Application of a CYP1B1-Targeted NIR Probe for Breast Cancer Diagnosis, Surgical Navigation, and CYP1B1-Associated Chemotherapy Resistance Monitoring
Zhihao Wu,
No information about this author
Tao Shi,
No information about this author
Qi Shao
No information about this author
et al.
Molecular Pharmaceutics,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 30, 2025
Early
detection
and
precise
treatment
for
breast
cancer
are
crucial,
given
its
high
global
incidence
rate.
Hence,
the
development
of
novel
imaging
targets
is
essential
diagnosing
monitoring
resistance
to
chemotherapy,
which
pivotal
achieving
personalized
patients.
In
our
previous
work,
we
successfully
developed
a
near-infrared
(NIR)
probe
1
CYP1B1-targeted
imaging.
this
study,
aimed
investigate
utility
as
NIR
fluorescence
photoacoustic
dual-mode
surveillance
cancer.
Western
blotting
cell
lines
has
confirmed
that
CYP1B1
widely
expressed
in
gynecological
vitro
capability
tracking
CYP1B1-positive
tumor
cells
was
validated
by
using
confocal
microscopy.
Further
studies,
including
vivo
dual-model
ex
biological
distribution
analysis
on
triple-negative
xenograft
mouse
model,
demonstrated
selectively
accumulated
tissue
within
early
0.5
h
postinjection.
The
results
surgical
resection
experiment
revealed
could
be
entirely
removed
under
guidance
imaging,
thereby
indicating
probe's
efficacy
navigation.
expression
found
upregulated
adriamycin
(ADR)-resistant
cells,
MCF-7/ADR.
Consequently,
sensitivity
overexpressed
MCF-7/1B1,
ADR
significantly
reduced,
with
an
IC50
value
0.586
±
0.0934
μM,
compared
parental
MCF-7
0.183
0.0444
μM.
assays
conducted
MCF-7/ADR
tumor-bearing
mice
specifically
enriched
sites,
suggesting
potential
chemotherapy
This
study
expands
scope
application
1,
establishing
diagnosis
through
fluorescence-photoacoustic
resistance,
resection.
strategy
paves
way
approaches
Language: Английский
Novel GAL7-targeted fluorescent molecular imaging probe for high-grade squamous intraepithelial lesion and cervical cancer screening
EJNMMI Research,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: March 13, 2025
Early
detection
and
treatment
are
critical
for
improving
the
survival
prognosis
of
patients
with
cervical
cancer.
However,
there
is
a
notable
scarcity
targeted
imaging
probes
specifically
designed
to
detect
high-grade
squamous
intraepithelial
lesions
(HSIL)
Our
study
aimed
address
this
gap
by
identifying
validating
probe
these
conditions.
Using
bioinformatics
data,
we
identified
galectin-7
(GAL7)
as
highly
expressed
in
cell
carcinoma
endocervical
adenocarcinoma
(CESC).
Immunohistochemical
staining
biopsy
samples
from
30
HSIL
cancer
verified
high
specific
expression
GAL7.
Further
validation
was
performed
using
mouse
human
CESC
lines
tumor
xenografts,
confirming
consistent
Based
on
finding,
synthesized
GAL7-specific
antibody
conjugated
FITC,
creating
GAL7-FITC
fluorescence
probe.
Fluorescence
molecular
revealed
that
exhibited
binding
various
xenograft
models.
Additionally,
diagnostic
capability
demonstrated
fresh
specimens
cone
excisions,
validated
through
histopathology
immunohistochemical
analysis.
GAL7
target
successfully
developed
has
shown
promising
potential
clinical
application
early
CESC,
providing
rapid
diagnosis
without
observable
toxicity.
This
advancement
may
significantly
enhance
accuracy
speed
diagnostics,
ultimately
patient
outcomes.
Language: Английский
808 nm Light-Triggered Cyanine-Decorated Iridium(III) Complexes for Antibacterial Photodynamic Therapy in Deep-Tissue
Baraka Joseph Butuyuyu,
No information about this author
Jiqiang Liu,
No information about this author
Qihang Ding
No information about this author
et al.
Inorganic Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 11, 2025
Acute
bacterial
skin
and
structure
infections
(ABSSSIs)
pose
significant
global
health
challenges,
exacerbated
by
rising
antibiotic
resistance.
Antibacterial
photodynamic
therapy
(APDT)
has
emerged
as
a
promising
strategy
to
combat
these
utilizing
photosensitizer
(PS)
that
generates
reactive
oxygen
species
(ROS)
upon
light
activation.
However,
the
limited
tissue
penetration
of
conventional
organic
PSs,
which
primarily
absorb
in
UV-vis
spectra,
hindered
their
therapeutic
potential
for
deeper
infections.
Herein,
we
introduce
novel
iridium(III)-cyanine
complex
(Ir-cy)
with
strong
near-infrared
(NIR)
absorption
at
814
nm
(up
101
red-shifted
from
previous
reports),
specifically
designed
enhance
APDT.
Under
808
laser
irradiation,
Ir-cy
demonstrated
substantial
ROS
generation
capacity,
achieving
approximately
70%
reduction
Staphylococcus
aureus
(S.
aureus)
colonies
depth
7.2
mm
within
simulated
model.
Comprehensive
vitro
vivo
evaluations
further
confirmed
its
potent
antibacterial
efficacy
against
S.
while
maintaining
excellent
biocompatibility.
These
findings
highlight
highly
effective
NIR-active
PS,
paving
way
advanced
strategies
targeting
deep-tissue
ABSSSIs
through
optimized
Language: Английский