Egyptian Journal of Medical Human Genetics,
Journal Year:
2024,
Volume and Issue:
25(1)
Published: Oct. 12, 2024
Abstract
Background
Endometriosis
is
a
common
cause
of
endometrial-type
mucosa
outside
the
uterine
cavity
with
symptoms
such
as
painful
periods,
chronic
pelvic
pain,
pain
intercourse
and
infertility.
However,
early
diagnosis
endometriosis
still
restricted.
The
purpose
this
investigation
to
identify
validate
key
biomarkers
endometriosis.
Methods
Next-generation
sequencing
dataset
GSE243039
was
obtained
from
Gene
Expression
Omnibus
database,
differentially
expressed
genes
(DEGs)
between
normal
control
samples
were
identified.
After
screening
DEGs,
gene
ontology
(GO)
REACTOME
pathway
enrichment
analyses
performed.
Furthermore,
protein–protein
interaction
(PPI)
network
constructed
modules
analyzed
using
Human
Integrated
Protein–Protein
Interaction
rEference
database
Cytoscape
software,
hub
Subsequently,
miRNAs
genes,
TFs
miRNet
NetworkAnalyst
tool,
possible
predicted.
Finally,
receiver
operating
characteristic
curve
analysis
used
genes.
Results
A
total
958
including
479
upregulated
downregulated
screened
samples.
GO
DEGs
showed
that
they
mainly
involved
in
multicellular
organismal
process,
developmental
signaling
by
GPCR
muscle
contraction.
Further
PPI
identified
10
vcam1,
snca,
prkcb,
adrb2,
foxq1,
mdfi,
actbl2,
prkd1,
dapk1
actc1.
Possible
target
miRNAs,
hsa-mir-3143
hsa-mir-2110,
TFs,
tcf3
(transcription
factor
3)
clock
(clock
circadian
regulator),
predicted
constructing
miRNA-hub
regulatory
TF-hub
network.
Conclusions
This
bioinformatics
techniques
explore
potential
novel
biomarkers.
These
might
provide
new
ideas
methods
for
diagnosis,
treatment
monitoring
World Journal of Gastrointestinal Surgery,
Journal Year:
2025,
Volume and Issue:
17(2)
Published: Jan. 20, 2025
BACKGROUND
The
stearoyl-coenzyme
A
desaturase
(SCD
)
gene
influences
colorectal
cancer
(CRC)
pathogenesis,
with
its
expression
linked
to
tumor
cell
survival
and
resistance,
necessitating
further
investigation
into
role
in
CRC.
AIM
To
explore
the
clinical
pathological
significance
of
SCD
CRC
tissues
evaluate
affinity
between
nitidine
chloride
(NC)
as
a
target.
METHODS
Multi-center
high-throughput
data
related
were
integrated
calculate
standardized
mean
difference
mRNA
levels.
Immunohistochemical
staining
results,
Clustered
Regularly
Interspaced
Short
Palindromic
Repeats
knockout
screening
results
growth,
single-cell
sequencing
employed
verify
was
assessed
using
pooled
receiver
operating
characteristic
curves,
sensitivity,
specificity,
likelihood
ratios.
molecular
mechanism
NC
against
clarified
SwissTarget
Prediction
functional
enrichment,
docking
techniques
utilized
targeting
SCD.
RESULTS
Data
from
18
platforms,
including
2482
samples
1334
non-cancerous
tissue
controls.
significantly
upregulated
CRC,
2.05
[95%
confidence
interval
(CI):
1.69-2.41].
area
under
curve
0.95
(95%CI:
0.92-0.96),
sensitivity
0.86
0.81-0.90)
specificity
0.90
0.87-0.93).
Positive
negative
ratios
9.02
6.49-12.51)
0.15
0.10-0.22),
respectively.
High
protein
noted
208
patients,
associated
vascular
invasion
(P
<
0.001).
At
level,
overexpressed
cells
total
33
lines
depended
on
for
growth.
potential
might
involve
modulation
cycle,
positioning
target
NC.
CONCLUSION
promotes
growth
thus
acts
an
oncogenic
factor,
making
it
therapeutic
treatment.
Genes,
Journal Year:
2025,
Volume and Issue:
16(5), P. 498 - 498
Published: April 27, 2025
The
global
rise
in
obesity
and
its
associated
metabolic
disorders
underscores
the
need
for
a
deeper
investigation
into
their
underlying
molecular
mechanisms.
While
genetic
factors
are
well-established
contributors,
recent
research
has
increasingly
focused
on
epigenetic
regulators,
particularly
N6-methyladenosine
(m6A)—the
most
prevalent
internal
RNA
modification
eukaryotes.
This
post-transcriptional
plays
crucial
role
metabolism
by
regulating
mRNA
stability,
splicing,
nuclear
export,
translation
efficiency.
Notably,
emerging
evidence
implicates
m6A
both
adipogenesis
dysregulation.
In
this
review,
we
systematically
examine
three
key
dimensions:
(1)
mechanisms
of
modification,
including
writers,
erasers,
readers,
obesity;
(2)
dysregulated
patterns
obesity-related
pathologies,
such
as
type
2
diabetes
(T2D),
insulin
resistance,
dysfunction-associated
steatotic
liver
disease
(MASLD),
glycolysis
cancer
cells;
(3)
therapeutic
potential
targeting
regulators.
By
critically
assessing
advancements,
highlight
m6A’s
dual
sensor
modulator,
offering
novel
insights
strategies
combating
syndromes.
Genes,
Journal Year:
2024,
Volume and Issue:
15(3), P. 347 - 347
Published: March 9, 2024
Lipid
metabolism
participates
in
various
physiological
processes
and
has
been
shown
to
be
connected
the
development
progression
of
multiple
diseases,
especially
metabolic
hepatopathy.
Apolipoproteins
(Apos)
act
as
vectors
that
combine
with
lipids,
such
cholesterol
triglycerides
(TGs).
Despite
being
involved
lipid
transportation
metabolism,
critical
role
Apos
maintenance
still
not
fully
revealed.
This
study
sought
clarify
variations
related
m6A
methylome
ApoF
gene
knockout
mice
disordered
based
on
bioinformatics
method
transcriptome-wide
epitranscriptomics.
High-throughput
methylated
RNA
immunoprecipitation
sequencing
(MeRIP-seq)
was
conducted
both
wild-type
(WT)
(KO)
mice.
As
a
result,
liver
histopathology
presented
vacuolization
steatosis,
serum
biochemical
assays
reported
abnormal
content
KO
The
m6A-modified
mRNAs
were
conformed
consensus
sequenced
eukaryotes,
distribution
enriched
within
coding
sequences
3′
non-coding
regions.
In
mice,
functional
annotation
terms
differentially
expressed
genes
(DEGs)
included
cholesterol,
steroid
storage.
m6A-methylated
mRNAs,
TG,
long-chain
fatty
acid
processes;
transport;
development.
overlapping
DEGs
differential
also
disorder.
conclusion,
MeRIP
demonstrated
this
crucial
apolipoprotein
health
metabolism.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Sept. 16, 2024
Prostate
adenocarcinoma
(PRAD)
is
a
prevalent
global
malignancy
which
depends
more
on
lipid
metabolism
for
tumor
progression
compared
to
other
cancer
types.
Although
Stearoyl-coenzyme
A
desaturase
(SCD)
documented
regulate
in
multiple
cancers,
landscape
analysis
of
its
implications
PRAD
are
still
missing
at
present.
Here,
we
conducted
an
diverse
datasets
revealing
elevated
SCD
expression
the
cohort
both
mRNA
and
protein
levels.
Interestingly,
was
associated
with
promoter
hypermethylation
genetic
alterations,
notably
L134V
mutation.
Integration
comprehensive
immunological
genomic
data
revealed
robust
positive
correlation
between
levels
abundance
CD8
+
T
cells
macrophages.
Further
analyses
identified
significant
associations
various
immune
markers
microenvironment.
Single-cell
transcriptomic
profiling
unveiled
differential
patterns
across
distinct
cell
types
within
prostate
The
Gene
Ontology
Kyoto
Encyclopedia
Genes
Genome
showed
that
enriched
pathways
were
primarily
related
biosynthesis,
cholesterol
endoplasmic
reticulum
membrane
functions,
metabolic
pathways.
Set
Enrichment
Analysis
highlighted
involvement
crucial
cellular
processes,
including
cycle
biosynthesis
cofactors
In
functional
studies,
overexpression
promoted
proliferation,
metastasis
invasion
cells,
whereas
downregulation
inhibits
these
processes.
This
study
provides
insights
into
multifaceted
roles
pathogenesis,
underscoring
potential
as
therapeutic
target
prognostic
biomarker.
RNA Biology,
Journal Year:
2024,
Volume and Issue:
21(1), P. 49 - 61
Published: Sept. 30, 2024
N6-methyladenosine
(m6A)
is
widely
recognized
as
the
predominant
form
of
RNA
modification
in
higher
organisms,
with
capability
to
finely
regulate
metabolism,
thereby
influencing
a
series
crucial
physiological
and
pathological
processes.
These
processes
include
regulation
gene
expression,
cell
proliferation,
invasion
metastasis,
cycle
control,
programmed
death,
interactions
within
tumour
microenvironment,
energy
immune
regulation.
With
advancing
research
into
mechanisms
methylation,
pivotal
role
m6A
pathophysiology
reproductive
system
tumours,
particularly
cervical
cancer,
has
been
progressively
unveiled.
This
discovery
opened
new
avenues
presented
significant
potential
for
diagnosis,
prognostic
evaluation,
treatment
diseases.
review
delves
deeply
biological
functions
its
action
onset
progression
cancer.
Furthermore,
it
explores
prospects
precision
diagnosis
aiming
provide
perspectives
theoretical
basis
innovative
advanced
strategies
Expert Reviews in Molecular Medicine,
Journal Year:
2024,
Volume and Issue:
26
Published: Jan. 1, 2024
Abstract
Cervical
cancer
(CC),
one
of
the
most
prevalent
and
detrimental
gynaecologic
cancers,
evolves
through
genetic
epigenetic
alterations
resulting
in
promotion
oncogenic
activity
dysfunction
tumour-suppressing
mechanisms.
Despite
medical
advancement,
prognosis
for
advanced-stage
patients
remains
extremely
low
due
to
high
recurrence
rates
resistance
existing
treatments.
Thereby,
search
potential
prognostic
biomarkers
is
heightened
unravel
new
modalities
CC
pathogenesis
develop
novel
anti-cancer
therapies.
Epitranscriptomic
modifications,
reversible
RNA
regulate
various
biological
processes
by
deciding
fate
mediating
interactions.
This
narrative
review
provides
insight
into
cellular
molecular
roles
endogenous
RNA-editing
proteins
their
associated
epitranscriptomic
especially
N
6
-methyladenosine
(m
A),
5-methylcytosine
5
C)
1
governing
development,
progression
metastasis
CC.
We
discussed
in-depth
mechanisms
underlying
regulation
over
50
RNAs
responsible
tumorigenesis,
proliferation,
migration,
invasion,
survival,
autophagy,
stemness,
epithelial-mesenchymal
transition,
metabolism
(glucose,
lipid,
glutamate
glutamine),
(drug
radiation),
angiogenesis
Additionally,
we
provided
a
concise
overview
therapeutic
targeting
altered
expression
aberrant
deposition
modifications
on
both
coding
non-coding
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: May 8, 2024
Abstract
Endometriosis
is
a
common
cause
of
endometrial-type
mucosa
outside
the
uterine
cavity
with
symptoms
such
as
painful
periods,
chronic
pelvic
pain,
pain
intercourse
and
infertility.
However,
early
diagnosis
endometriosis
still
restricted.
The
purpose
this
investigation
to
identify
validate
key
biomarkers
endometriosis.
Next
generation
sequencing
(NGS)
dataset
GSE243039
was
obtained
from
Gene
Expression
Omnibus
(GEO)
database,
differentially
expressed
genes
(DEGs)
between
normal
control
samples
were
identified.
After
screening
DEGs,
gene
ontology
(GO)
REACTOME
pathway
enrichment
analyses
performed.
Furthermore,
protein-protein
interaction
(PPI)
network
constructed
modules
analysed
using
Human
Integrated
Protein-Protein
Interaction
rEference
(HIPIE)
database
Cytoscape
software,
hub
Subsequantely,
miRNAs
genes,
TFss
miRNet
NetworkAnalyst
tool,
possible
TFs
predicted.
Finally,
receiver
operating
characteristic
curve
(ROC)
analysis
used
genes.
A
total
958
including
479
up
regulated
down
screened
samples.
GO
DEGs
showed
that
they
mainly
involved
in
multicellular
organismal
process,
developmental
signaling
by
GPCR
muscle
contraction.
Further
PPI
identified
10
VCAM1,
SNCA,
PRKCB,
ADRB2,
FOXQ1,
MDFI,
ACTBL2,
PRKD1,
DAPK1
ACTC1.
Possible
target
miRNAs,
hsa-mir-3143
hsa-mir-2110,
TFs,
TCF3
CLOCK,
predicted
constructing
miRNA-hub
regulatory
TF-hub
network.
This
bioinformatics
techniques
explore
potential
novel
biomarkers.
These
might
provide
new
ideas
methods
for
diagnosis,
treatment,
monitoring