The
CXC
chemokine
receptor
4
(CXCR4,
CD184)
is
a
member
of
the
G
protein-coupled
family
that
expressed
in
most
leukocytes.
Overexpression
CXCR4
associated
with
poor
prognosis
not
only
hematopoietic
malignancy
but
also
solid
tumors.
Because
an
attractive
target
for
tumor
therapy,
reliable
preclinical
murine
models
using
anti-CXCR4
monoclonal
antibodies
(mAbs)
have
been
warranted.
This
study
established
novel
anti-mouse
(mCXCR4)
mAb
Cell-Based
Immunization
and
Screening
(CBIS)
method.
Flow
cytometric
analysis
showed
anti-mCXCR4
mAb,
Cx4Mab-1
(rat
IgG2a,
kappa),
recognized
mCXCR4-overexpressed
Chinese
hamster
ovary-K1
(CHO/mCXCR4)
cells
endogenously
mCXCR4-expressing
mouse
myeloma
P3X63Ag8U.1
(P3U1)
cells.
Furthermore,
did
recognize
mCXCR4-knockout
P3U1
dissociation
constants
CHO/mCXCR4
were
determined
as
6.4
×
10−9
M
2.3
10-9
M,
respectively,
indicating
possesses
high
affinity
to
both
endogenous
exogenous
These
results
indicate
could
be
useful
tool
models.
Military Medical Research,
Год журнала:
2025,
Номер
12(1)
Опубликована: Фев. 11, 2025
Abstract
Cancer
recurrence,
driven
by
the
phenomenon
of
tumor
dormancy,
presents
a
formidable
challenge
in
oncology.
Dormant
cancer
cells
have
ability
to
evade
detection
and
treatment,
leading
relapse.
This
review
emphasizes
urgent
need
comprehend
dormancy
its
implications
for
recurrence.
Despite
notable
advancements,
significant
gaps
remain
our
understanding
mechanisms
underlying
lack
reliable
biomarkers
predicting
provides
comprehensive
analysis
cellular,
angiogenic,
immunological
aspects
dormancy.
It
highlights
current
therapeutic
strategies
targeting
dormant
cells,
particularly
combination
therapies
immunotherapies,
which
hold
promise
preventing
By
elucidating
these
proposing
innovative
research
methodologies,
this
aims
deepen
ultimately
facilitating
development
more
effective
recurrence
improving
patient
outcomes.
Frontiers in Immunology,
Год журнала:
2025,
Номер
16
Опубликована: Март 13, 2025
Gastric
cancer
(GC)
ranks
as
the
fifth
most
prevalent
on
a
global
scale,
with
HER2-positive
GC
representing
distinct
subtype
that
exhibits
more
intricate
biological
characteristics.
Conventional
chemotherapy
typically
restricted
efficacy
in
management
of
GC.
In
light
incessant
advancement
molecular
targeted
therapies,
targeting
HER2
has
emerged
promising
therapeutic
approach
for
this
subtype.
The
advent
antibody-drug
conjugates
(ADCs)
and
chimeric
antigen
receptor
T-cell
therapy
(CAR-T)
furnished
novel
treatment
alternatives
Nevertheless,
owing
to
pronounced
heterogeneity
complex
tumor
microenvironment,
drug
resistance
frequently
emerges,
thereby
substantially
influencing
effectiveness
HER2-targeted
therapy.
This
article
comprehensively
summarizes
deliberates
upon
strategies
well
underlying
mechanisms.
Scientific Reports,
Год журнала:
2024,
Номер
14(1)
Опубликована: Май 28, 2024
Abstract
The
prognosis
for
patients
with
colorectal
cancer
(CRC)
remains
worse
than
expected
due
to
metastasis,
recurrence,
and
resistance
chemotherapy.
Colorectal
stem
cells
(CRCSCs)
play
a
vital
role
in
tumor
chemotherapy
resistance.
However,
there
are
currently
no
prognostic
markers
based
on
CRCSCs-related
genes
available
clinical
use.
In
this
study,
single-cell
transcriptome
sequencing
was
employed
distinguish
(CSCs)
the
CRC
microenvironment
analyze
their
properties
at
level.
Subsequently,
data
from
TCGA
GEO
databases
were
utilized
develop
risk
model
validate
its
diagnostic
performance.
Additionally,
functional
enrichment,
immune
response,
chemotherapeutic
drug
sensitivity
of
relevant
investigated.
Lastly,
key
gene
RPS17
identified
as
potential
marker
therapeutic
target
further
comprehensive
studies.
Our
findings
provide
new
insights
into
treatment
offer
novel
perspectives
systematic
understanding
development.
Biomedicines,
Год журнала:
2024,
Номер
12(8), С. 1809 - 1809
Опубликована: Авг. 9, 2024
Oral
cancer
(OC)
presents
a
significant
global
health
burden
with
rising
incidence
rates.
Despite
advancements
in
diagnosis
and
treatments,
the
survival
rate
for
OC
patients,
particularly
those
advanced
or
recurrent
disease,
remains
low
at
approximately
20%.
This
poor
prognosis
is
often
due
to
small
population
of
stem
cells
(CSCs)
that
are
capable
self-renewal
immune
evasion,
playing
pivotal
roles
proliferation,
tumor
initiation,
progression,
metastasis,
therapy
resistance.
Exosomes,
which
nano-sized
extracellular
vesicles
(EVs),
have
emerged
as
crucial
mediators
cell-to-cell
communication
within
microenvironment
(TME).
These
carry
diverse
molecules
such
DNA,
RNA,
proteins,
lipids,
metabolites,
influencing
various
cellular
processes.
Emerging
evidence
suggests
CSC-derived
EVs
significantly
promote
progression
metastasis
maintain
balance
between
CSCs
non-CSCs,
vital
intracellular
TME
oral
cancer.
Recent
reports
indicate
cell-derived
(OCSC-EVs)
influence
stemness,
angiogenesis,
reoccurrence,
drug
Understanding
OCSC-EVs
could
improve
diagnosis,
prognosis,
therapy.
In
this
mini-review,
we
explore
OCSC-derived
exosomes
cancer,
examining
their
potential
diagnostic
prognostic
biomarkers
reflect
CSC
characteristics,
delve
into
therapeutic
implications,
emphasizing
However,
despite
promising
potential,
several
challenges
remain,
including
need
standardize
isolation
characterization
methods
elucidate
exosome-mediated
mechanisms.
Thus,
comprehensive
understanding
pave
way
innovative
strategies
clinical
outcomes
patients.
Cells,
Год журнала:
2024,
Номер
13(11), С. 958 - 958
Опубликована: Июнь 1, 2024
Autophagy
is
a
globally
conserved
cellular
activity
that
plays
critical
role
in
maintaining
homeostasis
through
the
breakdown
and
recycling
of
constituents.
In
recent
years,
there
has
been
much
emphasis
given
to
its
complex
cancer
stem
cells
(CSCs)
cell
treatment.
This
study
examines
molecular
processes
support
autophagy
how
it
regulated
context
CSCs
Although
dual
management
CSCs,
affecting
their
removal
as
well
maintenance,
intricate
interaction
between
several
signaling
channels
control
survival
death
part
mechanism
not
elucidated.
Given
have
development,
progression,
resistance
treatment
tumors,
imperative
comprehend
biological
activities.
are
important
for
biology
because
they
also
show
tissue
regeneration
model
helps
with
organoid
regeneration.
other
words,
manipulation
viable
therapeutic
approach
therapy.
Both
synthetic
natural
substances
target
pathways
demonstrated
promise
improving
cell-based
therapies
eliminating
CSCs.
Nevertheless,
difficulties
associated
limitations
CSC
regulation,
including
mechanisms
off-target
effects.
Thus,
regulation
offers
versatile
strategy
focusing
on
enhancing
results
Therefore,
understanding
interactions
would
be
essential
creating
treatments
work
both
regenerative
medicine
International Journal of Molecular Sciences,
Год журнала:
2025,
Номер
26(5), С. 2108 - 2108
Опубликована: Фев. 27, 2025
Gliomas,
particularly
glioblastoma
(GBM),
are
among
the
most
challenging
brain
tumors
due
to
their
complex
and
dynamic
tumor
microenvironment
(TME).
The
TME
plays
a
pivotal
role
in
progression,
immune
evasion,
resistance
therapy
through
intricate
interactions
glioma
cells,
components,
neurons,
astrocytes,
extracellular
matrix,
blood-brain
barrier.
Targeting
has
demonstrated
potential,
with
immunotherapies
such
as
checkpoint
inhibitors
neoadjuvant
therapies
enhancing
responses.
Nonetheless,
overcoming
immunosuppressive
landscape
metabolic
adaptations
continues
pose
significant
challenges.
This
review
explores
diverse
cellular
molecular
mechanisms
that
shape
TME.
A
deeper
understanding
of
these
holds
promise
for
providing
novel
therapeutic
opportunities
improve
treatment
outcomes.
Targeted Oncology,
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 27, 2025
Soft-tissue
sarcomas
represent
a
diverse
group
of
rare
malignancies
originating
from
mesenchymal
tissue,
accounting
for
less
than
1%
adult
cancers
in
the
USA.
With
over
13,000
new
cases
and
around
5350
deaths
annually,
patients
with
metastatic
soft-tissue
face
limited
therapeutic
options
an
estimated
median
overall
survival
18
months.
While
immunotherapy
has
demonstrated
effectiveness
several
cancers,
its
application
remains
challenging
owing
to
tumors'
largely
"cold"
immunological
environment,
characterized
by
low
levels
tumor-infiltrating
lymphocytes
lack
sarcoma-specific
biomarkers.
This
review
examines
potential
mechanisms
underlying
resistance
sarcomas,
including
complex
interplay
between
innate
adaptive
immunity,
tumor
microenvironment,
role
immune-related
genes.
Despite
preliminary
findings
suggesting
correlations
immune
profiles
histological
subtypes,
consistent
biomarkers
predicting
immunotherapeutic
responses
across
sarcoma
types
are
absent.
Emerging
strategies
focus
on
converting
tumors
"hot"
tumors,
enhancing
their
susceptibility
immunologic
activation.
research
is
ongoing,
personalized
treatment
approaches
may
offer
hope
overcoming
inherent
heterogeneity
seen
ultimately
aiming
improve
outcomes
affected
patients.