The Interplay between Heat Shock Proteins and Cancer Pathogenesis: A Novel Strategy for Cancer Therapeutics
Cancers,
Journal Year:
2024,
Volume and Issue:
16(3), P. 638 - 638
Published: Feb. 1, 2024
Heat
shock
proteins
(HSPs)
are
developmentally
conserved
families
of
protein
found
in
both
prokaryotic
and
eukaryotic
organisms.
HSPs
engaged
a
diverse
range
physiological
processes,
including
molecular
chaperone
activity
to
assist
the
initial
folding
or
promote
unfolding
refolding
misfolded
intermediates
acquire
normal
native
conformation
its
translocation
prevent
aggregation
as
well
immunity,
apoptosis,
autophagy.
These
chaperonins
classified
into
various
according
their
size
weight,
encompassing
small
(e.g.,
HSP10
HSP27),
HSP40,
HSP60,
HSP70,
HSP90,
category
large
that
include
HSP100
ClpB
proteins.
The
overexpression
is
induced
counteract
cell
stress
at
elevated
levels
variety
solid
tumors,
anticancer
chemotherapy,
closely
related
worse
prognosis
therapeutic
resistance
cancer
cells.
also
involved
anti-apoptotic
properties
associated
with
processes
progression
development,
such
metastasis,
invasion,
proliferation.
This
review
outlines
previously
mentioned
significant
involvement
mechanisms
tumor
advancement
contribution
identifying
potential
targets
for
interventions.
Language: Английский
Synergistic effects of 6-shogaol and hyperthermia on ACHN renal cancer cells: modulation of ROS and heat shock pro-teins in cancer therapy
Frontiers in Pharmacology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 20, 2025
Renal
cancer
is
known
for
its
aggressive
progression
and
resistance
to
standard
treatments,
underscoring
the
need
novel
therapeutic
strategies.
This
study
explores
potential
of
combining
6-shogaol
(6-SHO),
a
bioactive
compound
derived
from
ginger
(Zingiber
officinale),
with
hyperthermia
enhance
anticancer
efficacy
in
ACHN
renal
cells.
cells
were
treated
6-SHO
exposed
hyperthermic
conditions.
We
evaluated
combined
effects
on
apoptosis,
cell
cycle
arrest,
proliferation,
as
well
role
reactive
oxygen
species
(ROS)
heat
shock
proteins
(HSPs)
mediating
these
responses.
The
combination
significantly
increased
induced
G2/M
phase
reduced
proliferation
more
effectively
than
either
treatment
alone.
ROS
played
critical
effects,
modulation
HSPs
factor
1
(HSF1)
further
disrupting
survival
mechanisms.
These
findings
highlight
synergistic
approach
treatment,
supporting
research
clinical
evaluation.
Language: Английский
Chemoradiotherapy Combined With Modulated Electro‐Hyperthermia (mEHT) Converts Initially Inoperable Esophageal Cancer to Operable Disease
Deng‐Yu Kuo,
No information about this author
Pei‐Wei Shueng,
No information about this author
Shan‐Ying Wang
No information about this author
et al.
Thoracic Cancer,
Journal Year:
2025,
Volume and Issue:
16(6)
Published: March 1, 2025
ABSTRACT
This
case
report
demonstrated
the
effectiveness
of
combining
chemoradiotherapy
(CCRT)
with
modulated
electro‐hyperthermia
(mEHT)
in
converting
initially
inoperable
esophageal
cancer
into
an
operable
condition.
A
60‐year‐old
male
stage
IVB
lower
third
squamous
cell
carcinoma
(cT3N2M1)
experienced
significant
tumor
shrinkage
(ypT2N0M0)
and
a
notable
metabolic
response,
which
enabled
successful
surgical
removal.
treatment
approach
highlights
potential
mEHT
as
valuable
addition
to
comprehensive
management
cancer.
Language: Английский
Heat shock factor 1 inhibition enhances the effects of modulated electro hyperthermia in a triple negative breast cancer mouse model
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: April 8, 2024
Female
breast
cancer
is
the
most
diagnosed
worldwide.
Triple
negative
(TNBC)
aggressive
type
and
there
no
existing
endocrine
or
targeted
therapy.
Modulated
electro-hyperthermia
(mEHT)
a
non-invasive
complementary
therapy
using
an
electromagnetic
field
generated
by
amplitude
modulated
13.56
MHz
frequency
that
induces
tumor
cell
destruction.
However,
we
have
demonstrated
strong
induction
of
heat
shock
response
(HSR)
mEHT,
which
can
result
in
thermotolerance.
We
hypothesized
inhibition
factor
1
(HSF1)
synergize
with
mEHT
enhance
cell-killing.
Thus,
either
knocked
down
HSF1
gene
CRISPR/Cas9
lentiviral
construct
inhibited
specific
small
molecule
inhibitor:
KRIBB11
vivo.
Wild
HSF1-knockdown
4T1
TNBC
cells
were
inoculated
into
mammary
gland's
fat
pad
BALB/c
mice.
Four
treatments
performed
every
second
day
growth
was
followed
ultrasound
caliper.
administrated
intraperitoneally
at
50
mg/kg
daily
for
8
days.
Hsp70
expression
assessed.
knockdown
sensitized
transduced
to
reduced
growth.
mRNA
significantly
KO
group
when
compared
empty
vector
group,
consequently
mEHT-induced
upregulation
diminished
group.
Immunohistochemistry
(IHC)
confirmed
HSF1-KO
Demonstrating
translational
potential
inhibition,
combined
mass
monotherapy.
Inhibition
also
supported
qPCR
IHC.
In
conclusion,
suggest
mEHT-therapy
be
possible
new
strategy
treatment
great
potential.
Language: Английский
Regulation of transcription factor function by purinergic signalling in cardiovascular diseases
Hao Tang,
No information about this author
Qihang Kong,
No information about this author
Zhewei Zhang
No information about this author
et al.
Purinergic Signalling,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 31, 2024
Language: Английский
Case report: Combinations of immune checkpoint inhibitor, chemotherapy, and hyperthermia therapy avoid lymphatic recurrence in cholangiocarcinoma
Frontiers in Oncology,
Journal Year:
2024,
Volume and Issue:
14
Published: Oct. 24, 2024
Cholangiocarcinoma
is
a
malignancy
known
for
its
aggressiveness
and
limited
treatment
options.
The
malignant
tumor
behaviors
include
intrahepatic
recurrence,
regional
lymph
node
(LN)
metastasis,
peritoneal
carcinomatosis,
lung
metastasis.
Herein,
we
reported
case
of
lymphatic
recurrence
in
an
cholangiocarcinoma
patient
after
surgery,
adjuvant
concurrent
chemoradiotherapy
(CCRT),
who
experienced
remarkable
response
to
combination
therapy.
However,
the
failed
undergo
radiotherapy
or
other
invasive
local
therapy
therefore
received
Opdivo
(nivolumab)
with
chemotherapy
(FOLFOX)
modulated
electro-hyperthermia.
Notably,
these
medical
interventions,
this
had
complete
(CR)
treatments,
which
no
metastasis
occurred,
significantly
decreased
marker,
CA
19-9,
level
was
found.
This
highlights
potential
multiple
anti-tumor
therapies,
including
immune
checkpoint
inhibitors,
chemotherapy,
hyperthermia,
managing
challenging
cases.
Language: Английский
Ivermectin Synergizes with Modulated Electro-hyperthermia and Improves Its Anticancer Effects in a Triple-Negative Breast Cancer Mouse Model
ACS Pharmacology & Translational Science,
Journal Year:
2024,
Volume and Issue:
7(8), P. 2496 - 2506
Published: July 17, 2024
Triple-negative
breast
cancer
(TNBC)
is
the
most
aggressive
subtype,
with
limited
treatment
options.
Modulated
electro-hyperthermia
(mEHT)
a
novel
adjuvant
therapy
that
induces
selective
damage.
However,
mEHT
upregulates
heat
shock
protein
beta
1
(HSPB1),
cancer-promoting
stress
chaperone
molecule.
Thus,
we
investigated
whether
ivermectin
(IVM),
an
anthelmintic
drug,
may
synergize
and
enhance
its
anticancer
effects
by
inhibiting
HSPB1
phosphorylation.
Isogenic
4T1
TNBC
cells
were
inoculated
into
BALB/c
mice
treated
mEHT,
IVM,
or
combination
of
both.
IVM
synergistically
improved
tumor
growth
inhibition
achieved
mEHT.
Moreover,
downregulated
mEHT-induced
strongest
tissue
damage
was
observed
in
+
IVM-treated
tumors,
coupled
apoptosis
induction
proliferation
inhibition.
In
addition,
there
no
significant
body
weight
loss
indicating
this
well-tolerated.
conclusion,
combined
new,
effective,
safe
option
for
TNBC.
Language: Английский