Antioxidants,
Journal Year:
2021,
Volume and Issue:
10(11), P. 1801 - 1801
Published: Nov. 11, 2021
Multi-drug
resistance
(MDR)
is
a
leading
cause
of
cancer-related
death,
and
it
continues
to
be
major
barrier
cancer
treatment.
The
tumour
microenvironment
(TME)
has
proven
play
an
essential
role
in
not
only
progression
metastasis,
but
also
the
development
chemotherapy.
Despite
significant
advances
efficacy
anti-cancer
therapies,
drug
remains
impediment
therapeutic
success.
This
review
highlights
interplay
between
various
factors
within
TME
that
collectively
initiate
or
propagate
MDR.
key
TME-mediated
mechanisms
MDR
regulation
will
discussed
herein
include
(1)
altered
metabolic
processing
reactive
oxygen
species
(ROS)-hypoxia
inducible
factor
(HIF)
axis;
(2)
changes
stromal
cells;
(3)
increased
cell
survival
via
autophagy
failure
apoptosis;
(4)
delivery,
uptake,
efflux
(5)
induction
stem
(CSC)
phenotype.
discusses
thought-provoking
ideas
may
assist
overcoming
TME-induced
We
conclude
stressors
from
exposure
chemotherapeutic
agents
are
strongly
linked
cells.
Therefore,
there
vast
area
for
potential
research
further
elicit
existing
both
outside
TME.
Elucidating
this
network
developing
new
strategies
less
prone
due
Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: Jan. 16, 2023
Abstract
Microorganisms,
including
bacteria,
viruses,
fungi,
and
other
eukaryotes,
play
critical
roles
in
human
health.
An
altered
microbiome
can
be
associated
with
complex
diseases.
Intratumoral
microbial
components
are
found
multiple
tumor
tissues
closely
correlated
cancer
initiation
development
therapy
efficacy.
The
intratumoral
microbiota
may
contribute
to
promotion
of
the
progression
cancers
by
DNA
mutations,
activating
carcinogenic
pathways,
promoting
chronic
inflammation,
complement
system,
initiating
metastasis.
Moreover,
not
only
enhance
antitumor
immunity
via
mechanisms
STING
signaling
activation,
T
NK
cell
TLS
production,
microbiota-derived
antigen
presenting,
but
also
decrease
immune
responses
promote
through
pathways
upregulation
ROS,
an
anti-inflammatory
environment,
inactivation,
immunosuppression.
effect
on
is
dependent
composition,
crosstalk
between
cancer,
status
cancers.
regulate
physiology
response
different
β-catenin,
TLR,
ERK,
NF-κB,
STING,
among
others.
These
viewpoints
help
identify
as
diagnosis
or
prognosis
evaluation
cancers,
new
therapeutic
strategy
potential
targets
for
therapy.
Journal of Biomedical Science,
Journal Year:
2022,
Volume and Issue:
29(1)
Published: Sept. 26, 2022
The
major
concept
of
"oxidative
stress"
is
an
excess
elevated
level
reactive
oxygen
species
(ROS)
which
are
generated
from
vigorous
metabolism
and
consumption
oxygen.
precise
harmonization
oxidative
stresses
between
mitochondria
other
organelles
in
the
cell
absolutely
vital
to
survival.
Under
stress,
ROS
produced
mediator
for
tumorigenesis
different
aspects,
such
as
proliferation,
migration/invasion,
angiogenesis,
inflammation,
immunoescape
allow
cancer
cells
adapt
rigorous
environment.
Accordingly,
dynamic
balance
not
only
orchestrate
complex
signaling
events
but
also
affect
components
tumor
microenvironment
(TME).
Immune
cells,
M2
macrophages,
dendritic
T
immunosuppressive
TME
ROS-induced
inflammation.
Based
on
this
notion,
numerous
strategies
mitigate
tumors
have
been
tested
prevention
or
therapies;
however,
these
manipulations
devised
sources
mechanisms
without
established
effectiveness.
Herein,
we
integrate
current
progress
regarding
impact
mitochondrial
TME,
immune
discuss
combination
emerging
ROS-modulating
with
immunotherapies
achieve
antitumor
effects.
Molecular Cancer,
Journal Year:
2023,
Volume and Issue:
22(1)
Published: Aug. 10, 2023
Abstract
The
reversible
oxidation-reduction
homeostasis
mechanism
functions
as
a
specific
signal
transduction
system,
eliciting
related
physiological
responses.
Disruptions
to
redox
can
have
negative
consequences,
including
the
potential
for
cancer
development
and
progression,
which
are
closely
linked
series
of
processes,
such
adjustment
reactive
oxygen
species
(ROS)
levels
species,
changes
in
antioxidant
capacity,
differential
effects
ROS
on
downstream
cell
fate
immune
capacity.
tumor
microenvironment
(TME)
exhibits
complex
interplay
between
immunity
regulatory
death,
especially
autophagy
apoptosis,
is
crucially
regulated
by
ROS.
present
study
aims
investigate
multi-source
affects
autophagy,
anti-tumor
response
TME
mutual
crosstalk
these
three
processes.
Given
intricate
role
controlling
immunity,
we
will
further
examine
relationship
traditional
therapy
It
worth
noting
that
discuss
some
ROS-related
treatment
options
future
studies.
Journal of Hematology & Oncology,
Journal Year:
2024,
Volume and Issue:
17(1)
Published: June 11, 2024
Abstract
Macrophages
infiltrating
tumour
tissues
or
residing
in
the
microenvironment
of
solid
tumours
are
known
as
tumour-associated
macrophages
(TAMs).
These
specialized
immune
cells
play
crucial
roles
growth,
angiogenesis,
regulation,
metastasis,
and
chemoresistance.
TAMs
encompass
various
subpopulations,
primarily
classified
into
M1
M2
subtypes
based
on
their
differentiation
activities.
macrophages,
characterized
by
a
pro-inflammatory
phenotype,
exert
anti-tumoural
effects,
while
with
an
anti-inflammatory
function
protumoural
regulators.
highly
versatile
respond
to
stimuli
from
other
constituents
within
(TME),
such
growth
factors,
cytokines,
chemokines,
enzymes.
induce
polarization
towards
one
phenotype
another,
leading
complex
interactions
TME
components
influencing
both
pro-tumour
anti-tumour
processes.
This
review
comprehensively
deeply
covers
literature
origin
well
intricate
interplay
between
TME,
dual
nature
promoting
pro-
Moreover,
delves
primary
pathways
implicated
macrophage
polarization,
examining
diverse
that
regulate
this
process.
role
shaping
functions
macrophages.
In
addition,
advantages
limitations
current
clinical
interventions
reviewed,
including
enhancing
TAM
phagocytosis,
inducing
exhaustion,
inhibiting
recruitment,
polarizing
M1-like
phenotype.
conclusion,
treatment
strategies
targeting
precision
medicine
show
promise,
overcoming
several
obstacles
is
still
necessary
achieve
accessible
efficient
immunotherapy.
Deleted Journal,
Journal Year:
2024,
Volume and Issue:
2(2)
Published: May 1, 2024
Abstract
The
precision
treatment
of
tumors
with
minimal
side
effects
is
associated
improved
human
health
and
quality
life.
In
recent
years,
phototherapy
has
attracted
significant
attention
in
tumor
therapy
due
to
its
versatility,
spatiotemporal
controllability,
non‐resistance,
effects.
Carbon
dots
(CDs)
are
considered
promising
reagents
because
their
simple
preparation,
facilitated
surface
modification,
tunable
energy
bands,
excellent
electron‐transfer
capabilities,
remarkable
photoelectric
photothermal
conversion
properties,
outstanding
biocompatibility.
This
review
summarizes
advancements
photo‐responsive
CDs
for
photodynamic
the
emerging
photocatalytic
tumors.
Finally,
article
discusses
main
challenges
development
oncology
therapeutics
strategies
overcome
these
challenges.
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: Aug. 4, 2023
Radiotherapy
(RT)
is
an
effective
treatment
option
for
cancer
patients,
which
induces
the
production
of
reactive
oxygen
species
(ROS)
and
causes
oxidative
stress
(OS),
leading
to
death
tumor
cells.
OS
not
only
apoptosis,
autophagy
ferroptosis,
but
also
affects
immune
response.
The
combination
RT
immunotherapy
has
revolutionized
management
various
cancers.
In
this
process,
caused
by
ROS
plays
a
critical
role.
Specifically,
RT-induced
can
promote
release
tumor-associated
antigens
(TAAs),
regulate
infiltration
differentiation
cells,
manipulate
expression
checkpoints,
change
microenvironment
(TME).
review,
we
briefly
summarize
several
ways
in
IR
cell
discuss
interrelationship
between
antitumor
immunity,
with
focus
on
interaction
ferroptosis
immunogenic
death.
We
potential
mechanisms
regulates
checkpoint
expression,
cells
activity,
differentiation.
addition,
conclude
therapeutic
opportunity
improving
radiotherapy
regulating
OS,
may
be
beneficial
clinical
treatment.
Journal of Cancer Research and Clinical Oncology,
Journal Year:
2024,
Volume and Issue:
150(5)
Published: May 7, 2024
Abstract
Background
Tumor
growth
is
closely
linked
to
the
activities
of
various
cells
in
tumor
microenvironment
(TME),
particularly
immune
cells.
During
progression,
circulating
monocytes
and
macrophages
are
recruited,
altering
TME
accelerating
growth.
These
adjust
their
functions
response
signals
from
stromal
Tumor-associated
(TAMs),
similar
M2
macrophages,
key
regulators
TME.
Methods
We
review
origins,
characteristics,
TAMs
within
This
analysis
includes
mechanisms
through
which
facilitate
evasion
promote
metastasis.
Additionally,
we
explore
potential
therapeutic
strategies
that
target
TAMs.
Results
instrumental
mediating
malignant
behaviors.
They
release
cytokines
inhibit
effector
attract
additional
immunosuppressive
primarily
T
cells,
inducing
exhaustion
directly,
influencing
activity
indirectly
cellular
interactions,
or
suppressing
checkpoints.
directly
involved
proliferation,
angiogenesis,
invasion,
Summary
Developing
innovative
tumor-targeted
therapies
immunotherapeutic
currently
a
promising
focus
oncology.
Given
pivotal
role
evasion,
several
approaches
have
been
devised
them.
include
leveraging
epigenetics,
metabolic
reprogramming,
engineering
repolarize
TAMs,
inhibiting
recruitment
activity,
using
as
drug
delivery
vehicles.
Although
some
these
remain
distant
clinical
application,
believe
future
targeting
will
offer
significant
benefits
cancer
patients.