PLoS ONE,
Год журнала:
2018,
Номер
13(9), С. e0203030 - e0203030
Опубликована: Сен. 5, 2018
The
tumor
microenvironment
comprising
of
the
immune
cells
and
cytokines
acts
as
'soil'
that
nourishes
a
developing
tumor.
Lack
comprehensive
study
interactions
this
with
heterogeneous
sub-population
arise
from
differentiation
Cancer
Stem
Cells
(CSC),
i.e.
'seed',
has
limited
our
understanding
development
drug
resistance
treatment
failures
in
Cancer.
Based
on
seed
soil
hypothesis,
for
very
first
time,
we
have
captured
concept
CSC
tumor-immune
interaction
into
generic
model
been
validated
known
experimental
data.
Using
report
shifts
symmetric
to
asymmetric
pattern,
resistant
cancer
start
accumulating
makes
it
refractory
therapeutic
interventions.
Model
analyses
unveiled
presence
feedback
loops
establish
dual
role
M2
macrophages
regulating
proliferation.
further
revealed
oscillations
sub-populations
TH1
derived
IFN-γ
eliminates
CSC;
IL10
regulation
TH1/TH2
ratio.
These
expose
important
observations
are
indicative
prognosis.
Further,
used
testing
protocols
explore
reasons
failure
conventional
strategies
propose
an
improvised
protocol
shows
promising
results
suppressing
proliferation
all
cellular
restoring
healthy
ratio
assures
better
remission.
International Journal of Environmental Research and Public Health,
Год журнала:
2020,
Номер
17(6), С. 2078 - 2078
Опубликована: Март 20, 2020
Triple-negative
breast
cancer
(TNBC)
cells
are
deficient
in
estrogen,
progesterone
and
ERBB2
receptor
expression,
presenting
a
particularly
challenging
therapeutic
target
due
to
their
highly
invasive
nature
relatively
low
response
therapeutics.
There
is
an
absence
of
specific
treatment
strategies
for
this
tumor
subgroup,
hence
TNBC
managed
with
conventional
therapeutics,
often
leading
systemic
relapse.
In
terms
histology
transcription
profile
these
cancers
have
similarities
BRCA-1-linked
cancers,
it
hypothesized
that
BRCA1
pathway
non-functional
type
cancer.
review
article,
we
discuss
the
different
receptors
expressed
by
as
well
diversity
signaling
pathways
targeted
example,
Notch,
Hedgehog,
Wnt/b-Catenin
TGF-beta
pathways.
Additionally,
many
epidermal
growth
factor
(EGFR),
poly
(ADP-ribose)
polymerase
(PARP)
mammalian
rapamycin
(mTOR)
inhibitors
effectively
inhibit
TNBCs,
but
they
face
challenges
either
resistance
drugs
or
The
agents
has
helped
advancement
advanced
approaches
including
hyperthermia,
photodynamic
therapy,
nanomedicine-based
therapeutics
drugs,
miRNA,
siRNA,
aptamers,
which
will
also
be
discussed.
Artificial
intelligence
another
tool
presented
enhance
diagnosis
TNBC.
International Journal of Cancer,
Год журнала:
2016,
Номер
140(1), С. 10 - 22
Опубликована: Июль 8, 2016
Cancer
stem-like
cells
(CSCs)
are
thought
to
be
the
main
cause
of
tumor
occurrence,
progression
and
therapeutic
resistance.
Strong
research
efforts
in
last
decade
have
led
development
several
tailored
approaches
target
CSCs
with
some
very
promising
clinical
trials
underway;
however,
until
now
no
anti-CSC
therapy
has
been
approved
for
use.
Given
recent
improvement
our
understanding
how
onco-proteins
can
manipulate
cellular
metabolic
networks
promote
tumorigenesis,
cancer
metabolism
may
well
lead
innovative
strategies
identify
novel
regulators
downstream
mediators
CSC
maintenance.
Interfering
distinct
stages
CSC-associated
metabolics
elucidate
novel,
more
efficient
this
highly
malignant
cell
population.
Here
discoveries
regarding
properties
attributed
glioblastoma
(GBM)
colorectal
(CRC)
were
summarized.
The
association
between
stem
markers,
response
hypoxia
other
environmental
stresses
including
insults
as
developmentally
conserved
signaling
pathways
alterations
bioenergetic
also
discussed.
developments
imaging
This
summary
should
comprehensively
update
basic
scientists
on
traits
GBM
CRC.
Oncotarget,
Год журнала:
2015,
Номер
6(33), С. 35023 - 35039
Опубликована: Сен. 16, 2015
//
Fang
Wei
1,
6,
*
,
Xiao-Xiang
Rong
3,
Rao-Ying
Xie
Li-Ting
Jia
5
Hui-Yan
Wang
1
Yu-Juan
Qin
Lin
Chen
Hong-Fen
Shen
Xiao-Lin
Jie
Yang
Sheng
Wei-Chao
Hao
Yan
Sheng-Jun
Xiao
Hui-Rong
Zhou
Tao-Yan
Yu-Shuang
Sun
4
Kai-Tai
Yao
Dong
2
Cancer
Research
Institute,
Southern
Medical
University,
Guangzhou
510515,
China
Institute
of
Comparative
Medicine
&
Laboratory
Animal
Center,
3
Department
Oncology,
Nanfang
Hospital,
Children's
Hospital
Boston,
Harvard
School,
Massachusetts
02115,
USA
Pathology,
Guilin
College,
541001,
6
Digestive
Disease
First
People's
510180,
These
authors
have
contributed
equally
to
this
work
Correspondence
to:
Xiao,
e-mail:
[email protected]
Yao,
[email protected]
Keywords:
nasopharyngeal
carcinoma,
cytokine-induced
killer
cells,
cancer
stem
promoter-reporter
gene
strategy,
time-lapse
imaging
Received:
May
27,
2015
Accepted:
September
04,
Published:
16,
2015
ABSTRACT
cells
(CSCs)
are
considered
be
the
root
cause
for
treatment
failure.
Thus,
there
remains
an
urgent
need
more
potent
and
safer
therapies
against
CSCs
curing
cancer.
In
study,
antitumor
activity
(CIK)
putative
carcinoma
(NPC)
was
fully
evaluated
in
vitro
vivo
.
To
visualize
by
fluorescence
imaging,
image
quantify
tumor
xenograft-bearing
mice
bioluminescence
NPC
were
engineered
with
CSC
detector
vector
encoding
GFP
luciferase
(Luc)
under
control
Nanog
promoter.
Our
study
reported
intense
tumor-killing
CIK
NPC,
as
revealed
percentage
analysis
side
population
tumorsphere
formation
assay
Nanog-promoter-GFP-Luc
reporter
strategy
plus
recording.
Additionally,
firstly
illustrated
that
GFP-labeled
or
PKH26-labeled
tumorspheres
usually
attacked
simultaneously
many
finally
killed
suggesting
necessity
achieving
sufficient
effector-to-target
ratios.
We
confirmed
NKG2D
blockade
anti-NKG2D
antibody
significantly
but
partially
abrogated
cell-mediated
cytolysis
CSCs.
More
importantly,
intravenous
infusion
delayed
growth
NOD/SCID
mice,
accompanied
a
remarkable
reduction
number
monitored
whole-body
imaging.
Taken
together,
our
findings
suggest
demonstrate
at
least
part,
NKG2D-ligands
recognition.
results
indicate
cell-based
therapeutic
presents
promising
safe
approach
treatment.
Cancer Medicine,
Год журнала:
2023,
Номер
12(18), С. 18960 - 18980
Опубликована: Сен. 1, 2023
Abstract
Accumulating
data
reveals
that
tumors
possess
a
specialized
subset
of
cancer
cells
named
stem
(CSCs),
responsible
for
metastasis
and
recurrence
malignancies,
with
various
properties
such
as
self‐renewal,
heterogenicity,
capacity
drug
resistance.
Some
signaling
pathways
or
processes
like
Notch,
epithelial
to
mesenchymal
transition
(EMT),
Hedgehog
(Hh),
Wnt,
well
CSCs'
surface
markers
CD44,
CD123,
CD133,
cell
adhesion
molecule
(EpCAM)
have
pivotal
roles
in
acquiring
CSCs
properties.
Therefore,
targeting
CSC‐related
might
effectively
eradicate
pave
the
way
survival.
Since
current
treatments
chemotherapy
radiation
therapy
cannot
all
tumor
relapse
may
happen
following
temporary
recovery,
improving
novel
more
efficient
therapeutic
options
combine
is
required.
Immunotherapy
strategies
are
new
modalities
promising
results
CSCs.
Here,
we
review
by
immunotherapy
dendritic
(DC)
vaccines,
chimeric
antigen
receptors
(CAR)‐engineered
immune
cells,
natural
killer‐cell
(NK‐cell)
therapy,
monoclonal
antibodies
(mAbs),
checkpoint
inhibitors,
use
oncolytic
viruses
(OVs)
pre‐clinical
clinical
studies.
This
will
mainly
focus
on
blood
malignancies
but
also
describe
solid
cancers.
Materials Today Bio,
Год журнала:
2025,
Номер
31, С. 101601 - 101601
Опубликована: Фев. 20, 2025
Over
the
last
two
decades,
molecular
biology
advances
have
revealed
gut
microbiota's
active
and
crucial
role
in
colorectal
cancer
(CRC)
pathogenesis
its
dysregulation
during
tumorigenesis.
This
understanding
has
underscored
urgency
of
exploring
novel
therapeutic
approaches
to
address
challenges
posed
by
CRC.
Among
these
approaches,
nanosynergistic
therapies,
with
their
potential
modulate
microbiota,
increase
drug
bioavailability
stability,
reduce
side
effects,
emerged
as
a
promising
avenue.
Furthermore,
efficacy
nanotechnology-based
can
be
enhanced
combining
them
different
methods,
including
chemotherapy,
radiotherapy,
immunotherapy,
photothermal
therapy,
sonodynamic
therapy.
Herein,
recent
progress
nano
synergistic
therapy
been
reviewed,
focusing
on
synergy
between
microbiota
nanotechnology
CRC
treatment.
Additionally,
diverse
applications
nanoparticles
analyzed
provide
innovative
ideas
effective
solutions
for
developing
highly
treatment
strategies.
Cancers,
Год журнала:
2023,
Номер
15(15), С. 3836 - 3836
Опубликована: Июль 28, 2023
Cancer
is
an
impending
bottleneck
in
the
advanced
scientific
workflow
to
achieve
diagnostic,
prognostic,
and
therapeutic
success.
Most
cancers
are
refractory
conventional
diagnostic
chemotherapeutics
due
their
limited
targetability,
specificity,
solubility,
side
effects.
The
inherent
ability
of
each
cancer
evolve
through
various
genetic
epigenetic
transformations
metabolic
reprogramming
underlies
limitations.
Though
tumor
microenvironments
(TMEs)
quite
well
understood
some
cancers,
microenvironment
differs
from
other
internal
perturbations
skew
thereby
impeding
development
appropriate
diagnostics,
drugs,
vaccines,
therapies.
associated
bioenergetics
modulations
regulate
TME,
angiogenesis,
immune
evasion,
generation
resistant
niches
progression,
a
thorough
understanding
crucial
However,
this
remains
missing
element
theranostics,
necessitating
modalities
that
can
be
adapted
for
diagnostics
therapeutics.
In
challenging
scenario,
nanomaterials
modular
platforms
TME
achieving
successful
theranostics.
Several
nanoscale
particles
have
been
successfully
researched
animal
models,
few
reached
clinical
trials,
achieved
Nanoparticles
exhibit
intrinsic
capability
interact
with
diverse
biomolecules
modulate
functions.
Furthermore,
nanoparticles
functionalized
receptors,
modulators,
drugs
facilitate
specific
targeting
reduced
toxicity.
This
review
discusses
current
different
theranostic
nanosystems,
synthesis,
functionalization,
targetability
modulation
bioenergetics,
microenvironment.
We
highlight
potential
nanosystems
enhanced
chemotherapeutic
success
emphasizing
questions
remain
unanswered.