Frontiers in Oncology,
Journal Year:
2023,
Volume and Issue:
13
Published: Jan. 27, 2023
Cyclooxygenases-2
(COX-2)
and
Prostaglandin
E2
(PGE2),
which
are
important
in
chronic
inflammatory
diseases,
can
increase
tumor
incidence
promote
growth
metastasis.
PGE2
binds
to
various
prostaglandin
E
receptors
activate
specific
downstream
signaling
pathways
such
as
PKA
pathway,
β-catenin
NF-κB
pathway
PI3K/AKT
all
of
play
roles
biological
pathological
behavior.
Nonsteroidal
anti-inflammatory
drugs
(NSAIDs),
COX-2
inhibitors,
EP
antagonists
anti-tumor
immune
evasion.
The
COX-2-PGE2
promotes
evasion
by
regulating
myeloid-derived
suppressor
cells,
lymphocytes
(CD8+
T
CD4+
cells
natural
killer
cells),
antigen
presenting
(macrophages
dendritic
cells).
Based
on
conventional
treatment,
the
addition
inhibitors
or
may
enhance
immunotherapy
response
escape.
However,
there
still
a
lot
challenges
cancer
immunotherapy.
In
this
review,
we
focus
how
affects
tumor-associated
cells.
Molecular Cancer,
Journal Year:
2023,
Volume and Issue:
22(1)
Published: Feb. 21, 2023
Abstract
Lung
cancer
is
the
primary
cause
of
mortality
in
United
States
and
around
globe.
Therapeutic
options
for
lung
treatment
include
surgery,
radiation
therapy,
chemotherapy,
targeted
drug
therapy.
Medical
management
often
associated
with
development
resistance
leading
to
relapse.
Immunotherapy
profoundly
altering
approach
owing
its
tolerable
safety
profile,
sustained
therapeutic
response
due
immunological
memory
generation,
effectiveness
across
a
broad
patient
population.
Different
tumor-specific
vaccination
strategies
are
gaining
ground
cancer.
Recent
advances
adoptive
cell
therapy
(CAR
T,
TCR,
TIL),
clinical
trials
on
cancer,
hurdles
discussed
this
review.
patients
(without
targetable
oncogenic
driver
alteration)
reveal
significant
responses
when
treated
programmed
death-1/programmed
death-ligand
1
(PD-1/PD-L1)
checkpoint
blockade
immunotherapies.
Accumulating
evidence
indicates
that
loss
effective
anti-tumor
immunity
tumor
evolution.
vaccines
combined
immune
inhibitors
(ICI)
can
achieve
better
effects.
To
end,
present
article
encompasses
detailed
overview
recent
developments
immunotherapeutic
landscape
targeting
small
(SCLC)
non-small
(NSCLC).
Additionally,
review
also
explores
implication
nanomedicine
immunotherapy
as
well
combinatorial
application
traditional
along
regimens.
Finally,
ongoing
trials,
obstacles,
future
outlook
strategy
highlighted
boost
further
research
field.
Signal Transduction and Targeted Therapy,
Journal Year:
2024,
Volume and Issue:
9(1)
Published: July 17, 2024
Traditional
therapeutic
approaches
such
as
chemotherapy
and
radiation
therapy
have
burdened
cancer
patients
with
onerous
physical
psychological
challenges.
Encouragingly,
the
landscape
of
tumor
treatment
has
undergone
a
comprehensive
remarkable
transformation.
Emerging
fervently
pursued
modalities
are
small
molecule
targeted
agents,
antibody-drug
conjugates
(ADCs),
cell-based
therapies,
gene
therapy.
These
cutting-edge
not
only
afford
personalized
precise
targeting,
but
also
provide
enhanced
comfort
potential
to
impede
disease
progression.
Nonetheless,
it
is
acknowledged
that
these
strategies
still
harbour
untapped
for
further
advancement.
Gaining
understanding
merits
limitations
holds
promise
offering
novel
perspectives
clinical
practice
foundational
research
endeavours.
In
this
review,
we
discussed
different
modalities,
including
drugs,
peptide
antibody
cell
therapy,
It
will
detailed
explanation
each
method,
addressing
their
status
development,
challenges,
solutions.
The
aim
assist
clinicians
researchers
in
gaining
deeper
diverse
options,
enabling
them
carry
out
effective
advance
more
efficiently.
Signal Transduction and Targeted Therapy,
Journal Year:
2022,
Volume and Issue:
7(1)
Published: Oct. 8, 2022
Abstract
Gastric
cancer
(GC)
ranks
fifth
in
global
diagnosis
and
fourth
cancer-related
death.
Despite
tremendous
progress
therapeutic
strategies
significant
improvements
patient
survival,
the
low
malignancy
stage
is
relatively
asymptomatic
many
GC
cases
are
diagnosed
at
advanced
stages,
which
leads
to
unsatisfactory
prognosis
high
recurrence
rates.
With
recent
advances
genome
analysis,
biomarkers
have
been
identified
that
clinical
importance
for
diagnosis,
treatment,
prognosis.
Modern
molecular
classifications
uncovered
vital
roles
signaling
pathways,
including
EGFR/HER2,
p53,
PI3K,
immune
checkpoint
cell
adhesion
molecules,
play
tumorigenesis,
progression,
metastasis,
responsiveness.
These
open
way
more
precise
diagnoses
treatments
patients.
Nevertheless,
relative
significance,
temporal
activation,
interaction
with
risk
factors,
crosstalk
between
these
pathways
not
well
understood.
Here,
we
review
regulatory
of
potential
biomarkers,
targets
an
emphasis
on
discoveries.
Current
therapies,
signaling-based
immunotherapies
exploited
past
decade,
development
treatment
GC,
particularly
challenges
developing
precision
medications,
discussed.
provide
a
direction
integration
clinical,
molecular,
genomic
profiles
improve
treatments.
Journal for ImmunoTherapy of Cancer,
Journal Year:
2022,
Volume and Issue:
10(12), P. e005755 - e005755
Published: Dec. 1, 2022
Patients
with
advanced
melanoma
have
limited
treatment
options
after
progression
on
immune
checkpoint
inhibitors
(ICI).
Lifileucel,
a
one-time
autologous
tumor-infiltrating
lymphocyte
(TIL)
cell
therapy,
demonstrated
an
investigator-assessed
objective
response
rate
(ORR)
of
36%
in
66
patients
who
progressed
ICI
and
targeted
therapy.
Herein,
we
report
independent
review
committee
(IRC)-assessed
outcomes
153
treated
lifileucel
large
multicenter
Phase
2
therapy
trial
melanoma.Eligible
had
that
where
appropriate.
Melanoma
lesions
were
resected
(resected
tumor
diameter
≥1.5
cm)
shipped
to
central
good
manufacturing
practice
facility
for
22-day
manufacturing.
received
non-myeloablative
lymphodepletion
regimen,
single
infusion,
up
six
doses
high-dose
interleukin-2.
The
primary
endpoint
was
IRC-assessed
ORR
(Response
Evaluation
Criteria
Solid
Tumors
V.1.1).The
Full
Analysis
Set
consisted
lifileucel,
including
longer-term
follow-up
the
previously
reported.
median
3.0
lines
prior
(81.7%
both
anti-programmed
death
protein
1
anti-cytotoxic
lymphocyte-associated
4)
high
disease
burden
at
baseline
(median
target
lesion
sum
diameters
(SOD):
97.8
mm;
lactate
dehydrogenase
(LDH)
>upper
limit
normal:
54.2%).
31.4%
(95%
CI:
24.1%
39.4%),
8
complete
responses
40
partial
responses.
Median
duration
not
reached
study
27.6
months,
41.7%
maintained
≥18
months.
overall
survival
progression-free
13.9
4.1
respectively.
Multivariable
analyses
adjusted
Eastern
Cooperative
Oncology
Group
performance
status
elevated
LDH
SOD
>median
independently
correlated
(p=0.008);
normal
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: June 16, 2022
γδ
T-cells
directly
recognize
and
kill
transformed
cells
independently
of
HLA-antigen
presentation,
which
makes
them
a
highly
promising
effector
cell
compartment
for
cancer
immunotherapy.
Novel
T-cell-based
immunotherapies,
primarily
focusing
on
the
two
major
T-cell
subtypes
that
infiltrate
tumors
(
i.e.
Vδ1
Vδ2),
are
being
developed.
The
subset
is
enriched
in
tissues
contains
both
as
well
regulatory
with
tumor-promoting
potential.
Vδ2
T-cells,
contrast,
circulation
consist
large,
relatively
homogeneous,
pro-inflammatory
subset.
Healthy
individuals
typically
harbor
order
50-500
million
Vγ9Vδ2
peripheral
blood
alone
(1-10%
total
CD3
+
population),
can
rapidly
expand
upon
stimulation.
receptor
senses
intracellular
phosphorylated
metabolites,
accumulate
result
mevalonate
pathway
dysregulation
or
pharmaceutical
intervention.
Early
clinical
studies
investigating
therapeutic
potential
were
based
either
ex
vivo
expansion
adoptive
transfer
their
systemic
activation
aminobisphosphonates
synthetic
phosphoantigens,
combined
low
dose
IL-2.
Immune-related
adverse
events
(irAE)
generally
\mild,
but
efficacy
these
approaches
provided
overall
limited
benefit.
In
recent
years,
critical
advances
have
renewed
excitement
Here,
we
review
strategies
discuss
prospects
those
currently
evaluated
patients
future
therapies
might
arise
from
current
pre-clinical
results.
ACS Nano,
Journal Year:
2021,
Volume and Issue:
15(11), P. 17080 - 17123
Published: Oct. 26, 2021
Cell
membrane-coated
(CMC)
mimics
are
micro/nanosystems
that
combine
an
isolated
cell
membrane
and
a
template
of
choice
to
mimic
the
functions
cell.
The
design
exploits
its
physicochemical
biological
properties
for
therapeutic
applications.
demonstrate
excellent
compatibility,
enhanced
biointerfacing
capabilities,
physical,
chemical,
tunability,
ability
retain
cellular
properties,
immune
escape,
prolonged
circulation
time,
protect
encapsulated
drug
from
degradation
active
targeting.
These
ease
adapting
them
personalized
clinical
medicine
have
generated
significant
research
interest
over
past
decade.
This
review
presents
detailed
overview
recent
advances
in
development
mimics.
primary
focus
is
collate
discuss
components,
fabrication
methodologies,
significance
physiochemical
characterization
techniques
validating
CMC
mimic.
We
present
critical
analysis
two
main
components
mimics:
mapped
their
use
scenarios.
In
addition,
we
emphasized
on
challenges
associated
with
translation.
Overall,
this
up
date
toolbox
researchers
can
benefit
while
designing
characterizing
Journal of Experimental & Clinical Cancer Research,
Journal Year:
2022,
Volume and Issue:
41(1)
Published: Jan. 6, 2022
Abstract
The
immune
checkpoint
molecule
CD70
and
its
receptor
CD27
are
aberrantly
expressed
in
many
hematological
solid
malignancies.
Dysregulation
of
the
CD70-CD27
axis
within
tumor
microenvironment
is
associated
with
progression
immunosuppression.
This
contrast
to
physiological
conditions,
where
tightly
controlled
expression
plays
a
role
co-stimulation
responses.
In
malignancies,
cancer
cells
co-express
promoting
stemness,
proliferation
survival
malignancy.
tumors,
only
present
on
which
can
facilitate
evasion
through
microenvironment.
discovery
these
immunosuppressive
effects
has
unfolded
novel
target
field
oncology,
CD70.
this
review,
we
thoroughly
discuss
current
insights
into
patterns
effect
(pre)clinical
therapeutic
strategies.