Cells,
Journal Year:
2024,
Volume and Issue:
13(5), P. 447 - 447
Published: March 4, 2024
Tumors
are
composed
of
heterogeneous
populations
dysregulated
cells
that
grow
in
specialized
niches
support
their
growth
and
maintain
properties.
Tumor
heterogeneity
metastasis
among
the
major
hindrances
exist
while
treating
cancer
patients,
leading
to
poor
clinical
outcomes.
Although
factors
determine
tumor
complexity
remain
largely
unknown,
several
genotypic
phenotypic
changes,
including
DNA
mutations
metabolic
reprograming
provide
with
a
survival
advantage
over
host
resistance
therapeutics.
Furthermore,
presence
specific
population
within
mass,
commonly
known
as
stem
(CSCs),
is
thought
initiate
formation,
maintenance,
resistance,
recurrence.
Therefore,
these
CSCs
have
been
investigated
detail
recently
potential
targets
treat
prevent
Understanding
molecular
mechanisms
involved
CSC
proliferation,
self-renewal,
dormancy
may
important
clues
for
developing
effective
therapeutic
strategies.
Autophagy,
catabolic
process,
has
long
recognized
regulate
various
physiological
pathological
processes.
In
addition
regulating
cells,
recent
studies
identified
critical
role
autophagy
functions.
Autophagy
activated
under
adverse
conditions
promotes
cellular
survival,
even
cell
death.
Thus,
it
intriguing
address
whether
or
inhibits
functions
modulation
can
be
used
functions,
either
alone
combination.
This
review
describes
roles
regulation
proliferation
quiescence
CSCs,
its
during
stress.
The
further
highlights
autophagy-associated
pathways
could
CSCs.
Overall,
present
will
help
rationalize
translational
approaches
involve
autophagy-mediated
controlling
progression,
metastasis,
MedComm – Oncology,
Journal Year:
2025,
Volume and Issue:
4(1)
Published: Jan. 10, 2025
Abstract
The
success
of
cancer
therapy
has
been
significantly
hampered
by
various
mechanisms
therapeutic
resistance.
Chief
among
these
is
the
presence
clonal
heterogeneity
within
an
individual
tumor
mass.
introduction
concept
stem
cells
(CSCs)—a
rare
and
immature
subpopulation
with
tumorigenic
potential
that
contributes
to
intratumoral
heterogeneity—has
deepened
our
understanding
drug
Given
characteristics
CSCs,
such
as
increased
drug‐efflux
activity,
enhanced
DNA‐repair
capacity,
high
metabolic
plasticity,
adaptability
oxidative
stress,
and/or
upregulated
detoxifying
aldehyde
dehydrogenase
(ALDH)
enzymes,
CSCs
have
recognized
a
theoretical
reservoir
for
resistant
diseases.
Implicit
in
this
recognition
possibility
CSC‐targeted
strategies
might
offer
breakthrough
overcoming
resistance
patients.
Herein,
we
summarize
generation
current
underlying
CSC‐mediated
This
extended
knowledge
progressively
translated
into
novel
anticancer
enriched
available
options
combination
treatments,
all
which
are
anticipated
improve
clinical
outcomes
patients
experiencing
CSC‐related
relapse.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 6, 2025
Cancer
stem
cells
(CSCs)
are
a
small
subset
within
the
tumor
mass
significantly
contributing
to
cancer
progression
through
dysregulation
of
various
oncogenic
pathways,
driving
growth,
chemoresistance
and
metastasis
formation.
The
aggressive
behavior
CSCs
is
guided
by
several
intracellular
signaling
pathways
such
as
WNT,
NF-kappa-B,
NOTCH,
Hedgehog,
JAK-STAT,
PI3K/AKT1/MTOR,
TGF/SMAD,
PPAR
MAPK
kinases,
well
extracellular
vesicles
exosomes,
molecules
cytokines,
chemokines,
pro-angiogenetic
growth
factors,
which
finely
regulate
CSC
phenotype.
In
this
scenario,
microenvironment
(TME)
key
player
in
establishment
permissive
niche,
where
engage
intricate
communications
with
diverse
immune
cells.
"oncogenic"
mainly
represented
B
T
lymphocytes,
NK
cells,
dendritic
Among
macrophages
exhibit
more
plastic
adaptable
phenotype
due
their
different
subpopulations,
characterized
both
immunosuppressive
inflammatory
phenotypes.
Specifically,
tumor-associated
(TAMs)
create
an
milieu
production
plethora
paracrine
factors
(IL-6,
IL-12,
TNF-alpha,
TGF-beta,
CCL1,
CCL18)
promoting
acquisition
stem-like,
invasive
metastatic
TAMs
have
demonstrated
ability
communicate
via
direct
ligand/receptor
(such
CD90/CD11b,
LSECtin/BTN3A3,
EPHA4/Ephrin)
interaction.
On
other
hand,
exhibited
capacity
influence
creating
favorable
for
progression.
Interestingly,
bidirectional
TME
leads
epigenetic
reprogramming
sustains
malignant
transformation.
Nowadays,
integration
biological
computational
data
obtained
cutting-edge
technologies
(single-cell
RNA
sequencing,
spatial
transcriptomics,
trajectory
analysis)
has
improved
comprehension
biunivocal
multicellular
dialogue,
providing
comprehensive
view
heterogeneity
dynamics
CSCs,
uncovering
alternative
mechanisms
evasion
therapeutic
resistance.
Moreover,
combination
biology
will
lead
development
innovative
target
therapies
dampening
CSC-TME
Here,
we
aim
elucidate
most
recent
insights
on
complex
interactions
specifically
TAMs,
tracing
exhaustive
scenario
from
primary
Cancers,
Journal Year:
2022,
Volume and Issue:
14(4), P. 970 - 970
Published: Feb. 15, 2022
Tumor
heterogeneity
represents
an
important
limitation
to
the
development
of
effective
cancer
therapies.
The
presence
stem
cells
(CSCs)
and
their
differentiation
hierarchies
contribute
complexity
confer
tumors
ability
grow,
resist
treatment,
survive
unfavorable
conditions,
invade
neighboring
distant
tissues.
A
large
body
research
is
currently
focusing
on
understanding
properties
CSCs,
including
cellular
molecular
origin,
as
well
biological
behavior
in
different
tumor
types.
In
turn,
this
knowledge
informs
strategies
for
targeting
these
initiating
related
stemness.
Cancer
stemness
modulated
by
microenvironment,
which
influences
CSC
function
survival.
Several
advanced
vitro
models
are
being
developed
study
order
advance
new
key
pathways
involved
self-renewal
dormancy,
mimic
patients'
pre-clinical
drug
testing.
review,
we
discuss
CSCs
modulation
factors
signaling
pathways.
addition,
introduce
current
that
allow
targeted
Cancers,
Journal Year:
2022,
Volume and Issue:
14(2), P. 381 - 381
Published: Jan. 13, 2022
Cancer
stem
cells
(CSCs)
are
a
subset
of
the
tumor
population
that
play
critical
roles
in
tumorigenicity,
metastasis,
and
relapse.
A
key
feature
CSCs
is
their
resistance
to
numerous
therapeutic
strategies
which
include
chemotherapy,
radiation,
immune
checkpoint
inhibitors.
In
recent
years,
there
growing
body
literature
suggests
link
between
CSC
maintenance
autophagy,
mechanism
recycle
intracellular
components
during
moments
environmental
stress,
especially
since
thrive
microenvironment
plagued
with
hypoxia,
acidosis,
lack
nutrients.
Autophagy
activation
has
been
shown
aid
upkeep
stemness
state
along
bolstering
cancer
treatment.
However,
studies
have
also
suggested
autophagy
double-edged
sword
anti-tumorigenic
properties
under
certain
circumstances.
This
review
summarizes
integrates
what
published
terms
role
plays
more
complex
interplay
apoptosis
involves
multiple
pathways
regulation.
Future
therapy
needed
eradicate
this
resistant
cell
through
Seminars in Cancer Biology,
Journal Year:
2022,
Volume and Issue:
87, P. 48 - 83
Published: Nov. 5, 2022
Cell
identity
is
largely
determined
by
its
transcriptional
profile.
In
tumour,
deregulation
of
transcription
factor
expression
and/or
activity
enables
cancer
cell
to
acquire
a
stem-like
state
characterised
capacity
self-renew,
differentiate
and
form
tumours
in
vivo.
These
cells
are
highly
metastatic
therapy
resistant,
thus
warranting
more
complete
understanding
the
molecular
mechanisms
downstream
factors
that
mediate
establishment
stemness
state.
Here,
we
review
recent
research
findings
provide
mechanistic
link
between
commonly
deregulated
cancer.
particular,
describe
role
master
(SOX,
OCT4,
NANOG,
KLF,
BRACHYURY,
SALL,
HOX,
FOX
RUNX),
signalling-regulated
(SMAD,
β-catenin,
YAP,
TAZ,
AP-1,
NOTCH,
STAT,
GLI,
ETS
NF-κB)
unclassified
(c-MYC,
HIF,
EMT
P53)
across
diverse
tumour
types,
thereby
yielding
comprehensive
overview
identifying
shared
targets,
highlighting
unique
discussing
complexities.
Acta Pharmaceutica Sinica B,
Journal Year:
2023,
Volume and Issue:
13(12), P. 4688 - 4714
Published: Aug. 12, 2023
Beclin-1
is
the
firstly-identified
mammalian
protein
of
autophagy
machinery,
which
functions
as
a
molecular
scaffold
for
assembly
PI3KC3
(class
III
phosphatidylinositol
3
kinase)
complex,
thus
controlling
induction
and
other
cellular
trafficking
events.
Notably,
there
mounting
evidence
establishing
implications
in
diverse
tumorigenesis
processes,
including
tumor
suppression
progression
well
resistance
to
cancer
therapeutics
CSC
(cancer
stem-like
cell)
maintenance.
More
importantly,
has
been
confirmed
potential
target
treatment
multiple
cancers.
In
this
review,
we
provide
comprehensive
survey
structure,
functions,
regulations
Beclin-1,
discuss
recent
advances
understanding
controversial
roles
oncology.
Moreover,
focus
on
summarizing
targeted
Beclin-1-regulating
strategies
therapy,
providing
novel
insights
into
promising
strategy
regulating
improve
future.
Biomedicine & Pharmacotherapy,
Journal Year:
2023,
Volume and Issue:
161, P. 114487 - 114487
Published: March 22, 2023
Treatment
resistance
is
one
of
the
major
barriers
for
therapeutic
strategies
in
hepatocellular
carcinoma
(HCC).
Many
studies
have
indicated
that
chemotherapy
and
radiotherapy
induce
autophagy
machinery
(cell
protective
autophagy)
HCC
cells.
In
addition,
many
experiments
report
a
remarkable
crosstalk
between
treatment
pathways.
Thus,
could
be
key
factors
enabling
tumor
cells
to
hinder
induced
cell
death
after
medical
interventions.
Therefore,
extensive
research
on
molecular
pathways
involved
induction
been
conducted
achieve
desired
response.
The
related
therapy
are
TGF-β,
MAPK,
NRF2,
NF-κB,
non-coding
RNAs.
EMT,
drug
transports,
apoptosis
evasion,
DNA
repair,
cancer
stem
cells,
hypoxia
considerable
impact
hepatoma
cell's
response
therapies.
These
mechanisms
protect
against
various
treatments
shown
each
them
connected
HCC.
Hence,
inhibition
may
an
effective
strategy
improve
outcome
patients.
this
review,
we
further
highlight
how
leads
poor
during
through
complex
network
it
enhances
primary
liver
cancer.
We
propose
combinational
regimens
approved
protocols
plus
inhibitors
overcome
therapy.
Biomedicine & Pharmacotherapy,
Journal Year:
2023,
Volume and Issue:
160, P. 114336 - 114336
Published: Feb. 2, 2023
SOX2
is
a
transcription
factor
involved
in
multiple
stages
of
embryonic
development.
In
related
reports,
was
found
to
be
abnormally
expressed
tumor
tissues
and
correlated
with
clinical
features
such
as
TNM
staging,
grade,
prognosis
patients
various
cancer
types.
most
types,
tumor-promoting
that
regulates
progression
metastasis
primarily
by
maintaining
the
stemness
cells.
addition,
also
proliferation,
apoptosis,
invasion,
migration,
ferroptosis
drug
resistance
However,
acts
suppressor
some
cases
certain
gastric
lung
cancer.
These
key
regulatory
functions
involve
complex
networks,
including
protein-protein
protein-nucleic
acid
interactions
through
signaling
pathways
noncoding
RNA
interactions,
modulating
expression
may
potential
therapeutic
strategy
for
patients.
Therefore,
we
sorted
out
phenotypes
cancer,
hoping
provide
basis
further
translation.