International Journal of Colorectal Disease,
Journal Year:
2024,
Volume and Issue:
39(1)
Published: Nov. 20, 2024
Abstract
Purpose
Colorectal
cancer
cells
containing
mobile
lipids
are
said
to
be
an
early
indicator
of
chemotherapy
effects.
The
objective
the
study
was
examine
frequency
and
clinical
relevance
intratumoral
fat
deposition
in
colorectal
liver
metastases
(CRLM)
post-chemotherapy
using
dual-echo
chemical
shift
gradient-echo
magnetic
resonance
imaging
(MRI).
Methods
A
retrospective
analysis
98
patients
with
CRLM
diagnosed
between
2017
2022
(69
M,
mean
age
62.87
±
10.73
years
old)
who
had
MRI
after
performed.
On
MRI,
evaluated.
signal
intensity
drop
≥
12%
opposed-phase
images
vs.
in-phase
indicated
fat.
After
chemotherapy,
presence
correlated
patients’
overall
survival.
Results
Before
0
(0%)
29
(29.59%)
exhibited
number
ranged
from
1
25
a
median
3
size
32.58
22.95
mm.
groups
statistically
different
survival
times.
Overall
shorter
for
(32
months
(24–60,
95%
CI))
than
without
(48
(36–NA,
CI)).
Conclusion
In
our
group,
nearly
30%
chemotherapy.
Patients
have
time.
correlates
poor
long-term
prognosis.
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer,
Journal Year:
2025,
Volume and Issue:
unknown, P. 189259 - 189259
Published: Jan. 1, 2025
As
immunosuppressive
cells,
Regulatory
T
cells
(Tregs)
exert
their
influence
on
tumor
immune
escape
within
the
microenvironment
(TME)
by
effectively
suppressing
activity
of
other
thereby
significantly
impeding
anti-tumor
response.
In
recent
years,
metabolic
characteristics
Tregs
have
become
a
focus
research,
especially
important
role
lipid
metabolism
in
maintaining
function
Tregs.
Consequently,
targeted
interventions
aimed
at
modulating
been
recognized
as
an
innovative
and
promising
approach
to
enhance
effectiveness
immunotherapy.
This
review
presents
comprehensive
overview
pivotal
regulating
Tregs,
with
specific
targeting
augment
responses.
Furthermore,
we
discuss
potential
opportunities
challenges
associated
this
strategy,
aiming
provide
novel
insights
for
enhancing
efficacy
cancer
Frontiers in Cell and Developmental Biology,
Journal Year:
2024,
Volume and Issue:
12
Published: June 12, 2024
Lipids,
the
primary
constituents
of
cell
membrane,
play
essential
roles
in
nearly
all
cellular
functions,
such
as
cell-cell
recognition,
signaling
transduction,
and
energy
provision.
Lipid
metabolism
is
necessary
for
maintenance
life
since
it
regulates
balance
between
processes
synthesis
breakdown.
Increasing
evidence
suggests
that
cancer
cells
exhibit
abnormal
lipid
metabolism,
significantly
affecting
their
malignant
characteristics,
including
self-renewal,
differentiation,
invasion,
metastasis,
drug
sensitivity
resistance.
Prominent
oncogenic
pathways
modulate
metabolic
gene
expression
elevate
enzyme
activity
include
phosphoinositide
3-kinase
(PI3K)/AKT,
MAPK,
NF-kB,
Wnt,
Notch,
Hippo
pathway.
Conversely,
when
are
not
regulated,
they
can
lead
to
malfunctions
signal
transduction
pathways.
This,
turn,
enables
uncontrolled
growth
by
providing
energy,
building
blocks,
redox
potentials.
Therefore,
targeting
metabolism-associated
could
be
an
effective
therapeutic
approach
decrease
incidence
promote
survival.
This
review
sheds
light
on
interactions
reprogramming
cancer.
Exploring
a
target
provide
promising
creating
anticancer
treatments
identifying
inhibitors.
Additionally,
we
have
also
provided
overview
drugs
this
review.
ABSTRACT
Agaricus
blazei
Murill
polysaccharide
(ABMP)
has
been
found
to
exhibit
significant
immune
regulatory
effects,
making
them
a
promising
candidate
for
complementary
the
pharmacological
treatment
of
colorectal
cancer
immune‐related
diseases.
As
prevalence
among
younger
individuals
increases,
possible
age‐dependent
anticancer
modulatory
effect
ABMP
not
clarified.
This
study
evaluated
immunoregulatory
efficacy
polysaccharides
extraction
from
A.
in
colon
tumor.
Hematoxylin‐eosin
staining,
immunohistochemistry,
and
vibrational
spectroscopic
image
analysis
subcutaneous
tumor
tissues
after
preventive
intervention
14
weeks
were
analyzed
depth.
In
vivo
data
demonstrated
that
could
more
effectively
inhibit
growth
mice
at
8
compared
with
12
months
old
without
toxic
side
effect.
Concurrently,
Raman
imaging
spectroscopy
showed
significantly
reduce
lipid
content
microenvironment
(TME)
8‐month‐old
tumor‐bearing
mice,
suggesting
changes
TME
are
closely
related
activity.
These
results
stress
importance
considering
age
as
factor
adjuvant
therapy.
work
highlights
first
time
is
key
determinant
effectiveness
by
affecting
levels
thereby
exerting
Cells,
Journal Year:
2025,
Volume and Issue:
14(7), P. 488 - 488
Published: March 25, 2025
Inflammation
is
an
essential
component
of
the
immune
response
that
protects
host
against
pathogens
and
facilitates
tissue
repair.
Chronic
inflammation
a
critical
factor
in
cancer
development
progression.
It
affects
every
stage
tumor
development,
from
initiation
promotion
to
invasion
metastasis.
Tumors
often
create
inflammatory
microenvironment
induces
angiogenesis,
suppression,
malignant
growth.
Immune
cells
within
interact
actively
with
cells,
which
drives
progression
through
complex
molecular
mechanisms.
triggered
by
factors
such
as
infections,
obesity,
environmental
toxins
strongly
linked
increased
risk.
However,
acute
responses
can
sometimes
boost
antitumor
immunity;
thus,
presents
both
challenges
opportunities
for
therapeutic
intervention.
This
review
examines
how
contributes
biology,
emphasizing
its
dual
role
tumorigenesis
potential
target.
Discover Oncology,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: April 2, 2025
Immunotherapy
in
the
treatment
of
cancer,
with
immune
inhibitors
helps
many
cancer
types.
Many
patients
still
encounter
resistance
to
these
treatments,
though.
This
is
mediated
by
metabolic
changes
tumour
microenvironment
and
cells.
The
development
novel
treatments
overcome
boost
immunotherapy's
effectiveness
depends
on
changes.
review
concentrates
molecular
mechanisms
through
which
transformation
contributes
immunotherapy
resistance.
Additionally,
research
therapeutic
approaches
that
target
pathways
enhance
for
We
used
databases
available
PubMed,
Scopus,
Web
Science
perform
a
thorough
peer-reviewed
literature.
focusing
tumor
microenvironment,
mechanisms,
metabolism.
study
covers
oxidative
phosphorylation,
glycolysis,
lipid
metabolism,
amino
acid
An
immunosuppressive
produced
cells,
such
as
dysregulated
enhanced
glutaminolysis,
increased
glycolysis
(Warburg
effect).
Myeloid-derived
suppressor
cells
regulatory
T
are
promoted,
responses
suppressed,
cell
activity
impaired
when
lactate
other
metabolites
build
up.
metabolism
acids
arginine
tryptophan,
nutrients
crucial
function.
By
enhancing
their
function
alterations
aid
checkpoint
inhibitors.
Metabolic
change
plays
key
role
Gaining
knowledge
processes
can
help
develop
efficient
improve
effectiveness.
In
order
determine
best
targets
intervention,
future
studies
should
concentrate
patient-specific
profiling.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 22, 2025
This
study
focused
on
the
role
of
plasma
cells
in
multiple
myeloma
(MM)
and
associated
potential
mechanisms.
Transcriptomic
data
MM
various
gene
sets
from
several
public
databases
were
downloaded
for
subsequent
analyses.
Through
single-cell
sequencing,
10
major
cell
types
identified
annotated.
The
differential
expression
pathway
enrichment
between
different
subtypes
as
well
communication
analysis,
transcriptional
regulation
analysis
conjunction
with
malignant
subpopulation
performed.
Next,
samples
clustered
into
two
groups
by
applying
non-negative
matrix
factorization
(NMF).
Additional
revealed
notable
disparities
survival
clusters,
correlation
genes
involved
classical
metabolic
pathways
dysregulation,
thus
confirming
stability
validity
clustering.
Subsequently,
Weighted
Gene
Co-expression
Network
Analysis
was
performed
hub
modules
most
strongly
clustering
extracted.
We
then
constructed
a
prognostic
prediction
model
using
Least
Absolute
Shrinkage
Selection
Operator
multiCox
regression
analysis.
predictive
accuracy
evaluated
robustness
confirmed
separate
validation
cohort.
dysregulation
risk
analyzed.
Ultimately,
an
investigation
conducted
association
immunological
features,
terms
antitumor
immunotherapy,
tumor
microenvironment,
immune
checkpoints.
provides
in-depth
mechanisms
underlying
development
offers
new
directions
to
improve
therapeutic
approaches
enhance
patient
outcomes.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(16), P. 8836 - 8836
Published: Aug. 14, 2024
Colorectal
cancer
(CRC)
affects
approximately
2
million
people
worldwide.
Obesity
is
the
major
risk
factor
for
CRC.
In
addition,
obesity
contributes
to
a
chronic
inflammatory
stage
that
enhances
tumor
progression
through
secretion
of
proinflammatory
cytokines.
addition
an
increased
response,
obesity-associated
presents
accrued
molecular
factors
related
characteristics,
such
as
genome
instability,
sustained
cell
proliferation,
telomere
dysfunctions,
angiogenesis,
and
microbial
alteration,
among
others.
Despite
evidence
accumulated
over
last
few
years,
treatments
CRC
do
not
differ
from
in
normal-weight
individuals.
this
review,
we
summarize
current
knowledge
on
cancer,
including
its
epidemiology,
factors,
treatments.
Finally,
enumerate
possible
new
therapeutic
targets
may
improve
conditions
obese
patients.
key
development
CRC,
resulting
reversal
should
be
considered
strategy
improving
antineoplastic
therapies.
Breast Cancer Research,
Journal Year:
2024,
Volume and Issue:
26(1)
Published: Nov. 25, 2024
The
clinically
high
comorbidity
between
polycystic
ovary
syndrome
(PCOS)
and
breast
cancer
(BC)
has
been
extensively
reported.
However,
limited
knowledge
exists
regarding
their
shared
genetic
basis
underlying
mechanisms.
Leveraging
summary
statistics
from
the
largest
genome-wide
association
studies
(GWASs)
to
date,
we
conducted
a
comprehensive
cross-trait
analysis
of
PCOS
BC.
A
variety
statistical
methods
were
employed
uncover
potential
causes.
Our
revealed
overlap
three
trait
pairs.
After
partitioning
genome
into
2,495
independent
regions,
identified
two
loci,
chr8:
75,011,700–76,295,483
chr17:
6,305,079–7,264,458,
with
significant
localized
correlations.
Pleiotropic
under
composite
null
hypothesis
1,183
pleiotropic
single
nucleotide
polymorphisms
(SNPs)
across
FUMA
mapped
26
regions
16q12.2
6q25.1
duplicated
all
pairs,
while
COLOC
detected
loci
colocalization
evidence.
Gene-based
23
unique
candidate
genes,
including
FTO
by
as
well
SER1,
RALB,
others
in
Pathway
enrichment
further
highlighted
key
biological
pathways,
primarily
involving
pathways
metabolism
regulation
autophagy,
cellular
catabolic
process,
positive
process.
Latent
Heritable
Confounder
Mendelian
randomization
(LHC-MR)
supported
causal
relationship
both
BCALL
ERPBC
but
not
ERNBC.
In
conclusion,
our
BC,
specific
identical
mechanisms
causality
various
BC
subtypes,
which
could
better
explains
genetics
co-morbidity
rather
than
These
findings
provide
new
insights
these
complex
diseases,
have
important
implications
for
clinical
disease
intervention,
treatment,
improved
prognosis.