Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Dec. 23, 2024
Colorectal
cancer
(CRC),
as
one
of
the
malignant
tumors
with
highest
incidence
and
mortality
rates
worldwide
in
recent
years,
originating
primarily
from
mucosal
tissues
colon
or
rectum,
has
potential
to
rapidly
develop
into
invasive
cancer.
Its
pathogenesis
is
complex,
involving
a
multitude
factors
including
genetic
background,
lifestyle,
dietary
habits.
Early
detection
treatment
are
key
improving
survival
for
patients
CRC.
However,
pervasive
problem
that
can
become
severely
resistant
treatment,
which
greatly
increases
complexity
challenge
treatment.
Therefore,
unraveling
overcoming
resistance
CRC
focus
research.
Mitochondria,
energy
centers
cell,
play
crucial
role
cellular
metabolism,
supply,
apoptosis
process.
In
CRC,
Mitochondrial
dysfunction
not
only
impairs
normal
cell
function
but
also
promotes
tumor
resistance.
deep
understanding
relationship
between
mitochondrial
mechanisms
development,
well
by
it
chemotherapy
drugs,
development
targeted
therapies,
enhancing
drug
efficacy,
outcomes
quality
life
patients.
Molecular Cancer,
Journal Year:
2024,
Volume and Issue:
23(1)
Published: Sept. 2, 2024
Programmed
death
receptor-1
(PD-1)
and
its
ligand,
programmed
ligand-1
(PD-L1)
are
essential
molecules
that
key
in
modulating
immune
responses.
PD-L1
is
constitutively
expressed
on
various
cells,
epithelial
cancer
where
it
functions
as
a
co-stimulatory
molecule
capable
of
impairing
T-cell
mediated
Upon
binding
to
PD-1
activated
T-cells,
the
PD-1/PD-L1
interaction
triggers
signaling
pathways
can
induce
apoptosis
or
anergy,
thereby
facilitating
escape
tumors.
In
urological
cancers,
including
bladder
(BCa),
renal
cell
carcinoma
(RCC),
prostate
(PCa),
upregulation
has
been
demonstrated.
It
linked
poor
prognosis
enhanced
tumor
evasion.
Recent
studies
have
highlighted
significant
role
axis
mechanisms
cancers.
The
between
T-cells
further
contributes
immunosuppression
by
inhibiting
activation
proliferation.
Clinical
applications
checkpoint
inhibitors
shown
promising
efficacy
treating
advanced
significantly
improving
patient
outcomes.
However,
resistance
these
therapies,
either
intrinsic
acquired,
remains
challenge.
This
review
aims
provide
comprehensive
overview
pathway
We
summarize
regulatory
mechanism
underlying
expression
activity,
genetic,
epigenetic,
post-transcriptional,
post-translational
modifications.
Additionally,
we
discuss
current
clinical
research
inhibitors,
their
therapeutic
potential,
challenges
associated
with
resistance.
Understanding
crucial
for
developing
new
strategies
overcome
limitations
enhance
immunotherapy.
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: Sept. 3, 2024
The
aim
of
this
study
was
to
evaluate
the
prognostic
value
peripheral
blood
inflammation
indexes
in
patients
with
metastatic
Colorectal
Cancer
(CRC)
and
establish
a
predictive
scoring
system.
A
total
324
CRC
diagnosed
through
pathological
examination
from
January
2017
July
2022
at
Third
Affiliated
Hospital
Kunming
Medical
University
were
included.
prognosis
examined,
correlation
between
IL-10
expression
tissues
serum
analyzed.
results
showed
that
poorer
when
metastasis
occurred
(P
<
0.001).
Additionally,
highly
expressed
group
=
0.018),
positively
correlated
0.037).
neutrophil-to-lymphocyte
ratio
(NLR),
lymphocyte-to-white
cell
(LWR),
aggregate
index
systemic
(AISI),
monocyte-to-lymphocyte
(MLR),
inflammatory
response
(SIRI),
nutritional
(PNI),
advanced
lung
cancer
(ALI),
interleukin-10
(IL-10)
calculated
determined
by
ROC
curve.
critical
values
2.135,
3.735,
353.745,
0.265,
1.025,
52.975,
353.635,
11.25,
respectively.
Inflammatory
an
AUC
more
than
0.6
selected,
each
colorectal
patient
any
these
risk
factors
assigned
score
one.
then
divided
into
two
groups:
0–4
for
low-risk
4–8
high-risk
group.
occurrence
distant
metastases
groups
statistically
OS
PFS
significantly
superior
those
0.05).
These
findings
indicate
NLR,
LWR,
AISI,
MLR,
SIRI,
PNI,
ALI,
are
patients.
Therefore,
prediction
scores
can
be
used
effectively
CRC.
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: Feb. 18, 2025
Seven
compounds
were
isolated
from
ethyl
acetate
extract
of
Alcea
rosea
and
examined
for
their
cytotoxicity
against
HCT116,
HT29
SW480
colon
cancer
cells.
It
was
found
that
two
(C4
C5)
exhibited
strong
anti-colon
activities.
These
used
to
study
properties
include
MTT
activity
(with
IC50
C4
as
74.71,
129.0
131.4
µg/ml
in
respectively,
whereas
C5
128.1,
168.4
225.8
cells
respectively),
colony
formation
activity,
wound
healing
spheroid
DAPI-PI
staining,
acridine-orange
ethidium
bromide
ROS
measurement,
rhodamine-123
staining
both
HCT116
Both
the
showed
significant
increase
apoptosis
visualized
by
4′,6-diamidino-2-phenylindol/propidium
iodide
(DAPI-PI)
acridine
orange/ethidium
(AO/EtBr)
staining.
The
induction
further
confirmed
expressions
cleaved
PARP
caspase
3.
generation
its
effect
on
MMP
measured
with
Dichloro-dihydro-fluorescein
diacetate
(DCFH-DA)
Rhodamine.
Expression
levels
EMT
associated
markers
like
Cyclin
D1,
Slug,
Vimentin,
E-Cadherin
also
studied.
down
regulate
protein
Vimentin
a
concentration-dependent
manner.
Eeffect
key
signaling
Wnt3a,
Notch1,
Shh
evaluated.
Additionally,
mRNA
these
genes
analyzed.
best
binding
affinity
when
docked
Wnt3a
Notch1.
Similarly,
−
8.8,
-8.2
7.6
kcal⋅mol−
1
Shh,
present
findings
provide
insight
immense
scientific
support
integrity
piece
indigenous
knowledge.
However,
validation
living
organisms
is
necessary
before
progressing
clinical
trials
advancing
it
into
marketable
pharmaceutical
product.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(8), P. 3733 - 3733
Published: April 15, 2025
The
gut
microbiome,
a
complex
community
of
microorganisms
residing
in
the
intestinal
tract,
plays
dual
role
colorectal
cancer
(CRC)
development,
acting
both
as
contributing
risk
factor
and
protective
element.
This
review
explores
mechanisms
by
which
microbiota
contribute
to
CRC,
emphasizing
inflammation,
oxidative
stress,
immune
evasion,
production
genotoxins
microbial
metabolites.
Fusobacterium
nucleatum,
Escherichia
coli
(pks+),
Bacteroides
fragilis
promote
tumorigenesis
inducing
chronic
generating
reactive
oxygen
species,
producing
virulence
factors
that
damage
host
DNA.
These
can
also
evade
antitumor
response
suppressing
cytotoxic
T
cell
activity
increasing
regulatory
populations.
Additionally,
microbial-derived
metabolites
such
secondary
bile
acids
trimethylamine-N-oxide
(TMAO)
have
been
linked
carcinogenic
processes.
Conversely,
microbiota,
including
Lactobacillus,
Bifidobacterium,
Faecalibacterium
prausnitzii,
homeostasis
short-chain
fatty
(SCFAs)
like
butyrate,
exhibit
anti-inflammatory
anti-carcinogenic
properties.
beneficial
microbes
enhance
barrier
integrity,
modulate
responses,
inhibit
tumor
proliferation.
Understanding
dynamic
interplay
between
pathogenic
is
essential
for
developing
microbiome-based
interventions,
probiotics,
prebiotics,
fecal
transplantation,
prevent
or
treat
CRC.
Future
research
should
focus
on
identifying
biomarkers
early
CRC
detection
exploring
personalized
microbiome-targeted
therapies.
A
deeper
understanding
host–microbiota
interactions
may
lead
innovative
strategies
management
improved
patient
outcomes.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: April 5, 2024
Worldwide,
gastrointestinal
(GI)
cancer
is
recognized
as
one
of
the
leading
malignancies
diagnosed
in
both
genders,
with
mortality
largely
attributed
to
metastatic
dissemination.
It
has
been
identified
that
GI
cancer,
a
variety
signaling
pathways
and
key
molecules
are
modified,
emergence
an
immunotolerance
phenotype.
Such
modifications
pivotal
malignancy’s
evasion
immune
detection.
Thus,
thorough
analysis
contributing
cancer’s
vital
for
advancing
our
comprehension
propelling
creation
efficacious
pharmacological
treatments.
In
response
this
necessity,
review
illuminates
selection
groundbreaking
cellular
associated
including
Phosphoinositide
3-kinases/Akt,
Janus
kinase/Signal
Transducer
Activator
Transcription
3,
Nuclear
Factor
kappa-light-chain-enhancer
activated
B
cells,
Transforming
Growth
Factor-beta/Smad,
Notch,
Programmed
Death-1/Programmed
Death-Ligand
1,
Wingless
INT-1/beta-catenin-Interleukin
10.
Additionally,
we
examine
array
pertinent
like
Indoleamine-pyrrole
2,3-dioxygenase,
Human
Leukocyte
Antigen
G/E,
Glycoprotein
A
Repetitions
Predominant,
Clever-1,
Interferon
regulatory
factor
8/Osteopontin,
T-cell
immunoglobulin
mucin-domain
containing-3,
Carcinoembryonic
antigen-related
cell
adhesion
molecule
Cell
division
control
protein
42
homolog,
caspases-1
-12.
Experimental Hematology and Oncology,
Journal Year:
2024,
Volume and Issue:
13(1)
Published: Nov. 13, 2024
Abstract
Adoptive
T
cell
therapy
is
a
pivotal
strategy
in
cancer
immunotherapy,
demonstrating
potent
clinical
efficacy.
However,
its
limited
durability
often
results
primary
resistance.
High-throughput
screening
technologies,
which
include
both
genetic
and
non-genetic
approaches,
facilitate
the
optimization
of
adoptive
therapies
by
enabling
selection
biologically
significant
targets
or
substances
from
extensive
libraries.
In
this
review,
we
examine
advancements
high-throughput
technologies
their
applications
therapies.
We
highlight
use
for
cells,
tumor
other
promising
combination
strategies,
elucidate
role
identifying
small
molecules
targeted
delivery
systems
relevant
to
therapies,
providing
guidance
future
research
applications.
Frontiers in Cell and Developmental Biology,
Journal Year:
2024,
Volume and Issue:
12
Published: June 3, 2024
Cancer
remains
a
significant
global
challenge,
with
escalating
incidence
rates
and
substantial
burden
on
healthcare
systems
worldwide.
Herein,
we
present
an
in-depth
exploration
of
the
intricate
interplay
between
cancer
cell
death
pathways
tumor
immunity
within
microenvironment
(TME).
We
begin
by
elucidating
epidemiological
landscape
cancer,
highlighting
its
pervasive
impact
premature
mortality
pronounced
in
regions
such
as
Asia
Africa.
Our
analysis
centers
pivotal
concept
immunogenic
(ICD),
whereby
cells
succumbing
to
specific
stimuli
undergo
transformation
that
elicits
robust
anti-tumor
immune
responses.
scrutinize
mechanisms
underpinning
ICD
induction,
emphasizing
release
damage-associated
molecular
patterns
(DAMPs)
tumor-associated
antigens
(TAAs)
key
triggers
for
dendritic
(DC)
activation
subsequent
T
priming.
Moreover,
explore
contributions
non-apoptotic
RCD
pathways,
including
necroptosis,
ferroptosis,
pyroptosis,
TME.
Emerging
evidence
suggests
these
alternative
modalities
possess
properties
can
synergize
conventional
treatments
bolster
Furthermore,
discuss
therapeutic
implications
targeting
TME
treatment,
strategies
harness
manipulate
benefit.
By
crosstalk
modulation
TME,
this
review
aims
pave
way
development
novel
therapies
exploit
overcome
Challenges
Development
implementation
Novel
Therapies.