HER2-targeted therapies beyond breast cancer — an update
Nature Reviews Clinical Oncology,
Journal Year:
2024,
Volume and Issue:
21(9), P. 675 - 700
Published: July 22, 2024
Language: Английский
Unlocking the power of imidazoquinolines: recent advances in anticancer and immunotherapeutic strategies
Ranjini Jenifer R,
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Badruzzaman Choudhury,
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Mohammed Mujahid Alam
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et al.
Future Medicinal Chemistry,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1 - 17
Published: April 15, 2025
The
challenges
in
drug
discovery
aiming
to
mitigate
cancer
progression
are
the
thrust
area
of
scientific
research
for
several
decades.
Since
advent
heterocyclic
chemistry,
programs
have
made
significant
achievements
that
lead
development
numerous
drugs
with
broad
spectrum
potencies,
contributing
both
diagnostic
and
therapeutic
advancements.
Till
date,
efforts
discover
more
potent
efficient
candidates
underway
minimize
adverse
side
effects
existing
chemotherapeutics.
In
view
above,
small-molecule
agonists
can
interact
different
immune
modulators
like
toll
receptor-7
(TLR-7)
TLR-8
being
investigated
explored.
These
expected
display
profound
effect
on
anti-tumoral
activity
by
enhancing
production
proinflammatory
cytokines.
Recently,
imidazoquinoline
derivatives
proven
TLR
agonist
activities
emerged
as
promising
anticancer
therapeutics.
With
advancements
technology
evolution
new
scopes
discovery,
strategies
adopted,
particularly
help
nanotechnology,
immune-technology,
combination
etc.,
curb
various
types
cancers.
Herein,
novel
therapeutics
imidazoquinolines
reported
last
5
years,
their
structure-activity
relationship
along
important
synthetic
schemes
agonists,
discussed.
Language: Английский
Receptor tyrosine kinases in breast cancer treatment: unraveling the potential
Qi Yu,
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Shumin Deng,
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Kuan-Song Wang
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et al.
American Journal of Cancer Research,
Journal Year:
2024,
Volume and Issue:
14(9), P. 4172 - 4196
Published: Jan. 1, 2024
Breast
cancer
is
a
multifactorial
disease
driven
by
acquired
genetic
and
epigenetic
changes
that
lead
to
aberrant
regulation
of
cellular
signaling
pathways.
Receptor
tyrosine
kinases
(RTKs),
class
critical
receptors,
are
involved
in
the
initiation
progression
breast
cancer.
RTKs
cell
surface
receptors
with
unique
structures
biological
characteristics,
which
respond
environmental
signals
initiating
cascades
such
as
mitogen-activated
protein
kinase
(MAPK)
pathway,
Janus
(JAK)/signal
transducer,
activator
transcription
(STAT)
phosphoinositide
3-kinase
(PI3K)/AKT
pathway.
The
role
makes
them
suitable
targets
for
treatment.
Targeted
therapies
against
have
been
developed
recent
years,
evaluated
clinical
trials,
approved
several
types,
including
However,
displays
molecular
heterogeneity
exhibits
different
therapeutic
responses
various
drug
leading
limited
effectiveness
targeted
therapy
RTKs.
In
this
review,
we
summarize
structural
functional
characteristics
selected
discuss
mechanisms
current
status
involving
progression.
Language: Английский
The Complexity and Significance of Fibroblast Growth Factor (FGF) Signaling for FGF-Targeted Cancer Therapies
A. Nguyen,
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Caroline O. Facey,
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Bruce M. Boman
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et al.
Cancers,
Journal Year:
2024,
Volume and Issue:
17(1), P. 82 - 82
Published: Dec. 30, 2024
Fibroblast
growth
factors
(FGFs)
have
diverse
functions
in
the
regulation
of
cell
proliferation
and
differentiation
development,
tissue
maintenance,
wound
repair,
angiogenesis.
The
goal
this
review
paper
is
to
(i)
deliberate
on
role
FGFs
FGF
receptors
(FGFRs)
different
cancers,
(ii)
present
advances
FGF-targeted
cancer
therapies,
(iii)
explore
signaling
mechanisms
that
explain
how
expression
becomes
dysregulated
during
development.
often
mutated
overexpressed
FGFR
isoforms
unique
patterns
distinct
roles
cancers.
Among
members,
15/19
subfamily
particularly
interesting
because
its
protein
structure
endocrine
function.
abnormal
types
(breast,
colorectal,
hepatobiliary,
bronchogenic,
others)
examined
correlated
with
patient
prognosis.
classification
ligands
based
their
mode
action,
whether
autocrine,
paracrine,
endocrine,
or
intracrine,
illustrated,
an
analysis
binding
specificity
FGFRs
also
provided.
Moreover,
latest
therapeutic
strategies
involving
small
molecules,
ligand
traps,
monoclonal
antibody-based
inhibitors
are
presented.
Lastly,
we
discuss
dysregulation
affects
Language: Английский