Chemical Society Reviews,
Journal Year:
2021,
Volume and Issue:
50(7), P. 4629 - 4683
Published: Jan. 1, 2021
This
review
offers
a
holistic
perspective
on
Hf
and
Ce(iv)
based
metal–organic
frameworks
(MOFs),
with
focus
Hf/Ce(iv)-clusters,
topologies,
ligand
structures,
synthetic
strategies,
practical
applications
of
these
promising
MOFs.
Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: Aug. 7, 2023
Cancer
remains
a
highly
lethal
disease
in
the
world.
Currently,
either
conventional
cancer
therapies
or
modern
immunotherapies
are
non-tumor-targeted
therapeutic
approaches
that
cannot
accurately
distinguish
malignant
cells
from
healthy
ones,
giving
rise
to
multiple
undesired
side
effects.
Recent
advances
nanotechnology,
accompanied
by
our
growing
understanding
of
biology
and
nano-bio
interactions,
have
led
development
series
nanocarriers,
which
aim
improve
efficacy
while
reducing
off-target
toxicity
encapsulated
anticancer
agents
through
tumor
tissue-,
cell-,
organelle-specific
targeting.
However,
vast
majority
nanocarriers
do
not
possess
hierarchical
targeting
capability,
their
indices
often
compromised
poor
accumulation,
inefficient
cellular
internalization,
inaccurate
subcellular
localization.
This
Review
outlines
current
prospective
strategies
design
organelle-targeted
nanomedicines,
highlights
latest
progress
technologies
can
dynamically
integrate
these
three
different
stages
static
maximize
outcomes.
Finally,
we
briefly
discuss
challenges
future
opportunities
for
clinical
translation
nanomedicines.
Advanced Science,
Journal Year:
2021,
Volume and Issue:
9(1)
Published: Nov. 19, 2021
Abstract
The
past
decades
have
witnessed
great
progress
in
cancer
immunotherapy,
which
has
profoundly
revolutionized
oncology,
whereas
low
patient
response
rates
and
potential
immune‐related
adverse
events
remain
major
clinical
challenges.
With
the
advantages
of
controlled
delivery
modular
flexibility,
nanomedicine
offered
opportunities
to
strengthen
antitumor
immune
responses
sensitize
tumor
immunotherapy.
Furthermore,
tumor‐microenvironment
(TME)‐responsive
been
demonstrated
achieve
specific
localized
amplification
tissue
a
safe
effective
manner,
increasing
immunotherapy
reducing
side
effects
simultaneously.
Here,
recent
TME‐responsive
for
is
summarized,
responds
signals
TME,
such
as
weak
acidity,
reductive
environment,
high‐level
reactive
oxygen
species,
hypoxia,
overexpressed
enzymes,
adenosine
triphosphate.
Moreover,
combine
nanomedicine‐based
therapy
immunotherapeutic
strategies
overcome
each
step
cancer‐immunity
cycle
enhance
discussed.
Finally,
existing
challenges
further
perspectives
this
rising
field
with
hope
improved
development
applications
are
Frontiers in Pharmacology,
Journal Year:
2022,
Volume and Issue:
13
Published: May 24, 2022
Recently,
in
the
field
of
cancer
treatment,
paradigm
has
changed
to
immunotherapy
that
activates
immune
system
induce
attacks.
Among
them,
checkpoint
inhibitors
(ICI)
are
attracting
attention
as
excellent
and
continuous
clinical
results.
However,
it
shows
not
only
limitations
such
efficacy
some
patients
or
indications,
but
also
side-effects
resistance
occur.
Therefore,
is
necessary
understand
factors
tumor
microenvironment
(TME)
affect
immunotherapy,
is,
mechanism
by
which
grows
while
evading
suppressing
attacks
from
within
TME.
Tumors
can
evade
through
various
mechanisms
restricting
antigen
recognition,
inhibiting
system,
inducing
T
cell
exhaustion.
In
addition,
tumors
inhibit
accumulating
specific
metabolites
signal
TME
limiting
nutrients
available
cells.
order
overcome
develop
effective
treatments
therapeutic
strategies,
an
approach
needed
functions
cells
integrated
manner
based
on
this
review,
we
will
examine
effects
cells,
especially
how
anti-cancer
strategies
Molecular Cancer,
Journal Year:
2022,
Volume and Issue:
21(1)
Published: Feb. 21, 2022
Abstract
Clustered
regularly
interspaced
short
palindromic
repeats
(CRISPR)
system
provides
adaptive
immunity
against
plasmids
and
phages
in
prokaryotes.
This
inspires
the
development
of
a
powerful
genome
engineering
tool,
CRISPR/CRISPR-associated
nuclease
9
(CRISPR/Cas9)
editing
system.
Due
to
its
high
efficiency
precision,
CRISPR/Cas9
technique
has
been
employed
explore
functions
cancer-related
genes,
establish
tumor-bearing
animal
models
probe
drug
targets,
vastly
increasing
our
understanding
cancer
genomics.
Here,
we
review
current
status
gene
technology
oncological
research.
We
first
explain
basic
principles
introduce
several
new
CRISPR-based
modes.
next
detail
rapid
progress
CRISPR
screening
revealing
tumorigenesis,
metastasis,
resistance
mechanisms.
In
addition,
delivery
vectors
finally
demonstrate
potential
enhance
effect
adoptive
T
cell
therapy
(ACT)
reduce
adverse
reactions.
Experimental & Molecular Medicine,
Journal Year:
2022,
Volume and Issue:
54(10), P. 1670 - 1694
Published: Oct. 12, 2022
Abstract
Since
the
initial
clinical
approval
in
late
1990s
and
remarkable
anticancer
effects
for
certain
types
of
cancer,
molecular
targeted
therapy
utilizing
small
molecule
agents
or
therapeutic
monoclonal
antibodies
acting
as
signal
transduction
inhibitors
has
served
a
fundamental
backbone
precision
medicine
cancer
treatment.
These
approaches
are
now
used
clinically
first-line
various
human
cancers.
Compared
to
conventional
chemotherapy,
have
efficient
with
fewer
side
effects.
However,
emergence
drug
resistance
is
major
drawback
therapy,
several
strategies
been
attempted
improve
efficacy
by
overcoming
such
resistance.
Herein,
we
summarize
current
knowledge
regarding
agents,
including
classification,
brief
biology
target
kinases,
mechanisms
action,
examples
perspectives
future
development.
Clinical Cancer Research,
Journal Year:
2021,
Volume and Issue:
27(17), P. 4669 - 4679
Published: April 7, 2021
Abstract
Epithelial–mesenchymal
transition
(EMT)
has
been
shown
to
play
a
critical
role
in
tumor
development
from
initiation
metastasis.
EMT
could
be
regarded
as
continuum,
with
intermediate
hybrid
epithelial
and
mesenchymal
phenotypes
having
high
plasticity.
Classical
is
characterized
by
the
phenotype
change
of
cells
properties,
but
also
associated
multiple
other
molecular
processes,
including
immune
evasion.
Some
previous
studies
have
that
cell
number
immunosuppressive
cells,
such
myeloid-derived
suppressor
expression
checkpoints,
programmed
death-ligand
1,
several
cancer
types.
At
level,
transcriptional
factors,
Snail,
Zeb1,
Twist1,
produce
or
attract
promote
checkpoint
molecules
via
chemokine
production,
leading
microenvironment.
In
turn,
factors
induce
cells.
This
feedback
loop
between
immunosuppression
promotes
progression.
For
therapy
directly
targeting
challenging,
elucidation
interactive
regulation
desirable
for
developing
new
therapeutic
approaches
cancer.
The
combination
inhibitors
immunotherapy
promising
EMT.