Cancers,
Journal Year:
2021,
Volume and Issue:
13(11), P. 2668 - 2668
Published: May 28, 2021
Background:
Circulating
tumor
cells
(CTC)
have
relevance
as
prognostic
markers
in
breast
cancer.
However,
the
functional
properties
of
CTCs
or
their
molecular
characterization
not
been
well-studied.
Experimental
models
indicate
that
only
a
few
can
survive
circulation
and
eventually
metastasize.
Thus,
it
is
essential
to
identify
these
surviving
capable
forming
such
metastases.
Methods:
We
isolated
viable
from
50
peripheral
blood
samples
obtained
35
patients
with
advanced
metastatic
cancer
using
RosetteSepTM
for
ex
vivo
culture.
The
were
seeded
monitored
on
plates
under
low
adherence
conditions
media
supplemented
growth
factors
Nanoemulsions.
Phenotypic
analysis
was
performed
by
immunofluorescence
gene
expression
RT-PCR
counting
Cellsearch®
system.
Results:
found
75%
CTC
cultures
lasted
more
than
23
days,
predicting
shorter
Progression-Free
Survival
patients,
independently
having
≥5
Cellsearch®.
also
observed
before
after
culture
showed
different
profile.
Conclusions:
cultivability
predictive
factor.
Furthermore,
subset
growing
show
stem
mesenchymal
features
may
represent
population
potential
vivo.
Frontiers in Cell and Developmental Biology,
Journal Year:
2023,
Volume and Issue:
11
Published: May 5, 2023
Metastatic
progression
is
the
deadliest
feature
of
cancer.
Cancer
cell
growth,
invasion,
intravasation,
circulation,
arrest/adhesion
and
extravasation
require
specific
mechanical
properties
to
allow
survival
completion
metastatic
cascade.
Circulating
tumor
cells
(CTCs)
come
into
contact
with
capillary
bed
during
extravasation/intravasation
at
beginning
However,
CTC
mechanobiology
strategies
in
bloodstream,
specifically
microcirculation,
are
not
well
known.
A
fraction
CTCs
can
extravasate
colonize
distant
areas
despite
biomechanical
constriction
forces
that
exerted
by
microcirculation
strongly
decrease
survival.
Furthermore,
accumulating
evidence
shows
several
adaptations,
via
molecular
factors
interactions
blood
components
(e.g.,
immune
platelets
inside
capillaries),
may
promote
metastasis
formation.
To
better
understand
journey
as
part
cascade,
we
reviewed
how
interaction
other
types
bloodstream
help
them
survive
harsh
conditions
circulatory
system
metastasize
organs.
Clinical Chemistry,
Journal Year:
2024,
Volume and Issue:
70(1), P. 81 - 89
Published: Jan. 1, 2024
Abstract
Background
Metastasis
is
the
leading
cause
of
cancer-related
deaths.
Most
studies
have
focused
on
primary
tumor
or
overt
metastatic
lesions,
leaving
a
significant
knowledge
gap
concerning
blood-borne
cancer
cell
dissemination,
major
step
in
cascade.
Circulating
cells
(CTCs)
blood
patients
with
solid
can
now
be
enumerated
and
investigated
at
molecular
level,
giving
unexpected
information
biology
Content
Here,
we
reviewed
recent
advances
basic
translational/clinical
research
CTCs
as
key
elements
Summary
Findings
from
translational
elucidated
complexity
process.
Fully
understanding
this
process
will
open
new
potential
avenues
for
therapeutic
diagnostic
strategies
to
propose
precision
medicine
all
patients.
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: Jan. 31, 2025
Abstract
Cell
lines
derived
from
circulating
tumor
cells
(CTCs)
in
the
blood
provide
important
biological
information
on
cancer
metastasis.
CTC-ITB-01
is
a
CTC
cell
line
patient
with
metastatic
estrogen
receptor-alpha
(ER-alpha)
positive
breast
two
months
before
death
of
patient.
After
LC-MC/MS
based
proteomics
analysis
CTC-ITB-01,
we
found
extraordinary
high
levels
poorly
characterized
protein
SUSD2
(sushi
domain-containing
2)
CTC-ITB-01.
Expression
subsets
CTCs
was
validated
clinical
samples
patients
cancer.
SUSD2-positive
could
be
captured
specifically
by
MACS-based
approach.
We
overexpressed
poorly-metastatic
MCF-7.
This
resulted
upregulation
ER-alpha,
progression
GRP78
(78-kDa
glucose-regulated
protein)
and
downregulation
suppressor
PDCD4
(programmed
4).
observed
after
hypoxia
simulation
re-oxygenation
MCF-7
MDA-MB-468,
while
remained
unchanged,
only
downregulated
under
hypoxia.
In
conclusion,
show,
for
first
time,
that
expressed
appears
to
affect
key
proteins
survival.
Molecular Cancer,
Journal Year:
2021,
Volume and Issue:
20(1)
Published: Feb. 8, 2021
Abstract
The
characterization
of
circulating
tumor
cells
(CTCs)
holds
promises
for
precision
medicine
because
these
are
an
important
clinical
indicator
treatment
efficacy.
We
established
the
first
and
still
only
nine
permanent
colon
CTC
lines
from
peripheral
blood
samples
a
patient
with
metastatic
cancer
collected
at
different
time
points
during
progression.
study
objectives
were
(
i
)
to
compare
gene
expression
profiles
lines,
ii
determine
main
features
acquired
treatment.
number
upregulated
genes
was
higher
in
obtained
after
treatment,
indicating
that
they
properties
escape
pressure.
Among
genes,
some
involved
mTOR
PI3K/AKT
signaling
pathways.
Moreover,
cytidine
deaminase
significantly
increased
failure
first-
second-line
5-fluorouracile-based
treatments,
suggesting
CTCs
can
eliminate
this
specific
drug
resist
therapy.
Several
enzymes
xenobiotic
metabolism
also
activation
detoxification
mechanisms
response
chemotherapy.
Finally,
significant
aldolase
B
four
six
withdrawal
progression
indicated
clones
originated
liver
metastases.
In
conclusion,
generated
single
characterized
by
deregulation
promote
resistance,
energy
metabolism,
iii
stem
cell
plasticity.
Cancers,
Journal Year:
2021,
Volume and Issue:
13(11), P. 2668 - 2668
Published: May 28, 2021
Background:
Circulating
tumor
cells
(CTC)
have
relevance
as
prognostic
markers
in
breast
cancer.
However,
the
functional
properties
of
CTCs
or
their
molecular
characterization
not
been
well-studied.
Experimental
models
indicate
that
only
a
few
can
survive
circulation
and
eventually
metastasize.
Thus,
it
is
essential
to
identify
these
surviving
capable
forming
such
metastases.
Methods:
We
isolated
viable
from
50
peripheral
blood
samples
obtained
35
patients
with
advanced
metastatic
cancer
using
RosetteSepTM
for
ex
vivo
culture.
The
were
seeded
monitored
on
plates
under
low
adherence
conditions
media
supplemented
growth
factors
Nanoemulsions.
Phenotypic
analysis
was
performed
by
immunofluorescence
gene
expression
RT-PCR
counting
Cellsearch®
system.
Results:
found
75%
CTC
cultures
lasted
more
than
23
days,
predicting
shorter
Progression-Free
Survival
patients,
independently
having
≥5
Cellsearch®.
also
observed
before
after
culture
showed
different
profile.
Conclusions:
cultivability
predictive
factor.
Furthermore,
subset
growing
show
stem
mesenchymal
features
may
represent
population
potential
vivo.