Bridging epigenomics and tumor immunometabolism: molecular mechanisms and therapeutic implications
Molecular Cancer,
Journal Year:
2025,
Volume and Issue:
24(1)
Published: March 8, 2025
Epigenomic
modifications—such
as
DNA
methylation,
histone
acetylation,
and
methylation—and
their
implications
in
tumorigenesis,
progression,
treatment
have
emerged
a
pivotal
field
cancer
research.
Tumors
undergo
metabolic
reprogramming
to
sustain
proliferation
metastasis
nutrient-deficient
conditions,
while
suppressing
anti-tumor
immunity
the
tumor
microenvironment
(TME).
Concurrently,
immune
cells
within
immunosuppressive
TME
adaptations,
leading
alterations
function.
The
complicated
interplay
between
metabolites
epigenomic
modulation
has
spotlighted
significance
of
regulation
immunometabolism.
In
this
review,
characteristics
modification
associated
with
tumors
are
systematically
summarized
alongside
regulatory
roles
Classical
emerging
approaches
delineated
broaden
boundaries
research
on
crosstalk
immunometabolism
epigenomics.
Furthermore,
we
discuss
potential
therapeutic
strategies
that
target
modulate
modifications,
highlighting
burgeoning
synergy
therapies
immunotherapy
promising
avenue
for
treatment.
Language: Английский
Single-cell RNA sequencing elucidates cellular plasticity in esophageal small cell carcinoma following chemotherapy treatment
Frontiers in Genetics,
Journal Year:
2025,
Volume and Issue:
15
Published: Jan. 9, 2025
Small
cell
carcinoma
of
the
esophagus
(SCCE)
is
a
rare
and
aggressively
progressing
malignancy
that
presents
considerable
clinical
challenges.Although
chemotherapy
can
effectively
manage
symptoms
during
earlystages
SCCE,
its
long-term
effectiveness
notably
limited,
with
theunderlying
mechanisms
remaining
largely
undefined.
In
this
study,
weemployed
single-cell
RNA
sequencing
(scRNA-seq)
to
analyze
SCCE
samplesfrom
single
patient
both
before
after
treatment.
Our
analysisrevealed
significant
cellular
plasticity
alterations
in
tumormicroenvironment's
composition.
Notably,
we
observed
an
increase
intumor
diversity
coupled
reductions
T
cells,
B
myeloid-likecells.
The
pre-treatment
samples
predominantly
featured
cells
amiddle
transitional
state,
while
post-treatment
exhibited
expandedpresence
terminal,
initial-to-terminal
(IniTerm),
universally
alteredstates.
Further
analysis
highlighted
dynamic
interactions
between
tumor
andimmune
changes
detected
key
signaling
pathways,
suchas
TIGIT-PVR
MDK-SDC4.
This
study
elucidates
complex
dynamics
cellplasticity
following
chemotherapy,
providing
new
insights
identifyingpotential
therapeutic
targets
enhance
treatment
efficacy.
Language: Английский
Hi-C profiling in tissues reveals 3D chromatin-regulated breast tumor heterogeneity informing a looping-mediated therapeutic avenue
Lavanya Choppavarapu,
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Kun Fang,
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Tianxiang Liu
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et al.
Cell Reports,
Journal Year:
2025,
Volume and Issue:
44(4), P. 115450 - 115450
Published: March 18, 2025
Language: Английский
Role of Tumor-Associated Macrophages in Breast Cancer Immunotherapy
Yan He,
No information about this author
Quan Liu,
No information about this author
Zhuo-wa Luo
No information about this author
et al.
Frontiers in Bioscience-Landmark,
Journal Year:
2025,
Volume and Issue:
30(4)
Published: April 23, 2025
Breast
cancer
(BC)
is
the
second
leading
cause
of
death
among
women
worldwide.
Immunotherapy
has
become
an
effective
treatment
for
BC
patients
due
to
rapid
development
medical
technology.
Considerable
breakthroughs
have
been
made
in
research,
marking
beginning
a
new
era
treatment.
Among
them,
various
immunotherapies
such
as
immune
checkpoint
inhibitors
(ICIs),
vaccines,
and
adoptive
cell
transfer
are
good
prospects.
The
tumor
microenvironment
(TME)
plays
crucial
role
determining
outcomes
immunotherapy.
Tumor-associated
macrophages
(TAMs)
key
component
TME,
with
immunomodulatory
effect
closely
related
evasion
cells,
thereby
affecting
malignant
progression.
TAMs
also
significantly
affect
therapeutic
ICIs
(such
programmed
1/programmed
ligand
1
(PD-1/PD-L1)
inhibitors).
composed
multiple
heterogeneous
subpopulations,
including
M1
phenotypes
(M1)
M2
(M2).
Furthermore,
they
mainly
play
M2-like
moderate
variety
harmful
consequences
angiogenesis,
immunosuppression,
metastasis.
Therefore,
area
focus
therapies.
However,
several
immunotherapy
studies
demonstrated
that
only
small
number
solid
cancers,
still
faces
relevant
challenges
tumors.
This
review
explores
immunotherapy,
summarizing
their
involvement
development.
It
explains
classification
functions
TAMs,
outlines
current
approaches
combination
therapies,
discusses
potential
strategies
immuno-oncology
treatments.
Language: Английский