Journal of Cancer,
Journal Year:
2024,
Volume and Issue:
16(3), P. 700 - 707
Published: Dec. 31, 2024
Developing
new
drug
delivery
systems
is
crucial
for
enhancing
the
efficacy
of
oncolytic
virus
(OV)
therapies
in
cancer
treatment.
In
this
study,
mesenchymal
stem
cell
(MSC)-derived
vesicles
and
viruses
are
exploited
to
construct
a
novel
formulation.
It
has
been
hypothesized
that
vesicle-coated
OVs
could
amplify
cytotoxic
effects
through
superior
internalization
by
tumor
cells.
MSC
possess
natural
homing
ability
biocompatibility,
which
can
enhance
targeting,
uptake,
therapeutic
on
Experimental
results
indicated
treatment
system
increased
apoptosis
Furthermore,
flow
cytometry
analysis
demonstrated
uptake
cells
coated
with
soared
away
compared
uncoated
OVs,
being
1.5
times
than
group.
Additionally,
confocal
laser
scanning
microscopy
also
showed
fluorescence
intensity
within
pretreated
MSC-coated
was
greater.
Meanwhile,
propidium
iodide
(PI)
staining
revealed
Ovs
exposed
accelerating
latter.
According
statistics,
number
dead
increased,
testified
OV
group
as
high
23.78%.
These
findings
highlight
potential
therapy,
providing
promising
strategy
Cancers,
Journal Year:
2024,
Volume and Issue:
16(17), P. 2975 - 2975
Published: Aug. 27, 2024
Malignant
gliomas
present
great
difficulties
in
treatment,
with
little
change
over
the
past
30
years
median
survival
time
of
15
months.
Current
treatment
options
include
surgery,
radiotherapy
(RT),
and
chemotherapy.
New
therapies
aimed
at
suppressing
formation
new
vasculature
(antiangiogenic
treatments)
or
destroying
formed
tumor
(vascular
disrupting
agents)
show
promise.
This
study
summarizes
existing
knowledge
regarding
processes
by
which
glioblastoma
(GBM)
tumors
acquire
resistance
to
antiangiogenic
treatments.
The
discussion
encompasses
activation
redundant
proangiogenic
pathways,
heightened
cell
invasion
metastasis,
induced
hypoxia,
creation
vascular
mimicry
channels,
regulation
immune
microenvironment.
Subsequently,
we
explore
potential
strategies
overcome
this
resistance,
such
as
combining
other
methods,
personalizing
treatments
for
each
patient,
focusing
on
therapeutic
targets,
incorporating
immunotherapy,
utilizing
drug
delivery
systems
based
nanoparticles.
Additionally,
would
like
discuss
limitations
methods
future
directions
enhance
beneficial
effects
patients
GBM.
Therefore,
review
aims
research
outcome
GBM
provide
a
more
promising
opportunity
thoroughly
exploring
mechanisms
investigating
novel
strategies.
Biology,
Journal Year:
2024,
Volume and Issue:
13(5), P. 307 - 307
Published: April 28, 2024
Cancer
immune
evasion
represents
a
leading
hallmark
of
cancer,
posing
significant
obstacle
to
the
development
successful
anticancer
therapies.
However,
landscape
cancer
treatment
has
significantly
evolved,
transitioning
into
era
immunotherapy
from
conventional
methods
such
as
surgical
resection,
radiotherapy,
chemotherapy,
and
targeted
drug
therapy.
Immunotherapy
emerged
pivotal
component
in
treatment,
harnessing
body’s
system
combat
offering
improved
prognostic
outcomes
for
numerous
patients.
The
remarkable
success
spurred
efforts
enhance
clinical
efficacy
existing
agents
strategies.
Several
immunotherapeutic
approaches
have
received
approval
treatments,
while
others
are
currently
preclinical
trials.
This
review
explores
recent
progress
unraveling
mechanisms
evaluates
effectiveness
diverse
strategies,
including
vaccines,
adoptive
cell
therapy,
antibody-based
treatments.
It
encompasses
both
established
treatments
those
under
investigation,
providing
comprehensive
overview
through
immunological
approaches.
Additionally,
article
emphasizes
current
developments,
limitations,
challenges
immunotherapy.
Furthermore,
by
integrating
analyses
resistance
exploring
combination
strategies
personalized
approaches,
it
offers
valuable
insights
crucial
novel
International Journal of Nanomedicine,
Journal Year:
2024,
Volume and Issue:
Volume 19, P. 4533 - 4568
Published: May 1, 2024
Until
now,
there
has
been
a
lack
of
effective
strategies
for
cancer
treatment.
Immunotherapy
high
potential
in
treating
several
cancers
but
its
efficacy
is
limited
as
monotherapy.
Chemoimmunotherapy
(CIT)
holds
promise
to
be
widely
used
Therefore,
identifying
their
involvement
and
synergy
CIT
approaches
decisive.
Nano-based
drug
delivery
systems
(NDDSs)
are
ideal
because
they
can
simultaneously
target
immune
cells
cells,
promoting
accumulation,
reducing
the
toxicity
drug.
In
this
review,
we
first
introduce
five
current
immunotherapies,
including
checkpoint
blocking
(ICB),
adoptive
cell
transfer
therapy
(ACT),
vaccines,
oncolytic
virus
(OVT)
cytokine
therapy.
Subsequently,
immunomodulatory
effects
chemotherapy
by
inducing
immunogenic
death
(ICD),
tumor
killer
infiltration,
down-regulating
immunosuppressive
inhibiting
checkpoints
have
described.
Finally,
NDDSs-mediated
collaborative
introduced
detail,
development
nanoparticles
prospected.
Frontiers in Oncology,
Journal Year:
2025,
Volume and Issue:
15
Published: Feb. 7, 2025
Oncolytic
viruses
represent
a
distinct
class
of
that
selectively
infect
and
destroy
tumor
cells
while
sparing
normal
cells.
Despite
their
potential,
oncolytic
encounter
several
challenges
as
standalone
therapies.
Consequently,
the
combination
with
other
therapeutic
modalities
has
emerged
prominent
research
focus.
This
paper
summarizes
tumor-killing
mechanisms
viruses,
explores
integration
radiotherapy,
chemotherapy,
immune
checkpoint
inhibitors,
CAR-T,
CAR-NK
therapies,
provides
an
overview
related
clinical
trials.
By
synthesizing
these
advancements,
this
study
seeks
to
offer
valuable
insights
for
translation
virus
World Neurosurgery,
Journal Year:
2025,
Volume and Issue:
194, P. 123595 - 123595
Published: Jan. 23, 2025
The
authors
present
a
comprehensive
review
on
the
history
and
development
of
oncolytic
herpes
simplex
viral
therapies
for
malignant
glioma
with
focus
mechanisms
delivery
in
prior
ongoing
clinical
trials.
This
highlights
advancements
made
regard
to
delivering
these
highly
complex
immunologic
environment
setting
blood
brain
tumor
barrier
safe
effective
manner.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: July 2, 2024
Non-small
cell
lung
cancer
(NSCLC)
remains
an
unsolved
challenge
in
oncology,
signifying
a
substantial
global
health
burden.
While
considerable
progress
has
been
made
recent
years
through
the
emergence
of
immunotherapy
modalities,
such
as
immune
checkpoint
inhibitors
(ICIs),
monotherapies
often
yield
limited
clinical
outcomes.
The
rationale
behind
combining
various
immunotherapeutic
or
other
anticancer
agents,
mechanistic
underpinnings,
and
evidence
supporting
their
utilization
is
crucial
NSCLC
therapy.
Regarding
synergistic
potential
combination
immunotherapies,
this
study
aims
to
provide
insights
help
landscape
treatment
improve
In
addition,
review
article
discusses
challenges
considerations
regimens,
including
toxicity
management
patient
selection.
Pathogens,
Journal Year:
2025,
Volume and Issue:
14(2), P. 140 - 140
Published: Feb. 3, 2025
Ovarian
cancer
(OC)
remains
the
most
lethal
gynecologic
malignancy
with
limited
effective
treatment
options.
Oncolytic
viruses
(OVs)
have
emerged
as
a
promising
therapeutic
approach
for
treatment,
capable
of
selectively
infecting
and
lysing
cells
while
stimulating
anti-tumor
immune
responses.
Preclinical
studies
demonstrated
significant
tumor
regression
prolonged
survival
in
OC
models
using
various
OVs,
such
herpes
simplex.
Early-phase
clinical
trials
shown
favorable
safety
profile,
though
impact
on
patient
has
been
modest.
Current
research
focuses
combining
OVs
other
treatments
like
checkpoint
inhibitors
to
enhance
their
efficacy.
We
provide
comprehensive
overview
current
understanding
future
directions
utilizing
management
OC.
Cancers,
Journal Year:
2025,
Volume and Issue:
17(5), P. 715 - 715
Published: Feb. 20, 2025
Pancreatic
ductal
adenocarcinoma
(PDAC)
is
a
lethal
malignancy
with
poor
prognosis.
Currently,
chemotherapy
the
only
option
for
most
patients
advanced-stage
PDAC.
Further,
conventional
immunotherapies
and
targeted
therapies
improve
survival
outcomes
in
rare
PDAC
patient
subgroups.
To
date,
combinatory
immunotherapeutic
strategies
to
overcome
immune-hostile
tumor
microenvironment
(TME)
have
resulted
limited
efficacy
clinical
studies.
However,
efforts
are
ongoing
develop
new
treatment
evolving
knowledge
of
TME,
molecular
characterization,
immune
resistance
mechanisms.
growing
arsenal
various
agents,
including
novel
classes
checkpoint
inhibitors
oncolytic,
chimeric
antigen
receptor
T
cell,
vaccine
therapies,
reinforces
these
efforts.
This
review
will
focus
on
place
immunotherapy
future
possible
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(5), P. 2167 - 2167
Published: Feb. 28, 2025
Due
to
the
minimal
survival
benefits
of
existing
therapies
for
pediatric
diffuse
midline
glioma
(DMG)
patients,
new
therapeutic
modalities
are
being
investigated.
Immunotherapies
such
as
CAR-T
cells
and
oncolytic
viruses
(OVs)
part
these
efforts,
evidenced
by
increasing
number
clinical
trials.
αβ
T
engineered
with
a
high-affinity
γ9δ2
T-cell
receptor
(TEGs)
immune
designed
target
metabolic
changes
in
malignant
or
virally
infected
via
BTN2A1
BTN3A.
Because
expression
BTN3A
can
be
altered
tumor
cells,
combining
TEGs
OVs
could
potentially
enhance
anti-tumor
response.
We
investigated
this
hypothesis
following
study.
demonstrate
that
indeed
DMG,
which
expresses
at
varying
levels,
further
BTN3A-but
not
BTN2A1-in
DMG.
Functionally,
killed
DMG
cell
cultures,
killing
was
increased
after
OV
infection
DMGs
either
adenovirus
Δ24-RGD
reovirus
R124
under
suboptimal
conditions.
However,
additive
effect
lost
when
TCR-ligand
interaction
boosted
pamidronate.
This
study
demonstrates
Vγ9Vδ2
TCR-engineered
conditions
supports
combination
strategy
efficacy
both
modalities.