Colorectal
cancer
(CRC)
has
one
of
the
highest
rates
mortality
worldwide.
Despite
progress
in
improving
screening
rates,
approximately
35%
CRC
patients
are
diagnosed
with
stage
IV
(metastatic)
disease
which
poor
prognosis.
In
vitro
3D
models
have
been
developed
provide
useful
platforms
to
explore
biomolecular
processes
pre-clinical
studies
and
metastasis,
enabling
characterisation
mechanisms
can
then
be
applied
improvement
diagnosis,
prognosis
treatment.
Extracellular
vesicles
(EVs)
now
known
play
a
critical
role
progression.
Not
only
do
they
support
progression
towards
but
as
carriers
bioactive
cargo,
also
show
promise
potential
biomarkers.
this
study,
organotypic
mimicking
invasion
pre-metastatic
niche
(PMN)
lung
were
EVs
advanced
stages
evaluate
their
prognostic
markers.
After
validating
transwell
system
an
effective
model,
work
establishes
that
induce
cells
stage-dependent
manner,
metastatic
SW620
driving
more
aggressive
phenotype
than
SW480
EVs.
Proteomic
profiling
PMN
showed
differences
protein
content
upon
treatment
list
m/z
signals
able
distinguish
between
EV
was
obtained
by
multivariate
analysis.
induced
α-smooth
muscle
actin
(α-SMA)
expression
fibroblasts,
demonstrating
activation
fibroblasts
model.
Expression
activity
TG2,
multifunctional
enzyme
involved
progression,
increased
after
model
invasion.
This
led
exploration
cell-specific
TG2
cells/fibroblasts
co-culture,
EV-mediated
increase
on
surface
non-EV
mediated
decrease
fibroblast
surface.
further
explored
hepatic
stellate
cells,
crucial
cellular
components
liver
metastasis.
Finally,
pilot
biomarker
study
small
cohort
performed,
using
analysis
cell
responses
plasma-derived
separate
according
stage.
The
established
validated
provided
information
about
complex
milieu
factors
including
EVs,
thus
confirming
importance
culture
modelling
research.
Moreover,
demonstrate
key
roles
activities
could
translated
for
development
alternative
approaches
may
application
early
diagnosis
CRC.
Molecular Cancer,
Journal Year:
2023,
Volume and Issue:
22(1)
Published: Oct. 9, 2023
Abstract
The
use
of
nanotechnology
has
the
potential
to
revolutionize
detection
and
treatment
cancer.
Developments
in
protein
engineering
materials
science
have
led
emergence
new
nanoscale
targeting
techniques,
which
offer
renewed
hope
for
cancer
patients.
While
several
nanocarriers
medicinal
purposes
been
approved
human
trials,
only
a
few
authorized
clinical
cells.
In
this
review,
we
analyze
some
formulations
discuss
challenges
translating
findings
from
lab
clinic.
This
study
highlights
various
compounds
that
can
be
used
selective
tumor
inherent
difficulties
therapy.
Nanotechnology
provides
promising
platform
improving
future,
but
further
research
is
needed
overcome
current
limitations
translation.
Graphical
Journal of Translational Medicine,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: May 13, 2024
Abstract
Extracellular
vesicles
(EVs)
are
lipid
bilayer
structures
released
by
all
cells
and
widely
distributed
in
biological
fluids.
EVs
implicated
diverse
physiopathological
processes
orchestrating
cell–cell
communication.
Colorectal
cancer
(CRC)
is
one
of
the
most
common
cancers
worldwide,
with
metastasis
being
leading
cause
mortality
CRC
patients.
contribute
significantly
to
advancement
spread
transferring
their
cargo,
which
includes
lipids,
proteins,
RNAs,
DNAs,
neighboring
or
distant
cells.
Besides,
they
can
serve
as
non-invasive
diagnostic
prognostic
biomarkers
for
early
detection
be
harnessed
effective
carriers
delivering
therapeutic
agents.
Autophagy
an
essential
cellular
process
that
serves
remove
damaged
proteins
organelles
lysosomal
degradation
maintain
homeostasis.
EV
release
coordinately
activated
tumor
share
factors
regulatory
mechanisms.
Although
significance
autophagy
well
established,
exact
mechanism
interplay
development
obscure.
This
review
focuses
on
examining
specific
functions
various
aspects
CRC,
including
progression,
metastasis,
immune
regulation,
therapy
resistance.
Further,
we
overview
emerging
discoveries
relevant
crosstalk
CRC.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(17), P. 9463 - 9463
Published: Aug. 30, 2024
Colorectal
cancer
(CRC)
represents
a
significant
global
health
burden,
with
high
incidence
and
mortality
rates
worldwide.
Recent
progress
in
research
highlights
the
distinct
clinical
molecular
characteristics
of
colon
versus
rectal
cancers,
underscoring
tumor
location's
importance
treatment
approaches.
This
article
provides
comprehensive
review
our
current
understanding
CRC
epidemiology,
risk
factors,
pathogenesis,
management
strategies.
We
also
present
intricate
cellular
architecture
colonic
crypts
their
roles
intestinal
homeostasis.
carcinogenesis
multistep
processes
are
described,
covering
conventional
adenoma-carcinoma
sequence,
alternative
serrated
pathways,
influential
Vogelstein
model,
which
proposes
sequential
Journal of Experimental & Clinical Cancer Research,
Journal Year:
2025,
Volume and Issue:
44(1)
Published: Jan. 8, 2025
Abstract
Background
Circulating
tumour
cells
(CTCs)
and
tumour-derived
extracellular
vesicles
(tdEVs)
have
great
potential
for
monitoring
therapy
response
early
detection
of
relapse,
facilitating
personalized
adjuvant
therapeutic
strategies.
However,
their
low
abundance
in
peripheral
blood
limits
informative
value.
In
this
study,
we
explored
the
presence
CTCs
tdEVs
collected
intraoperatively
from
a
tumour-draining
vein
(DV)
via
central
venous
catheter
(CVC)
prior
to
resection.
Methods
CellSearch
analyses
395
samples
306
patients
with
gastrointestinal
tumours
93
healthy
donors
were
used
establish
validate
gates
automated
ACCEPT
software
R
scripts.
The
selected
gate
settings
applied
227
142
colorectal
cancer
(CRC)
two
independent
collectives.
Phenotypic
features
obtained
numeric
analysis
fluorescence
signals
(e.g.
size,
shape,
intensity)
calculating
diversity
using
Shannon
index
(SI)
clusters
generated
k-means
algorithm
after
Uniform
Manifold
Approximation
Projection
(UMAP)
pre-processing,
standard
deviation
(SD).
Results
more
abundant
DV
compared
CVC
(
p
<
0.05).
detected
higher
numbers
than
both
compartments.
Importantly,
CVCs
associated
tumor
spread,
whereas
DVs
linked
size.
compartments,
prognostic
value
overall
survival
(OS)
surpassed
that
CTCs,
as
demonstrated
by
univariate,
multivariate,
Kaplan-Meier
analyses.
phenotypically
distinct,
being
larger,
eccentric,
displaying
stronger
cytokeratin
intensities
0.05)
those
samples.
Furthermore,
increased
CTC
tdEV
phenotypes
was
significantly
shorter
survival,
validating
relevance
SD-diversity
metric.
Conclusion
Our
study
demonstrates
sampling
enhances
prognostically
relevant
CRC
patients,
underscoring
superior
significance
CTCs.
combined
phenotypic
markers
emerges
powerful
biomarker
enumeration
alone.
These
findings
suggest
comprehensive,
may
open
new
avenues
tailoring
individualized
therapies
patients.
Journal of Biochemical and Molecular Toxicology,
Journal Year:
2025,
Volume and Issue:
39(4)
Published: March 31, 2025
ABSTRACT
Colorectal
cancer
(CRC)
is
a
prevalent
malignancy
of
the
digestive
system.
Here,
we
explored
role
M2
macrophage‐derived
extracellular
vesicles
(EVs)
carrying
long
non‐coding
RNA‐nuclear
paraspeckle
assembly
transcript
1
(lncRNA‐NEAT1)
in
promoting
CRC
progression
via
regulation
miR‐204‐5p/regulator
ribosome
synthesis
(RRS1)
axis
and
cell
cycle
dynamics.
Firstly,
differentiated
WTHP‐1
cells
into
M0
macrophages
transfected
with
sh‐NEAT1
lentivirus
plasmids.
EVs
were
isolated
from
administered
to
SW480
along
miR‐204‐5p
inhibitors
or
si‐RRS1
for
24
h.
M2‐EVs‐derived
lncRNA‐NEAT1
enhanced
proliferation,
migration,
invasion,
viability
while
reducing
apoptosis.
This
was
accompanied
by
increased
expression
RRS1,
WEE1
G2
checkpoint
kinase
(WEE1),
cyclin‐dependent
(CDK1),
CyclinB1,
reduced
levels,
lower
proportion
G2/M
phase.
Knockdown
reversed
these
effects.
Mechanistically,
functioned
as
competing
endogenous
RNA
(ceRNA),
sponging
upregulate
RRS1
expression.
In
summary,
promote
development
modulating
miR‐204‐5p/RRS1
axis,
influencing
These
findings
provide
insights
tumor‐promoting
mechanisms
CRC.
Environmental Toxicology,
Journal Year:
2024,
Volume and Issue:
39(7), P. 3790 - 3798
Published: March 18, 2024
Abstract
Chondrosarcoma
is
a
malignant
bone
tumor
that
arises
from
abnormalities
in
cartilaginous
tissue
and
associated
with
lung
metastases.
Extracellular
vesicles
called
exosomes
are
primarily
used
as
mediators
of
intercellular
signal
transmission
to
control
metastasis.
Visfatin
an
adipokine
reported
enhance
metastasis,
but
its
relationship
exosome
generation
chondrosarcoma
motility
remains
undetermined.
Our
results
found
overexpressing
visfatin
augments
the
production
cells.
Visfatin‐treated
educate
macrophage
polarization
towards
M2
not
M1
phenotype.
Interestingly,
macrophages
polarized
by
return
cells
facilitate
cell
motility.
According
these
findings,
emit
more
when
treated
visfatin.
The
stimulation
polarizes
enhances
chondrosarcoma.
Technology in Cancer Research & Treatment,
Journal Year:
2023,
Volume and Issue:
22
Published: Jan. 1, 2023
Extracellular
vesicles
(EVs)
are
a
class
of
spherical
that
produced
by
active
secretion
cells
and
encapsulated
phospholipid
bilayers.
In
recent
years,
numerous
studies
have
shown
EVs
play
pivotal
roles
in
the
regulation
intercellular
communication
between
colorectal
cancer
(CRC)
target
cells,
can
regulate
proliferation,
metastasis,
infiltration
tumor
regulating
microenvironment
cells.
carry
specific
molecular
substances
source
CRC
expected
to
serve
as
new
markers
for
detection
cancers.
This
review
highlights
current
state
research
progress
potentially
incorporating
diagnosis
treatment
CRC.
Aging,
Journal Year:
2023,
Volume and Issue:
15(22), P. 13163 - 13175
Published: Nov. 21, 2023
Chondrosarcoma
is
a
primary
malignant
bone
tumor.
Traditional
therapy
not
very
effective,
and
it
prone
to
metastasis
in
the
late
stage.
The
tumor
microenvironment
(TME)
plays
key
role
progression
of
chondrosarcoma,
hypoxia
one
factors
formation
TME.
However,
detailed
mechanism
how
affects
chondrosarcoma
still
fully
understood.
In
this
study,
we
focused
on
interaction
between
hypoxic
cells
(SW1353)
macrophages.
Our
results
suggest
that
enhances
release
exosomes
from
cells.
These
hypoxia-induced
promoted
macrophage
polarization
towards
M2
phenotype,
characterized
by
expression
CD163
CD206,
but
M1
CD86
expression.
Further
analysis
revealed
macrophages
polarized
expressed
arginase-1
feedback
promote
migration.
secrete
more
microenvironment,
these
hypoxia-derived
induce
into
an
ultimately
promoting
metastatic
behavior