Photoinduced Actin Aggregation Involves Cell Death: A Mechanism of Cancer Cell Cytotoxicity after Near-Infrared Photoimmunotherapy
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 18, 2025
Near-infrared
photoimmunotherapy
(NIR-PIT)
is
a
cancer
treatment
modality
that
uses
antibody-photoabsorber
(IR700)
conjugates
to
destroy
specific
cells.
The
reaction
between
the
antibody
and
photoabsorber
triggered
by
NIR-light,
this
alters
shape
hydrophilicity
of
conjugate.
This
photochemical
responsible
for
NIR-PIT-induced
cell
death;
however,
detailed
mechanism
underlying
effect
remains
unknown.
In
study,
we
demonstrated
actin
filaments
underneath
membrane
play
an
important
role
in
death
IR700
mediates
conjugates,
leading
filament
aggregation
upon
NIR-light
irradiation.
destruction
cortical
beneath
plasma
allows
water
flow
into
based
on
osmotic
conditions,
resulting
rupture.
sequence
events
may
constitute
death,
making
NIR-PIT
promising
modality.
Language: Английский
Contrast-enhanced ultrasound imaging for monitoring the efficacy of near-infrared photoimmunotherapy
Kohei Matsuoka,
No information about this author
Mizuki Yamada,
No information about this author
Noriaki Fukatsu
No information about this author
et al.
EBioMedicine,
Journal Year:
2023,
Volume and Issue:
95, P. 104737 - 104737
Published: Aug. 7, 2023
Near-infrared
photoimmunotherapy
(NIR-PIT)
is
a
promising
cancer
therapy
combining
NIR-light
irradiation
with
an
antibody
and
IR700DX,
light-sensitive
substance,
to
destroy
tumours.
However,
homogeneous
difficult
because
the
light
varies
depending
on
distance
tissue
environment.
Therefore,
markers
that
indicate
sufficient
are
necessary.
Nanoparticles
sized
10∼200
nm
show
enhanced
permeation
retention
within
tumours,
which
further
via
NIR-PIT
(super
permeability
retention,
SUPR).
We
aimed
monitor
effectiveness
of
by
measuring
SUPR.A
xenograft
mouse
tumour
model
was
established
inoculating
human
cells
in
both
buttocks
Balb/C-nu/nu
mice,
performed
only
one
side.
To
evaluate
SUPR,
fluorescent
signal
examination
using
QD800-fluorescent
nanoparticles
NIR-fluorescent
poly
(d,l-lactide-co-glycolic
acid)
(NIR-PLGA)
microparticles.
Harmonic
signals
were
evaluated
micro-bubbles
contrast
agent
Sonazoid
contrast-enhanced
ultrasound
(CEUS)
imaging.
The
correlation
between
SUPR
immediately
after
treatment
day
evaluated.QD800
persisted
treated
intensity
remaining
showed
high
positive
therapeutic
effect.
NIR-PLGA
Sonazoid-derived
harmonic
remained
for
longer
time
tumours
than
controls,
kE
value
two-compartment
correlated
effectiveness.SUPR
measurement
CEUS
imaging
could
be
easily
adapted
clinical
use
as
image-based
biomarker
monitoring
confirming
efficacy.This
research
supported
ARIM
JAPAN
MEXT,
Program
Developing
Next-generation
Researchers
(Japan
Science
Technology
Agency),
KAKEN
(18K15923,
21K07217)
(JSPS),
CREST
(JPMJCR19H2,
JST),
FOREST-Souhatsu
(JST).
Mochida
Memorial
Foundation
Medical
Pharmaceutical
Research;
Takeda
Foundation;
Japan
Health
Princess
Takamatsu
Cancer
Research
Fund.
Funders
provided
financial
support
had
no
role
study
design,
data
collection,
analysis,
interpretation,
writing
report.
Language: Английский
近红外光免疫治疗策略靶向肿瘤微环境的研究进展
崔瀛书 Cui Yingshu,
No information about this author
李怡 Li Yi,
No information about this author
李晓松 Li Xiaosong
No information about this author
et al.
Chinese Journal of Lasers,
Journal Year:
2024,
Volume and Issue:
51(9), P. 0907010 - 0907010
Published: Jan. 1, 2024
近红外光免疫治疗(NIR-PIT)是一种结合抗体和光吸收剂IRDye700DX的新型肿瘤疗法,它既能够激活局部免疫效应,又能够增强肿瘤靶向性,已在不同肿瘤类型的治疗中显示出巨大的应用潜力。大量研究已经证实肿瘤微环境是导致肿瘤不断发展的重要原因,因此NIR-PIT中的光免疫偶联物靶点也已经扩展至肿瘤微环境中非肿瘤细胞的表面蛋白中。利用NIR-PIT局部消除肿瘤微环境中某些具有特定标志物的免疫抑制细胞、血管或肿瘤成纤维细胞,将解除免疫抑制,最大效率发挥机体的正常免疫功能,取得最佳的疗效。主要综述了NIR-PIT的治疗策略和靶向肿瘤微环境的最新研究进展。