Cell Death Discovery,
Journal Year:
2024,
Volume and Issue:
10(1)
Published: March 7, 2024
Abstract
Colorectal
cancer
(CRC)
is
a
malignancy
that
widely
prevalent
worldwide.
Due
to
its
unsatisfactory
treatment
outcome
and
extremely
poor
prognosis,
many
studies
on
the
molecular
mechanisms
pathological
of
CRC
have
been
published
in
recent
years.
The
tumor
microenvironment
(TME)
an
important
feature
tumorigenesis
one
hallmarks
development.
Metabolic
reprogramming
currently
hot
topic
research,
this
provided
insights
into
In
particular,
metabolic
causes
changes
composition
energy
nutrients
TME.
Furthermore,
it
can
alter
complex
crosstalk
between
immune
cells
associated
factors,
such
as
macrophages
T
cells,
which
play
roles
TME,
turn
affecting
escape
tumors
by
altering
surveillance.
review,
we
summarize
several
metabolism-related
processes
tumors.
Our
results
showed
regulated
influences
development
CRC.
Frontiers in Immunology,
Journal Year:
2020,
Volume and Issue:
11
Published: Dec. 3, 2020
Tumor-associated
macrophages
(TAMs)
represent
one
of
the
main
tumor-infiltrating
immune
cell
types
and
are
generally
categorized
into
either
two
functionally
contrasting
subtypes,
namely
classical
activated
M1
alternatively
M2
macrophages.
The
former
typically
exerts
anti-tumor
functions,
including
directly
mediate
cytotoxicity
antibody-dependent
cell-mediated
(ADCC)
to
kill
tumor
cells;
latter
can
promote
occurrence
metastasis
cells,
inhibit
T
response,
angiogenesis,
lead
progression.
Both
have
high
degree
plasticity
thus
be
converted
each
other
upon
microenvironment
changes
or
therapeutic
interventions.
As
relationship
between
TAMs
malignant
tumors
becoming
clearer,
become
a
promising
target
for
developing
new
cancer
treatment.
In
this
review,
we
summarize
origin
TAMs,
interaction
with
microenvironment,
up-to-date
treatment
strategies
targeting
TAMs.
Cell Death and Disease,
Journal Year:
2020,
Volume and Issue:
11(2)
Published: Feb. 6, 2020
Lipid
droplets
(also
known
as
lipid
bodies)
are
lipid-rich,
cytoplasmic
organelles
that
play
important
roles
in
cell
signaling,
metabolism,
membrane
trafficking,
and
the
production
of
inflammatory
mediators.
droplet
biogenesis
is
a
regulated
process,
accumulation
these
within
leukocytes,
epithelial
cells,
hepatocytes,
other
nonadipocyte
cells
frequently
observed
phenotype
several
physiologic
or
pathogenic
situations
thoroughly
described
during
conditions.
Moreover,
recent
years,
studies
have
an
increase
intracellular
different
neoplastic
processes,
although
it
not
clear
whether
directly
involved
establishment
types
malignancies.
This
review
discusses
current
evidence
related
to
biogenesis,
composition
functions
hallmarks
cancer:
inflammation,
increased
proliferation,
escape
from
death,
hypoxia.
potential
markers
disease
targets
for
novel
anti-inflammatory
antineoplastic
therapies
will
be
discussed.
Theranostics,
Journal Year:
2020,
Volume and Issue:
11(3), P. 1016 - 1030
Published: Nov. 6, 2020
Macrophages
phagocytize
pathogens
to
initiate
innate
immunity
and
products
from
the
tumor
microenvironment
(TME)
mediate
immunity.
The
loss
of
tumor-associated
macrophage
(TAM)-mediated
immune
responses
results
in
suppression.
To
reverse
this
disorder,
regulatory
mechanism
TAMs
TME
needs
be
clarified.
Immune
molecules
(cytokines
chemokines)
have
been
widely
accepted
as
mutual
mediators
signal
transduction
past
few
decades.
Recently,
researchers
tried
seek
intrinsic
TAM
phenotypic
functional
changes
through
metabolic
connections.
Numerous
metabolites
derived
identified
that
induce
cell-cell
crosstalk
with
TAMs.
bulk
cells,
stromal
cells
produce
are
involved
regulation
Meanwhile,
some
regulate
biological
functions
well.
Here,
we
review
recent
reports
demonstrating
between
MedComm,
Journal Year:
2020,
Volume and Issue:
2(1), P. 27 - 59
Published: Dec. 24, 2020
Dysregulated
lipid
metabolism
represents
an
important
metabolic
alteration
in
cancer.
Fatty
acids,
cholesterol,
and
phospholipid
are
the
three
most
prevalent
lipids
that
act
as
energy
producers,
signaling
molecules,
source
material
for
biogenesis
of
cell
membranes.
The
enhanced
synthesis,
storage,
uptake
contribute
to
cancer
progression.
rewiring
has
been
linked
activation
oncogenic
pathways
cross
talk
with
tumor
microenvironment.
resulting
activity
favors
survival
proliferation
cells
harsh
conditions
within
tumor.
Lipid
also
plays
a
vital
role
immunogenicity
via
effects
on
function
noncancer
microenvironment,
especially
immune-associated
cells.
Targeting
altered
shown
potential
promising
anticancer
therapy.
Here,
we
review
recent
evidence
implicating
contribution
reprogramming
progression,
discuss
molecular
mechanisms
underlying
cancer,
therapeutic
strategies
directed
toward
This
sheds
new
light
fully
understanding
context
provides
valuable
clues
targeting
Nature Communications,
Journal Year:
2022,
Volume and Issue:
13(1)
Published: Oct. 2, 2022
Liver
metastasis
is
highly
aggressive
and
treatment-refractory,
partly
due
to
macrophage-mediated
immune
suppression.
Understanding
the
mechanisms
leading
functional
reprogramming
of
macrophages
in
tumor
microenvironment
(TME)
will
benefit
cancer
immunotherapy.
Herein,
we
find
that
scavenger
receptor
CD36
upregulated
metastasis-associated
(MAMs)
deletion
MAMs
attenuates
liver
mice.
contain
more
lipid
droplets
have
unique
capability
engulfing
cell-derived
long-chain
fatty
acids,
which
are
carried
by
extracellular
vesicles.
The
lipid-enriched
vesicles
preferentially
partitioned
into
via
CD36,
fuel
trigger
their
tumor-promoting
activities.
In
patients
with
metastases,
high
expression
correlates
protumoral
M2-type
infiltration,
creating
a
immunosuppressive
TME.
Collectively,
our
findings
uncover
mechanism
cells
metabolically
interact
TME,
suggest
therapeutic
potential
targeting
as
immunotherapy
for
metastasis.
Frontiers in Immunology,
Journal Year:
2021,
Volume and Issue:
12
Published: April 23, 2021
Macrophages
are
crucial
innate
immune
cells
that
maintain
tissue
homeostasis
and
defend
against
pathogens;
however,
their
infiltration
into
tumors
has
been
associated
with
adverse
outcomes.
Tumor-associated
macrophages
(TAMs)
represent
a
significant
component
of
the
inflammatory
infiltrate
in
breast
tumors,
extensive
TAMs
linked
to
poor
prognosis
cancer.
Here,
we
detail
how
impede
productive
tumor
immunity
cycle
by
limiting
antigen
presentation
reducing
activation
cytotoxic
T
lymphocytes
(CTLs)
while
simultaneously
supporting
cell
survival,
angiogenesis,
metastasis.
There
is
an
urgent
need
overcome
TAM-mediated
suppression
for
durable
anti-tumor
To
date,
failure
fully
characterize
TAM
biology
classify
multiple
subsets
hindered
advancement
therapeutic
targeting.
In
this
regard,
complexity
recently
taken
center
stage
owing
subset
diversity
tightly
regulated
molecular
metabolic
phenotypes.
review,
reveal
major
gaps
our
knowledge
functional
phenotypic
characterization
cancer,
before
after
treatment.
Future
work
subsets,
location,
crosstalk
neighboring
will
be
critical
counteract
pro-tumor
functions
identify
novel
TAM-modulating
strategies
combinations
likely
enhance
current
therapies
chemo-
immuno-therapy
resistance.