Cancer Research,
Journal Year:
2023,
Volume and Issue:
83(21), P. 3529 - 3543
Published: Aug. 21, 2023
As
a
safe,
feasible,
and
inexpensive
dietary
intervention,
fasting-mimicking
diet
(FMD)
exhibits
excellent
antitumor
efficacy
by
regulating
metabolism
boosting
immunity.
A
better
understanding
of
the
specific
mechanisms
underlying
immunoregulatory
functions
FMD
could
help
improve
expand
clinical
application
FMD-mediated
immunotherapeutic
strategies.
In
this
study,
we
aimed
to
elucidate
role
metabolic
reprogramming
induced
in
activation
immunity
against
colorectal
cancer.
Single-cell
RNA
sequencing
analysis
intratumoral
immune
cells
revealed
that
tumor-infiltrating
IgA+
B
were
significantly
reduced
treatment,
leading
tumor
regression
murine
cancer
models.
Mechanistically,
delayed
growth
repressing
B-cell
class
switching
IgA.
Therefore,
FMD-induced
reduction
overcame
suppression
CD8+
T
cells.
The
effects
intervention
reversed
transfer.
Moreover,
boosted
fatty
acid
oxidation
(FAO)
trigger
RUNX3
acetylation,
thus
inactivating
Cα
gene
transcription
IgA
switching.
expansion
was
also
impeded
patients
placed
on
FMD,
while
expression
carnitine
palmitoyl
transferase
1A
(CPT1A),
rate-limiting
enzyme
FAO,
increased.
Furthermore,
CPT1A
negatively
correlated
with
both
secretion
within
Together,
these
results
highlight
holds
great
promise
for
treating
degree
cell
infiltration
FAO-associated
status
are
potential
biomarkers
evaluating
efficacy.Metabolic
suppresses
production
activate
inhibit
growth.
See
related
commentary
Bush
Perry,
p.
3493.
Immunological Reviews,
Journal Year:
2023,
Volume and Issue:
321(1), P. 20 - 32
Published: Sept. 7, 2023
Summary
Cancer
cells
undergoing
immunogenic
cell
death
(ICD)
can
initiate
adaptive
immune
responses
against
dead
cell‐associated
antigens,
provided
that
(1)
said
antigens
are
not
perfectly
covered
by
central
tolerance
(antigenicity),
(2)
occurs
along
with
the
emission
of
immunostimulatory
cytokines
and
damage‐associated
molecular
patterns
(DAMPs)
actively
engage
effector
mechanisms
(adjuvanticity),
(3)
microenvironment
dying
is
permissive
for
initiation
immunity.
Finally,
ICD‐driven
only
operate
exert
cytotoxic
functions
if
target
cancer
enables
infiltration
activity.
Multiple
forms
radiation,
including
non‐ionizing
(ultraviolet)
ionizing
elicit
bona
fide
ICD
as
they
increase
both
antigenicity
adjuvanticity
cells.
Here,
we
review
determinants
elicited
radiation
critically
discuss
strategies
to
reinforce
immunogenicity
succumbing
clinically
available
strategies.
Cancers,
Journal Year:
2023,
Volume and Issue:
15(15), P. 3898 - 3898
Published: July 31, 2023
The
remodeled
cancer
cell
metabolism
affects
the
tumor
microenvironment
and
promotes
an
immunosuppressive
state
by
changing
levels
of
macro-
micronutrients
releasing
hormones
cytokines
that
recruit
immune
cells.
Novel
dietary
interventions
such
as
amino
acid
restriction
periodic
fasting
mimicking
diets
can
prevent
or
dampen
formation
acting
systemically
on
release
growth
factors,
inhibiting
proinflammatory
cytokines,
remodeling
vasculature
extracellular
matrix.
Here,
we
discuss
latest
research
effects
these
therapeutic
immunometabolism
response
future
scenarios
pertaining
to
how
could
contribute
therapy.
Cancer Research,
Journal Year:
2023,
Volume and Issue:
83(21), P. 3529 - 3543
Published: Aug. 21, 2023
As
a
safe,
feasible,
and
inexpensive
dietary
intervention,
fasting-mimicking
diet
(FMD)
exhibits
excellent
antitumor
efficacy
by
regulating
metabolism
boosting
immunity.
A
better
understanding
of
the
specific
mechanisms
underlying
immunoregulatory
functions
FMD
could
help
improve
expand
clinical
application
FMD-mediated
immunotherapeutic
strategies.
In
this
study,
we
aimed
to
elucidate
role
metabolic
reprogramming
induced
in
activation
immunity
against
colorectal
cancer.
Single-cell
RNA
sequencing
analysis
intratumoral
immune
cells
revealed
that
tumor-infiltrating
IgA+
B
were
significantly
reduced
treatment,
leading
tumor
regression
murine
cancer
models.
Mechanistically,
delayed
growth
repressing
B-cell
class
switching
IgA.
Therefore,
FMD-induced
reduction
overcame
suppression
CD8+
T
cells.
The
effects
intervention
reversed
transfer.
Moreover,
boosted
fatty
acid
oxidation
(FAO)
trigger
RUNX3
acetylation,
thus
inactivating
Cα
gene
transcription
IgA
switching.
expansion
was
also
impeded
patients
placed
on
FMD,
while
expression
carnitine
palmitoyl
transferase
1A
(CPT1A),
rate-limiting
enzyme
FAO,
increased.
Furthermore,
CPT1A
negatively
correlated
with
both
secretion
within
Together,
these
results
highlight
holds
great
promise
for
treating
degree
cell
infiltration
FAO-associated
status
are
potential
biomarkers
evaluating
efficacy.Metabolic
suppresses
production
activate
inhibit
growth.
See
related
commentary
Bush
Perry,
p.
3493.