Unraveling the tumor microenvironment: Insights into cancer metastasis and therapeutic strategies
Cancer Letters,
Journal Year:
2024,
Volume and Issue:
591, P. 216894 - 216894
Published: April 16, 2024
This
comprehensive
review
delves
into
the
pivotal
role
of
tumor
microenvironment
(TME)
in
cancer
metastasis
and
therapeutic
response,
offering
fresh
insights
intricate
interplay
between
cells
their
surrounding
milieu.
The
TME,
a
dynamic
ecosystem
comprising
diverse
cellular
acellular
elements,
not
only
fosters
progression
but
also
profoundly
affects
efficacy
conventional
emerging
therapies.
Through
nuanced
exploration,
this
illuminates
multifaceted
nature
elucidating
its
capacity
to
engender
drug
resistance
via
mechanisms
such
as
hypoxia,
immune
evasion,
establishment
physical
barriers
delivery.
Moreover,
it
investigates
innovative
approaches
aimed
at
targeting
including
stromal
reprogramming,
modulation,
extracellular
matrix
(ECM)-targeting
agents,
personalized
medicine
strategies,
highlighting
potential
augment
treatment
outcomes.
Furthermore,
critically
evaluates
challenges
posed
by
complexity
heterogeneity
which
contribute
variable
responses
potentially
unintended
consequences.
underscores
need
identify
robust
biomarkers
advance
predictive
models
anticipate
outcomes,
well
advocate
for
combination
therapies
that
address
multiple
facets
TME.
Finally,
emphasizes
necessity
an
interdisciplinary
approach
integration
cutting-edge
technologies
unravel
intricacies
thereby
facilitating
development
more
effective,
adaptable,
treatments.
By
providing
critical
current
state
TME
research
implications
future
oncology,
highlights
evolving
landscape
field.
Language: Английский
Role of Exosomes in Cancer and Aptamer-Modified Exosomes as a Promising Platform for Cancer Targeted Therapy
Yating Wu,
No information about this author
Yue Cao,
No information about this author
Li Chen
No information about this author
et al.
Biological Procedures Online,
Journal Year:
2024,
Volume and Issue:
26(1)
Published: May 27, 2024
Abstract
Exosomes
are
increasingly
recognized
as
important
mediators
of
intercellular
communication
in
cancer
biology.
can
be
derived
from
cells
well
cellular
components
tumor
microenvironment.
After
secretion,
the
exosomes
carrying
a
wide
range
bioactive
cargos
ingested
by
local
or
distant
recipient
cells.
The
released
act
through
variety
mechanisms
to
elicit
multiple
biological
effects
and
impact
most
if
not
all
hallmarks
cancer.
Moreover,
owing
their
excellent
biocompatibility
capability
being
easily
engineered
modified,
currently
exploited
promising
platform
for
targeted
therapy.
In
this
review,
we
first
summarize
current
knowledge
roles
risk
etiology,
initiation
progression
cancer,
underlying
molecular
mechanisms.
aptamer-modified
exosome
therapy
is
then
briefly
introduced.
We
also
discuss
future
directions
emerging
biology
perspective
Language: Английский
Induction Radiochemotherapy for Esophageal Cancer: Long-Term Outcomes from a Single-Center Study
Journal of Clinical Medicine,
Journal Year:
2025,
Volume and Issue:
14(2), P. 394 - 394
Published: Jan. 10, 2025
Background/Objectives:
The
management
of
esophageal
cancer
(EC)
remains
a
significant
clinical
challenge,
particularly
in
optimizing
therapeutic
strategies
for
different
stages
and
subgroups.
This
study
assessed
the
impact
preoperative
radiochemotherapy
(CRT)
on
staging
identified
subgroups
whom
definitive
CRT
(dCRT)
may
provide
favorable
alternative
to
surgery.
Methods:
Sixty-one
patients
with
adenocarcinoma
or
squamous
cell
carcinoma
were
enrolled.
Pre-treatment
included
computed
tomography,
gastroscopy
biopsy,
comprehensive
laboratory
evaluations.
Patients
received
following
CROSS
dCRT
protocols
based
tumor
stage.
Surgical
approaches
staged
esophagectomy
single-stage
Ivor
Lewis
procedures.
Four
declined
surgery
treated
dCRT.
Postoperative
outcomes
evaluated
using
pTNM
classification.
Follow-up
imaging
endoscopic
surveillance.
Statistical
analyses
changes
factors
influencing
treatment
outcomes.
Results:
significantly
reduced
T
stage
across
entire
cohort
(p
=
0.0002),
complete
pathological
response
(pT0N0M0)
observed
54.5%
induction
0.0001).
Male
demonstrated
reduction
0.0008),
while
similar
trend
females
was
not
0.068).
Among
declining
surgery,
acceptable
oncologic
control
over
mean
follow-up
4
±
0.79
years.
Conclusions:
Preoperative
effectively
downstages
EC
achieves
high
rates
response,
especially
male
patients.
Therefore,
be
viable
selected
patients,
emphasizing
need
individualized
optimize
These
findings
underscore
importance
refining
multimodal
care.
Language: Английский
Impact of Timing the Combination of Radiotherapy and PD-1 Inhibitors on Outcomes in Patients with Hepatocellular Carcinoma
Journal of Hepatocellular Carcinoma,
Journal Year:
2025,
Volume and Issue:
Volume 12, P. 123 - 134
Published: Jan. 1, 2025
Purpose:The
optimal
timing
for
combining
radiotherapy
with
immunotherapy
in
patients
hepatocellular
carcinoma
(HCC)
remains
uncertain
and
affects
treatment
efficacy
patient
outcomes.This
study
aimed
to
evaluate
compare
the
treatment-related
adverse
events
(TRAEs)
of
synchronously
administered
programmed
cell
death
protein
(PD)-1
inhibitors
sequential
administration
HCC.Patients
Methods:
We
retrospectively
enrolled
67
HCC
who
were
undergoing
liver
PD-1
inhibitor
therapy
at
two
medical
centers
between
July
2017
April
2023.Additionally,
we
created
an
experimental
tumor
model
using
6-week-old
female
mice
validate
our
findings.Results:
In
concurrent
group,
median
overall
survival
was
indefinite;
however,
it
13
months
group
(95%
confidence
interval
[CI]
6.7-19.3months,
P=0.010).The
progression-free
significantly
longer
(12
months,
95%
CI
9.5-14.5
months)
than
(7
1.3-12.7
months;
P=0.043).Grade
3/4
TRAEs
occurred
30.4%
(concurrent)
28.6%
(sequential)
without
any
deaths.In
mouse
model,
synchronous
inhibited
growth
compared
(293.4±45.18mm
3
versus
602.7
±41.68
mm
;
P=0.001).Flow
cytometry
revealed
increased
Tregs/CD3
+
T
ratio
a
decreased
CD8
/Treg
postradiotherapy,
suggesting
immunosuppressive
microenvironment.Conclusion:
Synchronous
demonstrated
superior
treating
treatment,
manageable
events.The
rapid
increase
Tregs
after
may
contribute
reduced
plus
inhibitors.
Language: Английский
The Role of cGAS-STING in Remodeling the Tumor Immune Microenvironment Induced by Radiotherapy
Qingyu Jiang,
No information about this author
Zhiheng Chen,
No information about this author
Jin Jiang
No information about this author
et al.
Critical Reviews in Oncology/Hematology,
Journal Year:
2025,
Volume and Issue:
209, P. 104658 - 104658
Published: Feb. 15, 2025
Language: Английский
Immunological Effects of Proton Radiotherapy: New Opportunities and Challenges in Cancer Therapy
Anhang Zhang,
No information about this author
L. T. Fan,
No information about this author
Qi Liu
No information about this author
et al.
Cancer Innovation,
Journal Year:
2025,
Volume and Issue:
4(2)
Published: March 7, 2025
ABSTRACT
Radiation
therapy
can
be
categorised
by
particle
type
into
photon,
proton
and
heavy
ion
therapies.
Proton
radiotherapy
is
highlighted
due
to
its
unique
physical
properties,
such
as
the
Bragg
peak
minimal
exit
dose,
which
offer
superior
dose
distribution.
This
makes
especially
advantageous
for
treating
tumours
near
vital
organs
with
complex
structures,
gliomas
brain,
nasopharyngeal
carcinoma
brainstem
mediastinal
heart.
irradiation
induce
distant
effects
through
immunogenicity
within
target
area.
The
reduced
low‐dose
zone
outside
provides
better
lymphatic
system
protection
immune
benefits.
Additionally,
combining
immunotherapy
may
further
biological
advantages.
These
features
make
a
promising
option
in
cancer
treatment.
article
aid
understanding
of
lead
new
effective
options
tumour
Language: Английский
Nanoparticle-based drug delivery systems: opportunities and challenges in the treatment of esophageal squamous cell carcinoma (ESCC)
Linjia Peng,
No information about this author
Zixuan Gao,
No information about this author
Yan‐Feng Liang
No information about this author
et al.
Nanoscale,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Esophageal
squamous
cell
carcinoma
(ESCC)
is
an
aggressive
malignancy
characterized
by
limited
treatment
options
and
poor
prognosis.
Nanoparticle-based
drug
delivery
systems
have
emerged
as
a
promising
strategy
to
enhance
cancer
therapy
efficacy
improving
targeting,
reducing
toxicity,
enabling
multifunctional
applications.
This
review
highlights
some
key
types
of
nanoparticles,
including
liposomes,
polymeric
metallic
dendrimers,
quantum
dots,
which
could
effectively
improve
the
various
drugs
used
in
chemotherapy,
radiotherapy,
immunotherapy,
offering
more
precise
effective
options.
With
ability
stability
overcome
biological
barriers,
nanoparticle-based
represent
transformative
for
ESCC
treatment.
Despite
challenges,
such
biocompatibility
scalability,
future
holds
great
promise,
particularly
development
personalized
nanomedicine
novel
therapeutic
approaches
targeting
tumor
microenvironment.
ongoing
advancements,
hold
immense
potential
revolutionize
patient
outcomes.
Language: Английский
Tumor Microenvironment Dynamics of Triple-Negative Breast Cancer Under Radiation Therapy
Suryakant Niture,
No information about this author
Subhajit Ghosh,
No information about this author
Jerry J. Jaboin
No information about this author
et al.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(6), P. 2795 - 2795
Published: March 20, 2025
Triple-negative
breast
cancer
(TNBC)
is
an
aggressive
subtype
of
characterized
by
the
absence
estrogen
receptors
(ER),
progesterone
(PR),
and
HER2
expression.
While
TNBC
relatively
less
common,
accounting
for
only
10–15%
initial
diagnosis,
due
to
its
nature,
it
carries
a
worse
prognosis
in
comparison
hormone
receptor-positive
counterparts.
Despite
significant
advancements
screening,
treatment
cancer,
remains
important
public
health
burden.
Following
with
chemotherapy,
surgery,
radiation,
over
40%
patients
experience
relapse
within
3
years
achieve
least
benefit
from
post-mastectomy
radiation.
The
tumor
microenvironment
environment
(TME)
pivotal
initiation,
progression,
immune
evasion,
resistance,
prognosis.
TME
complex
network
that
consists
cells,
non-immune
soluble
factors
located
region
adjacent
modulates
therapeutic
response
differentially
between
TNBC.
mechanisms
underlying
radiation
resistance
remain
unclear,
immunosuppressive
has
been
implicated
chemotherapeutic
resistance.
Radiation
therapy
(RT)
known
alter
TME;
however,
changes
elicited
are
poorly
date,
whether
these
contribute
unknown.
This
review
delves
into
distinct
characteristics
TME,
explores
how
RT
influences
dynamics,
examines
radiosensitization,
radioresistance,
responses.
Language: Английский
A Boolean network model of hypoxia, mechanosensing and TGF-β signaling captures the role of phenotypic plasticity and mutations in tumor metastasis
GL Greene,
No information about this author
Ian Zonfa,
No information about this author
Erzsébet Ravasz Regan
No information about this author
et al.
PLoS Computational Biology,
Journal Year:
2025,
Volume and Issue:
21(4), P. e1012735 - e1012735
Published: April 16, 2025
The
tumor
microenvironment
aids
cancer
progression
by
promoting
several
hallmarks,
independent
of
cancer-related
mutations.
Biophysical
properties
this
environment,
such
as
the
stiffness
matrix
cells
adhere
to
and
local
cell
density,
impact
proliferation,
apoptosis,
epithelial
mesenchymal
transition
(EMT).
latter
is
a
rate-limiting
step
for
invasion
metastasis,
enhanced
in
hypoxic
environments
but
hindered
soft
matrices
and/or
high
densities.
As
these
influences
are
often
studied
isolation,
crosstalk
between
hypoxia,
biomechanical
signals,
classic
EMT
driver
TGF-β
not
well
mapped,
limiting
our
ability
predict
anticipate
behaviors
changing
environments.
To
address
this,
we
built
Boolean
regulatory
network
model
that
integrates
signaling
with
mechanosensitive
EMT,
which
includes
EMT-promoting
mitogens
cycle
control,
apoptosis.
Our
reproduces
requirement
Hif-1α
anti-proliferative
effects
strong
stabilization
during
protection
from
anoikis,
hypoxia-driven
EMT.
We
offer
experimentally
testable
predictions
about
effect
VHL
loss
on
or
without
secondary
oncogene
activation.
Taken
together,
serves
predictive
framework
synthesize
responses
associated
metastasis
healthy
vs.
mutant
cells.
single-cell
key
towards
more
extensive
models
cover
damage-response
senescence,
integrating
most
cell-autonomous
hallmarks
into
single
can,
turn,
control
behavior
silico
within
tissue
homeostasis
carcinoma.
Language: Английский
A new target of radiotherapy combined with immunotherapy: regulatory T cells
Dongmei Song,
No information about this author
Yun Ding
No information about this author
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
14
Published: Jan. 8, 2024
Radiotherapy
is
one
important
treatment
for
malignant
tumours.
It
widely
believed
today
that
radiotherapy
has
not
only
been
used
as
a
local
tumour
method,
but
also
can
induce
systemic
anti-tumour
responses
by
influencing
the
microenvironment,
its
efficacy
limited
immunosuppression
microenvironment.
With
advancement
of
technology,
immunotherapy
entered
golden
age
rapid
development,
gradually
occupying
place
in
clinical
treatment.
Regulatory
T
cells
(Tregs)
distributing
microenvironment
play
an
role
mediating
development.
This
article
analyzes
immunotherapy,
interaction
between
Tregs,
tumours
and
radiotherapy.
briefly
introduces
immunotherapies
targeting
aiming
to
provide
new
strategies
combined
with
Immunotherapy.
Language: Английский