Current Cancer Reports,
Journal Year:
2024,
Volume and Issue:
6(1), P. 193 - 204
Published: July 2, 2024
Aims:
Nanotherapeutics
are
being
explored
as
a
potential
solution
to
treat
inflammation-induced
cancer.
enhance
innate
immune
cells'
immunity,
enabling
them
fight
tumors
effectively.
These
cells
secrete
specific
chemicals
like
cytokines,
allowing
replicate
quickly
and
respond
future
threats,
making
suitable
for
immunotherapy.Methods:
Nanotechnology
can
significantly
improve
human
health
by
enhancing
infection
detection,
prevention,
treatment.
Nanomedicines,
composed
of
restorative
imaging
compounds
in
submicrometer-sized
materials,
aim
deliver
effective
treatments
limit
inflammation
healthy
body
areas.
Combining
nanotechnology
clinical
sciences,
nanoparticles
gene
therapy
have
been
developed
treating
various
diseases,
including
cancer,
cardiovascular,
diabetes,
pulmonary,
inflammatory
diseases.Results:
Neutrophils
their
offspring,
films
extracellular
vehicles,
crucial
drug
transporters
enhanced
growth
therapy.
Tumor
microenvironment
inputs
modify
tumor-associated
neutrophils
(TANs),
which
essential
tumor
healing.
Human
intratumor
heterogeneity
is
Nanomedicines
shown
targeted
delivery,
toxicity
reduction,
therapeutic
effectiveness
enhancement.
However,
relevance
efficacy
remain
inadequate
due
lack
understanding
the
interaction
between
nanomaterials,
nanomedicine,
biology.
The
diverse
biological
milieu
impacts
dynamic
bioidentity
nanoformulations,
interactions
function
or
cellular
absorption.Conclusion:
holds
great
promise
improving
detecting,
preventing,
infections.
fusion
sciences
nanotechnology,
use
transporter
materials
delivery
reducing
contamination.
Nanoparticles'
small
size
high
surface-to-volume
ratio
benefit
Research
has
led
wide
range
nanomedicine
products
globally.
Journal of Hematology & Oncology,
Journal Year:
2025,
Volume and Issue:
18(1)
Published: Jan. 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.
MedComm,
Journal Year:
2025,
Volume and Issue:
6(2)
Published: Jan. 21, 2025
Abstract
Neutrophils,
the
most
abundant
circulating
leukocytes,
have
long
been
recognized
as
key
players
in
innate
immunity
and
inflammation.
However,
recent
discoveries
unveil
their
remarkable
heterogeneity
plasticity,
challenging
traditional
view
of
neutrophils
a
homogeneous
population
with
limited
functional
repertoire.
Advances
single‐cell
technologies
assays
revealed
distinct
neutrophil
subsets
diverse
phenotypes
functions
ability
to
adapt
microenvironmental
cues.
This
review
provides
comprehensive
overview
multidimensional
landscape
heterogeneity,
discussing
various
axes
along
which
diversity
manifests,
including
maturation
state,
density,
surface
marker
expression,
polarization.
We
highlight
molecular
mechanisms
underpinning
focusing
on
complex
interplay
signaling
pathways,
transcriptional
regulators,
epigenetic
modifications
that
shape
responses.
Furthermore,
we
explore
implications
plasticity
physiological
processes
pathological
conditions,
host
defense,
inflammation,
tissue
repair,
cancer.
By
integrating
insights
from
cutting‐edge
research,
this
aims
provide
framework
for
understanding
multifaceted
roles
potential
therapeutic
targets
wide
range
diseases.
Molecular Cancer,
Journal Year:
2025,
Volume and Issue:
24(1)
Published: Jan. 16, 2025
Neutrophils,
traditionally
considered
as
non-specific
components
of
the
innate
immune
system,
have
garnered
considerable
research
interest
due
to
their
dual
roles
in
both
promoting
and
inhibiting
tumor
progression.
This
paper
seeks
clarify
specific
mechanisms
by
which
neutrophils
play
a
bidirectional
role
immunity
factors
that
influence
these
roles.
By
conducting
comprehensive
analysis
synthesis
vast
array
relevant
literature,
it
has
become
evident
can
development
invasive
migration
through
various
mechanisms,
thereby
exerting
anti-tumor
effects.
Conversely,
they
also
facilitate
tumorigenesis
proliferation,
well
affect
normal
physiological
functions
other
cells,
thus
pro-tumor
Moreover,
are
influenced
cells
unique
microenvironment,
turn
affects
heterogeneity
plasticity.
Neutrophils
interact
with
regulate
aspects
life
activities
precisely.
identifies
unresolved
issues
concerning
development,
offering
new
opportunities
challenges
for
advancing
our
understanding.
This,
turn,
aid
proper
application
insights
clinical
treatment
strategies.
Cancers,
Journal Year:
2025,
Volume and Issue:
17(3), P. 384 - 384
Published: Jan. 24, 2025
Neutrophils,
the
most
abundant
circulating
white
blood
cells,
are
essential
for
initial
immune
response
to
infection
and
injury.
Emerging
research
reveals
a
dualistic
function
of
neutrophils
in
cancer,
where
they
can
promote
or
inhibit
tumor
progression.
This
dichotomy
is
influenced
by
microenvironment,
with
capable
remodeling
extracellular
matrix,
promoting
angiogenesis,
alternatively
inducing
cancer
cell
death
enhancing
responses.
An
intriguing
yet
poorly
understood
aspect
neutrophil–cancer
interactions
phenomenon
neutrophil
engulfment
which
has
been
observed
across
various
cancers.
process,
potentially
mediated
LC3-associated
phagocytosis
(LAP),
raises
questions
about
whether
it
serves
as
mechanism
evasion
contributes
through
pathways
like
ferroptosis.
review
examines
current
knowledge
on
development,
their
roles
mechanisms
LAP
cells.
We
discuss
how
manipulating
impacts
progression
may
represent
therapeutic
strategy.
also
explore
neutrophils’
potential
delivery
vehicles
agents.
Understanding
complex
functions
tumor-associated
(TANs)
molecular
underlying
open
new
avenues
effective
interventions
mitigate
risks.
Journal of Experimental & Clinical Cancer Research,
Journal Year:
2025,
Volume and Issue:
44(1)
Published: March 15, 2025
Abstract
In
the
last
two
decades,
novel
and
promising
cell-based
therapies
have
populated
treatment
landscape
for
haematological
tumors.
However,
commonly
exploited
T
NK
show
limited
applicability
to
solid
This
is
mainly
given
by
impaired
tumor
trafficking
capability
effector
activity
of
these
cells
within
a
highly
immunosuppressive
microenvironment.
Myeloid
spontaneously
home
tumors
can
thus
be
reprogrammed
and/or
engineered
directly
attack
or
locally
selectively
deliver
therapeutically
relevant
payloads
that
may
improve
efficacy
immunotherapy
against
difficult-to-access
context
myeloid
therapies,
adoptive
transfer
monocytes
has
often
been
overshadowed
infusion
differentiated
macrophages
hematopoietic
stem
cell
transplantation
despite
their
therapeutic
potential.
Here,
we
summarize
recent
improvements
benefits
using
tumors,
current
clinical
applications
challenges
use
as
well
some
possible
strategies
overcome
them.
Advanced Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 12, 2025
Abstract
Tumor
heterogeneity
remains
a
formidable
obstacle
in
targeted
cancer
therapy,
often
leading
to
suboptimal
treatment
outcomes.
This
study
presents
an
innovative
approach
that
harnesses
controlled
inflammation
guide
neutrophil‐mediated
drug
delivery,
effectively
overcoming
the
limitations
imposed
by
tumor
heterogeneity.
By
inducing
localized
within
tumors
using
lipopolysaccharide,
it
significantly
amplify
recruitment
of
drug‐laden
neutrophils
sites,
irrespective
specific
markers.
strategy
not
only
enhances
delivery
but
also
triggers
release
neutrophil
extracellular
traps,
further
potentiating
anti‐tumor
effect.
Crucially,
this
demonstrates
potential
systemic
inflammatory
responses
can
be
mitigated
through
transfusion,
ensuring
safety
and
clinical
viability
approach.
In
murine
breast
model,
method
impedes
growth
compared
conventional
treatments.
work
offers
versatile
for
precise
across
diverse
types.
The
findings
pave
way
more
effective
broadly
applicable
treatments,
potentially
addressing
long‐standing
challenge
Advanced Healthcare Materials,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 15, 2025
Immune
cells
show
enormous
potential
for
targeted
nanoparticle
delivery
due
to
their
intrinsic
tumor-homing
skills.
However,
the
immune
can
internalize
nanoparticles,
leading
cellular
functional
impairments,
degradation
of
and
delayed
release
drugs
from
cells.
To
address
these
issues,
this
study
introduces
an
approach
synthesis
freshly
derived
neutrophils
(NUs)-based
nanocarriers
system
where
NUs
are
surfaced
by
dialdehyde
alginate-coated
self-assembled
micelles
loaded
with
mitoxantrone
(MIT)
indocyanine
green
(ICG)
(i.e.,
dA(MI@IPM)s)
stimuli-responsive
tumor-targeted
therapy.
Here,
dA(MI@IPM)s
not
internalized
NUs,
but
they
anchored
on
membrane
via
distearoylphosphatidylethanolamine-polyethylene
glycol-polyethylenimine
anchors.
Owing
natural
recruitment
ability
tumor
microenvironment,
NUs-anchored
accumulation
is
higher
at
site
than
free
dA(MI@IPM)s,
readily
detach
get
in
The
disassembles
inside
cancer
upon
near-infrared
irradiation
photosensitizing
effect
ICG,
releasing
MIT
significantly
inhibiting
growth.
This
simple
fast
prepare,
opening
up
exciting
possibilities
personalized
treatment
using
patient's
autologous
NUs.