Cell Reports Medicine,
Год журнала:
2024,
Номер
5(7), С. 101626 - 101626
Опубликована: Июнь 28, 2024
Solid
tumor
pathology,
characterized
by
abnormalities
in
the
microenvironment
(TME),
challenges
therapeutic
effectiveness.
Mechanical
factors,
including
increased
stiffness
and
accumulation
of
intratumoral
forces,
can
determine
success
cancer
treatments,
defining
tumor's
"mechanopathology"
profile.
These
cause
extensive
vascular
compression,
leading
to
hypoperfusion
hypoxia.
Hypoperfusion
hinders
drug
delivery,
while
hypoxia
creates
an
unfavorable
TME,
promoting
progression
through
immunosuppression,
heightened
metastatic
potential,
resistance,
chaotic
angiogenesis.
Strategies
targeting
TME
mechanopathology,
such
as
stroma
normalization,
hold
promise
enhancing
therapies
with
some
already
advancing
clinic.
Normalization
be
achieved
using
anti-angiogenic
agents,
mechanotherapeutics,
immune
checkpoint
inhibitors,
engineered
bacterial
therapeutics,
metronomic
nanomedicine,
ultrasound
sonopermeation.
Here,
we
review
methods
developed
rectify
which
have
even
led
cures
preclinical
models,
discuss
their
bench-to-bedside
translation,
derivation
biomarkers
from
mechanopathology
for
personalized
therapy.
Frontiers in Pharmacology,
Год журнала:
2022,
Номер
13
Опубликована: Май 24, 2022
Recently,
in
the
field
of
cancer
treatment,
paradigm
has
changed
to
immunotherapy
that
activates
immune
system
induce
attacks.
Among
them,
checkpoint
inhibitors
(ICI)
are
attracting
attention
as
excellent
and
continuous
clinical
results.
However,
it
shows
not
only
limitations
such
efficacy
some
patients
or
indications,
but
also
side-effects
resistance
occur.
Therefore,
is
necessary
understand
factors
tumor
microenvironment
(TME)
affect
immunotherapy,
is,
mechanism
by
which
grows
while
evading
suppressing
attacks
from
within
TME.
Tumors
can
evade
through
various
mechanisms
restricting
antigen
recognition,
inhibiting
system,
inducing
T
cell
exhaustion.
In
addition,
tumors
inhibit
accumulating
specific
metabolites
signal
TME
limiting
nutrients
available
cells.
order
overcome
develop
effective
treatments
therapeutic
strategies,
an
approach
needed
functions
cells
integrated
manner
based
on
this
review,
we
will
examine
effects
cells,
especially
how
anti-cancer
strategies
Cancers,
Год журнала:
2023,
Номер
15(8), С. 2323 - 2323
Опубликована: Апрель 16, 2023
Metastatic
tumors
cause
the
most
deaths
in
cancer
patients.
Treating
metastasis
remains
primary
goal
of
current
research.
Although
immune
system
prevents
and
kills
tumor
cells,
function
metastatic
has
been
unappreciated
for
decades
because
are
able
to
develop
complex
signaling
pathways
suppress
responses,
leading
them
escape
detection
elimination.
Studies
showed
NK
cell-based
therapies
have
many
advantages
promise
fighting
cancers.
We
here
review
progression,
specifically
focusing
on
ability
cells
antimetastasis,
how
cell
attack,
as
well
recent
development
effective
antimetastatic
immunotherapies.
British Journal of Cancer,
Год журнала:
2023,
Номер
129(8), С. 1212 - 1224
Опубликована: Июль 15, 2023
Abstract
Immune
checkpoint
therapies
(ICT)
can
reinvigorate
the
effector
functions
of
anti-tumour
T
cells,
improving
cancer
patient
outcomes.
Anti-tumour
cells
are
initially
formed
during
their
first
contact
(priming)
with
tumour
antigens
by
antigen-presenting
(APCs).
Unfortunately,
many
patients
refractory
to
ICT
because
tumours
considered
be
‘cold’
tumours—i.e.,
they
do
not
allow
generation
(so-called
‘desert’
tumours)
or
infiltration
existing
(T-cell-excluded
tumours).
Desert
disturb
antigen
processing
and
priming
targeting
APCs
suppressive
factors
derived
from
genetic
instabilities.
In
contrast,
T-cell-excluded
characterised
blocking
effective
lymphocytes
infiltrating
masses
obstacles,
such
as
fibrosis
tumour-cell-induced
immunosuppression.
This
review
delves
into
critical
mechanisms
which
induce
T-cell
‘desertification’
‘exclusion’
in
tumours.
Filling
gaps
our
knowledge
regarding
these
pro-tumoral
will
aid
researchers
developing
novel
class
immunotherapies
that
aim
at
restoring
more
efficient
leukocyte
trafficking.
Such
developments
expected
unleash
clinical
benefit
patients.
Cancers,
Год журнала:
2023,
Номер
15(13), С. 3474 - 3474
Опубликована: Июль 3, 2023
Non-small
cell
lung
cancer
(NSCLC)
is
a
significant
public
health
concern
with
high
mortality
rates.
Recent
advancements
in
genomic
data,
bioinformatics
tools,
and
the
utilization
of
biomarkers
have
improved
possibilities
for
early
diagnosis,
effective
treatment,
follow-up
NSCLC.
Biomarkers
play
crucial
role
precision
medicine
by
providing
measurable
indicators
disease
characteristics,
enabling
tailored
treatment
strategies.
The
integration
big
data
artificial
intelligence
(AI)
further
enhances
potential
personalized
through
advanced
biomarker
analysis.
However,
challenges
remain
impact
new
on
efficacy
due
to
limited
evidence.
Data
analysis,
interpretation,
adoption
approaches
clinical
practice
pose
additional
emphasize
technologies
such
as
analysis
(AI),
which
enhance
Despite
these
obstacles,
into
has
shown
promising
results
NSCLC,
improving
patient
outcomes
targeted
therapies.
Continued
research
discovery,
utilization,
evidence
generation
are
necessary
overcome
medicine.
Addressing
obstacles
will
contribute
continued
improvement
non-small
cancer.
Abstract
Cancer
nanovaccines
represent
a
promising
frontier
in
cancer
immunotherapy,
utilizing
nanotechnology
to
augment
traditional
vaccine
efficacy.
This
review
comprehensively
examines
the
current
state‐of‐the‐art
nanovaccine
development,
elucidating
innovative
strategies
and
technologies
employed
their
design.
It
explores
both
preclinical
clinical
advancements,
emphasizing
key
studies
demonstrating
potential
elicit
robust
anti‐tumor
immune
responses.
The
study
encompasses
various
facets,
including
integrating
biomaterial‐based
nanocarriers
for
antigen
delivery,
adjuvant
selection,
impact
of
nanoscale
properties
on
performance.
Detailed
insights
into
complex
interplay
between
tumor
microenvironment
responses
are
provided,
highlighting
challenges
opportunities
optimizing
therapeutic
outcomes.
Additionally,
presents
thorough
analysis
ongoing
trials,
presenting
snapshot
landscape.
By
curating
latest
scientific
findings
developments,
this
aims
serve
as
comprehensive
resource
researchers
clinicians
engaged
advancing
immunotherapy.
Integrating
design
holds
immense
promise
revolutionizing
treatment
paradigms,
provides
timely
update
evolving
landscape
nanovaccines.
Journal of Hematology & Oncology,
Год журнала:
2025,
Номер
18(1)
Опубликована: Янв. 13, 2025
The
tumor
microenvironment
(TME)
is
integral
to
cancer
progression,
impacting
metastasis
and
treatment
response.
It
consists
of
diverse
cell
types,
extracellular
matrix
components,
signaling
molecules
that
interact
promote
growth
therapeutic
resistance.
Elucidating
the
intricate
interactions
between
cells
TME
crucial
in
understanding
progression
challenges.
A
critical
process
induced
by
epithelial-mesenchymal
transition
(EMT),
wherein
epithelial
acquire
mesenchymal
traits,
which
enhance
their
motility
invasiveness
progression.
By
targeting
various
components
TME,
novel
investigational
strategies
aim
disrupt
TME's
contribution
EMT,
thereby
improving
efficacy,
addressing
resistance,
offering
a
nuanced
approach
therapy.
This
review
scrutinizes
key
players
emphasizing
avenues
therapeutically
components.
Moreover,
article
discusses
implications
for
resistance
mechanisms
highlights
current
toward
modulation
along
with
potential
caveats.
Cancer Biology & Therapy,
Год журнала:
2024,
Номер
25(1)
Опубликована: Фев. 22, 2024
While
the
emergence
of
immunotherapies
has
fundamentally
altered
management
solid
tumors,
cancers
exploit
many
complex
biological
mechanisms
that
result
in
resistance
to
these
agents.
These
encompass
a
broad
range
cellular
activities
-
from
modification
traditional
paradigms
immunity
via
antigen
presentation
and
immunoregulation
metabolic
modifications
manipulation
tumor
microenvironment.
Intervening
on
intricate
processes
may
provide
clinical
benefit
patients
with
tumors
by
overcoming
immunotherapies,
which
is
why
it
become
an
area
tremendous
research
interest
practice-changing
implications.
This
review
details
major
ways
avoid
both
natural
through
primary
(innate)
secondary
(acquired)
resistance,
considers
available
emerging
therapeutic
approaches
immunotherapy
resistance.
Journal of the American Chemical Society,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 2, 2025
Despite
the
promising
clinical
applications
of
immunotherapy,
its
effectiveness
is
often
limited
by
low
immune
responses
and
tumor
escape.
In
this
study,
we
introduce
a
simple
drug-free
inorganic
nanomaterial,
sodium
succinate
(C4H4Na2O4
NPs),
prepared
using
rapid
microemulsion
method
to
enhance
cancer
immunotherapy.
The
synthesized
C4H4Na2O4
NPs
can
release
high
concentrations
Na+
ions
into
cells,
leading
an
increase
in
intracellular
osmolarity.
This
triggers
pyroptosis
pathway,
resulting
cellular
contents,
inflammatory
factors,
damage-associated
molecular
patterns,
which
ultimately
boost
responses.
Furthermore,
inhibit
escape
through
upregulating
major
histocompatibility
complex-I
(MHC-I)
expression.
Collectively,
significantly
growth
metastasis
pyroptosis-induced
activation
MHC-I
expression
upregulation-remitted
research
offers
novel
approach
treatment
that
leverages
pyroptosis,
demonstrating
potential
for
application
Journal of Inflammation Research,
Год журнала:
2025,
Номер
Volume 18, С. 895 - 909
Опубликована: Янв. 1, 2025
Ovarian
cancer
(OC)
remains
one
of
the
most
lethal
gynecological
malignancies,
largely
due
to
its
late-stage
diagnosis
and
high
recurrence
rates.
Chronic
inflammation
is
a
critical
driver
OC
progression,
contributing
immune
evasion,
tumor
growth,
metastasis.
Inflammatory
cytokines,
including
IL-6,
TNF-α,
IL-8,
as
well
key
signaling
pathways
such
nuclear
factor
kappa
B
(NF-kB)
signal
transducer
activator
transcription
3
(STAT3),
are
upregulated
in
OC,
promoting
tumor-promoting
environment.
The
microenvironment
(TME)
characterized
by
cells
like
tumor-associated
macrophages
(TAMs)
regulatory
T
(Tregs),
which
suppress
anti-tumor
responses,
facilitating
evasion.
Furthermore,
utilize
checkpoint
pathways,
PD-1/PD-L1,
inhibit
cytotoxic
cell
activity.
Targeting
these
inflammatory
evasion
mechanisms
offers
promising
therapeutic
strategies.
COX-2
inhibitors,
Janus
kinase/signal
(JAK/STAT)
pathway
blockers,
NF-kB
inhibitors
have
shown
potential
preclinical
studies,
while
targeting
PD-1/PD-L1
CTLA-4
been
explored
with
mixed
results
OC.
Additionally,
emerging
research
on
microbiome
inflammation-related
biomarkers,
microRNAs
(miRNAs)
exosomes,
points
new
opportunities
for
early
detection
precision
medicine.
Future
approaches
treatment
must
focus
personalized
strategies
that
target
TME,
integrating
anti-inflammatory
therapies
immunotherapy
enhance
patient
outcomes.
Continued
into
interplay
between
essential
developing
effective,
long-lasting
treatments.