Journal of Immunology Research,
Journal Year:
2021,
Volume and Issue:
2021, P. 1 - 12
Published: Aug. 26, 2021
Tumor
immunotherapy
is
the
fourth
therapy
after
surgery,
chemotherapy,
and
radiotherapy.
It
has
made
great
breakthroughs
in
treatment
of
some
epithelial
tumors
hematological
tumors.
However,
its
adverse
reactions
are
common
or
even
more
serious,
response
rate
solid
not
satisfactory.
With
maturity
genomics
metabolomics
technologies,
effect
intestinal
microbiota
tumor
development
gradually
been
recognized.
The
may
affect
immunity
by
regulating
host
immune
system
microenvironment.
Some
bacteria
help
fight
activating
immunity,
while
mediate
immunosuppression
to
cancer
cells
escape
from
system.
More
studies
have
revealed
that
effects
complications
related
composition
gut
microbiota.
sensitive
prone
certain
characteristics.
These
characteristics
be
used
as
biomarkers
predict
prognosis
also
developed
“immune
potentiators”
assist
immunotherapy.
clinical
preclinical
proved
microbial
intervention,
including
transplantation,
can
improve
sensitivity
reduce
a
extent.
gene
editing
technology
nanotechnology,
design
engineered
contribute
become
new
research
hotspot.
Based
on
relationship
between
immunotherapy,
correct
mining
information
reasonable
feasible
intervention
methods
expected
optimize
large
extent
bring
treatment.
Molecular Cancer,
Journal Year:
2023,
Volume and Issue:
22(1)
Published: March 11, 2023
The
malignant
tumor
is
a
multi-etiological,
systemic
and
complex
disease
characterized
by
uncontrolled
cell
proliferation
distant
metastasis.
Anticancer
treatments
including
adjuvant
therapies
targeted
are
effective
in
eliminating
cancer
cells
but
limited
number
of
patients.
Increasing
evidence
suggests
that
the
extracellular
matrix
(ECM)
plays
an
important
role
development
through
changes
macromolecule
components,
degradation
enzymes
stiffness.
These
variations
under
control
cellular
components
tissue
via
aberrant
activation
signaling
pathways,
interaction
ECM
to
multiple
surface
receptors,
mechanical
impact.
Additionally,
shaped
regulates
immune
which
results
suppressive
microenvironment
hinders
efficacy
immunotherapies.
Thus,
acts
as
barrier
protect
from
supports
progression.
Nevertheless,
profound
regulatory
network
remodeling
hampers
design
individualized
antitumor
treatment.
Here,
we
elaborate
on
composition
ECM,
discuss
specific
mechanisms
remodeling.
Precisely,
highlight
impact
development,
proliferation,
anoikis,
metastasis,
angiogenesis,
lymphangiogenesis,
escape.
Finally,
emphasize
"normalization"
potential
strategy
for
anti-malignant
International Journal of Molecular Sciences,
Journal Year:
2021,
Volume and Issue:
22(12), P. 6262 - 6262
Published: June 10, 2021
Colorectal
carcinoma
(CRC)
is
one
of
the
most
frequently
diagnosed
carcinomas
and
leading
causes
cancer-related
death
worldwide.
Metabolic
reprogramming,
a
hallmark
cancer,
closely
related
to
initiation
progression
carcinomas,
including
CRC.
Accumulating
evidence
shows
that
activation
oncogenic
pathways
loss
tumor
suppressor
genes
regulate
metabolic
reprogramming
mainly
involved
in
glycolysis,
glutaminolysis,
one-carbon
metabolism
lipid
metabolism.
The
abnormal
program
provides
cells
with
abundant
energy,
nutrients
redox
requirements
support
their
malignant
growth
metastasis,
which
accompanied
by
impaired
flexibility
microenvironment
(TME)
dysbiosis
gut
microbiota.
crosstalk
between
cells,
components
TME
intestinal
microbiota
further
facilitates
CRC
cell
proliferation,
invasion
metastasis
leads
therapy
resistance.
Hence,
target
dysregulated
metabolism,
microbiota,
novel
preventive
therapeutic
applications
are
required.
In
this
review,
dysregulation
programs,
molecular
pathways,
addressed.
Possible
strategies,
inhibition
immune
CRC,
as
well
modulation
aberrant
discussed.
Advanced Science,
Journal Year:
2023,
Volume and Issue:
10(15)
Published: March 23, 2023
Abstract
Gut
microbiota‐derived
metabolites
are
key
hubs
connecting
the
gut
microbiome
and
cancer
progression,
primarily
by
remodeling
tumor
microenvironment
regulating
signaling
pathways
in
cells
multiple
immune
cells.
The
use
of
microbial
radiotherapy
chemotherapy
mitigates
severe
side
effects
from
treatment
improves
efficacy
treatment.
Immunotherapy
combined
with
effectively
activates
system
to
kill
tumors
overcomes
drug
resistance.
Consequently,
various
novel
strategies
have
been
developed
modulate
metabolites.
Manipulation
genes
involved
metabolism
using
synthetic
biology
approaches
directly
affects
levels
metabolites,
while
fecal
transplantation
phage
affect
altering
composition
microbiome.
However,
some
harbor
paradoxical
functions
depending
on
context
(e.g.,
type
cancer).
Furthermore,
metabolic
microorganisms
certain
anticancer
drugs
such
as
irinotecan
gemcitabine,
render
ineffective
or
exacerbate
their
adverse
effects.
Therefore,
a
personalized
comprehensive
consideration
patient's
condition
is
required
when
employing
treat
cancer.
purpose
this
review
summarize
correlation
between
cancer,
provide
fresh
ideas
for
future
scientific
research.
Pharmaceutics,
Journal Year:
2023,
Volume and Issue:
15(4), P. 1143 - 1143
Published: April 4, 2023
Cancer
immunotherapy
is
a
type
of
treatment
that
harnesses
the
power
immune
systems
patients
to
target
cancer
cells
with
better
precision
compared
traditional
chemotherapy.
Several
lines
have
been
approved
by
US
Food
and
Drug
Administration
(FDA)
led
remarkable
success
in
solid
tumors,
such
as
melanoma
small-cell
lung
cancer.
These
immunotherapies
include
checkpoint
inhibitors,
cytokines,
vaccines,
while
chimeric
antigen
receptor
(CAR)
T-cell
has
shown
responses
hematological
malignancies.
Despite
these
breakthrough
achievements,
response
variable
among
patients,
only
small
percentage
gained
from
this
treatment,
depending
on
histological
tumor
other
host
factors.
develop
mechanisms
avoid
interacting
circumstances,
which
an
adverse
effect
how
effectively
they
react
therapy.
arise
either
due
intrinsic
factors
within
or
microenvironment
(TME).
When
scenario
used
therapeutic
setting,
term
“resistance
immunotherapy”
applied;
“primary
resistance”
denotes
failure
respond
start,
“secondary
relapse
following
initial
immunotherapy.
Here,
we
provide
thorough
summary
internal
external
underlying
resistance
Furthermore,
variety
are
briefly
discussed,
along
recent
developments
employed
prevent
relapses
focus
upcoming
initiatives
improve
efficacy
for
patients.
Molecular Cancer,
Journal Year:
2025,
Volume and Issue:
24(1)
Published: Jan. 15, 2025
The
last
decade
has
witnessed
unprecedented
succusses
with
the
use
of
immune
checkpoint
inhibitors
in
treating
cancer.
Nevertheless,
proportion
patients
who
respond
favorably
to
treatment
remained
rather
modest,
partially
due
resistance.
This
fueled
a
wave
research
into
potential
mechanisms
resistance
which
can
be
classified
primary
or
acquired
after
an
initial
response.
In
current
review,
we
summarize
what
is
known
so
far
about
terms
being
tumor-intrinsic
tumor-extrinsic
taking
account
multimodal
crosstalk
between
tumor,
system
compartment
and
other
host-related
factors.
Cell Death and Disease,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: Feb. 7, 2025
Abstract
Gastric
cancer
(GC)
remains
a
leading
cause
of
cancer-related
mortality
worldwide,
with
limited
treatment
options
in
advanced
stages.
Immunotherapy,
particularly
immune
checkpoint
inhibitors
(ICIs)
targeting
PD1/PD-L1,
has
emerged
as
promising
therapeutic
approach.
However,
significant
proportion
patients
exhibit
primary
or
acquired
resistance,
limiting
the
overall
efficacy
immunotherapy.
This
review
provides
comprehensive
analysis
mechanisms
underlying
immunotherapy
resistance
GC,
including
role
tumor
microenvironment,
dynamic
PD-L1
expression,
compensatory
activation
other
checkpoints,
and
genomic
instability.
Furthermore,
explores
GC-specific
factors
such
molecular
subtypes,
unique
evasion
mechanisms,
impact
Helicobacter
pylori
infection.
We
also
discuss
emerging
strategies
to
overcome
combination
therapies,
novel
immunotherapeutic
approaches,
personalized
based
on
genomics
microenvironment.
By
highlighting
these
key
areas,
this
aims
inform
future
research
directions
clinical
practice,
ultimately
improving
outcomes
for
GC
undergoing
Molecular Therapy,
Journal Year:
2022,
Volume and Issue:
31(3), P. 631 - 646
Published: Dec. 5, 2022
Human
mucosal-associated
invariant
T
(MAIT)
cells
are
characterized
by
their
expression
of
an
TCR
α
chain
Vα7.2-Jα33/Jα20/Jα12
paired
with
a
restricted
β
chain.
MAIT
recognize
microbial
peptides
presented
the
highly
conserved
MHC
class
I-like
molecule
MR1
and
bridge
innate
acquired
immune
systems
to
mediate
augmented
responses.
Upon
activation,
rapidly
proliferate,
produce
variety
cytokines
cytotoxic
molecules,
trigger
efficient
antitumor
immunity.
Administration
representative
cell
ligand
5-OP-RU
effectively
activates
enhances
capacity.
In
this
review,
we
introduce
biology
importance
in
immunity,
summarize
current
development
peripheral
blood
mononuclear
cell-derived
stem
products
for
cancer
treatment,
discuss
potential
genetic
engineering
off-the-shelf
immunotherapy.