Thiophene engineering of near-infrared D-π-A nano-photosensitizers for enhanced multiple phototheranostics and inhibition of tumor metastasis
Journal of Colloid and Interface Science,
Год журнала:
2025,
Номер
685, С. 291 - 303
Опубликована: Янв. 17, 2025
Язык: Английский
Metal ion interference therapy: metal-based nanomaterial-mediated mechanisms and strategies to boost intracellular “ion overload” for cancer treatment
Materials Horizons,
Год журнала:
2024,
Номер
11(18), С. 4275 - 4310
Опубликована: Янв. 1, 2024
This
comprehensive
review
systematically
summarizes
the
intrinsic
mechanism
of
different
metal
ion
(such
as
Fe
3+
/Fe
2+
,
Cu
/Cu
+
Ca
Zn
Mn
Na
/K
and
Mg
)-mediated
interference
therapies
their
research
progress
in
cancer
treatment.
Язык: Английский
MicroRNA‐Triggered Programmable DNA‐Encoded Pre‐PROTACs for Cell‐Selective and Controlled Protein Degradation
Angewandte Chemie International Edition,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 9, 2024
Abstract
Proteolysis‐targeting
chimeras
(PROTACs)
have
accelerated
drug
development;
however,
some
challenges
still
exist
owing
to
their
lack
of
tumor
selectivity
and
on‐demand
protein
degradation.
Here,
we
developed
a
miR
NA‐
i
nitiated
ssembled
pre‐PRO
TAC
(miRiaTAC)
platform
that
enables
the
activation
termination
target
degradation
in
cell
type‐specific
manner.
Using
miRNA‐21
as
model,
engineered
DNA
hairpins
labeled
with
JQ‐1
pomalidomide
facilitated
modular
assembly
DNA‐encoded
pre‐PROTACs
through
hybridization
chain
reaction.
This
configuration
promoted
selective
polyubiquitination
BRD4
upon
miR‐21
initiation,
highlighting
significant
minimal
systemic
toxicity.
Furthermore,
incorporates
photolabile
groups,
enabling
precise
optical
control
during
assembly/disassembly,
mitigating
risk
excessive
Additionally,
by
introducing
secondary
ligand
targeting
CDK6,
these
were
used
scaffold
for
programmable
active
miRiaTACs
containing
two
different
warheads
exact
stoichiometry,
orthogonal
multitarget
The
integration
near‐infrared
light‐mediated
photodynamic
therapy
an
upconversion
nanosystem
further
enhanced
efficacy
potent
vivo
anticancer
activity.
We
anticipate
miRiaTAC
represents
intersection
between
dynamic
nanotechnology
PROTAC,
potentially
expanding
versatility
PROTAC
toolkit
cancer
therapy.
Язык: Английский
A diselenide MOF-based nanomotor dual-driven by carbon monoxide and near-infrared-II light for multimodal tumor-targeted therapy
Science China Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 7, 2024
Язык: Английский
MicroRNA‐Triggered Programmable DNA‐Encoded Pre‐PROTACs for Cell‐Selective and Controlled Protein Degradation
Angewandte Chemie,
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 9, 2024
Abstract
Proteolysis‐targeting
chimeras
(PROTACs)
have
accelerated
drug
development;
however,
some
challenges
still
exist
owing
to
their
lack
of
tumor
selectivity
and
on‐demand
protein
degradation.
Here,
we
developed
a
miR
NA‐
i
nitiated
ssembled
pre‐PRO
TAC
(miRiaTAC)
platform
that
enables
the
activation
termination
target
degradation
in
cell
type‐specific
manner.
Using
miRNA‐21
as
model,
engineered
DNA
hairpins
labeled
with
JQ‐1
pomalidomide
facilitated
modular
assembly
DNA‐encoded
pre‐PROTACs
through
hybridization
chain
reaction.
This
configuration
promoted
selective
polyubiquitination
BRD4
upon
miR‐21
initiation,
highlighting
significant
minimal
systemic
toxicity.
Furthermore,
incorporates
photolabile
groups,
enabling
precise
optical
control
during
assembly/disassembly,
mitigating
risk
excessive
Additionally,
by
introducing
secondary
ligand
targeting
CDK6,
these
were
used
scaffold
for
programmable
active
miRiaTACs
containing
two
different
warheads
exact
stoichiometry,
orthogonal
multitarget
The
integration
near‐infrared
light‐mediated
photodynamic
therapy
an
upconversion
nanosystem
further
enhanced
efficacy
potent
vivo
anticancer
activity.
We
anticipate
miRiaTAC
represents
intersection
between
dynamic
nanotechnology
PROTAC,
potentially
expanding
versatility
PROTAC
toolkit
cancer
therapy.
Язык: Английский