Intracellular Photocatalytic NADH/NAD(P)H Oxidation for Cancer Drug Development
Ashish Yadav,
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Samya Banerjee,
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Arif Ali Mandal
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et al.
Journal of the American Chemical Society,
Journal Year:
2025,
Volume and Issue:
147(9), P. 7161 - 7181
Published: Feb. 20, 2025
Photocatalytic
cancer
therapy
(PCT)
has
emerged
as
a
cutting-edge
anticancer
mechanism
of
action,
harnessing
light
energy
to
mediate
the
catalytic
oxidation
intracellular
substrates.
PCT
is
significant
current
importance
due
its
potential
address
limitations
conventional
chemotherapy,
particularly
drug
resistance
and
side
effects.
This
approach
offers
noninvasive,
targeted
treatment
option
by
utilizing
metal-based
photocatalysts
induce
redox
metabolic
disorders
within
cells.
The
disrupt
cell
metabolism
converting
NADH/NAD(P)H
NAD+/NAD(P)+
via
photoredox
processes,
altering
NAD+/NADH
or
NAD(P)+/NAD(P)H
ratios,
which
are
crucial
for
cellular
metabolism.
Ir(III),
Ru(II),
Re(I),
Os(II)
demonstrated
promising
efficacy.
Despite
these
developments,
gaps
remain
in
literature
translating
this
new
into
clinical
trials.
Perspective
critically
examines
developments
research
area
provides
future
directions
designing
efficient
PCT.
Language: Английский
Exploring Anticancer Activity and DNA Binding of Metal (II) Salicylaldehyde Schiff Base Complexes: A Convergence of Experimental and Computational Perspectives
Applied Organometallic Chemistry,
Journal Year:
2025,
Volume and Issue:
39(5)
Published: April 9, 2025
ABSTRACT
Metal
complexes
derived
from
salicylaldehyde‐based
Schiff
bases
are
among
the
frontrunners
in
pursuit
of
precise
and
potent
cancer
treatments
due
to
their
remarkable
prowess.
In
this
study,
base
(
HL
)
was
prepared
via
a
reaction
between
2‐amino‐5‐benzonitrile
salicylaldehyde.
Subsequently,
further
reacted
with
Ni
(II),
Co
Cu
(II)
Pd
ions
using
respective
metal
salts
obtain
homoleptic
mononuclear
C1
–
C4
).
The
composition
were
determined
1
H
13
C
NMR,
UV–Vis,
FTIR,
CHN,
SEM–EDX
HRMS
analyses.
addition,
structural
geometries
,
C3
solid
state
single
crystal
X‐ray
diffraction
analysis
corroborate
mentioned
characterization
techniques
employed.
stability
compounds
assessed
through
time‐dependent
UV–vis
spectroscopy,
revealing
that
C2
exhibited
highest
under
experimental
conditions.
anticancer
effects
tested
on
breast
cell
lines
(MCF‐7)
MTT,
LDH
ATP
assays.
Both
displayed
potential
cytotoxicity
MCF‐7
line,
which
better
inhibition
effect
than
standard
chemotherapeutic
agent,
doxorubicin
(DOX),
IC
50
43.08
μM.
We
postulate
mechanism
by
may
function
is
binding
DNA
=
0.114
(±
0.02)
×
10
4
intercalation
(shown
UV‐CD
UV‐LD
spectroscopy)
at
AT
rich
sites.
These
data
corroborated
silico
extra
precision
(XP)
docking
molecular
dynamic
(MD)
simulations.
Language: Английский
A mechanism – based perspective on the interplay of new drug candidate with biomolecules
Journal of Molecular Structure,
Journal Year:
2024,
Volume and Issue:
1321, P. 139700 - 139700
Published: Aug. 23, 2024
Language: Английский
Recent advances in Rh(III)-based anticancer complexes
Souvik Saha,
No information about this author
Rajesh Kushwaha,
No information about this author
Apurba Mandal
No information about this author
et al.
Coordination Chemistry Reviews,
Journal Year:
2024,
Volume and Issue:
525, P. 216306 - 216306
Published: Nov. 22, 2024
Language: Английский
Gold(I) Complexes of the Type [AuL{κC-2-C6H4P(S)Ph2}] [L = PTA, PPh3, PPh2(C6H4-3-SO3Na) and PPh2(2-py)]: Synthesis, Characterisation, Crystal Structures, and In Vitro and In Vivo Anticancer Properties.
T. Srinivasa Reddy,
No information about this author
Steven H. Privér,
No information about this author
Ruchika Ojha
No information about this author
et al.
European Journal of Medicinal Chemistry,
Journal Year:
2024,
Volume and Issue:
281, P. 117007 - 117007
Published: Oct. 30, 2024
Language: Английский
Exploring Sex-Based Neuropsychological Outcomes in Pediatric Brain Cancer Survivors: A Pilot Study
Diseases,
Journal Year:
2024,
Volume and Issue:
12(11), P. 289 - 289
Published: Nov. 11, 2024
Background:
The
increasing
survival
rates
among
pediatric
cancer
patients
underscore
the
critical
need
to
understand
long-term
psychosocial
impacts
of
treatments,
such
as
cisplatin
and
carboplatin.
While
these
treatments
are
lifesaving,
they
may
pose
risks
neurodevelopmental
processes.
Despite
substantial
body
research
highlighting
cognitive
impairments
associated
with
there
remains
a
gap
in
understanding
how
effects
differ
by
sex.
As
sex
differences
could
inform
tailored
interventions
support
mechanisms
for
affected
individuals,
this
pilot
study
aimed
examine
neuropsychological
outcomes
treated
brain
and/or
Methods:
Our
employed
rigorous/structured
assessments
evaluate
executive
functions
survivors
We
utilized
BRIEF
TOL
tests
assess
key
domains
function,
including
inhibitory
control,
flexibility,
problem-solving
abilities.
Additionally,
factors
were
evaluated
using
Resiliency
Scale
measure
resilience
PAT
test
family
risk.
Results:
In
our
cohort
17
patients,
significant
emerged,
where
males
outperformed
females
areas
impulse
regulation,
strategic
planning.
Conclusions:
These
findings
highlight
complexity
survivors.
Understanding
sex-specific
is
essential
developing
that
optimize
outcomes.
Future
should
focus
on
larger
cohorts
longitudinal
studies
validate
guide
targeted
improve
survivorship
Language: Английский
Novel Pt (II) Complexes With Anticancer Activity Against Pancreatic Ductal Adenocarcinoma Cells
Bioinorganic Chemistry and Applications,
Journal Year:
2024,
Volume and Issue:
2024(1)
Published: Jan. 1, 2024
Pancreatic
ductal
adenocarcinoma
(PDAC)
is
a
highly
aggressive
type
of
solid
tumor
that
becoming
more
common.
cis
‐[PtCl
2
(NH
3
)
]
(in
short
cisplatin
or
CDDP)
has
been
shown
to
be
effective
in
treating
various
cancers,
including
PDAC.
However,
the
development
resistance
chemotherapy
drugs
created
need
for
synthesis
new
anticancer
agents.
Platinum‐based
containing
bidentate
ligand
phenanthroline
have
found
strong
antitumor
activity
due
their
ability
cause
DNA
damage.
In
this
study,
we
examined
two
Pt
(II)
cationic
complexes,
[Pt(
η
1
‐C
H
4
OR)
(DMSO)
(phen)]
+
Pt‐EtORSOphen;
R
=
Me,
;
Et,
),
inhibit
growth
and
spread
BxPC‐3
PDAC
cells,
comparison
CDDP.
The
length
alkyl
chain
its
associated
lipophilic
properties
did
not
affect
effects
complexes
cells.
it
appear
influence
rapid
loss
mitochondrial
membrane
potential
(ΔΨ
M
suggesting
these
could
potentially
used
as
mitochondria‐targeted
cations
therapy.
Language: Английский