Frontiers in Oncology,
Journal Year:
2020,
Volume and Issue:
10
Published: Aug. 20, 2020
Kidney
renal
clear
cell
carcinoma
(KIRC)
is
the
predominant
pathological
subtype
of
(RCC)
in
adults.
Long
non-coding
RNAs
(lncRNAs)
are
an
important
class
gene
expression
regulators
and
serve
fundamental
roles
immune
regulation.
The
intent
this
study
to
develop
a
novel
immune-related
lncRNA
signature
accurately
predict
prognosis
for
KIRC
patients.
Here,
we
performed
genome-wide
comparative
analysis
profiles
537
patients
from
Cancer
Genome
Atlas
(TCGA)
database.
Cox
regression
model-identified
lncRNAs
were
extracted
constructing
five
(AC008105.3,
LINC02084,
AC243960.1,
AC093278.2,
AC108449.2)
with
ability
Univariate
multivariate
analyses
demonstrated
that
could
act
as
independent
prognostic
predictor
overall
survival
(OS).
With
further
investigation
on
different
clinicopathological
parameters,
found
divide
samples
into
high-risk
groups
shorter
OS
low-risk
longer
subgroups.
Principal
component
suggested
drew
distinction
between
high-
based
lncRNAs.
status
two
was
observed
set
enrichment
ESTIMATE
algorithm.
Except
expressions
other
four
significantly
upregulated
tumor
tissues.
In
summary,
identified
immune-lncRNA
had
clinical
implications
prediction
be
exploited
underlying
therapeutic
targets
Cancer Communications,
Journal Year:
2020,
Volume and Issue:
41(2), P. 109 - 120
Published: Oct. 29, 2020
Abstract
Altered
metabolism
is
a
hallmark
of
cancer,
and
the
reprogramming
energy
has
historically
been
considered
general
phenomenon
tumors.
It
well
recognized
that
long
noncoding
RNAs
(lncRNAs)
regulate
in
cancer.
However,
lncRNA‐mediated
posttranslational
modifications
metabolic
are
unclear
at
present.
In
this
review,
we
summarized
current
understanding
interactions
between
alterations
cancer‐associated
enzymes,
transcription
factors,
other
proteins
involved
pathways.
addition,
discuss
mechanisms
through
which
these
contribute
to
tumor
initiation
progression,
key
roles
clinical
significance
functional
lncRNAs.
We
believe
an
in‐depth
cancer
can
help
identify
cellular
vulnerabilities
be
exploited
for
diagnosis
therapy.
Nature Communications,
Journal Year:
2022,
Volume and Issue:
13(1)
Published: Feb. 10, 2022
Long
noncoding
RNAs
(lncRNAs)
are
recently
implicated
in
modifying
immunology
colorectal
cancer
(CRC).
Nevertheless,
the
clinical
significance
of
immune-related
lncRNAs
remains
largely
unexplored.
In
this
study,
we
develope
a
machine
learning-based
integrative
procedure
for
constructing
consensus
lncRNA
signature
(IRLS).
IRLS
is
an
independent
risk
factor
overall
survival
and
displays
stable
powerful
performance,
but
only
demonstrates
limited
predictive
value
relapse-free
survival.
Additionally,
possesses
distinctly
superior
accuracy
than
traditional
variables,
molecular
features,
109
published
signatures.
Besides,
high-risk
group
sensitive
to
fluorouracil-based
adjuvant
chemotherapy,
while
low-risk
benefits
more
from
bevacizumab.
Notably,
abundant
lymphocyte
infiltration,
high
expression
CD8A
PD-L1,
response
pembrolizumab.
Taken
together,
could
serve
as
robust
promising
tool
improve
outcomes
individual
CRC
patients.
Briefings in Bioinformatics,
Journal Year:
2021,
Volume and Issue:
23(1)
Published: Nov. 5, 2021
Abstract
Long
non-coding
ribonucleic
acids
(RNAs)
(lncRNAs)
are
key
players
in
tumorigenesis
and
immune
responses.
The
nature
of
their
cell
type-specific
gene
expression
other
functional
evidence
support
the
idea
that
lncRNAs
have
distinct
cellular
functions
tumor
microenvironment
(TIME).
To
date,
majority
lncRNA
studies
heavily
relied
on
bulk
RNA-sequencing
data
which
various
types
contribute
to
an
averaged
signal,
limiting
discovery
functions.
Single-cell
(scRNA-seq)
is
a
potential
solution
for
tackling
this
limitation
despite
lack
annotations
low
abundance
yet
lncRNAs.
Hence,
updated
further
understanding
will
be
necessary
characterizing
genes
TIME.
In
review,
we
discuss
specifically
expressed
cells,
summarize
regulatory
at
type
level
highlight
how
scRNA-seq
approach
can
help
study
TIME
Proceedings of the National Academy of Sciences,
Journal Year:
2021,
Volume and Issue:
118(15)
Published: April 7, 2021
Simultaneous
profiling
of
multiomic
modalities
within
a
single
cell
is
grand
challenge
for
single-cell
biology.
While
there
have
been
impressive
technical
innovations
demonstrating
feasibility-for
example,
generating
paired
measurements
transcriptome
(single-cell
RNA
sequencing
[scRNA-seq])
and
chromatin
accessibility
assay
transposase-accessible
using
[scATAC-seq])-widespread
application
joint
challenging
due
to
its
experimental
complexity,
noise,
cost.
Here,
we
introduce
BABEL,
deep
learning
method
that
translates
between
the
profiles
cell.
Leveraging
an
interoperable
neural
network
model,
BABEL
can
predict
expression
directly
from
cell's
scATAC-seq
vice
versa
after
training
on
relevant
data.
This
makes
it
possible
computationally
synthesize
when
only
one
modality
experimentally
available.
Across
several
ATAC
gene
datasets
in
human
mouse,
validate
accurately
these
individual
cells.
also
generalizes
well
types
new
biological
contexts
not
seen
during
training.
Starting
patient-derived
basal
carcinoma
(BCC),
generated
enabled
fine-grained
classification
complex
states,
despite
having
never
BCC
These
predictions
are
comparable
analyses
scRNA-seq
data
diverse
related
BABEL's
We
further
show
incorporate
additional
modalities,
such
as
protein
epitope
profiling,
thus
enabling
translation
across
chromatin,
RNA,
protein.
offers
powerful
approach
exploration
hypothesis
generation.
Frontiers in Oncology,
Journal Year:
2023,
Volume and Issue:
13
Published: March 9, 2023
Most
of
our
transcribed
RNAs
are
represented
by
non-coding
sequences.
Long
(lncRNAs)
transcripts
with
no
or
very
limited
protein
coding
ability
and
a
length
>200nt.
They
can
be
epigenetically
modified.
N6-methyladenosine
(m6A),
N1-methyladenosine
(m1A),
5-methylcytosine
(m5C),
7-methylguanosine
(m7G)
2’-O-methylation
(Nm)
some
the
lncRNAs
epigenetic
modifications.
The
modifications
RNA
controlled
three
classes
enzymes,
each
playing
role
in
specific
phase
modification.
These
enzymes
defined
as
“writers”,
“readers”
“erasers”.
m6A
m5C
most
studied
RNA.
alter
structure
properties,
thus
modulating
functions
interactions
lncRNAs.
aberrant
expression
several
is
linked
to
development
variety
cancers
signatures
m6A-
m5C-related
increasingly
recognized
potential
biomarkers
prognosis,
predictors
disease
stage
overall
survival.
In
present
manuscript,
up
date
literature
reviewed
focus
on
their
significance
cancer.
Clinical and Translational Medicine,
Journal Year:
2021,
Volume and Issue:
11(4)
Published: April 1, 2021
Abstract
Lung
cancer
remains
a
major
threat
to
human
health.
Low
dose
CT
scan
(LDCT)
has
become
the
main
method
of
early
screening
for
lung
due
low
sensitivity
chest
X‐ray.
However,
LDCT
not
only
high
false
positive
rate,
but
also
entails
risks
overdiagnosis
and
cumulative
radiation
exposure.
In
addition,
by
subsequent
follow‐up
can
increase
risk
cancer.
Many
studies
have
shown
that
long
noncoding
RNAs
(lncRNAs)
remain
stable
in
blood,
profiling
blood
advantages
being
noninvasive,
readily
accessible
inexpensive.
Serum
or
plasma
assay
lncRNAs
be
used
as
novel
detection
assist
while
improving
accuracy
screening.
LncRNAs
participate
regulation
various
biological
processes.
A
large
number
researches
reported
are
key
regulators
involved
progression
cancers
through
multiple
action
models.
Especially,
some
affect
hallmarks
addition
their
diagnostic
value,
possess
promising
potential
other
clinical
applications
toward
predictive
markers
chemosensitivity,
radiosensitivity,
epidermal
growth
factor
receptor
(EGFR)‐targeted
therapy,
well
prognosis.
Different
been
implicated
regulate
EGFR‐targeted
therapy
diverse
mechanisms.
Although
many
challenges
need
addressed
future,
bright
prospects
an
adjunct
radiographic
methods
management
Aging,
Journal Year:
2020,
Volume and Issue:
unknown
Published: Nov. 18, 2020
Long
noncoding
RNAs
(lncRNAs)
have
multiple
functions
in
the
cancer
immunity
response
and
tumor
microenvironment.To
investigate
immune-related
lncRNA
(IRlncRNA)
signature
for
predicting
prognosis
immunotherapeutic
bladder
(BLCA),
we
extracted
BLCA
data
from
The
Cancer
Genome
Atlas
(TCGA)
database.Finally,
a
total
of
405
cases
were
enrolled
8
prognostic
IRlncRNAs
(MIR181A2HG,
AC114730.3,LINC00892,
PTPRD-AS1,
LINC01013,
MRPL23-AS1,
LINC01395,
AC002454.1)were
identified
training
set.Risk
scores
calculated
to
divide
patients
into
high-risk
low-risk
groups,
tended
poor
overall
survival
(OS).Multivariate
Cox
regression
analysis
confirmed
that
IRlncRNA
could
be
an
independent
factor.The
results
subsequently
validating
set.Additionally,
this
8-IRlncRNA
classifier
was
related
recurrence
free
(RFS)
BLCA.Functional
characterization
revealed
mediated
phenotype.This
also
associated
with
immune
cell
infiltration
(i.e.,
macrophages
M0,
M2,
Tregs,
CD8
T
cells,
neutrophils)
checkpoint
inhibitors
(ICIs)
immunotherapy-related
biomarkers
[mismatch
repair
(MMR)
genes,
mutation
burden
(TMB)
genes].The
present
study
highlighted
value
as
predictor
BLCA.
Cancers,
Journal Year:
2021,
Volume and Issue:
13(7), P. 1587 - 1587
Published: March 30, 2021
Immunotherapy
is
presently
one
of
the
most
promising
areas
investigation
and
development
for
treatment
cancer.
While
immune
checkpoint-blocking
monoclonal
antibodies
chimeric
antigen
receptor
(CAR)
T-cell-based
therapy
have
recently
provided
in
some
cases
valuable
therapeutic
options,
goal
cure
has
not
yet
been
achieved
malignancies
more
efforts
are
urgently
needed.
Noncoding
RNAs
(ncRNA),
including
microRNAs
(miRNAs)
long
noncoding
(lncRNAs),
regulate
several
biological
processes
via
selective
targeting
crucial
molecular
signaling
pathways.
Recently,
key
roles
miRNA
lncRNAs
as
regulators
immune-response
cancer
progressively
emerged,
since
they
may
act
(i)
by
shaping
intrinsic
tumor
cell
microenvironment
(TME)
properties;
(ii)
regulating
angiogenesis,
immune-escape,
epithelial-to-mesenchymal
transition,
invasion,
drug
resistance;
(iii)
acting
potential
biomarkers
prognostic
assessment
prediction
response
to
immunotherapy.
In
this
review,
we
provide
an
overview
on
role
ncRNAs
modulating
TME.
We
discuss
use
or
targets
clinical
translation
new
therapeutics.
Finally,
combinatory
approaches
based
ncRNA
agents
immune-checkpoint
inhibitor
CAR-T
experimental
human