Advances in Ferroptosis Research: A Comprehensive Review of Mechanism Exploration, Drug Development, and Disease Treatment
Pharmaceuticals,
Journal Year:
2025,
Volume and Issue:
18(3), P. 334 - 334
Published: Feb. 26, 2025
In
recent
years,
ferroptosis,
as
an
emerging
modality
of
programmed
cell
death,
has
captured
significant
attention
within
the
scientific
community.
This
comprehensive
review
meticulously
canvasses
pertinent
literature
past
few
spanning
multiple
facets.
It
delves
into
intricate
mechanisms
underpinning
tracks
evolution
its
inducers
and
inhibitors,
dissects
roles
in
a
diverse
array
diseases,
well
resultant
therapeutic
implications.
A
profound
exploration
is
conducted
functional
ferroptosis-related
molecules,
intracellular
pathways,
metabolic
cascades,
signaling
transduction
routes.
Novel
ferroptosis
inhibitors
are
introduced
detail,
covering
their
design
blueprints,
synthetic
methodologies,
bioactivity
profiles.
Moreover,
exhaustive
account
provided
regarding
involvement
malignancies,
neurodegenerative
disorders,
cardiovascular
ailments,
other
pathologies.
By
highlighting
pivotal
status
potential
regimens
various
this
aspires
to
furnish
thorough
reference
framework
for
future
investigations
clinical
translations
domain.
Language: Английский
Naphthalene peri-Diselenide-Based BODIPY Probe for the Detection of Hydrogen Peroxide, tert-Butylhydroperoxide, Hydroxyl Radical, and Peroxynitrite Ion
Babli Chhillar,
No information about this author
Nikhil Sodhi,
No information about this author
Rajni Kadian
No information about this author
et al.
ACS Omega,
Journal Year:
2025,
Volume and Issue:
10(7), P. 6396 - 6405
Published: Feb. 13, 2025
Dimethoxynaphthalene
peri-diselenide-based
BODIPY
(4,4-difluoro-4-bora-3a,4a-diaza-s-indacene)
probe
has
been
synthesized.
The
demonstrated
selectivity
and
sensitivity
for
hydrogen
peroxide
(H2O2)
tert-butylhydroperoxide
(t-BuOOH),
hydroxyl
radical
(•OH),
peroxynitrite
ion
(ONOO–)
detection
reversibility
upon
treatment
with
glutathione.
limits
of
the
were
observed
to
be
0.40
μM
H2O2,
0.41
t-BuOOH,
0.95
•OH,
0.46
ONOO–,
respectively.
A
proposed
mechanism
"turn-on"
event
suggested
corroborated
by
spectroscopic
computational
data.
It
that
electron
transfer
occurred
from
Se
center
moiety,
followed
photoinduced
(PET)
mechanism.
Language: Английский
Synthetic Benzylic Diselenides and Disulfides: Potential Anticancer Activities via Modulation of the ROS‐dependent Akt/β‐Catenin Signaling Pathway
Pallavi Barman,
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Roopjyoti Misra,
No information about this author
Nikita Pal
No information about this author
et al.
ChemMedChem,
Journal Year:
2024,
Volume and Issue:
19(22)
Published: Aug. 1, 2024
Abstract
The
natural
and
synthetic
organodiselenides
have
garnered
much
research
attention
due
to
their
chemotherapeutic
chemopreventive
activities.
Herein,
we
describe
the
synthesis
of
a
series
benzylic
diselenides,
which
were
synthesized
by
coupling
in
situ
generated
disodium
diselenide
with
corresponding
halides.
diselenides
evaluated
for
anticancer
activities
highly
aggressive
triple‐negative
breast
cancer
cells.
Preliminary
anti‐proliferative
indicated
4‐cyano‐substituted
7
be
most
potent
an
IC
50
value
1.9±0.3
μM.
Detailed
mechanistic
investigations
showed
that
induces
apoptosis
causes
G1
phase
arrest
cell
cycle.
It
exhibits
activity
suppressing
Akt/β‐catenin
signaling
pathway.
Further
control
experiments
LiCl
(inhibitor
GSK‐3β)
revealed
down‐regulation
β‐catenin
was
promoted
GSK‐3β‐induced
phosphorylation
its
subsequent
proteasomal
degradation.
Moreover,
intracellular
ROS
found
act
as
upstream
mediator
inactivation
present
study
describing
efficient
towards
cells
through
modulation
ROS‐dependent
pathway
would
certainly
helpful
future
development
small‐molecule
organoselenium
compounds
treatment
cancer.
Language: Английский