
lymphocytes
(TIL)
one
form
ACT
involving
administration
activated
autologous
derived
from
surgically
resected
tissues
reinfusion
into
holds
great
potential
for
cancer.
In
this
review,
TIL
introduced
its
suitability
discussed.
Then
historical
clinical
developments
are
summarized,
methods
developed
up-to-date
identify
tumor-recognizing
TILs
optimize
composition.
Some
perspectives
toward
future
also
provided.
Language: Английский
Breaking the mold: 3D cell cultures reshaping the future of cancer research
Frontiers in Cell and Developmental Biology,
Journal Year:
2024,
Volume and Issue:
12
Published: Nov. 26, 2024
Despite
extensive
efforts
to
unravel
tumor
behavior
and
develop
anticancer
therapies,
most
treatments
fail
when
advanced
clinical
trials.
The
main
challenge
in
cancer
research
has
been
the
absence
of
predictive
models,
accurately
mimicking
tumoral
processes
response
treatments.
microenvironment
(TME)
shows
several
human-specific
physical
chemical
properties,
which
cannot
be
fully
recapitulated
by
conventional
2D
cell
cultures
or
Language: Английский