European Journal of Nuclear Medicine and Molecular Imaging,
Journal Year:
2022,
Volume and Issue:
49(13), P. 4616 - 4641
Published: July 5, 2022
Abstract
Targeted
radionuclide
theranostics
is
becoming
more
and
prominent
in
clinical
oncology.
Currently,
most
nuclear
medicine
compounds
researched
for
cancer
are
directed
towards
targets
expressed
only
a
small
subset
of
types,
limiting
applicability.
The
identification
cancer-specific
that
(more)
universally
will
allow
patients
to
benefit
from
these
personalized
medicine–based
interventions.
A
tumor
not
merely
collection
cells,
it
also
comprises
supporting
stromal
cells
embedded
an
altered
extracellular
matrix
(ECM),
together
forming
the
microenvironment
(TME).
Since
TME
less
genetically
unstable
than
phenotypes
can
be
shared
between
offers
expressed.
characterized
by
presence
processes
such
as
hypoxia,
acidity,
increased
metabolism.
Next
ECM,
consists
cancer-associated
fibroblasts
(CAFs),
macrophages,
endothelial
neo-vasculature,
immune
adipocytes
(CAAs).
Radioligands
at
processes,
cellular
components
have
been
developed
evaluated
preclinical
studies
targeted
imaging
and/or
therapy.
In
this
review,
we
provide
overview
their
corresponding
radioligands.
addition,
discuss
what
developments
needed
further
explore
target
theranostics,
with
hopes
stimulating
development
novel
radioligands
multi-cancer,
or
some
cases
even
pan-cancer,
application.
Biomedicine & Pharmacotherapy,
Journal Year:
2023,
Volume and Issue:
165, P. 115199 - 115199
Published: July 28, 2023
Chronic
wounds
and
scar
formation
are
widespread
due
to
limited
suitable
remedies.
The
macrophage
is
a
crucial
regulator
in
wound
healing,
controlling
the
onset
termination
of
inflammation
regulating
other
processes
related
healing.
current
breakthroughs
developing
new
medications
drug
delivery
methods
have
enabled
accurate
targeting
macrophages
oncology
rheumatic
disease
therapies
through
clinical
trials.
These
successes
cleared
way
utilize
drugs
various
disorders.
This
review
thus
summarizes
involvement
normal
pathologic
It
further
details
targets
available
for
intervention
therapeutic
strategies
behavior
tissue
repair
regeneration.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(14), P. 11251 - 11251
Published: July 8, 2023
Neuroinflammation
is
a
common
pathological
feature
of
amyotrophic
lateral
sclerosis
(ALS).
Although
scientific
evidence
to
date
does
not
allow
defining
neuroinflammation
as
an
ALS
trigger,
its
role
in
exacerbating
motor
neuron
(MNs)
degeneration
and
disease
progression
attracting
research
interest.
Activated
CNS
(Central
Nervous
System)
glial
cells,
proinflammatory
peripheral
infiltrated
T
lymphocytes
monocytes/macrophages,
well
the
immunoreactive
molecules
they
release,
represent
active
players
for
immune
dysregulation
enhancing
neuroinflammation.
The
crosstalk
between
cells
significantly
correlates
with
survival
patients
since
modification
macrophages
can
downregulate
inflammation
at
periphery
along
nerves
CNS.
As
putative
vehicles
misfolded
protein
inflammatory
mediators
extracellular
vesicles
(EVs)
have
also
drawn
particular
attention
field
ALS.
Both
release
EVs,
which
are
able
modulate
behavior
neighboring
recipient
cells;
unfortunately,
mechanisms
involved
EVs-mediated
communication
remain
unclear.
This
review
aims
synthesize
current
literature
regarding
EV-mediated
cell-to-cell
brain
under
ALS,
point
view
on
responding
understand
biological
process
exploit
it
management.
Frontiers in Oncology,
Journal Year:
2021,
Volume and Issue:
10
Published: Feb. 24, 2021
Hepatocellular
carcinoma
(HCC)
is
the
most
common
primary
malignancy
of
liver
and
a
leading
cause
death
in
US
worldwide.
HCC
remains
global
health
problem
highly
aggressive
with
unfavorable
prognosis.
Even
surgical
interventions
newer
medical
treatment
regimens,
patients
have
poor
survival
rates.
These
limited
therapeutic
strategies
mechanistic
understandings
immunopathogenesis
urgently
warrant
non-palliative
measures.
Irrespective
multitude
etiologies,
microenvironment
intricately
associated
chronic
necroinflammation,
progressive
fibrosis,
cirrhosis
as
precedent
events
along
dysregulated
innate
adaptive
immune
responses.
Central
to
these
immunological
networks
complement
cascade
(CC),
fundamental
defense
system
inherent
which
tightly
regulates
humoral
cellular
responses
noxious
stimuli.
Importantly,
source
for
biosynthesis
>80%
components
expresses
variety
receptors.
Recent
studies
implicate
inflammation,
abnormal
regenerative
responses,
carcinogenesis,
development
HCC.
Although
activation
differentially
promotes
immunosuppressive,
stimulant,
angiogenic
microenvironments
conducive
development,
it
under-investigated.
Here,
we
review
derangement
specific
proteins
context
altered
regulatory
factors,
immune-activating
components,
their
implications
disease
pathogenesis.
We
also
summarize
how
molecules
regulate
cancer
stem
cells
(CSCs),
interact
complement-coagulation
cascades,
provide
opportunities
targeted
intervention
Oral Oncology,
Journal Year:
2022,
Volume and Issue:
135, P. 106227 - 106227
Published: Nov. 3, 2022
Head
and
neck
squamous
cell
carcinoma
(HNSCC)
is
an
immunogenic
cancer
type,
tumor
associated
macrophages
(TAMs)
are
a
major
component
of
the
microenvironment
(TME).
In
this
systematic
review
meta-analysis,
studies
assessing
infiltration
with
CD68+,
iNOS+,
HLA-DR+,
CD11b+,
CD163+,
CD206+,
CD204+TAMs
were
included,
correlation
to
survival
hazard
was
studied.
A
low
number
CD68+TAMs
correlated
better
overall
(OS)
in
multivariate
analysis
(HR
1.36
95
%CI
(1.07-1.72)
P
=
.01).
did
not
correlate
disease
free
(DFS),
specific
(DSS),
progression
(PFS),
or
recurrence
(RFS).
CD163+TAMs
OS
uni-
(resp.
HR
2.65
(1.57-4.46)
.01
2.42
(1.72-3.41)
<
.001).
also
DFS
PFS,
whereas
only
PFS.
While
IHC
pan
macrophage
marker
CD68
M2-like
CD163
both
show
prognostic
utility
OS,
stronger
prognosticator,
as
indicated
by
meta-analysis.
PFS;
outcomes
that
more
relevant
patients,
thus
showing
promising
results
for
future
clinical
implementation.
European Journal of Nuclear Medicine and Molecular Imaging,
Journal Year:
2022,
Volume and Issue:
49(13), P. 4616 - 4641
Published: July 5, 2022
Abstract
Targeted
radionuclide
theranostics
is
becoming
more
and
prominent
in
clinical
oncology.
Currently,
most
nuclear
medicine
compounds
researched
for
cancer
are
directed
towards
targets
expressed
only
a
small
subset
of
types,
limiting
applicability.
The
identification
cancer-specific
that
(more)
universally
will
allow
patients
to
benefit
from
these
personalized
medicine–based
interventions.
A
tumor
not
merely
collection
cells,
it
also
comprises
supporting
stromal
cells
embedded
an
altered
extracellular
matrix
(ECM),
together
forming
the
microenvironment
(TME).
Since
TME
less
genetically
unstable
than
phenotypes
can
be
shared
between
offers
expressed.
characterized
by
presence
processes
such
as
hypoxia,
acidity,
increased
metabolism.
Next
ECM,
consists
cancer-associated
fibroblasts
(CAFs),
macrophages,
endothelial
neo-vasculature,
immune
adipocytes
(CAAs).
Radioligands
at
processes,
cellular
components
have
been
developed
evaluated
preclinical
studies
targeted
imaging
and/or
therapy.
In
this
review,
we
provide
overview
their
corresponding
radioligands.
addition,
discuss
what
developments
needed
further
explore
target
theranostics,
with
hopes
stimulating
development
novel
radioligands
multi-cancer,
or
some
cases
even
pan-cancer,
application.