International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(20), P. 15332 - 15332
Published: Oct. 18, 2023
Breast
cancer
(BC),
one
of
the
most
widespread
and
devastating
diseases
affecting
women
worldwide,
presents
a
significant
public
health
challenge.
This
review
explores
emerging
frontiers
research
focused
on
deciphering
intricate
interplay
between
BC
cells
immune
microenvironment.
Understanding
role
system
in
is
critical
as
it
holds
promise
for
novel
therapeutic
approaches
precision
medicine
strategies.
delves
into
current
literature
regarding
microenvironment's
contribution
to
initiation,
progression,
metastasis.
It
examines
complex
mechanisms
by
which
interact
with
various
cell
populations,
including
tumor-infiltrating
lymphocytes
(TILs)
tumor-associated
macrophages
(TAMs).
Furthermore,
this
highlights
impact
immune-related
factors,
such
cytokines
checkpoint
molecules.
Additionally,
comprehensive
analysis
sheds
light
potential
biomarkers
associated
response
BC,
enabling
early
diagnosis
prognostic
assessment.
The
implications
targeting
microenvironment
are
also
explored,
encompassing
immunotherapeutic
strategies
combination
therapies
enhance
treatment
efficacy.
significance
lies
its
pave
way
interventions,
providing
clinicians
researchers
essential
knowledge
design
targeted
personalized
regimens
patients.
Frontiers in Chemistry,
Journal Year:
2021,
Volume and Issue:
9
Published: Aug. 2, 2021
Photodynamic
therapy
(PDT)
has
been
used
as
an
anti-tumor
treatment
method
for
a
long
time
and
photosensitizers
(PS)
can
be
in
various
types
of
tumors.
Originally,
light
is
effective
tool
that
the
diseases
ages.
The
effects
combination
specific
dyes
with
illumination
was
demonstrated
at
beginning
20th
century
novel
PDT
approaches
have
developed
ever
since.
Main
strategies
current
studies
are
to
reduce
off-target
improve
pharmacokinetic
properties.
Given
high
interest
vast
literature
about
topic,
approval
first
drug/device
by
FDA
should
come
no
surprise.
consists
two
stages
treatment,
combining
energy
PS
order
destruct
tumor
cells
after
activation
light.
In
general,
fewer
side
toxicity
than
chemotherapy
and/or
radiotherapy.
addition
purpose
several
PSs
diagnostic
purposes
Such
called
photodynamic
diagnosis
(PDD).
this
Review,
we
provide
general
overview
clinical
applications
cancer,
including
therapeutic
approaches.
Assessment
efficacy
clinic
will
discussed,
since
identifying
predictors
determine
response
crucial.
addition,
examples
tumors
discussed.
Furthermore,
other
modalities
such
chemotherapy,
radiotherapy,
surgery
immunotherapy
emphasized,
seem
promising
terms
enhancing
effectiveness
against
tumor.
treatments
may
yield
better
results
single
treatments.
Moreover,
utilization
lower
doses
setting
cause
less
therapy.
A
understanding
well
optimization
complex
multimodal
expand
PDT.
Molecular Cancer,
Journal Year:
2022,
Volume and Issue:
21(1)
Published: Nov. 2, 2022
Tumors
are
comprised
of
both
cancer
cells
and
surrounding
stromal
components.
As
an
essential
part
the
tumor
microenvironment,
stroma
is
highly
dynamic,
heterogeneous
commonly
tumor-type
specific,
it
mainly
includes
noncellular
compositions
such
as
extracellular
matrix
unique
cancer-associated
vascular
system
well
a
wide
variety
cellular
components
including
activated
fibroblasts,
mesenchymal
cells,
pericytes.
All
these
elements
operate
with
each
other
in
coordinated
fashion
collectively
promote
initiation,
progression,
metastasis
therapeutic
resistance.
Over
past
few
decades,
numerous
studies
have
been
conducted
to
study
interaction
crosstalk
between
neoplastic
cells.
Meanwhile,
we
also
witnessed
exponential
increase
investigation
recognition
critical
roles
solid
tumors.
A
series
clinical
trials
targeting
launched
continually.
In
this
review,
introduce
discuss
current
advances
understanding
various
their
cancers.
We
elaborate
on
potential
novel
approaches
for
tumor-stroma-based
targeting,
aim
leap
from
bench
bedside.
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: Feb. 13, 2023
The
tumor
microenvironment
(TME)
in
pancreatic
ductal
adenocarcinoma
(PDAC)
is
a
complex
ecosystem
that
drives
progression;
however,
in-depth
single
cell
characterization
of
the
PDAC
TME
and
its
role
response
to
therapy
lacking.
Here,
we
perform
single-cell
RNA
sequencing
on
freshly
collected
human
samples
either
before
or
after
chemotherapy.
Overall,
find
heterogeneous
mixture
basal
classical
cancer
subtypes,
along
with
distinct
cancer-associated
fibroblast
macrophage
subpopulations.
Strikingly,
basal-like
cells
exhibit
similar
transcriptional
responses
chemotherapy
do
not
demonstrate
shift
towards
program
among
treated
samples.
We
observe
decreased
ligand-receptor
interactions
samples,
particularly
between
TIGIT
CD8
+
T
receptor
cells,
identify
as
major
inhibitory
checkpoint
molecule
cells.
Our
results
suggest
profoundly
impacts
may
promote
resistance
immunotherapy.
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: Nov. 16, 2023
Cancer
progression
is
primarily
caused
by
interactions
between
transformed
cells
and
the
components
of
tumor
microenvironment
(TME).
TAMs
(tumor-associated
macrophages)
make
up
majority
invading
immune
components,
which
are
further
categorized
as
anti-tumor
M1
pro-tumor
M2
subtypes.
While
known
to
have
anti-cancer
properties,
recognized
extend
a
protective
role
tumor.
As
result,
manipulates
TME
in
such
way
that
it
induces
macrophage
infiltration
switching
bias
secure
its
survival.
This
M2-TAM
promotes
cancer
cell
proliferation,
neoangiogenesis,
lymphangiogenesis,
epithelial-to-mesenchymal
transition,
matrix
remodeling
for
metastatic
support,
manipulation
an
immunosuppressive
state.
additionally
promote
emergence
stem
(CSCs),
their
ability
originate,
metastasize,
relapse
into
tumors.
CSCs
also
help
revealing
escape
survival
strategies
during
initiation
phases.
review
describes
reasons
immunotherapy
failure
and,
thereby,
devises
better
impair
tumor-TAM
crosstalk.
study
will
shed
light
on
understudied
TAM-mediated
address
much-needed
holistic
approach
therapy,
encompasses
targeting
cells,
CSCs,
all
at
same
time.
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: Sept. 19, 2023
Abstract
The
tumor
microenvironment
(TME)
is
comprised
of
non-malignant
cells
that
interact
with
each
other
and
cancer
cells,
critically
impacting
biology.
TME
complex,
understanding
it
requires
simplifying
approaches.
Here
we
provide
an
experimental-mathematical
approach
to
decompose
the
into
small
circuits
interacting
cell
types.
We
find,
using
female
breast
single-cell-RNA-sequencing
data,
a
hierarchical
network
interactions,
cancer-associated
fibroblasts
(CAFs)
at
top
secreting
factors
primarily
tumor-associated
macrophages
(TAMs).
This
composed
repeating
circuit
motifs.
isolate
strongest
two-cell
motif
by
culturing
in-vitro,
analyze
their
dynamics
transcriptomes.
isolated
recapitulates
hierarchy
in-vivo
enables
testing
effect
ligand-receptor
interactions
on
function,
as
demonstrate
identifying
mediator
CAF-TAM
-
RARRES2,
its
receptor
CMKLR1.
Thus,
complexity
may
be
simplified
circuits,
facilitating
development
strategies
modulate
TME.
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: April 6, 2022
The
tumor
microenvironment
(TME)
plays
a
critical
role
in
tumorigenesis
and
is
comprised
of
different
components,
including
cells,
stromal
immune
cells.
Among
them,
the
relationship
between
each
mediator
involved
construction
TME
can
be
understood
by
focusing
on
secreting
or
expressing
factors
from
Therefore,
understanding
various
interactions
cellular
component
necessary
for
precise
therapeutic
approaches.
In
carcinoma,
cells
are
well
known
to
influence
extracellular
matrix
(ECM)
formation
progression
through
multiple
mediators.
Immune
respond
causing
cytotoxicity
inflammatory
responses.
However,
they
escape
immunoregulatory
mechanisms.
general,
anti-cancer
therapy
has
mainly
been
focused
cancer
themselves
specific
cell
components.
directly
indirectly
other
partners,
members
such
as
also
participate
organization
their
mutual
communication.
this
review,
we
summarized
discussed
positive
negative
relationships
point
view
development
use
research
applications
strategies.
Frontiers in Cell and Developmental Biology,
Journal Year:
2023,
Volume and Issue:
11
Published: Jan. 30, 2023
Stromal
heterogeneity
of
tumor
microenvironment
(TME)
plays
a
crucial
role
in
malignancy
and
therapeutic
resistance.
Cancer-associated
fibroblasts
(CAFs)
are
one
the
major
players
stroma.
The
heterogeneous
sources
origin
subsequent
impacts
crosstalk
with
breast
cancer
cells
flaunt
serious
challenges
before
current
therapies
to
cure
triple-negative
(TNBC)
other
cancers.
positive
reciprocal
feedback
CAFs
induce
dictates
their
mutual
synergy
establishing
malignancy.
Their
substantial
creating
tumor-promoting
niche
has
reduced
efficacy
several
anti-cancer
treatments,
including
radiation,
chemotherapy,
immunotherapy,
endocrine
therapy.
Over
years,
there
been
an
emphasis
on
understanding
CAF-induced
resistance
order
enhance
therapy
results.
CAFs,
majority
cases,
employ
crosstalk,
stromal
management,
strategies
generate
resilience
surrounding
cells.
This
emphasizes
significance
developing
novel
that
target
particular
CAF
subpopulations,
which
will
improve
treatment
sensitivity
impede
growth.
In
this
review,
we
discuss
progression,
altering
response
agents
cancer.
addition,
also
potential
possible
approaches
for
CAF-mediated
therapies.
Frontiers in Pharmacology,
Journal Year:
2023,
Volume and Issue:
14
Published: March 14, 2023
Cancer
immunotherapy
has
opened
a
new
landscape
in
cancer
treatment,
however,
the
poor
specificity
and
resistance
of
most
targeted
therapeutics
have
limited
their
therapeutic
efficacy.
In
recent
years,
role
CAFs
immune
regulation
been
increasingly
noted
as
more
evidence
uncovered
regarding
link
between
cancer-associated
fibroblasts
(CAFs)
evolutionary
process
tumor
progression.
interact
with
cells
to
shape
microenvironment
(TIME)
that
favors
malignant
progression,
crosstalk
leads
failure
immunotherapies.
this
review,
we
outline
advances
immunosuppressive
function
CAFs,
highlight
mechanisms
CAFs-immune
cell
interactions,
discuss
current
CAF-targeted
strategies
for
future
study.