Leveraging Single-Cell Multi-Omics to Decode Tumor Microenvironment Diversity and Therapeutic Resistance
Pharmaceuticals,
Journal Year:
2025,
Volume and Issue:
18(1), P. 75 - 75
Published: Jan. 10, 2025
Recent
developments
in
single-cell
multi-omics
technologies
have
provided
the
ability
to
identify
diverse
cell
types
and
decipher
key
components
of
tumor
microenvironment
(TME),
leading
important
advancements
toward
a
much
deeper
understanding
how
heterogeneity
contributes
cancer
progression
therapeutic
resistance.
These
are
able
integrate
data
from
molecular
genomic,
transcriptomic,
proteomics,
metabolomics
studies
cells
at
resolution
scale
that
give
rise
full
cellular
complexity
TME.
Understanding
complex
sometimes
reciprocal
relationships
among
cells,
CAFs,
immune
ECs
has
led
novel
insights
into
their
immense
functions,
which
can
consequences
on
behavior.
In-depth
uncovered
evasion
mechanisms,
including
exhaustion
T
metabolic
reprogramming
response
hypoxia
cells.
Single-cell
also
revealed
resistance
such
as
stromal
cell-secreted
factors
physical
barriers
extracellular
matrix.
Future
examining
specific
pathways
targeting
approaches
reduce
TME
will
likely
lead
better
outcomes
with
immunotherapies,
drug
delivery,
etc.,
for
treatments.
incorporate
data,
spatial
micro-environments,
translation
personalized
therapies.
This
review
emphasizes
provide
TME,
revealing
reprogramming,
influences.
aim
guide
development
targeted
therapies,
highlighting
role
diversity
shaping
behavior
treatment
outcomes.
Language: Английский
Cross-Talk Between Cancer and Its Cellular Environment—A Role in Cancer Progression
Cells,
Journal Year:
2025,
Volume and Issue:
14(6), P. 403 - 403
Published: March 10, 2025
The
tumor
microenvironment
is
a
dynamic
and
complex
three-dimensional
network
comprising
the
extracellular
matrix
diverse
non-cancerous
cells,
including
fibroblasts,
adipocytes,
endothelial
cells
various
immune
(lymphocytes
T
B,
NK
dendritic
monocytes/macrophages,
myeloid-derived
suppressor
innate
lymphoid
cells).
A
constantly
rapidly
growing
number
of
studies
highlight
critical
role
these
in
shaping
cancer
survival,
metastatic
potential
therapy
resistance.
This
review
provides
synthesis
current
knowledge
on
modulating
cellular
progression
response
to
treatment.
Language: Английский
Role of emodin to prevent gastrointestinal cancers: recent trends and future prospective
Falak Thakral,
No information about this author
Bhairav Prasad,
No information about this author
Rippin Sehgal
No information about this author
et al.
Discover Oncology,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: April 5, 2025
Abstract
Gastrointestinal
malignancies
are
responsible
for
approximately
35%
of
all
cancer-related
deaths,
underscoring
the
critical
need
to
explore
pharmacologically
active
molecules
chemoprevention.
Emodin
(1,3,8-trihydroxy-6-methylanthraquinone),
a
natural
compound
derived
from
traditional
Chinese
and
Japanese
medicine,
has
recently
garnered
significant
attention
its
potential
anticancer
properties.
exerts
chemoprotective
effects
through
combination
antioxidative,
anti-inflammatory,
anti-proliferative
mechanisms.
Research
indicates
that
emodin
inhibits
cancer
metastasis,
disrupts
cell
cycle
progression,
impairs
survival.
These
mediated
activation
p38
MAPK/JNK1/2
signaling
pathway,
upregulation
pro-apoptotic
factors
such
as
Bax/Bcl-2
caspases,
enhancement
reactive
oxygen
species
(ROS)
levels
(Supplementary
Fig.
1).
To
optimize
emodin’s
therapeutic
potential,
it
is
crucial
further
investigate
underlying
mechanisms
action
develop
advanced
nano-targeted
delivery
systems
enhance
bioavailability.
This
review
highlights
promise
chemopreventive
agent
gastrointestinal
cancers
emphasizes
development
into
novel
clinical
formulation.
Language: Английский
Aryl hydrocarbon receptor dynamics in esophageal squamous cell carcinoma: From immune modulation to therapeutic opportunities
Mina Rahmati,
No information about this author
Hassan Moghtaderi,
No information about this author
Saeed Mohammadi
No information about this author
et al.
World Journal of Experimental Medicine,
Journal Year:
2024,
Volume and Issue:
14(3)
Published: Aug. 28, 2024
Esophageal
squamous
cell
carcinoma
(ESCC)
is
a
substantial
global
health
burden.
Immune
escape
mechanisms
are
important
in
ESCC
progression,
enabling
cancer
cells
to
the
surveillance
of
host
immune
system.
One
key
player
this
process
Aryl
Hydrocarbon
Receptor
(AhR),
which
influences
multiple
cellular
processes,
including
proliferation,
differentiation,
metabolism,
and
regulation.
Dysregulated
AhR
signaling
participates
development
by
stimulating
carcinogenesis,
epithelial-mesenchymal
transition,
escape.
Targeting
potential
therapeutic
approach
for
ESCC,
with
ligands
showing
efficacy
preclinical
studies.
Additionally,
modification
combination
therapies
present
new
opportunities
intervention.
This
review
aims
address
knowledge
gap
related
role
pathogenesis
Language: Английский
Tumor-Infiltrating Lymphocytes in Resected Esophageal and Gastric Adenocarcinomas Do Not Correlate with Tumor Regression Score After Neoadjuvant Chemotherapy: Results of a Case-Series Study
Cancers,
Journal Year:
2024,
Volume and Issue:
16(21), P. 3694 - 3694
Published: Nov. 1, 2024
:
Adenocarcinomas
of
the
esophagogastric
junction
and
stomach
present
clinical
entities
with
significant
cancer-related
morbidity
mortality,
often
requiring
multimodal
treatments.
Preoperative
chemotherapy,
mainly
FLOT
regimen,
is
increasingly
being
utilized
in
neoadjuvant
setting
for
treatment
these
malignancies,
varying
degrees
tumor
response.
Language: Английский