A cutting-edge investigation of the multifaceted role of SOX family genes in cancer pathogenesis through the modulation of various signaling pathways
Functional & Integrative Genomics,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: Jan. 4, 2025
Language: Английский
Intervention of epithelial mesenchymal transition against colon cancer cell growth and metastasis based on SOX21/POU4F2/Hedgehog signaling axis
Qiaochang Cao,
No information about this author
Yangyang Gao,
No information about this author
Chenxi Zhou
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et al.
Life Sciences,
Journal Year:
2024,
Volume and Issue:
352, P. 122905 - 122905
Published: July 9, 2024
Language: Английский
TCF4 promotes apoptosis and Wnt/β-catenin signaling pathway in acute kidney injury via transcriptional regulation of COX7A2L
Minhui Xi,
No information about this author
Jingyuan Lu,
No information about this author
Hualin Qi
No information about this author
et al.
PLoS ONE,
Journal Year:
2024,
Volume and Issue:
19(11), P. e0307667 - e0307667
Published: Nov. 5, 2024
Background
Acute
kidney
injury
(AKI)
is
still
a
serious
illness
with
high
morbidity
and
death
rates,
it’s
crucial
to
comprehend
the
underlying
molecular
causes.
Methods
Bioinformatics
analysis
was
performed
on
GSE139061
GSE30718
data
sets,
COX7A2L
screened
out.
The
role
of
in
H/R-treated
cells
its
transcriptional
regulation
TCF4
were
assessed.
In
vitro
experiments
analyzed
proliferation,
apoptosis,
Wnt/β-catenin
signaling
pathway
cells.
Results
as
hub
gene
downregulated
AKI
samples.
cells,
overexpression
inhibited
apoptosis
promoted
cell
while
knockdown
proliferation.
Notably,
exhibited
significant
positive
correlation
COX7A2L.
overexpression-induced
lessened
improved
proliferation
countered
by
knockdown,
according
rescue
study
findings.
Besides,
we
discovered
that
increased
expression
proteins
linked
(c-myc,
β-catenin,
cyclin
D1),
underexpression
counteracted
this
effect.
Conclusion
revealed
pivotal
AKI,
which
regulated
modulates
pathway,
highlighting
potential
therapeutic
target.
Language: Английский
Transcriptomics Revealed Differentially Expressed Transcription Factors and MicroRNAs in Human Diabetic Foot Ulcers
Proteomes,
Journal Year:
2024,
Volume and Issue:
12(4), P. 32 - 32
Published: Nov. 5, 2024
Non-healing
diabetic
foot
ulcers
(DFUs)
not
only
significantly
increase
morbidity
and
mortality
but
also
cost
a
lot
drain
healthcare
resources.
Persistent
inflammation,
decreased
angiogenesis,
altered
extracellular
matrix
remodeling
contribute
to
delayed
healing
or
non-healing.
Recent
studies
suggest
an
increasing
trend
of
DFUs
in
diabetes
patients,
non-healing
DFYs
the
incidence
amputation.
Despite
current
treatment
with
offloading,
dressing,
antibiotics
use,
oxygen
therapy,
risk
amputation
persists.
Thus,
there
is
need
understand
molecular
cellular
factors
regulating
DFUs.
The
ongoing
research
based
on
proteomics
transcriptomics
has
predicted
multiple
potential
targets,
no
definitive
therapy
enhance
chronic
Increased
expression
various
proteins
encoded
by
genes,
whose
transcriptionally
post-transcriptionally
regulated
transcription
(TFs)
microRNAs
(miRs),
regulates
DFU
healing.
For
this
study,
RNA
sequencing
was
conducted
20
samples
ulcer
tissue
non-ulcerated
nearby
healthy
tissues.
IPA
analysis
revealed
activated
inhibited
microRNAs.
Further
network
interactions
between
TFs
miRs
targets
these
miRs.
30
differentially
expressed
(21
9
inhibited),
two
translational
regulators
(RPSA
EIF4G2),
seven
miRs,
including
mir-486,
mir-324,
mir-23,
mir-186,
mir-210,
mir-199,
mir-338
upstream
(
Language: Английский