International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(14), P. 7959 - 7959
Published: July 21, 2024
Esophageal
cancer
ranks
the
seventh
in
incidence
and
sixth
death.
squamous
cell
carcinoma
(ESCC)
accounts
for
approximately
90%
of
total
cases
esophageal
cancer.
Chemotherapy
is
most
effective
drug-based
method
treatment
However,
severe
side
effects
traditional
chemotherapy
limit
its
efficacy.
Targeted
can
deliver
chemotherapeutic
drugs
to
cells
specifically
kill
these
with
reduced
effects.
In
work,
bivalent
aptamer-DNA
carrier
(BAD)
was
designed
by
using
an
ESCC
cell-specific
aptamer
as
recognition
molecule
a
GC
base-rich
DNA
sequence
drug
carrier.
With
doxorubicin
(Dox)
drugs,
aptamer-DNA-Dox
conjugate
(BADD)
constructed
targeted
killing
cells.
Firstly,
truncated
A2(35)
retained
binding
ability
obtained
through
optimization
intact
A2(80)
used
fuse
sequences
constructing
BAD
simple
hybridization.
The
results
gel
electrophoresis
flow
cytometry
analysis
showed
that
successfully
had
stronger
affinity
than
monovalent
A2(35).
Then,
loaded
Dox
construct
BADD
noncovalent
intercalation.
fluorescence
spectra
assays
bind
target
strongly.
Confocal
imaging
further
displayed
be
internalized
into
release
Dox.
CCK-8
assays,
Calcein
AM/PI
staining,
wound
healing
demonstrated
cells,
but
not
control
Our
demonstrate
developed
selectively
offering
potentially
strategy
ESCC.
ACS Sensors,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 17, 2025
This
study
focuses
on
the
surface
functionalization
of
citrate-stabilized
gold
nanoparticles
(AuNPs)
with
disease-specific
aptamers
to
enhance
detection
multifactorial
disease
(MD)
biomarkers.
MDs,
characterized
by
complex
pathophysiology
involving
multiple
genetic
and
environmental
factors,
present
significant
diagnostic
challenges.
Aptamers,
which
are
short,
single-stranded
oligonucleotides
high
specificity
affinity
for
target
molecules,
have
emerged
as
promising
tools
biomarker
detection.
By
utilizing
response
methodology
(RSM)
face-centered
central
composite
design
(FCCCD),
this
research
systematically
optimized
bioconjugation
process
AuNPs
different
aptamer
sequences,
focusing
parameters
such
AuNP
size
concentration.
The
developed
protocol
in
demonstrated
that
aptamer-functionalized
can
be
yield,
efficiency,
stability,
coverage,
making
them
suitable
applications,
particularly
surface-enhanced
Raman
spectroscopy
(SERS).
findings
provide
a
foundation
development
customizable
nanoprobes
adapted
various
biomarkers
associated
potentially
improving
early
diagnosis
therapeutic
outcomes.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 17, 2025
Aptamer-based
immunotherapy
can
be
a
new
hope
for
treating
solid
tumors
with
personalized
and
specific
approaches
toward
cancer
therapies.
Aptamers
are
small
synthetic
single-stranded
nucleic
acids
that
may
bring
in
paradigm
shift
tumors.
These
highly
selective
drugs
applied
cellular
immunotherapy,
cytokine
modulation,
immune
checkpoint
suppression.
This
review
provides
an
overview
of
the
recent
advances
aptamer-based
technologies
key
clinical
trials
involving
AON-D21
AM003.
potently
active
regulation
tumor
targeting.
However,
aptamer
stability
bioavailability
seriously
compromised
by
issues
relating
to
renal
clearance
rapid
degradation
through
nucleases.
The
latter
reviewed
here
along
novel
improvements,
some
which
involve
chemical
modifications
greatly
enhance
prolong
circulation
time;
exemplary
such
PEGylation,
cholesterol
conjugation,
synthesis
circular
acids.
regulatory
aspect
is
also
crucial.
For
example,
addition
strategies
prevent
drug-drug
interactions
(DDIs)
remediation
medications,
this
paper
underscores
need
risk
assessment,
particularly
because
immunogenicity
organ
failure.
use
aptamers
expanded
development
SOMAmers,
X-aptamers,
bioinformatics.
To
make
major
part
treatment,
future
research
should
concentrate
more
on
resolving
existing
expanding
their
beneficial
uses.
ACS Omega,
Journal Year:
2025,
Volume and Issue:
10(16), P. 16123 - 16137
Published: April 16, 2025
Type
2
diabetes
mellitus
(T2DM)
has
led
to
a
considerable
increase
in
morbidity
and
mortality
worldwide.
Current
treatments
control
blood
glucose
but
cannot
reverse
the
disease,
making
it
important
identify
biomarkers
that
predict
T2DM
onset
progression.
This
study
explores
heme
oxygenase
1(HMOX1)
as
novel
biomarker
for
through
bioinformatics
experimental
validation.
Core
differentially
expressed
genes
(DEGs)
were
identified
using
Gene
Expression
Omnibus
database,
with
Ontology,
Kyoto
Encyclopedia
of
Genes
Genomes,
Set
Enrichment
Analysis
analyses
revealing
notable
pathways,
including
Toll-like
receptor
signaling
cytokine
interactions.
A
Nomogram
model
receiver
operating
characteristic
curves
demonstrated
strong
diagnostic
effectiveness
these
core
DEGs.
The
CIBERSORT
algorithm
assessed
relation
between
DEGs
immune
cell
infiltration,
showing
substantial
associations
several
types,
particularly
highlighting
HMOX1's
correlation
eight
cells
(p
<
0.05).
In
mouse
model,
db/db
mice
displayed
typical
diabetic
characteristics
lower
serum
HMOX1
levels
compared
db/m
controls
0.01).
Histological
analysis
confirmed
liver
damage
decreased
expression
NFE2L2
tissues
is
promising
T2DM,
its
downregulation
methods.
Biosensors,
Journal Year:
2025,
Volume and Issue:
15(5), P. 277 - 277
Published: April 29, 2025
Aptamers
have
emerged
as
powerful
molecular
recognition
elements
for
biosensing
applications,
offering
high
specificity,
stability,
and
adaptability.
This
review
explores
key
considerations
in
designing
aptamer-based
sensors
(aptasensors),
with
a
focus
on
biomarker
selection,
aptamer
design,
detection
immobilization
strategies.
However,
challenges
such
biofluid
stability
reversibility
must
be
addressed
to
improve
biosensor
performance.
In
this
study,
the
potential
of
platforms
diagnostics
is
explored,
emphasizing
their
advantages
future
applications.
Looking
ahead,
advances
multifunctional
aptamers,
integration
nanomaterials,
computational
optimization
are
highlighted
promising
directions
enhancing
effectiveness
biosensing.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: May 14, 2025
Head
and
neck
squamous
cell
carcinoma
(HNSCC)
is
a
highly
aggressive
malignancy
characterized
by
complex
tumor
microenvironment
(TME)
that
plays
pivotal
role
in
initiation,
progression,
immune
evasion.
Recent
advancements
have
highlighted
the
intricate
interplay
between
infiltration
patterns,
checkpoint
dysregulation,
metabolic
reprogramming
driving
HNSCC
escape.
Despite
these
insights,
significant
challenges
remain,
including
incomplete
understanding
of
specific
evasion
pathways
lack
personalized
therapeutic
strategies.
To
address
gaps,
this
review
introduces
novel
“Trinity”
regulatory
network
HNSCC,
encompassing:
(1)
reprogramming-mediated
modulation,
(2)
stromal
cell-driven
dysfunction,
(3)
epigenetic
remodeling
fostering
tolerance.
This
framework
provides
theoretical
foundation
for
development
multi-targeted
combination
therapies
offers
innovative
strategies
to
overcome
Additionally,
systematically
synthesizes
current
relationship
escape,
with
focus
on
emerging
immunotherapeutic
approaches
such
as
PD-1/PD-L1
inhibitors
CAR-T
therapy.
Leveraging
cutting-edge
single-cell
sequencing
spatial
transcriptomics,
we
elucidate
spatiotemporal
heterogeneity
landscape
propose
new
paradigm
“lineage
plasticity-driven
adaptation.”
These
insights
not
only
advance
our
biology
but
also
pave
way
precision
immunotherapies
aimed
at
improving
patient
survival
quality
life.
By
integrating
multidisciplinary
perspectives,
work
underscores
importance
targeting
TME
achieve
durable
clinical
responses
immunotherapy
resistance
HNSCC.
Bioconjugate Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 22, 2025
Targeted
delivery
of
cytostatic
drugs
is
a
powerful
approach
to
achieving
tumor
tissue
selectivity,
reducing
systemic
toxicity,
and
ultimately
improving
the
efficacy
anticancer
chemotherapy.
Targeting
can
be
achieved
using
wide
range
molecular
ligands,
with
DNA
aptamers
being
promising
representative.
In
this
work,
we
employed
flow
cytometry,
AuNP-aptasensor,
atomic-scale
computer
modeling
assess
affinity
several
(Anti-HER2,
HB5,
Apt-6,
HeA2_1,
HeA2_3)
for
human
epidermal
growth
factor
receptor
2
(HER2),
which
known
one
factors
that
promote
breast
cancer
cells.
Flow
cytometry
showed
short
(HeA2_1
had
higher
HER2
on
MDAMB453
cells
than
longer
(HB5,
Apt-6).
HER2-negative
MDA-MB-231
served
as
negative
control.
The
HeA2_3
aptamer
has
high
average
(HeA2_3:23.6,
HeA2_1:13.1,
Apt-6:3.6;
HB5:3.5;
Anti-HER2:3.2)
nearly
Gaussian
distribution
across
cells,
while
HeA2_1
forms
fraction
relatively
fluorescence
signal
intensity
(HeA2_1:11.6;
HeA2_3:5.9;
Apt-6:3.4;
HB5:3.1;
Anti-HER2:2.1).
Most
findings
also
hold
HER2-positive
small
extracellular
vesicles
studied
AuNP-aptasensor.
Computer
simulations
confirmed
are
characterized
by
stronger
binding
domain
HER2.
A
detailed
analysis
free
energy
allowed
us
show
first
time
tight
correlates
well-separated
hot
cold
spots
protein
surface.
For
meet
these
criteria
(HeA2_1,
HeA2_3,
Anti-HER2),
favorable
interactions
driven
local
attraction
nucleotides
arginine
lysine
residues
possibly
stabilized
intermolecular
hydrogen
bonds.
(Apt-6
HB5),
surface
overlap
much
weaker
binding.
Overall,
our
cannot
merely
dissociation
equilibrium
constant.
more
sophisticated
combines
experimental
computational
methods
unlock
mechanisms
behind
aptamer-HER2
bindings.
results
study
suggest
become
reliable
accurate
tool
prescreening
prior
laboratory
experiments.
International Journal of Translational Medicine,
Journal Year:
2024,
Volume and Issue:
4(2), P. 309 - 333
Published: May 31, 2024
Many
ailments
can
be
diagnosed
while
they
are
asymptomatic,
meaning
that
the
patient
has
no
signs
or
symptoms
of
a
progressing
disease.
If
caught
in
their
initial
stage
formation,
these
disorders
effectively
treated,
leading
to
successful
outcomes;
curative
therapies
halt
illnesses
from
advancing,
thus
improving
quality
life
and
long-term
survival
patient.
Still,
cutting-edge
upgrades
precision
technologies
necessary
for
early,
reliable,
affordable,
rapid
disease
detection,
but
also
vital
well-being
people
future
global
public
health.
The
emerging
role
utility
non-invasive
repeatable
diagnostic
test
approaches
detection
health
conditions
have
been
exemplified
by
liquid
biopsies
based
on
genomic
biomarkers.
As
such,
biological
fluids
permit
any
measurable
molecular
indicator
signature
(e.g.,
proteins)
provide
valuable
information
an
individual’s
wellness
and/or
Among
bodily
secretions
used
diagnostics
is
sputum,
complex
viscous
gel-like
biopolymeric
network
gained
growing
recognition
as
rich
source
biomarkers
airway
infections
pulmonary
diseases,
serves
determinant
reveal
other
illnesses.
per
World
Health
Organization,
burden
respiratory
exacerbated
factors
ranging
considerable
subjection
air
pollution
occupational
contaminants
tobacco
smoking
second-hand
smoke,
addition
poor
socio-economic
status.
Due
likely
increase
determinants,
tract
rise,
affecting
many
individuals,
putting
stress
healthcare
facilities
services
worldwide.
aim
this
study
was
perform
narrative
review
sputum
constituents
with
emphasis
proteins
glycoproteins
assessed
possible
lung
organ
diseases.
A
search
conducted
using
mucus,
proteomics,
biomarkers,
point-of-care
testing
keywords
employing
Google,
PubMed
(MEDLINE),
Web
Science,
selecting
most
referenced
related
papers
last
decade.
We,
therefore,
highlight
need
use
expectorated
induced
specimens
routine
sample
protein
diagnose
chronic
disorders,
predict
inflammation
progression,
well
monitor
effectiveness
treatments.
Further,
we
discuss
urgent
fast
reliable
methods
detect
quantify
crucial
specimens,
limitations
faced
when
dealing
matrices.