Journal for ImmunoTherapy of Cancer,
Journal Year:
2024,
Volume and Issue:
12(6), P. e009063 - e009063
Published: June 1, 2024
Cancer
immunotherapy
has
flourished
over
the
last
10–15
years,
transforming
practice
of
oncology
and
providing
long-term
clinical
benefit
to
some
patients.
During
this
time,
three
distinct
classes
immune
checkpoint
inhibitors,
chimeric
antigen
receptor-T
cell
therapies
specific
for
two
targets,
bispecific
T
engagers,
a
vaccine,
an
oncolytic
virus
have
joined
cytokines
as
standard
cancer
care.
At
same
scientific
progress
delivered
vast
amounts
new
knowledge.
For
example,
advances
in
technologies
such
single-cell
sequencing
spatial
transcriptomics
provided
deep
insights
into
immunobiology
tumor
microenvironment.
With
rapid
progress,
field
is
currently
at
critical
inflection
point,
with
potential
exponential
growth
next
decade.
Recognizing
this,
Society
Immunotherapy
convened
diverse
group
experts
representing
academia,
pharmaceutical
biotechnology
industries,
patient
advocacy,
regulatory
community
identify
current
opportunities
challenges
goal
prioritizing
areas
highest
impact.
The
consensus
identified
seven
high-priority
opportunity
field:
mechanisms
antitumor
activity
toxicity;
drug
resistance;
biomarkers
biospecimens;
unique
aspects
novel
therapeutics;
host
environmental
interactions;
premalignant
immunity,
interception,
immunoprevention;
trial
design,
endpoints,
conduct.
Additionally,
roadblocks
were
discussed,
several
topics
cross-cutting
tools
optimization,
each
impact
multiple
priority
areas.
These
include
preclinical
models,
data
curation
sharing,
biopsies
biospecimens,
diversification
funding
sources,
definitions
standards,
engagement.
Finally,
key
guiding
principles
that
will
both
optimize
maximize
field.
engaging
community;
cultivating
diversity,
equity,
inclusion,
accessibility;
leveraging
power
artificial
intelligence
accelerate
progress.
Here,
we
present
outcomes
these
discussions
strategic
vision
galvanize
decade
immunotherapy.
Foods,
Journal Year:
2023,
Volume and Issue:
12(4), P. 878 - 878
Published: Feb. 18, 2023
Oligosaccharides
derived
from
natural
resources
are
attracting
increasing
attention
as
both
food
and
nutraceutical
products
because
of
their
beneficial
health
effects
lack
toxicity.
During
the
past
few
decades,
many
studies
have
focused
on
potential
benefits
fucoidan.
Recently,
new
interest
has
emerged
in
fucoidan,
partially
hydrolysed
into
fuco-oligosaccharides
(FOSs)
or
low-molecular
weight
owing
to
superior
solubility
biological
activities
compared
with
There
is
considerable
development
for
use
functional
food,
cosmetic,
pharmaceutical
industries.
Therefore,
this
review
summarises
discusses
preparation
FOSs
fucoidan
using
mild
acid
hydrolysis,
enzymatic
depolymerisation,
radical
degradation
methods,
advantages
disadvantages
hydrolysis
methods.
Several
purification
steps
performed
obtain
(according
latest
reports)
also
reviewed.
Moreover,
FOS
that
human
summarised
based
evidence
vitro
vivo
studies,
possible
mechanisms
prevention
treatment
various
diseases
discussed.
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: Feb. 11, 2023
Abstract
Efficient
cancer
immunotherapy
depends
on
selective
targeting
of
high
bioactivity
therapeutic
agents
to
the
tumours.
However,
delivering
exogenous
medication
might
prove
difficult
in
clinical
practice.
Here
we
report
a
cooperative
Nano-CRISPR
scaffold
(Nano-CD)
that
utilizes
specific
sgRNA,
selected
from
functional
screen
for
triggering
endogenous
GDSME
expression,
while
releasing
cisplatin
initiate
immunologic
cell
death.
Mechanistically,
cascade-amplification
antitumor
immune
response
is
prompted
by
adjuvantic
properties
lytic
intracellular
content
and
enhanced
heightened
resulting
pyroptosis
release
tumor
associated
antigens.
Neither
single
components
provide
efficient
tumour
control,
growth
efficiently
inhibited
primary
recurrent
melanomas
due
combinatorial
effect
self-supplied
GSDME.
Moreover,
Nano-CD
combination
with
checkpoint
blockade
creates
durable
memory
strong
systemic
anti-tumor
response,
leading
disease
relapse
prevention,
lung
metastasis
inhibition
increased
survival
mouse
melanomas.
Taken
together,
our
approach
CRISPR-technology
enable
cell-intrinsic
protein
expression
immunotherapy,
using
as
prototypic
modulator.
This
nanoplatform
thus
can
be
applied
modulate
further
immunological
processes
benefit.
Cell Death Discovery,
Journal Year:
2023,
Volume and Issue:
9(1)
Published: Feb. 15, 2023
Abstract
Hepatocellular
carcinoma
(HCC),
one
of
the
most
malignant
tumors,
is
characterized
by
its
stubborn
immunosuppressive
microenvironment.
As
main
members
tumor
microenvironment
(TME)
HCC,
tumor-associated
macrophages
(TAMs)
play
a
critical
role
in
occurrence
and
development,
including
stimulating
angiogenesis,
enhancing
immunosuppression,
promoting
drug
resistance
cancer
metastasis.
This
review
describes
origin
as
well
phenotypic
heterogeneity
TAMs
their
potential
effects
on
development
HCC
also
discusses
about
various
adjuvant
therapy
based
strategies
that
can
be
used
for
targeting
TAMs.
In
addition,
we
have
highlighted
different
treatment
modalities
immunotherapy,
small
molecular
inhibitors,
immune
checkpoint
antibodies,
vaccines,
adoptive
cellular
nanocarriers
delivery,
to
explore
novel
combination
therapies
provide
feasible
therapeutic
options
clinically
improving
prognosis
quality
life
patients.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease,
Journal Year:
2023,
Volume and Issue:
1869(6), P. 166746 - 166746
Published: May 7, 2023
Cellular
and
stromal
components
including
tumor
cells,
immune
mesenchymal
cancer-linked
fibroblasts,
extracellular
matrix,
constituent
microenvironment
(TME).
TME
plays
a
crucial
role
in
reprogramming
initiation,
uncontrolled
proliferation,
invasion
metastasis
as
well
response
to
therapeutic
modalities.
In
recent
years
targeting
the
has
developed
potential
strategy
for
treatment
of
cancer
because
its
life-threatening
functions
restricting
development
modulating
responses
standard-of-care
medicines.
Cold
atmospheric
plasma,
oncolytic
viral
therapy,
bacterial
nano-vaccine,
repurposed
pharmaceuticals
with
combination
antiangiogenic
drugs,
immunotherapies
are
among
most
effective
therapies
directed
by
that
have
either
been
clinically
authorized
or
currently
being
studied.
This
article
discusses
above-mentioned
light
TME.
We
also
cover
problems
related
TME-targeted
therapies,
future
insights
practical
uses
this
rapidly
growing
field.
Journal of Hematology & Oncology,
Journal Year:
2024,
Volume and Issue:
17(1)
Published: June 11, 2024
Abstract
Macrophages
infiltrating
tumour
tissues
or
residing
in
the
microenvironment
of
solid
tumours
are
known
as
tumour-associated
macrophages
(TAMs).
These
specialized
immune
cells
play
crucial
roles
growth,
angiogenesis,
regulation,
metastasis,
and
chemoresistance.
TAMs
encompass
various
subpopulations,
primarily
classified
into
M1
M2
subtypes
based
on
their
differentiation
activities.
macrophages,
characterized
by
a
pro-inflammatory
phenotype,
exert
anti-tumoural
effects,
while
with
an
anti-inflammatory
function
protumoural
regulators.
highly
versatile
respond
to
stimuli
from
other
constituents
within
(TME),
such
growth
factors,
cytokines,
chemokines,
enzymes.
induce
polarization
towards
one
phenotype
another,
leading
complex
interactions
TME
components
influencing
both
pro-tumour
anti-tumour
processes.
This
review
comprehensively
deeply
covers
literature
origin
well
intricate
interplay
between
TME,
dual
nature
promoting
pro-
Moreover,
delves
primary
pathways
implicated
macrophage
polarization,
examining
diverse
that
regulate
this
process.
role
shaping
functions
macrophages.
In
addition,
advantages
limitations
current
clinical
interventions
reviewed,
including
enhancing
TAM
phagocytosis,
inducing
exhaustion,
inhibiting
recruitment,
polarizing
M1-like
phenotype.
conclusion,
treatment
strategies
targeting
precision
medicine
show
promise,
overcoming
several
obstacles
is
still
necessary
achieve
accessible
efficient
immunotherapy.
Molecular Cancer,
Journal Year:
2023,
Volume and Issue:
22(1)
Published: July 29, 2023
Abstract
Newly
growing
evidence
highlights
the
essential
role
that
epitranscriptomic
marks
play
in
development
of
many
cancers;
however,
little
is
known
about
and
implications
altered
epitranscriptome
deposition
prostate
cancer.
Here,
we
show
transfer
RNA
N
7
-methylguanosine
(m
G)
transferase
METTL1
highly
expressed
primary
advanced
tumours.
Mechanistically,
find
depletion
causes
loss
m
G
tRNA
methylation
promotes
biogenesis
a
novel
class
small
non-coding
RNAs
derived
from
5'tRNA
fragments.
5'tRNA-derived
steer
translation
control
to
favour
synthesis
key
regulators
tumour
growth
suppression,
interferon
pathway,
immune
effectors.
Knockdown
Mettl1
cancer
preclinical
models
increases
intratumoural
infiltration
pro-inflammatory
cells
enhances
responses
immunotherapy.
Collectively,
our
findings
reveal
therapeutically
actionable
METTL1-directed
cell
biology.
Journal of Cancer Research and Clinical Oncology,
Journal Year:
2024,
Volume and Issue:
150(5)
Published: May 7, 2024
Abstract
Background
Tumor
growth
is
closely
linked
to
the
activities
of
various
cells
in
tumor
microenvironment
(TME),
particularly
immune
cells.
During
progression,
circulating
monocytes
and
macrophages
are
recruited,
altering
TME
accelerating
growth.
These
adjust
their
functions
response
signals
from
stromal
Tumor-associated
(TAMs),
similar
M2
macrophages,
key
regulators
TME.
Methods
We
review
origins,
characteristics,
TAMs
within
This
analysis
includes
mechanisms
through
which
facilitate
evasion
promote
metastasis.
Additionally,
we
explore
potential
therapeutic
strategies
that
target
TAMs.
Results
instrumental
mediating
malignant
behaviors.
They
release
cytokines
inhibit
effector
attract
additional
immunosuppressive
primarily
T
cells,
inducing
exhaustion
directly,
influencing
activity
indirectly
cellular
interactions,
or
suppressing
checkpoints.
directly
involved
proliferation,
angiogenesis,
invasion,
Summary
Developing
innovative
tumor-targeted
therapies
immunotherapeutic
currently
a
promising
focus
oncology.
Given
pivotal
role
evasion,
several
approaches
have
been
devised
them.
include
leveraging
epigenetics,
metabolic
reprogramming,
engineering
repolarize
TAMs,
inhibiting
recruitment
activity,
using
as
drug
delivery
vehicles.
Although
some
these
remain
distant
clinical
application,
believe
future
targeting
will
offer
significant
benefits
cancer
patients.