Inhibition of lanosterol synthase linking with MAPK/JNK signaling pathway suppresses endometrial cancer
Liangjian Ma,
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Wunan Huang,
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Xiaolei Liang
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et al.
Cell Death Discovery,
Journal Year:
2025,
Volume and Issue:
11(1)
Published: Feb. 8, 2025
Abstract
Endometrial
cancer
(EC)
is
a
significant
health
threat
to
women,
with
recurrence
after
treatment
posing
major
challenge.
While
abnormal
cholesterol
metabolism
has
been
implicated
in
EC
progression,
the
underlying
mechanisms
remain
unclear.
In
this
study,
we
identified
lanosterol
synthase
(LSS)
as
key
mediator
associated
EC.
We
found
that
LSS
significantly
upregulated
tissues.
Functional
assays
revealed
promotes
cell
proliferation
and
migration,
inhibits
apoptosis,
drives
tumor
growth
vivo.
Mechanistically,
exerts
dual
effects
by
accumulating
esters,
thereby
enhancing
growth,
activating
MAPK/JNK
signaling
pathway.
Importantly,
inhibition
of
specific
inhibitor
Ro
48-8071
not
only
reduced
suppressed
xenograft
but
also
inhibited
patient-derived
tumor-like
clusters
(PTCs).
These
findings
establish
novel
oncogene
EC,
promoting
progression
through
activation
ester
accumulation,
highlight
therapeutic
potential
targeting
treatment.
Language: Английский
The metabolic dialogue between intratumoural microbes and cancer: implications for immunotherapy
Y. Situ,
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Pengpeng Zhang,
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Cangang Zhang
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et al.
EBioMedicine,
Journal Year:
2025,
Volume and Issue:
115, P. 105708 - 105708
Published: April 22, 2025
Language: Английский
Genetic association of lipids and lipid-lowering drug target genes with Endometrial carcinoma: a drug target Mendelian randomization study
Zhe-Han Yang,
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Jun-Pan Chen,
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Ming-Hao Wen
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et al.
Frontiers in Endocrinology,
Journal Year:
2024,
Volume and Issue:
15
Published: Aug. 13, 2024
Background
Aberrant
lipid
metabolism
is
intricately
linked
to
the
development
of
endometrial
cancer,
and
statin
lipid-lowering
medications
are
regarded
as
promising
adjunctive
therapies
for
future
management
this
malignancy.
This
study
employed
Mendelian
randomization
(MR)
explore
causal
association
between
traits
cancer
while
assessing
potential
impact
drug
targets
on
lower
lipids
cancer.
Method
Two-sample
was
probe
carcinoma.
Drug-target
also
utilized
identify
drug-target
genes
managing
In
instances
where
lipid-mediated
effects
through
particular
were
notable,
impacts
these
carcinoma
risk
factors
investigated
bolster
findings.
Result
No
genetically
predicted
(LDL-C,
TG,
TC,
HDL-C)
EC
found
in
two-sample
randomization.
target
randomization,
genetic
modeling
apolipoprotein
B
(APOB)
(OR
[95%CI]=0.31,
[0.16-0.60];
p
=4.73e-04)
cholesteryl
ester
transfer
protein
(CETP)
[95%CI]=1.83,
[1.38-2.43];
=2.91e-05)
mimicry
associated
with
non-endometrioid
Conclusion
The
results
our
MR
revealed
no
EC.
Among
six
targets,
we
observed
a
significant
APOB
levels
higher
CETP
an
increased
endometrioid
These
findings
provide
novel
insights
into
importance
regulation
individuals
carcinoma,
warranting
further
clinical
validation
mechanistic
investigations.
Language: Английский
Phospholipid Acyltransferases: Characterization and Involvement of the Enzymes in Metabolic and Cancer Diseases
Jan Korbecki,
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Mateusz Bosiacki,
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Maciej Pilarczyk
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et al.
Cancers,
Journal Year:
2024,
Volume and Issue:
16(11), P. 2115 - 2115
Published: May 31, 2024
This
review
delves
into
the
enzymatic
processes
governing
initial
stages
of
glycerophospholipid
(phosphatidylcholine,
phosphatidylethanolamine,
and
phosphatidylserine)
triacylglycerol
synthesis.
The
key
enzymes
under
scrutiny
include
GPAT
AGPAT.
Additionally,
as
most
AGPATs
exhibit
LPLAT
activity,
participating
in
Lands
cycle
with
similar
functions
are
also
covered.
begins
by
discussing
properties
these
enzymes,
emphasizing
their
specificity
reactions,
notably
incorporation
polyunsaturated
fatty
acids
(PUFAs)
such
arachidonic
acid
docosahexaenoic
(DHA)
phospholipids.
paper
sheds
light
on
intricate
involvement
various
diseases,
including
obesity,
insulin
resistance,
cancer.
To
underscore
relevance
cancer
processes,
a
bioinformatics
analysis
was
conducted.
expression
levels
described
were
correlated
overall
survival
patients
across
33
different
types
using
GEPIA
portal.
further
explores
potential
therapeutic
implications
inhibiting
treatment
metabolic
diseases
By
elucidating
pathways
involved
lipid
synthesis
impact
pathological
conditions,
this
contributes
to
comprehensive
understanding
targets.
Language: Английский