Journal of Hematology & Oncology,
Год журнала:
2022,
Номер
15(1)
Опубликована: Май 12, 2022
Abstract
Single-cell
sequencing
(SCS)
is
an
emerging
high-throughput
technology
that
can
be
used
to
study
the
genomics,
transcriptomics,
and
epigenetics
at
a
single
cell
level.
SCS
widely
in
diagnosis
treatment
of
various
diseases,
including
cancer.
Over
years,
has
gradually
become
effective
clinical
tool
for
exploration
tumor
metastasis
mechanisms
development
strategies.
Currently,
not
only
analyze
metastasis-related
malignant
biological
characteristics,
such
as
heterogeneity,
drug
resistance,
microenvironment,
but
also
construct
maps
predicting
monitoring
dynamics
metastasis.
identify
therapeutic
targets
related
it
provides
insights
into
distribution
subsets
gene
expression
differences
between
primary
metastatic
tumors.
Additionally,
techniques
combination
with
artificial
intelligence
(AI)
are
liquid
biopsy
circulating
cells
(CTCs),
thereby
providing
novel
strategy
treating
In
this
review,
we
summarize
potential
applications
field
discuss
prospects
limitations
provide
theoretical
basis
finding
International Journal of Molecular Sciences,
Год журнала:
2019,
Номер
20(24), С. 6249 - 6249
Опубликована: Дек. 11, 2019
MicroRNAs
(miRNAs)
are
small
non-coding
RNAs
with
the
capability
of
modulating
gene
expression
at
post-transcriptional
level
either
by
inhibiting
messenger
RNA
(mRNA)
translation
or
promoting
mRNA
degradation.
The
outcome
a
myriad
physiological
processes
and
pathologies,
including
cancer,
cardiovascular
metabolic
diseases,
relies
highly
on
miRNAs.
However,
deciphering
precise
roles
specific
miRNAs
in
these
pathophysiological
contexts
is
challenging
due
to
high
levels
complexity
their
actions.
Indeed,
regulation
frequently
cell/organ
specific;
dependent
stress
status
organism;
often
poorly
correlated
miRNA
levels.
Such
biological
features
suggest
that
various
regulatory
mechanisms
control
not
only
expression,
but
also
activity
and/or
bioavailability.
Several
have
been
described
modulate
action,
genetic
polymorphisms,
methylation
promoters,
asymmetric
strand
selection,
interactions
RNA-binding
proteins
(RBPs)
other
coding/non-coding
RNAs.
Moreover,
nucleotide
modifications
(A-to-I
C-to-U)
within
sequences
different
stages
maturation
critical
for
functionality.
This
mechanism
called
"RNA
editing"
involves
enzymes
adenosine/cytidine
deaminase
family,
which
trigger
single
changes
primary
These
greatly
influence
miRNA's
stability,
changing
its
specificity
towards
target
mRNAs.
Understanding
how
editing
events
impact
ability
regulate
responses
cells
organs,
development
e.g.,
diseases
should
deepen
our
knowledge
molecular
underlying
complex
can
facilitate
design
new
therapeutic
approaches
based
targeting.
Herein,
we
will
discuss
current
this
regulates
biogenesis
activity.
Frontiers in Immunology,
Год журнала:
2020,
Номер
11
Опубликована: Авг. 4, 2020
The
immunosuppressive
status
of
the
tumour
microenvironment
(TME)
remains
poorly
defined
due
to
a
lack
understanding
regarding
function
tumour-associated
macrophages
(TAMs),
which
are
abundant
in
TME.
TAMs
crucial
drivers
progression,
metastasis
and
resistance
therapy.
Intra-
inter-tumoural
spatial
heterogeneities
potential
keys
relationships
between
subpopulations
their
functions.
Antitumour
M1-like
pro-tumour
M2-like
coexist
within
tumours,
opposing
effects
these
M1/M2
on
tumours
directly
impact
current
strategies
improve
antitumour
immune
responses.
Recent
studies
have
found
significant
differences
among
monocytes
or
from
distinct
other
investigations
explored
existence
diverse
TAM
subsets
at
molecular
level.
In
this
review,
we
discuss
emerging
evidence
highlighting
redefinition
functions
TME
possibility
separating
macrophage
with
into
during
development
tumours.
Such
may
relate
differential
cellular
origin
monocyte
plasticity
heterogeneity
TAMs,
all
potentially
biomarkers
our
how
phenotypes
dictated
by
ontogeny,
activation
localization.
Therefore,
detailed
landscape
must
be
deciphered
integration
new
technologies,
such
as
multiplexed
immunohistochemistry
(mIHC),
mass
cytometry
time-of-flight
(CyTOF),
single-cell
RNA-seq
(scRNA-seq),
transcriptomics
systems
biology
approaches,
for
analyses
Biology,
Год журнала:
2023,
Номер
12(7), С. 997 - 997
Опубликована: Июль 13, 2023
The
advent
of
next-generation
sequencing
(NGS)
has
brought
about
a
paradigm
shift
in
genomics
research,
offering
unparalleled
capabilities
for
analyzing
DNA
and
RNA
molecules
high-throughput
cost-effective
manner.
This
transformative
technology
swiftly
propelled
advancements
across
diverse
domains.
NGS
allows
the
rapid
millions
fragments
simultaneously,
providing
comprehensive
insights
into
genome
structure,
genetic
variations,
gene
expression
profiles,
epigenetic
modifications.
versatility
platforms
expanded
scope
facilitating
studies
on
rare
diseases,
cancer
genomics,
microbiome
analysis,
infectious
population
genetics.
Moreover,
enabled
development
targeted
therapies,
precision
medicine
approaches,
improved
diagnostic
methods.
review
provides
an
insightful
overview
current
trends
recent
technology,
highlighting
its
potential
impact
areas
genomic
research.
delves
challenges
encountered
future
directions
including
endeavors
to
enhance
accuracy
sensitivity
data,
novel
algorithms
data
pursuit
more
efficient,
scalable,
solutions
that
lie
ahead.
F1000Research,
Год журнала:
2020,
Номер
9, С. 47 - 47
Опубликована: Янв. 27, 2020
Single-cell
sequencing
is
an
emerging
technology
in
the
field
of
immunology
and
oncology
that
allows
researchers
to
couple
RNA
quantification
other
modalities,
like
immune
cell
receptor
profiling
at
level
individual
cell.
A
number
workflows
software
packages
have
been
created
process
analyze
single-cell
transcriptomic
data.
These
allow
users
take
vast
dimensionality
data
generated
single-cell-based
experiments
distill
into
novel
insights.
Unlike
field,
there
a
lack
options
for
profiling.
Enabling
easily
combine
mRNA
profiling,
scRepertoire
was
built
derived
from
10x
Genomics
Chromium
Immune
Profiling
both
T-cell
(TCR)
immunoglobulin
(Ig)
enrichment
subsequently
interacts
with
popular
Seurat
R
package.
The
package
processed
are
open
source
available
on
GitHub
provides
in-depth
tutorials
capability
F1000Research,
Год журнала:
2020,
Номер
9, С. 47 - 47
Опубликована: Июнь 15, 2020
Single-cell
sequencing
is
an
emerging
technology
in
the
field
of
immunology
and
oncology
that
allows
researchers
to
couple
RNA
quantification
other
modalities,
like
immune
cell
receptor
profiling
at
level
individual
cell.
A
number
workflows
software
packages
have
been
created
process
analyze
single-cell
transcriptomic
data.
These
allow
users
take
vast
dimensionality
data
generated
single-cell-based
experiments
distill
into
novel
insights.
Unlike
field,
there
a
lack
options
for
profiling.
Enabling
easily
combine
mRNA
profiling,
scRepertoire
was
built
derived
from
10x
Genomics
Chromium
Immune
Profiling
both
T-cell
(TCR)
immunoglobulin
(Ig)
enrichment
subsequently
interacts
with
popular
R
expression,
such
as
Seurat.
The
package
processed
are
open
source
available
on
GitHub
provides
in-depth
tutorials
capability
package.
Circulation,
Год журнала:
2020,
Номер
142(14), С. 1374 - 1388
Опубликована: Окт. 5, 2020
Background:
Ascending
thoracic
aortic
aneurysm
(ATAA)
is
caused
by
the
progressive
weakening
and
dilatation
of
wall
can
lead
to
dissection,
rupture,
other
life-threatening
complications.
To
improve
our
understanding
ATAA
pathogenesis,
we
aimed
comprehensively
characterize
cellular
composition
ascending
identify
molecular
alterations
in
each
cell
population
human
tissues.
Methods:
We
performed
single-cell
RNA
sequencing
analysis
tissues
from
11
study
participants,
including
8
patients
with
(4
women
4
men)
3
control
subjects
(2
1
man).
Cells
extracted
tissue
were
analyzed
categorized
data
perform
cluster
identification.
ATAA-related
changes
then
examined
comparing
proportions
type
gene
expression
profiles
between
also
which
genes
may
be
critical
for
performing
integrative
publicly
available
genome-wide
association
studies.
Results:
identified
major
types
tissue;
high-resolution
reclustering
these
cells
further
divided
them
into
40
subtypes.
Multiple
subtypes
observed
smooth
muscle
cells,
macrophages,
T
lymphocytes,
suggesting
that
have
multiple
functional
populations
wall.
In
general,
had
fewer
nonimmune
more
immune
especially
than
did.
Differential
suggested
presence
extensive
mitochondrial
dysfunction
addition,
public
promoter
capture
Hi-C
erythroblast
transformation-specific
related
gene(
ERG
)
exerts
an
important
role
maintaining
normal
function.
Conclusions:
Our
provides
a
comprehensive
evaluation
reveals
how
landscape
altered
tissue.
The
information
this
makes
contributions
formation
progression.
Abstract
Rare
diseases
affect
30
million
people
in
the
USA
and
more
than
300–400
worldwide,
often
causing
chronic
illness,
disability,
premature
death.
Traditional
diagnostic
techniques
rely
heavily
on
heuristic
approaches,
coupling
clinical
experience
from
prior
rare
disease
presentations
with
medical
literature.
A
large
number
of
patients
remain
undiagnosed
for
years
many
even
die
without
an
accurate
diagnosis.
In
recent
years,
gene
panels,
microarrays,
exome
sequencing
have
helped
to
identify
molecular
cause
such
diseases.
These
technologies
allowed
diagnoses
a
sizable
proportion
(25–35%)
patients,
actionable
findings.
However,
these
undiagnosed.
this
review,
we
focus
that
can
be
adopted
if
is
unrevealing.
We
discuss
benefits
whole
genome
additional
benefit
may
offered
by
long-read
technology,
pan-genome
reference,
transcriptomics,
metabolomics,
proteomics,
methyl
profiling.
highlight
computational
methods
help
regionally
distant
similar
phenotypes
or
genetic
mutations.
Finally,
describe
approaches
automate
accelerate
genomic
analysis.
The
strategies
discussed
here
are
intended
serve
as
guide
clinicians
researchers
next
steps
when
encountering
non-diagnostic
exomes.