International Journal of Molecular Sciences,
Год журнала:
2020,
Номер
21(7), С. 2423 - 2423
Опубликована: Март 31, 2020
MicroRNAs
are
tiny
but
powerful
regulators
of
gene
expression
at
the
post-transcriptional
level.
Aberrant
oncogenic
and
tumor-suppressor
microRNAs
has
been
recognized
as
a
common
feature
human
cancers.
Colorectal
cancer
represents
major
clinical
challenge
in
developed
world
design
innovative
therapeutic
approaches
relies
on
identification
novel
biological
targets.
Here,
we
perform
functional
screening
colorectal
cells
using
library
locked
nucleic
acid
(LNA)-modified
anti-miRs
order
to
unveil
putative
whose
inhibition
yields
cytotoxic
effect.
We
identify
miR-1285-3p
further
explore
effect
its
targeting
both
commercial
cell
lines
primary
stem
cells,
finding
induction
cycle
arrest
apoptosis.
show
that
DAPK2,
known
tumor-suppressor,
is
miR-1285
target
mediates
anti-proliferative
pro-apoptotic
effects
depletion.
Altogether,
our
findings
uncover
microRNA
lay
foundation
for
studies
aiming
development
possible
strategies
based
targeting.
In
the
last
decades,
role
of
microenvironment
in
tumor
progression
and
therapeutic
outcome
has
gained
increasing
attention.
Cancer-associated
fibroblasts
(CAFs)
have
emerged
as
key
players
among
stromal
cells,
owing
to
their
abundance
most
solid
tumors
diverse
tumor-restraining/promoting
roles.
The
interplay
between
cells
neighboring
CAFs
takes
place
by
both
paracrine
signals
(cytokines,
exosomes
metabolites)
or
multifaceted
functions
surrounding
extracellular
matrix.
Here,
we
dissect
recent
identified
mechanisms
underlying
CAF-mediated
control
therapy
resistance,
which
include
induction
epithelial-to-mesenchymal
transition
(EMT),
activation
survival
pathways
stemness-related
programs
metabolic
reprogramming
cells.
Importantly,
recently
unveiled
heterogeneity
claims
tailored
efforts
aimed
at
eradicating
specific
subset
facilitating
progression,
resistance
relapse.
However,
despite
large
amount
pre-clinical
data,
much
effort
is
still
needed
translate
CAF-directed
anti-cancer
strategies
from
bench
clinic.
Cancers,
Год журнала:
2019,
Номер
11(5), С. 732 - 732
Опубликована: Май 27, 2019
Cancer
stem
cells
(CSCs)
are
subpopulations
of
tumor
with
the
ability
to
self-renew,
differentiate,
and
initiate
maintain
growth,
they
considered
be
main
drivers
intra-
inter-tumoral
heterogeneity.
While
conventional
chemotherapy
can
eradicate
majority
non-CSC
cells,
CSCs
often
drug-resistant,
leading
recurrence
metastasis.
The
heterogeneity
is
challenge
in
developing
CSC-targeting
therapy;
therefore,
we
other
investigators
have
focused
on
novel
therapeutic
strategies
that
combine
inhibitors
CSC-regulating
pathways.
Encouraging
preclinical
findings
suggested
CSC
pathway
blockade
indeed
enhance
cellular
sensitivity
non-targeted
therapy,
this
work
has
led
several
ongoing
clinical
trials
inhibitors.
Our
studies
bladder
cancer
lung
adenocarcinoma
demonstrated
a
crucial
role
YAP1,
transcriptional
regulator
genes
promote
cell
survival
proliferation,
regulating
phenotypes.
Moreover,
using
lines
patient-derived
xenograft
models,
showed
inhibition
YAP1
enhances
efficacy
therapies
by
attenuating
stemness
features.
In
review,
summarize
for
targeting
cancers
discuss
potential
challenges
approach.
The
role
of
fibronectin
(FN)
in
tumorigenesis
and
malignant
progression
has
been
highly
controversial.
Cancerous
FN
plays
a
tumor-suppressive
role,
whereas
it
is
pro-metastatic
associated
with
poor
prognosis.
Interestingly,
matrix
deposited
the
tumor
microenvironments
(TMEs)
promotes
but
paradoxically
related
to
better
Here,
we
justify
how
impacts
transformation
subsequently
metastatic
progression.
Next,
try
reconcile
rationalize
seemingly
conflicting
roles
cancer
TMEs.
Finally,
propose
future
perspectives
for
potential
FN-based
therapeutic
strategies.
Frontiers in Cell and Developmental Biology,
Год журнала:
2021,
Номер
9
Опубликована: Март 1, 2021
Cancer
is
a
disease
which
frequently
has
poor
prognosis.
Although
multiple
therapeutic
strategies
have
been
developed
for
various
cancers,
including
chemotherapy,
radiotherapy,
and
immunotherapy,
resistance
to
these
treatments
impedes
the
clinical
outcomes.
Besides
active
driven
by
genetic
epigenetic
alterations
in
tumor
cells,
microenvironment
(TME)
also
reported
be
crucial
regulator
tumorigenesis,
progression,
resistance.
Here,
we
propose
that
adaptive
mechanisms
of
are
closely
connected
with
TME
rather
than
depending
on
non-cell-autonomous
changes
response
treatment.
comprehensive
understanding
need
further
investigation
fully
elucidate
resistance,
many
targeting
successful.
In
this
review,
report
recent
advances
concerning
molecular
events
important
factors
involved
TME,
particularly
focusing
contributions
provide
insights
into
potential
methods
or
translational
medicine
overcome
therapy
Cancers,
Год журнала:
2019,
Номер
11(8), С. 1076 - 1076
Опубликована: Июль 30, 2019
PTEN
is
one
of
the
most
frequently
inactivated
tumor
suppressor
genes
in
cancer.
Loss
or
variation
gene/protein
levels
commonly
observed
a
broad
spectrum
human
cancers,
while
germline
mutations
cause
inherited
syndromes
that
lead
to
increased
risk
tumors.
restrains
tumorigenesis
through
different
mechanisms
ranging
from
phosphatase-dependent
and
independent
activities,
subcellular
localization
protein
interaction,
modulating
array
cellular
functions
including
growth,
proliferation,
survival,
DNA
repair,
cell
motility.
The
main
target
phosphatase
activity
significant
growth
pro-survival
signaling
pathway
cancer:
PI3K/AKT/mTOR.
Several
shreds
evidence
shed
light
on
critical
role
normal
cancer
stem
cells
(CSCs)
homeostasis,
with
its
loss
fostering
CSC
compartment
both
solid
hematologic
malignancies.
CSCs
are
responsible
for
propagation,
metastatic
spread,
resistance
therapy,
relapse.
Thus,
understanding
how
alterations
affect
hallmarks
could
be
crucial
development
successful
therapeutic
approaches.
Here,
we
discuss
findings
PTEN-mediated
control
state.
We
aim
unravel
regulation
key
specific
CSCs,
such
as
self-renewal,
quiescence/cell
cycle,
Epithelial-to-Mesenchymal-Transition
(EMT),
particular
focus
PTEN-based
therapy
their
exploitation
novel
approaches
treatment.
Advanced Healthcare Materials,
Год журнала:
2023,
Номер
12(18)
Опубликована: Март 11, 2023
Abstract
The
clinical
translations
of
drugs
and
nanomedicines
depend
on
coherent
pharmaceutical
research
based
biologically
accurate
screening
approaches.
Since
establishing
the
2D
in
vitro
cell
culture
method,
scientific
community
has
improved
cell‐based
drug
assays
models.
Those
advances
result
more
informative
biochemical
development
3D
multicellular
models
to
describe
biological
complexity
better
enhance
simulation
vivo
microenvironment.
Despite
overall
dominance
conventional
macroscopic
methods,
they
present
physicochemical
operational
challenges
that
impair
scale‐up
by
not
allowing
a
high
parallelization,
multidrug
combination,
high‐throughput
screening.
Their
combination
complementarity
with
microfluidic
platforms
enable
microfluidics‐based
unequivocal
advantages
therapies.
Thus,
this
review
presents
an
updated
consolidated
view
miniaturization's
physical,
chemical,
considerations
scenario.
It
clarifies
field
using
gradient‐based
microfluidics,
droplet‐based
printed‐based
digital‐based
SlipChip,
paper‐based
microfluidics.
Finally,
it
comparative
analysis
performance
methods
life
achieve
increased
precision
process.
Stem Cells International,
Год журнала:
2018,
Номер
2018, С. 1 - 15
Опубликована: Янв. 1, 2018
RNA-binding
proteins
(RBPs)
mediate
the
localization,
stability,
and
translation
of
target
transcripts
fine-tune
physiological
functions
encoded.
The
insulin-like
growth
factor
(IGF)
2
mRNA-binding
protein
(IGF2BP,
IMP)
family
comprises
three
RBPs,
IGF2BP1,
IGF2BP2,
IGF2BP3,
capable
associating
with
IGF2
other
mediating
their
processing.
IGF2BP2
represents
least
understood
member
this
RBPs;
however,
it
has
been
reported
to
participate
in
a
wide
range
processes,
such
as
embryonic
development,
neuronal
differentiation,
metabolism.
Its
dysregulation
is
associated
insulin
resistance,
diabetes,
carcinogenesis
may
potentially
be
powerful
biomarker
candidate
for
relevant
diseases.
This
review
summarizes
structural
features,
regulation,
association
cancer
stem
cells.
Stem Cell Research & Therapy,
Год журнала:
2020,
Номер
11(1)
Опубликована: Ноя. 18, 2020
Abstract
Over
the
last
decades,
cancer
survival
rate
has
increased
due
to
personalized
therapies,
discovery
of
targeted
therapeutics
and
novel
biological
agents,
application
palliative
treatments.
Despite
these
advances,
tumor
resistance
chemotherapy
radiation
rapid
progression
metastatic
disease
are
still
seen
in
many
patients.
Evidence
shown
that
stem
cells
(CSCs),
a
sub-population
share
common
characteristics
with
somatic
(SSCs),
contribute
this
therapeutic
failure.
The
most
critical
properties
CSCs
their
self-renewal
ability
capacity
for
differentiation
into
heterogeneous
populations
cells.
Although
only
constitute
low
percentage
total
mass,
can
regrow
mass
on
own.
Initially
identified
leukemia,
have
subsequently
been
found
cancers
breast,
colon,
pancreas,
brain.
Common
genetic
phenotypic
features
both
SSCs
CSCs,
including
upregulated
signaling
pathways
such
as
Notch,
Wnt,
Hedgehog,
TGF-β.
These
play
fundamental
roles
development
well
control
cell
fate
relevant
targeting
CSCs.
differences
expression
membrane
proteins
exosome-delivered
microRNAs
between
also
important
specifically
target
cancer.
Further
research
efforts
should
be
directed
toward
elucidation
improve
existing
therapies
generate
new
clinically
Nutrients,
Год журнала:
2020,
Номер
12(6), С. 1663 - 1663
Опубликована: Июнь 3, 2020
Saturated
fatty
acids
possess
few
health
benefits
compared
to
unsaturated
acids.
However,
increasing
experimental
evidence
demonstrates
the
nutritionally
beneficial
role
of
odd-chain
saturated
in
human
health.
In
this
study,
anti-cancer
effects
pentadecanoic
acid
were
evaluated
breast
carcinoma
MCF-7/stem-like
cells
(SC),
a
cell
line
with
greater
mobility,
invasiveness,
and
cancer
stem
properties
parental
MCF-7
cells.
Pentadecanoic
exerted
selective
cytotoxic
MCF-7/SC
Moreover,
reduced
stemness
suppressed
migratory
invasive
ability
as
evidenced
by
results
flow
cytometry,
mammosphere
formation
assay,
an
aldehyde
dehydrogenase
activity
Western
blot
experiments
conducted
analyze
expression
markers—CD44,
β-catenin,
MDR1,
MRP1—and
epithelial–mesenchymal
transition
(EMT)
markers—snail,
slug,
MMP9,
MMP2.
addition,
interleukin-6
(IL-6)-induced
JAK2/STAT3
signaling,
induced
cycle
arrest
at
sub-G1
phase,
promoted
caspase-dependent
apoptosis
MCF-7/SC.
These
findings
indicate
that
can
serve
novel
signaling
inhibitor
suggest
acid-rich
food
intake
during
treatments.
Frontiers in Immunology,
Год журнала:
2020,
Номер
11
Опубликована: Окт. 21, 2020
Cancer
cell
dormancy
is
a
common
feature
of
human
tumors
and
represents
major
clinical
barrier
to
the
long-term
efficacy
anticancer
therapies.
Dormant
cancer
cells,
either
in
primary
or
disseminated
secondary
organs,
may
reawaken
relapse
into
more
aggressive
disease.
The
mechanisms
underpinning
entry
exit
strongly
resemble
those
governing
stemness,
include
intrinsic
contextual
cues.
Cellular
molecular
components
tumor
microenvironment
persistently
interact
with
cells.
This
dialog
highly
dynamic,
as
it
evolves
over
time
space,
cooperates
nets,
governs
features
(like
quiescence
stemness)
fate
(survival
outgrowth).
Therefore,
deeper
insights
biology
dormant
(stem)
cells
regulating
equilibrium
quiescence-versus-proliferation
are
vital
our
pursuit
find
new
therapeutic
opportunities
that
prevent
from
ever
recurring.
Here,
we
review
discuss
microenvironmental
regulations
its
parallels
offer
view
strategies
adopted
lethal
recurrence,
by
eradicating
resident
maintaining
them
state