Research Square (Research Square),
Год журнала:
2021,
Номер
unknown
Опубликована: Сен. 7, 2021
Abstract
Non-coding
RNAs
(ncRNAs)
form
a
large
portion
of
the
mammalian
genome
however,
their
biological
functions
are
poorly
characterized
in
cancers.
In
this
study,
using
newly
developed
tool,
SomaGene,
we
analyze
de
novo
somatic
point
mutations
from
International
Cancer
Genome
Consortium
(ICGC)
whole-genome
sequencing
data
1,855
breast
We
identify
929
candidates
ncRNAs
that
significantly
and
explicitly
mutated
cancer
samples.
By
integrating
ENCODE
regulatory
features
FANTOM5
expression
atlas,
show
candidate
samples
enrich
for
active
chromatin
histone
marks
(1.9
times),
CTCF
binding
sites
(2.45
DNase
accessibility
(1.76
HMM
predicted
enhancers
(2.26
times)
eQTL
polymorphisms
(1.77
times).
Importantly,
contain
much
higher
level
(3.64
cancer-associated
genome-wide
association
(GWAS)
single
nucleotide
(SNPs)
than
expectation.
Such
enrichment
has
not
been
seen
with
GWAS
SNPs
other
diseases.
Using
tissue
related
Hi-C
then
82%
our
interact
promoter
protein-coding
genes,
including
previously
known
suggesting
critical
role
ncRNA
genes
activation
essential
regulators
development
differentiation
cancer.
provide
an
extensive
web-based
resource
(https://www.ihealthe.unsw.edu.au/research),
to
communicate
results
research
community.
Our
list
cancer-specific
potential
better
understanding
underlying
genetic
causes
Lastly,
tool
study
can
be
used
analysis
all
Abstract
Background
Breast
cancer
is
the
most
common
in
women
around
world,
and
molecular
mechanisms
of
breast
progression
metastasis
are
still
unclear.
This
study
aims
to
clarify
function
N6,2′-O-dimethyladenosine
(m6A)
regulation
lncRNA
MIR210HG
cancer.
Results
High
expression
was
confirmed
promoted
progression,
which
mediated
by
its
encoded
miR-210.
regulated
IGF2BP1
m6A
modification.
highly
expressed
induced
both
miR-210
expression,
contributed
progression.
In
addition,
transcript
stabilized
co-factor
ELAVL1.
a
direct
target
MYCN
via
E-box
binding
motif.
cells.
expressions
were
also
increased
MYCN.
Conclusions
cancer,
functions
as
an
oncogenic
lncRNA,
ELAVL1
enhance
stability
,
contributes
Interestingly,
directly
activated
MYCN,
explains
role
These
findings
related
mechanism
The
MYCN/IGF2BP1/
axis
may
serve
alternative
Journal of Pathology Informatics,
Год журнала:
2023,
Номер
14, С. 100341 - 100341
Опубликована: Янв. 1, 2023
Skin
cancer
is
among
the
most
common
types
worldwide.
Automatic
identification
of
skin
complicated
because
poor
contrast
and
apparent
resemblance
between
lesions.
The
rate
human
death
can
be
significantly
reduced
if
melanoma
could
detected
quickly
using
dermoscopy
images.
This
research
uses
an
anisotropic
diffusion
filtering
method
on
images
to
remove
multiplicative
speckle
noise.
To
do
this,
fast-bounding
box
(FBB)
applied
here
segment
region.
We
also
employ
2
feature
extractors
represent
first
one
Hybrid
Feature
Extractor
(HFE),
second
convolutional
neural
network
VGG19-based
CNN.
HFE
combines
3
extraction
approaches
namely,
Histogram-Oriented
Gradient
(HOG),
Local
Binary
Pattern
(LBP),
Speed
Up
Robust
(SURF)
into
a
single
fused
vector.
CNN
used
extract
additional
features
from
test
training
datasets.
2-feature
vector
then
design
classification
model.
proposed
employed
datasets
ISIC
2017
academic
torrents
dataset.
Our
achieves
99.85%,
91.65%,
95.70%
in
terms
accuracy,
sensitivity,
specificity,
respectively,
making
it
more
successful
than
previously
machine
learning
algorithms.
Skin
cancer
is
an
exquisite
disease
globally
nowadays.
Because
of
the
poor
contrast
and
apparent
resemblance
between
skin
lesions,
automatic
identification
complicated.
The
rate
human
death
can
be
massively
reduced
if
melanoma
detected
quickly
using
dermoscopy
images.
In
this
research,
anisotropic
diffusion
filtering
method
used
on
images
to
remove
multiplicative
speckle
noise
fast-bounding
box
(FBB)
applied
segment
region.
Furthermore,
paper
consists
two
feature
extractor
parts.
One
features
parts
hybrid
(HFE)
part
another
convolutional
neural
network
VGG19
based
CNN
part.
HFE
portion
combines
three
extraction
approaches
into
a
single
fused
vector:
Histogram-Oriented
Gradient
(HOG),
Local
Binary
Pattern
(LBP),
Speed
Up
Robust
Feature
(SURF).
also
extract
additional
from
test
training
datasets.
This
two-feature
vector
design
classification
model.
classifier
performs
whether
it
or
non-melanoma
cancer.
proposed
methodology
performed
ordinary
datasets
achieved
accuracy
99.85%,
sensitivity
91.65%,
specificity
95.70%,
which
makes
more
successful
than
previous
machine
learning
algorithms.
Frontiers in Molecular Biosciences,
Год журнала:
2023,
Номер
10
Опубликована: Янв. 16, 2023
Background:
Breast
cancer
(BC)
is
the
most
common
in
women.
The
incidence
and
morbidity
of
BC
are
expected
to
rise
rapidly.
stage
at
which
diagnosed
has
a
significant
impact
on
clinical
outcomes.
When
detected
early,
an
overall
5-year
survival
rate
up
90%
possible.
Although
numerous
studies
have
been
conducted
assess
prognostic
diagnostic
values
non-coding
RNAs
(ncRNAs)
breast
cancer,
their
potential
remains
unclear.
In
this
field
study,
there
various
systematic
reviews
meta-analysis
that
report
volumes
data.
we
tried
collect
all
these
order
re-analyze
data
without
any
restriction
or
RNA
type,
make
it
as
comprehensive
Methods:
Three
databases,
namely,
PubMed,
Scopus,
Web
Science
(WoS),
were
searched
find
relevant
studies.
After
thoroughly
searching,
screening
titles,
abstracts,
full-text
quality
included
assessed
using
AMSTAR
tool.
All
required
including
hazard
ratios
(HRs),
sensitivity
(SENS),
specificity
(SPEC)
extracted
for
further
analysis,
analyses
carried
out
Stata.
Results:
part,
our
initial
search
three
databases
produced
10,548
articles,
58
current
study.
We
correlation
(ncRNA)
expression
with
different
outcomes
patients:
(OS)
(HR
=
1.521),
disease-free
(DFS)
1.33),
recurrence-free
(RFS)
1.66),
progression-free
(PFS)
1.71),
metastasis-free
(MFS)
0.90),
disease-specific
(DSS)
0.37).
eliminating
low-quality
studies,
results
did
not
change
significantly.
22
articles
30
datasets
retrieved
from
8,453
articles.
was
determined.
bivariate
random-effects
models
used
value
ncRNAs.
area
under
curve
(AUC)
ncRNAs
differentiated
patients
0.88
(SENS:
80%
SPEC:
82%).
There
no
difference
single
combined
patients.
However,
microRNAs
(miRNAs)
higher
than
long
(lncRNAs).
No
evidence
publication
bias
found
Nine
miRNAs,
four
lncRNAs,
five
gene
targets
showed
OS
RFS
between
normal
based
pan-cancer
demonstrating
value.
Conclusion:
present
umbrella
review
ncRNAs,
lncRNAs
can
be
biomarkers
patients,
regardless
sample
sources,
ethnicity
subtype
cancer.
BMC Bioinformatics,
Год журнала:
2022,
Номер
23(1)
Опубликована: Апрель 19, 2022
Colorectal
cancer
(CRC)
is
one
of
the
leading
causes
cancer-related
deaths
worldwide.
Recent
studies
have
observed
causative
mutations
in
susceptible
genes
related
to
colorectal
10
15%
patients.
This
highlights
importance
identifying
for
early
detection
this
more
effective
treatments
among
high
risk
individuals.
Mutation
considered
as
key
point
research.
Many
performed
subtyping
based
on
type
frequently
mutated
genes,
or
proportion
mutational
processes.
However,
best
our
knowledge,
combination
these
features
has
never
been
used
together
task.
potential
introduce
better
and
inclusive
subtype
classification
approaches
using
wider
range
enable
biomarker
discovery
thus
inform
drug
development
CRC.In
study,
we
develop
a
new
pipeline
novel
concept
called
'gene-motif',
which
merges
gene
information
with
tri-nucleotide
motif
sites,
identification.
We
apply
International
Cancer
Genome
Consortium
(ICGC)
CRC
samples
identify,
first
time,
3131
gene-motif
combinations
that
are
significantly
536
ICGC
samples.
Using
features,
identify
seven
subtypes
distinguishable
phenotypes
biomarkers,
including
unique
signaling
pathways,
most
them
targeted
treatment
options
currently
available.
Interestingly,
also
several
multiple
but
sequence
contexts.Our
results
highlight
considering
both
mutation
identification
biomarkers.
The
presented
study
demonstrates
distinguished
phenotypic
properties
can
be
effectively
treatments.
By
knowing
associated
subtypes,
personalized
plan
developed
considers
specific
their
genomic
lesion.
Frontiers in Public Health,
Год журнала:
2022,
Номер
10
Опубликована: Июнь 23, 2022
Early
diagnosis,
prioritization,
screening,
clustering,
and
tracking
of
patients
with
COVID-19,
production
drugs
vaccines
are
some
the
applications
that
have
made
it
necessary
to
use
a
new
style
technology
involve,
manage,
deal
this
epidemic.
Strategies
backed
by
artificial
intelligence
(A.I.)
Internet
Things
(IoT)
been
undeniably
effective
understand
how
virus
works
prevent
from
spreading.
Accordingly,
main
aim
survey
is
critically
review
ML,
IoT,
integration
IoT
ML-based
techniques
in
related
diagnosis
disease
prediction
its
outbreak.
According
findings,
provided
prompt
efficient
approach
spread.
On
other
hand,
most
studies
developed
aimed
at
detection
handling
challenges
associated
COVID-19
pandemic.
Among
different
approaches,
Convolutional
Neural
Network
(CNN),
Support
Vector
Machine,
Genetic
CNN,
pre-trained
followed
ResNet
demonstrated
best
performances
compared
methods.
Frontiers in Immunology,
Год журнала:
2023,
Номер
14
Опубликована: Июнь 6, 2023
Long
noncoding
RNAs
(lncRNAs)
increase
in
genomes
of
complex
organisms
and
represent
the
largest
group
RNA
genes
transcribed
mammalian
cells.
Previously
considered
only
transcriptional
noise,
lncRNAs
comprise
a
heterogeneous
class
transcripts
that
are
emerging
as
critical
regulators
T
cell-mediated
immunity.
Here
we
summarize
lncRNA
expression
landscape
different
cell
subsets
highlight
recent
advances
role
regulating
differentiation,
function
exhaustion
during
homeostasis
cancer.
We
discuss
molecular
mechanisms
can
serve
novel
targets
to
modulate
or
improve
response
cancer
immunotherapies
by
modulating
immunosuppressive
tumor
microenvironment.
Non-Coding RNA,
Год журнала:
2023,
Номер
9(4), С. 44 - 44
Опубликована: Авг. 1, 2023
Lymphoid
cells
play
a
critical
role
in
the
immune
system,
which
includes
three
subgroups
of
T,
B,
and
NK
cells.
Recognition
complexity
human
genetics
transcriptome
lymphopoiesis
has
revolutionized
our
understanding
regulatory
potential
RNA
normal
lymphoid
malignancies.
Long
non-coding
RNAs
(lncRNAs)
are
class
molecules
greater
than
200
nucleotides
length.
LncRNAs
have
recently
attracted
much
attention
due
to
their
roles
various
biological
processes,
including
gene
regulation,
chromatin
organization,
cell
cycle
control.
can
also
be
used
for
differentiation
fate,
as
expression
patterns
often
specific
particular
types
or
developmental
stages.
Additionally,
lncRNAs
been
implicated
differentiation,
such
regulating
T-cell
B-cell
development,
linked
immune-associated
diseases
leukemia
lymphoma.
In
addition,
investigated
biomarkers
diagnosis,
prognosis,
therapeutic
response
disease
management.
this
review,
we
provide
an
overview
current
knowledge
about
physiopathology
processes
during
leukemia.