Scientific Reports,
Journal Year:
2023,
Volume and Issue:
13(1)
Published: July 13, 2023
In
the
current
study,
we
designed
and
synthesized
a
series
of
new
quinoline
derivatives
10a-p
as
antiproliferative
agents
targeting
cancer
through
inhibition
VEGFR-2.
Preliminary
molecular
docking
to
assess
interactions
with
binding
site
VEGFR-2
(PDB
code:
4ASD)
displayed
poses
comparable
sorafenib.
The
compounds
exhibited
inhibitory
activity
IC50
ranging
from
36
nM
2.23
μM
compared
sorafenib
(IC50
=
45
nM),
where
derivative
10i
was
most
potent.
Additionally,
were
evaluated
in
vitro
for
their
cytotoxic
against
HepG2
cell
line.
Seven
10a,
10c,
10d,
10e,
10i,
10n
10o
4.60,
4.14,
1.07,
0.88,
1.60,
2.88
2.76
respectively)
better
than
8.38
μM).
Compound
tested
Transformed
Human
Liver
Epithelial-2
normal
line
(THLE-2)
evaluate
its
selective
cytotoxicity.
Furthermore,
potent
representative
series,
assayed
apoptotic
cycle
kinetics'
influence
on
HepG2,
effects
gene
expression
VEGFR-2,
protein
markers
Caspase-7
Bax.
proved
have
potential
role
apoptosis
by
causing
significant
increase
early
late
quartiles,
remarkable
elevating
relative
Bax
reduction
expression.
Collectively,
obtained
results
indicate
that
compound
has
promising
lead
development
anticancer
agents.
Signal Transduction and Targeted Therapy,
Journal Year:
2024,
Volume and Issue:
9(1)
Published: Aug. 23, 2024
Abstract
Alzheimer’s
disease
(AD)
stands
as
the
predominant
form
of
dementia,
presenting
significant
and
escalating
global
challenges.
Its
etiology
is
intricate
diverse,
stemming
from
a
combination
factors
such
aging,
genetics,
environment.
Our
current
understanding
AD
pathologies
involves
various
hypotheses,
cholinergic,
amyloid,
tau
protein,
inflammatory,
oxidative
stress,
metal
ion,
glutamate
excitotoxicity,
microbiota-gut-brain
axis,
abnormal
autophagy.
Nonetheless,
unraveling
interplay
among
these
pathological
aspects
pinpointing
primary
initiators
require
further
elucidation
validation.
In
past
decades,
most
clinical
drugs
have
been
discontinued
due
to
limited
effectiveness
or
adverse
effects.
Presently,
available
primarily
offer
symptomatic
relief
often
accompanied
by
undesirable
side
However,
recent
approvals
aducanumab
(
1
)
lecanemab
2
Food
Drug
Administration
(FDA)
present
potential
in
disrease-modifying
Nevertheless,
long-term
efficacy
safety
need
Consequently,
quest
for
safer
more
effective
persists
formidable
pressing
task.
This
review
discusses
pathogenesis,
advances
diagnostic
biomarkers,
latest
updates
trials,
emerging
technologies
drug
development.
We
highlight
progress
discovery
selective
inhibitors,
dual-target
allosteric
modulators,
covalent
proteolysis-targeting
chimeras
(PROTACs),
protein-protein
interaction
(PPI)
modulators.
goal
provide
insights
into
prospective
development
application
novel
drugs.
Molecular Cancer,
Journal Year:
2022,
Volume and Issue:
21(1)
Published: Nov. 2, 2022
Tumors
are
comprised
of
both
cancer
cells
and
surrounding
stromal
components.
As
an
essential
part
the
tumor
microenvironment,
stroma
is
highly
dynamic,
heterogeneous
commonly
tumor-type
specific,
it
mainly
includes
noncellular
compositions
such
as
extracellular
matrix
unique
cancer-associated
vascular
system
well
a
wide
variety
cellular
components
including
activated
fibroblasts,
mesenchymal
cells,
pericytes.
All
these
elements
operate
with
each
other
in
coordinated
fashion
collectively
promote
initiation,
progression,
metastasis
therapeutic
resistance.
Over
past
few
decades,
numerous
studies
have
been
conducted
to
study
interaction
crosstalk
between
neoplastic
cells.
Meanwhile,
we
also
witnessed
exponential
increase
investigation
recognition
critical
roles
solid
tumors.
A
series
clinical
trials
targeting
launched
continually.
In
this
review,
introduce
discuss
current
advances
understanding
various
their
cancers.
We
elaborate
on
potential
novel
approaches
for
tumor-stroma-based
targeting,
aim
leap
from
bench
bedside.
Molecular Cancer,
Journal Year:
2023,
Volume and Issue:
22(1)
Published: Oct. 13, 2023
Cancer-associated
fibroblasts
(CAFs)
are
a
heterogeneous
cell
population
that
plays
crucial
role
in
remodeling
the
tumor
microenvironment
(TME).
Here,
through
integrated
analysis
of
spatial
and
single-cell
transcriptomics
data
across
six
common
cancer
types,
we
identified
four
distinct
functional
subgroups
CAFs
described
their
distribution
characteristics.
Additionally,
RNA
sequencing
(scRNA-seq)
from
three
additional
types
two
newly
generated
scRNA-seq
datasets
rare
namely
epithelial-myoepithelial
carcinoma
(EMC)
mucoepidermoid
(MEC),
expanded
our
understanding
CAF
heterogeneity.
Cell-cell
interaction
conducted
within
context
highlighted
pivotal
roles
matrix
(mCAFs)
angiogenesis
inflammatory
(iCAFs)
shaping
immunosuppressive
microenvironment.
In
patients
with
breast
(BRCA)
undergoing
anti-PD-1
immunotherapy,
iCAFs
demonstrated
heightened
capacity
facilitating
proliferation,
promoting
epithelial-mesenchymal
transition
(EMT),
contributing
to
establishment
an
Furthermore,
scoring
system
based
on
showed
significant
correlation
immune
therapy
response
melanoma
patients.
Lastly,
provided
web
interface
(
https://chenxisd.shinyapps.io/pancaf/
)
for
research
community
investigate
pan-cancer.
British Journal of Pharmacology,
Journal Year:
2023,
Volume and Issue:
unknown
Published: Sept. 8, 2023
Tumour
angiogenesis
is
the
formation
of
new
blood
vessels
to
support
growth
a
tumour.
This
process
critical
for
tumour
progression
and
metastasis,
making
it
an
attractive
approach
cancer
therapy.
Natural
products
derived
from
plants,
animals
or
microorganisms
exert
anti-angiogenic
properties
can
be
used
inhibit
progression.
In
this
review,
we
comprehensively
report
on
current
status
natural
against
four
perspectives
until
March
2023:
(1)
role
pro-angiogenic
factors
antiangiogenic
in
angiogenesis;
(2)
development
anti-tumour
therapy
(monoclonal
antibodies,
VEGFR-targeted
small
molecules
fusion
proteins);
(3)
summary
agents,
including
polyphenols,
polysaccharides,
alkaloids,
terpenoids,
saponins
their
mechanisms
action,
(4)
future
(bioavailability
improvement,
testing
dosage
side
effects,
combination
use
discovery
unique
natural-based
compounds).
Our
review
aims
better
understand
potential
drug
inhibiting
further
aid
effective
transition
these
outcomes
into
clinical
trials.
Cancers,
Journal Year:
2024,
Volume and Issue:
16(3), P. 505 - 505
Published: Jan. 24, 2024
Despite
significant
advancements
in
the
development
of
novel
therapies,
cancer
continues
to
stand
as
a
prominent
global
cause
death.
In
many
cases,
cornerstone
standard-of-care
therapy
consists
chemotherapy
(CT),
radiotherapy
(RT),
or
combination
both.
Notably,
hyperthermia
(HT),
which
has
been
clinical
use
last
four
decades,
proven
enhance
effectiveness
CT
and
RT,
owing
its
recognized
potency
sensitizer.
Furthermore,
HT
exerts
effects
on
all
steps
cancer–immunity
cycle
impact
key
oncogenic
pathways.
Most
recently,
there
noticeable
expansion
research
related
treatment
options
involving
immunotherapy
(IT)
targeted
(TT),
trend
also
visible
pipelines
pharmaceutical
companies.
However,
potential
results
arising
from
these
innovative
therapeutic
approaches
with
remain
largely
unexplored.
Therefore,
this
review
aims
explore
oncology
major
companies,
primary
objective
identifying
principal
targets
forthcoming
therapies
that
have
be
advantageous
for
patients
by
specifically
targeting
molecular
pathways
involved
HT.
The
ultimate
goal
is
pave
way
future
initiatives
trials
harness
synergy
between
emerging
IT
TT
medications
when
used
conjunction
Pharmacological Research,
Journal Year:
2024,
Volume and Issue:
201, P. 107101 - 107101
Published: Feb. 7, 2024
The
vascular
endothelial
growth
factors
(VEGFs)
and
their
cognate
receptors
(VEGFRs),
besides
well-known
involvement
in
physiological
angiogenesis/lymphangiogenesis
diseases
associated
to
pathological
vessel
formation,
play
multifaceted
functions
the
central
nervous
system
(CNS).
In
addition
shaping
brain
development,
by
controlling
cerebral
vasculogenesis
regulating
neurogenesis
as
well
astrocyte
differentiation,
VEGFs/VEGFRs
axis
exerts
essential
adult
both
contexts.
this
article,
after
describing
CNS,
we
focus
on
neurodegenerative
reviewing
current
literature
rather
complex
contribution
pathogenic
mechanisms
of
Alzheimer's
(AD)
Parkinson's
(PD)
diseases.
Thereafter,
based
outcome
targeting
animal
models
AD
PD,
discuss
factual
relevance
pharmacological
modulation
a
novel
potential
disease-modifying
approach
for
these
pathologies.
Specific
VEGFRs
targeting,
aimed
at
selective
VEGFR-1
inhibition,
while
preserving
VEGFR-2
signal
transduction,
appears
promising
strategy
hit
molecular
underlying
pathology.
Moreover,
therapeutic
VEGFs-based
approaches
can
be
proposed
PD
treatment,
with
aim
fine-tuning
levels
amplify
neurotrophic/neuroprotective
effects
limiting
an
excessive
impact
permeability.