Theranostics,
Journal Year:
2021,
Volume and Issue:
11(7), P. 3167 - 3182
Published: Jan. 1, 2021
Rationale:
Iron-saturated
Lf
(Holo-Lactoferrin,
Holo-Lf)
exhibits
a
superior
anticancer
property
than
low
iron-saturated
(Apo-Lf).
Ferroptosis
is
an
iron-dependent
cell
death
characterized
by
the
accumulation
of
lipid
peroxidation
products
and
lethal
reactive
oxygen
species
(ROS).
Radiotherapy
also
exerts
its
therapeutic
effect
through
ROS.
Methods:
The
different
on
ferroptosis
radiotherapy
were
tested
triple-negative
breast
cancer
(TNBC)
line
MDA-MB-231
non-TNBC
MCF-7.
Results:
Holo-Lf
significantly
increased
total
iron
content,
promoted
ROS
generation,
end
product,
malondialdehyde
(MDA),
enhanced
cells.
By
contrast,
Apo-Lf
upregulated
SLC7a11
expression,
GSH
generation
inhibited
However,
MCF-7
cells
resistant
to
Holo-Lf-induced
because
have
higher
redox
balance
capacity
More
importantly,
downregulated
HIF-1α
ameliorated
hypoxia
microenvironment
in
subcutaneous
tumors,
radiation-induced
DNA
damage
hypoxic
Finally,
efficacy
tumors
was
Holo-Lf.
Conclusion:
could
induce
sensitize
radiotherapy.
Chemical Reviews,
Journal Year:
2021,
Volume and Issue:
121(21), P. 13454 - 13619
Published: Sept. 28, 2021
This
review
presents
a
robust
strategy
to
design
photosensitizers
(PSs)
for
various
species.
Photodynamic
therapy
(PDT)
is
photochemical-based
treatment
approach
that
involves
the
use
of
light
combined
with
light-activated
chemical,
referred
as
PS.
Attractively,
PDT
one
alternatives
conventional
cancer
due
its
noninvasive
nature,
high
cure
rates,
and
low
side
effects.
PSs
play
an
important
factor
in
photoinduced
reactive
oxygen
species
(ROS)
generation.
Although
concept
photosensitizer-based
photodynamic
has
been
widely
adopted
clinical
trials
bioimaging,
until
now,
our
surprise,
there
no
relevant
article
on
rational
designs
organic
PDT.
Furthermore,
most
published
articles
focused
nanomaterials
nanotechnology
based
traditional
PSs.
Therefore,
this
aimed
at
reporting
recent
strategies
develop
innovative
enhanced
therapy,
each
example
described
detail
instead
providing
only
general
overview,
typically
done
previous
reviews
PDT,
provide
intuitive,
vivid,
specific
insights
readers.
Chemical Society Reviews,
Journal Year:
2020,
Volume and Issue:
50(2), P. 1111 - 1137
Published: Nov. 27, 2020
This
review
summarizes
the
recent
development
of
second
near-infrared
photothermal
combinational
nanotheranostics
for
cancer,
infectious
diseases
and
regenerative
medicine.
Advanced Materials,
Journal Year:
2021,
Volume and Issue:
33(48)
Published: Sept. 27, 2021
Photodynamic
therapy
(PDT)
has
aroused
great
research
interest
in
recent
years
owing
to
its
high
spatiotemporal
selectivity,
minimal
invasiveness,
and
low
systemic
toxicity.
However,
due
the
hypoxic
nature
characteristic
of
many
solid
tumors,
PDT
is
frequently
limited
therapeutic
effect.
Moreover,
consumption
O2
during
may
further
aggravate
tumor
condition,
which
promotes
proliferation,
metastasis,
invasion
resulting
poor
prognosis
treatment.
Therefore,
numerous
efforts
have
been
made
increase
content
with
goal
enhancing
efficacy.
Herein,
these
strategies
developed
past
decade
are
comprehensively
reviewed
alleviate
hypoxia,
including
1)
delivering
exogenous
directly,
2)
generating
situ,
3)
reducing
cellular
by
inhibiting
respiration,
4)
regulating
TME,
(e.g.,
normalizing
vasculature
or
disrupting
extracellular
matrix),
5)
hypoxia-inducible
factor
1
(HIF-1)
signaling
pathway
relieve
hypoxia.
Additionally,
-independent
Type-I
also
discussed
as
an
alternative
strategy.
By
reviewing
progress,
it
hoped
that
this
review
will
provide
innovative
perspectives
new
nanomaterials
designed
combat
hypoxia
avoid
associated
limitation
PDT.
Chemical Society Reviews,
Journal Year:
2021,
Volume and Issue:
50(16), P. 9152 - 9201
Published: Jan. 1, 2021
Photodynamic
therapy
(PDT)
has
been
extensively
investigated
for
decades
tumor
treatment
because
of
its
non-invasiveness,
spatiotemporal
selectivity,
lower
side-effects,
and
immune
activation
ability.
Accounts of Chemical Research,
Journal Year:
2020,
Volume and Issue:
53(4), P. 752 - 762
Published: Feb. 6, 2020
Cancer
therapy
is
routinely
performed
in
the
clinic
to
cure
cancer
and
control
its
progression,
wherein
therapeutic
agents
are
generally
used.
To
reduce
side
effects,
protherapeutic
that
can
be
activated
by
overexpressed
biomarkers
under
development.
However,
these
still
face
certain
extent
of
off-target
activation
normal
tissues,
stimulating
interest
design
external-stimuli
activatable
protherapeutics.
In
this
regard,
photoactivatable
have
been
utilized
for
treatments.
because
intrinsic
features
photolabile
moieties,
most
only
respond
ultraviolet-visible
light,
limiting
their
vivo
applications.
Thus,
near-infrared
(NIR)
light
with
minimal
phototoxicity
increased
tissue
penetration
highly
desired.In
Account,
we
summarize
our
semiconducting
polymer
nanomaterials
(SPNs)
as
NIR
treatment.
SPNs
transformed
from
π-conjugated
polymers
efficiently
convert
into
heat
or
singlet
oxygen
(1O2).
With
photothermal
photodynamic
properties,
directly
used
photomedicine
serve
transducers
activate
1O2-responsive
agents.The
heat-activatable
SPN-based
developed
loading
conjugating
(e.g.,
agonist,
gene,
enzyme).
For
instance,
photothermally
triggered
release
agonists
specifically
activates
protein
ion
channels
on
cellular
membrane,
leading
overinflux
induced
mitochondria
dysfunction
consequently
apoptosis
cells.
Moreover,
temperature-sensitive
bromelain
promote
situ
degradation
collagens
(the
major
components
extracellular
matrix),
resulting
an
improved
accumulation
tumor
tissues
thus
amplified
outcome.The
1O2-activatable
constructed
through
covalent
conjugation
caged
via
hypoxia-
1O2-cleavable
linkers.
Upon
photoirradiation,
consume
generate
1O2,
which
leads
(PDT),
meanwhile
breaks
linkers
on-demand
molecules
chemodrug,
enzyme,
inhibitor).
Such
remote
applied
induce
DNA
damage,
ribonucleic
acid
degradation,
inhibition
biosynthesis,
immune
system
tumors
living
animals.
By
synergizing
PDT
photoactivation
those
biological
actions,
effectively
eliminate
even
fully
inhibit
metastasis.This
Account
highlights
potential
construction
versatile
protherapeutics
treat
at
designated
times
locations
high
outcome
precision.
ACS Nano,
Journal Year:
2021,
Volume and Issue:
15(3), P. 5735 - 5751
Published: March 11, 2021
As
next-generation
artificial
enzymes,
nanozymes
have
shown
great
promise
for
tumor
catalytic
therapy.
In
particular,
their
peroxidase-like
activity
has
been
employed
to
catalyze
hydrogen
peroxide
(H2O2)
produce
highly
toxic
hydroxyl
radicals
(•OH)
kill
cells.
However,
limited
by
the
low
affinity
between
with
H2O2
and
level
of
in
microenvironment,
peroxidase
usually
produced
insufficient
•OH
cells
therapeutic
purposes.
Herein,
we
present
a
pyrite
nanozyme
ultrahigh
affinity,
resulting
4144-
3086-fold
increase
compared
that
classical
Fe3O4
natural
horseradish
peroxidase,
respectively.
We
found
also
possesses
intrinsic
glutathione
oxidase-like
activity,
which
catalyzes
oxidation
reduced
accompanied
generation.
Thus,
dual-activity
constitutes
self-cascade
platform
generate
abundant
deplete
glutathione,
induces
apoptosis
as
well
ferroptosis
Consequently,
it
killed
apoptosis-resistant
harboring
KRAS
mutation
inducing
ferroptosis.
The
exhibited
favorable
tumor-specific
cytotoxicity
biodegradability
ensure
its
biosafety.
These
results
indicate
high-performance
is
an
effective
reagent
may
aid
development
nanozyme-based
Small,
Journal Year:
2021,
Volume and Issue:
17(12)
Published: Feb. 12, 2021
Abstract
Nanotechnology
has
provided
great
opportunities
for
managing
neoplastic
conditions
at
various
levels,
from
preventive
and
diagnostic
to
therapeutic
fields.
However,
when
it
comes
clinical
application,
nanoparticles
(NPs)
have
some
limitations
in
terms
of
biological
stability,
poor
targeting,
rapid
clearance
the
body.
Therefore,
biomimetic
approaches,
utilizing
immune
cell
membranes,
are
proposed
solve
these
issues.
For
example,
macrophage
or
neutrophil
membrane
coated
NPs
developed
with
ability
interact
tumor
tissue
suppress
cancer
progression
metastasis.
The
functionality
particles
largely
depends
on
surface
proteins
cells
their
preserved
function
during
extraction
coating
process
NPs.
Proteins
outer
can
render
a
wide
range
activities
NPs,
including
prolonged
blood
circulation,
remarkable
competency
recognizing
antigens
enhanced
better
cellular
interactions,
gradual
drug
release,
reduced
toxicity
vivo.
In
this
review,
nano‐based
systems
cells‐derived
membranous
layers,
detailed
production
process,
applicability
treatment
discussed.
addition,
future
perspectives
challenges
translation
also
presented.
Journal of the American Chemical Society,
Journal Year:
2020,
Volume and Issue:
142(11), P. 5380 - 5388
Published: Feb. 27, 2020
Tumor
hypoxia
has
proven
to
be
the
major
bottleneck
of
photodynamic
therapy
(PDT)
clinical
transformation.
Different
from
traditional
O2
delivery
approaches,
here
we
describe
an
innovative
binary
O2-economizer
(PDOE)
tactic
reverse
hypoxia-driven
resistance
by
designing
a
superoxide
radical
(O2•–)
generator
targeting
mitochondria
respiration,
termed
SORgenTAM.
This
PDOE
system
is
able
block
intracellular
consumption
and
down-regulate
HIF-1α
expression,
which
successfully
rescues
cancer
cells
becoming
hypoxic
relieves
intrinsic
burden
tumors
in
vivo,
thereby
sparing
sufficient
endogenous
for
PDT
process.
Photosensitization
mechanism
studies
demonstrate
that
SORgenTAM
ideal
intersystem
crossing
rate
triplet
excited
state
lifetime
generating
O2•–
through
type-I
photochemistry,
generated
can
further
trigger
biocascade
reduce
PDT's
demand
O2-recycble
manner.
Furthermore,
also
serves
activate
AMPK
metabolism
signaling
pathway
inhibit
cell
repair
promote
death.
Consequently,
using
this
two-step
O2-economical
strategy,
under
relatively
low
light
dose
irradiation,
excellent
therapeutic
responses
toward
are
achieved.
study
offers
conceptual
while
practical
paradigm
overcoming
pitfalls
phototherapeutics.
Advanced Materials,
Journal Year:
2020,
Volume and Issue:
33(4)
Published: Dec. 16, 2020
Abstract
Immunotherapy
has
offered
new
treatment
options
for
cancer;
however,
the
therapeutic
benefits
are
often
modest
and
desired
to
be
improved.
A
semiconducting
polymer
nanoadjuvant
(SPN
II
R)
with
a
photothermally
triggered
cargo
release
second
near‐infrared
(NIR‐II)
photothermal
immunotherapy
is
reported
here.
SPN
R
consists
of
nanoparticle
core
as
an
NIR‐II
converter,
which
doped
toll‐like
receptor
(TLR)
agonist
adjuvant
coated
thermally
responsive
lipid
shell.
Upon
photoirradiation,
effectively
generates
heat
not
only
ablate
tumors
induce
immunogenic
cell
death
(ICD),
but
also
melt
layers
on‐demand
TLR
agonist.
The
combination
ICD
activation
TLR7/TLR8
enhances
maturation
dendritic
cells,
amplifies
anti‐tumor
immune
responses.
Thus,
single
R‐mediated
inhibits
growth
both
primary
distant
eliminates
lung
metastasis
in
murine
mouse
model.
This
study
thus
provides
remote‐controlled
smart
delivery
system
synergize
photomedicine
enhanced
cancer
treatment.