Research Square (Research Square),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Dec. 12, 2023
Abstract
Traditional
two-dimensional
(2D)
cell
culture
methodologies
exhibit
significant
limitations,
notably
their
failure
to
replicate
the
intricate
three-dimensional
(3D)
milieu
of
human
tissue
architecture.
This
discrepancy
has
catalyzed
exploration
advanced
drug
screening
platforms
that
more
faithfully
mimic
complex
3D
biological
environment.
To
this
end,
precision
medicine
research
increasingly
used
in
vitro
models
emulate
microenvironment
body.
In
study,
breast
cancer
lines
(MDA-MB-231
and
SK-BR-3)
were
co-cultured
with
adipose-derived
stem
cells
(ADSCs),
mimicking
tumor
multicellular
heterogeneous
nature
solid
tumors
compared
a
2D
only
system.
Additionally,
collagen
type
I
was
within
spheroid
platform,
enhancing
accuracy
platform
characteristics.
Significantly,
interactions
between
ADSCs
two
markedly
influenced
factors
such
as
elongation,
molecular
expression,
migration
patterns,
sensitivity.
The
integration
pivotal
simulating
microenvironment,
highlighting
even
same
line,
varying
microenvironmental
contexts
can
lead
vastly
different
experimental
results.
Thus,
study
provides
insights
into
role
cellular
substrates
akin
body
when
constructing
system
based
on
cells.
Military Medical Research,
Journal Year:
2025,
Volume and Issue:
12(1)
Published: Feb. 11, 2025
Abstract
Cancer
recurrence,
driven
by
the
phenomenon
of
tumor
dormancy,
presents
a
formidable
challenge
in
oncology.
Dormant
cancer
cells
have
ability
to
evade
detection
and
treatment,
leading
relapse.
This
review
emphasizes
urgent
need
comprehend
dormancy
its
implications
for
recurrence.
Despite
notable
advancements,
significant
gaps
remain
our
understanding
mechanisms
underlying
lack
reliable
biomarkers
predicting
provides
comprehensive
analysis
cellular,
angiogenic,
immunological
aspects
dormancy.
It
highlights
current
therapeutic
strategies
targeting
dormant
cells,
particularly
combination
therapies
immunotherapies,
which
hold
promise
preventing
By
elucidating
these
proposing
innovative
research
methodologies,
this
aims
deepen
ultimately
facilitating
development
more
effective
recurrence
improving
patient
outcomes.
Frontiers in Oncology,
Journal Year:
2024,
Volume and Issue:
14
Published: July 2, 2024
The
biophysical
and
biomechanical
properties
of
the
extracellular
matrix
(ECM)
are
crucial
in
processes
cell
differentiation
proliferation.
However,
it
is
unclear
to
what
extent
tumor
cells
influenced
by
changes
surrounding
microenvironment
how
this
response
varies
between
different
forms,
over
course
progression.
entire
ensemble
genes
encoding
ECM
associated
proteins
called
matrisome.
In
cancer,
evolves
become
highly
dysregulated,
rigid,
fibrotic,
serving
both
pro-tumorigenic
anti-tumorigenic
roles.
Tumor
desmoplasia
characterized
a
dramatic
increase
α-smooth
muscle
actin
expressing
fibroblast
deposition
hard
containing
collagen,
fibronectin,
proteoglycans,
hyaluronic
acid
common
many
solid
tumors.
review,
we
described
role
inflammation
inflammatory
cytokines,
desmoplastic
remodeling,
state
transition
driven
forces
signaling
pathways
mechanotransduction
as
potential
targeted
therapies,
focusing
on
impact
qualitative
quantitative
variations
regulation
development,
hypothesizing
presence
matrisome
drivers,
acting
alongside
cell-intrinsic
oncogenic
some
stages
neoplastic
progression
contexts,
such
pancreatic
carcinoma,
breast
lung
cancer
mesothelioma.
Clinical and Translational Medicine,
Journal Year:
2024,
Volume and Issue:
14(2)
Published: Feb. 1, 2024
Abstract
Tumour
cell
dormancy
is
critical
for
metastasis
and
resistance
to
chemoradiotherapy.
Polyploid
giant
cancer
cells
(PGCCs)
with
or
multiple
nuclei
high
DNA
content
have
the
properties
of
stem
single
PGCCs
can
individually
generate
tumours
in
immunodeficient
mice.
represent
a
dormant
form
that
survive
harsh
tumour
conditions
contribute
recurrence.
Hypoxic
mimics,
chemotherapeutics,
radiation
cytotoxic
traditional
Chinese
medicines
induce
formation
through
endoreduplication
and/or
fusion.
After
incubation,
recover
from
treatment
produce
daughter
strong
proliferative,
migratory
invasive
abilities
via
asymmetric
division.
Additionally,
resist
hypoxia
chemical
stress
distinct
protein
signature
involves
chromatin
remodelling
cycle
regulation.
Dormant
cellular
basis
therapeutic
resistance,
metastatic
cascade
disease
This
review
summarises
regulatory
mechanisms
governing
entry
exit
dormancy,
which
may
be
used
by
PGCCs,
potential
strategies
targeting
PGCCs.
Molecular Medicine,
Journal Year:
2025,
Volume and Issue:
31(1)
Published: March 3, 2025
Abstract
As
an
emerging
technology,
organoids
are
promising
new
tools
for
basic
and
translational
research
in
disease.
Currently,
the
culture
of
relies
mainly
on
a
type
unknown
composition
scaffold,
namely
Matrigel,
which
may
pose
problems
studying
effect
mechanical
properties
organoids.
Hydrogels,
material
with
adjustable
properties,
can
adapt
to
current
studies.
In
this
review,
we
summarized
synthesis
recent
advance
developing
definite
hydrogel
scaffolds
organoid
identified
critical
parameters
regulating
properties.
addition,
classified
by
different
like
stiffness
viscoelasticity,
concluded
development
tumor
We
hope
review
enhances
understanding
hydrogels
provides
more
practical
approaches
investigating
them.
Cancers,
Journal Year:
2023,
Volume and Issue:
15(23), P. 5497 - 5497
Published: Nov. 21, 2023
The
Hippo
pathway
is
conserved
across
species.
Key
mammalian
kinases,
including
MST1/2
and
LATS1/2,
inhibit
cellular
growth
by
inactivating
the
TEAD
coactivators,
YAP,
TAZ.
Extensive
research
has
illuminated
roles
of
signaling
in
cancer,
development,
regeneration.
Notably,
dysregulation
components
not
only
contributes
to
tumor
metastasis,
but
also
renders
tumors
resistant
therapies.
This
review
delves
into
recent
on
YAP/TAZ-TEAD-mediated
gene
regulation
biological
processes
cancer.
We
focus
several
key
areas:
newly
identified
molecular
patterns
YAP/TAZ
activation,
emerging
mechanisms
that
contribute
metastasis
cancer
therapy
resistance,
unexpected
suppression,
advances
therapeutic
strategies
targeting
this
pathway.
Moreover,
we
provide
an
updated
view
YAP/TAZ's
functions,
discuss
ongoing
controversies,
offer
perspectives
specific
debated
topics
rapidly
evolving
field.
Cancer Letters,
Journal Year:
2024,
Volume and Issue:
591, P. 216899 - 216899
Published: April 21, 2024
Tumor
cells
disseminate
in
various
distant
organs
at
early
stages
of
cancer
progression.
These
disseminated
tumor
(DTCs)
can
stay
dormant/quiescent
without
causing
patient
symptoms
for
years
or
decades.
dormant
survive
despite
curative
treatments
by
entering
growth
arrest,
escaping
immune
surveillance,
and/or
developing
drug
resistance.
However,
these
reactivate
to
proliferate,
metastatic
progression
relapse,
posing
a
threat
patients'
survival.
It's
unclear
how
maintain
dormancy
and
what
triggers
their
reactivation.
What
are
better
approaches
prevent
relapse
through
harnessing
dormancy?
To
answer
remaining
questions,
we
reviewed
the
studies
reactivation
types
using
different
model
systems,
including
brief
history
studies,
intrinsic
characteristics
cells,
external
cues
cellular
molecular
levels.
Furthermore,
discussed
future
directions
field
strategies
manipulating
recurrence.
Current Opinion in Cell Biology,
Journal Year:
2023,
Volume and Issue:
86, P. 102288 - 102288
Published: Dec. 5, 2023
Cell
adhesion
to
the
extracellular
matrix
(ECM)
is
required
for
normal
cell
cycle
progression
and
accurate
division.
However,
how
wide
range
of
ECM
proteins
found
in
human
tissues
influences
not
fully
understood.
The
composition
physical
properties
can
have
profound
effects
on
proliferation
but
also
promote
exit
quiescence.
Furthermore,
during
tumor
development
progression,
changes
drive
both
cancer
dormancy.
Cell-matrix
primarily
sensed
via
integrin-associated
complexes,
which
turn
are
regulated
by
machinery.
In
particular,
cyclin-dependent
kinase
1
(CDK1)
has
been
shown
play
a
crucial
role
regulating
complexes
interphase
entry
into
mitosis.
These
reciprocal
links
between
cell-matrix
interactions
now
being
identified.
Cells,
Journal Year:
2024,
Volume and Issue:
13(13), P. 1087 - 1087
Published: June 23, 2024
Tumors
are
a
heterogeneous
group
of
cell
masses
originating
in
various
organs
or
tissues.
The
cellular
composition
the
tumor
mass
interacts
an
intricate
manner,
influenced
by
humoral,
genetic,
molecular,
and
microenvironment
cues
that
dictate
growth
suppression.
As
result,
tumors
undergo
period
dormant
state
before
their
clinically
discernible
stage,
which
surpasses
clinical
dormancy
threshold.
Moreover,
as
genetically
imprinted
strategy,
early-seeder
cells,
distinct
population
break
off
to
dock
nearby
extravasate
into
blood
vessels
secondary
tissues,
where
they
form
disseminated
solitary
cells
with
reversible
capacity.
Among
mechanisms
underlying
formation,
heat
shock
proteins
(HSPs)
might
play
one
most
important
roles
how
program
plays
out.
It
is
known
numerous
aberrant
processes,
such
malignant
transformation,
cancer
stemness,
invasion,
metastasis,
angiogenesis,
signaling
pathway
maintenance,
HSPs.
An
accumulating
body
knowledge
suggests
HSPs
may
be
involved
angiogenic
switch,
immune
editing,
extracellular
matrix
(ECM)
remodeling
cascades,
crucial
strategies
initiation
maintenance
program.
In
this
review,
we
highlight
biological
events
orchestrate
work
has
been
conducted
on
dynamics
mass,
well
reactivation.
Additionally,
propose
conceptual
framework
could
possibly
underlie
reactivation
metastatic
relapse.
ACS Applied Bio Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 13, 2025
Among
the
secondary
target
organs
for
metastatic
breast
cancer,
brain
metastasis
is
extremely
aggressive
in
nature,
resulting
lower
survival
rates.
These
cancer
cells
have
potential
to
enter
a
dormant
state
brain,
allowing
them
survive
extended
time
periods.
The
microenvironment
plays
key
role
controlling
phenotype,
yet
how
various
components
of
this
influence
dormancy
not
well
understood.
In
work,
we
employed
hyaluronic
acid
(HA)-based
hydrogels
as
mimetic
tissue
environment
study
biochemical
cues,
specifically,
impact
laminin
and
laminin-derived
peptides
IKVAV
YIGSR
on
regulation
cell
versus
proliferation.
We
applied
varying
protein/peptide
concentrations
confirmed
functionalization
HA
hydrogel
surfaces.
then
seeded
10,000
surface
cultured
5
days.
found
that
presence
or
IKVAV,
MDA-MB-231Br
transitioned
from
rounded
spread
morphology
exhibited
enhanced
proliferation
laminin/IKVAV
concentration
increased.
contrast,
functionalized
with
YIGSR,
these
maintained
morphology,
no
concentrations.
involvement
αVβ3
integrin
mediating
tumor
phenotype
laminin.
By
evaluating
known
markers
proliferation,
direct
correlation
between
increased
phosphorylated
extracellular
signal-regulated
kinase
1/2
(p-ERK)
positivity,
along
decreased
p38
(p-p38)
while
levels
both
p-ERK
p-p38
remained
unaltered.
Finally,
demonstrated
when
were
transferred
IKVAV-deficient
IKVAV-rich
hydrogels,
induced
cellular
was
reversible.
Collectively,
our
findings
provide
insights
into
cues
regulate