EBioMedicine,
Journal Year:
2024,
Volume and Issue:
103, P. 105098 - 105098
Published: April 11, 2024
BackgroundThe
widespread
involvement
of
tumor-infiltrating
B
cells
highlights
their
potential
role
in
tumor
behavior.
However,
cell
heterogeneity
PDAC
remains
unexplored.
Studying
TIL-Bs
aims
to
identify
new
treatment
strategies.MethodsWe
performed
single-cell
RNA
sequencing
study
the
PDAC.
The
prognostic
and
immunologic
value
identified
CD38+
was
explored
FUSCC
(n
=
147)
TCGA
176)
cohorts.
Flow
cytometry
conducted
characterize
relationship
between
other
immune
cells,
as
well
phenotypic
features.
In
vitro
vivo
experiments
were
assess
putative
effect
on
antitumor
immunity.FindingsThe
presence
associated
with
unfavorable
clinicopathological
features
poorer
overall
survival
(p
<
0.001).
Increased
infiltration
accompanied
by
reduced
natural
killer
(NK)
0.021)
increased
regulatory
T
0.016).
Molecular
profiling
revealed
high
expression
IL-10,
IL-35,
TGF-β,
GZMB,
TIM-1,
CD5
CD21,
confirming
cell-like
Co-culture
demonstrated
suppression
NK
cytotoxicity
cell-derived
IL-10
Finally,
suggested
adoptive
transfer
immunity
administration
a
CD38
inhibitor
hampered
growth
0.001).InterpretationWe
discovered
an
independent
factor
use
may
provide
possibilities
for
immunotherapy.FundingThis
supported
National
Natural
Science
Foundation
China
(U21A20374),
Shanghai
Municipal
Technology
Major
Project
(21JC1401500),
Scientific
Innovation
Education
Committee
(2019-01-07-00-07-E00057),
Special
Clinical
Research
Health
Industry
Commission
(No.
20204Y0265)
(23ZR1479300).
Molecular Cancer,
Journal Year:
2024,
Volume and Issue:
23(1)
Published: May 6, 2024
Abstract
Background
Metabolic
reprogramming
and
epigenetic
alterations
contribute
to
the
aggressiveness
of
pancreatic
ductal
adenocarcinoma
(PDAC).
Lactate-dependent
histone
modification
is
a
new
type
mark,
which
links
glycolysis
metabolite
process
lactylation.
However,
role
lactylation
in
PDAC
remains
unclear.
Methods
The
level
was
identified
by
western
blot
immunohistochemistry,
its
relationship
with
overall
survival
evaluated
using
Kaplan-Meier
plot.
participation
growth
progression
confirmed
through
inhibition
inhibitors
or
lactate
dehydrogenase
A
(
LDHA
)
knockdown
both
vitro
vivo.
potential
writers
erasers
were
functional
experiments.
target
genes
H3K18
(H3K18la)
screened
CUT&Tag
RNA-seq
analyses.
candidate
TTK
protein
kinase
BUB1
mitotic
checkpoint
serine/threonine
B
BUB1B
validated
ChIP-qPCR,
RT-qPCR
Next,
effects
these
two
overexpression.
interaction
between
Co-IP
assay.
Results
Histone
lactylation,
especially
H3K18la
elevated
PDAC,
high
associated
poor
prognosis.
suppression
glycolytic
activity
different
kinds
contributed
anti-tumor
E1A
binding
p300
(P300)
deacetylase
2
writer
eraser
cells,
respectively.
enriched
at
promoters
activated
transcription
regulators
.
Interestingly,
could
elevate
expression
P300
turn
increased
glycolysis.
Moreover,
phosphorylated
tyrosine
239
(Y239)
LDHA,
subsequently
upregulated
levels.
Conclusions
glycolysis-H3K18la-TTK/BUB1B
positive
feedback
loop
exacerbates
dysfunction
PDAC.
These
findings
delivered
exploration
significant
inter-relationship
metabolic
regulation,
might
pave
way
toward
novel
treatment
strategies
therapy.
npj Precision Oncology,
Journal Year:
2024,
Volume and Issue:
8(1)
Published: Feb. 3, 2024
Abstract
The
relevance
of
KRAS
mutation
alleles
to
clinical
outcome
remains
inconclusive
in
pancreatic
adenocarcinoma
(PDAC).
We
conducted
a
retrospective
study
803
patients
with
PDAC
(42%
metastatic
disease)
at
MD
Anderson
Cancer
Center.
Overall
survival
(OS)
analysis
demonstrated
that
status
and
subtypes
were
prognostic
(
p
<
0.001).
Relative
wildtype
tumors
(median
OS
38
months),
G12R
had
similar
34
while
Q61
G12D
mutated
shorter
20
months
[HR:
1.9,
95%
CI
1.2–3.0,
=
0.006]
22
1.7,
1.3–2.3,
0.001],
respectively).
There
was
enrichment
(34%
vs
24%,
OR:
1.2–2.4,
0.001)
well
moderately
differentiated
(14%
9%,
1.05–2.99,
0.04).
Similar
findings
observed
the
external
validation
cohort
(PanCAN’s
Know
Your
Tumor®
dataset,
n
408).
Signal Transduction and Targeted Therapy,
Journal Year:
2024,
Volume and Issue:
9(1)
Published: Dec. 1, 2024
Cancer
has
a
high
mortality
rate
across
the
globe,
and
tissue
biopsy
remains
gold
standard
for
tumor
diagnosis
due
to
its
level
of
laboratory
standardization,
good
consistency
results,
relatively
stable
samples,
accuracy
results.
However,
there
are
still
many
limitations
drawbacks
in
application
tumor.
The
emergence
liquid
provides
new
ideas
early
prognosis
Compared
with
biopsy,
advantages
treatment
various
types
cancer,
including
non-invasive,
quickly
so
on.
Currently,
detection
received
widely
attention.
It
is
now
undergoing
rapid
progress,
it
holds
significant
potential
future
applications.
Around
now,
biopsies
encompass
several
components
such
as
circulating
cells,
DNA,
exosomes,
microRNA,
RNA,
platelets,
endothelial
cells.
In
addition,
advances
identification
indicators
have
significantly
enhanced
possibility
utilizing
clinical
settings.
this
review,
we
will
discuss
application,
challenges
some
common
tumors
from
perspective
diverse
systems
tumors,
look
forward
development
prospects
field
cancer
treatment.
Signal Transduction and Targeted Therapy,
Journal Year:
2024,
Volume and Issue:
9(1)
Published: May 22, 2024
Abstract
Immunotherapy
represented
by
anti-PD-(L)1
and
anti-CTLA-4
inhibitors
has
revolutionized
cancer
treatment,
but
challenges
related
to
resistance
toxicity
still
remain.
Due
the
advancement
of
immuno-oncology,
an
increasing
number
novel
immunoregulatory
targets
mechanisms
are
being
revealed,
with
relevant
therapies
promising
improve
clinical
immunotherapy
in
foreseeable
future.
Therefore,
comprehending
larger
picture
is
important.
In
this
review,
we
analyze
summarize
current
landscape
preclinical
translational
mechanistic
research,
drug
development,
trials
that
brought
about
next-generation
pharmacological
anti-cancer
agents
candidates
beyond
classical
immune
checkpoint
inhibitors.
Along
further
clarification
immunobiology
advances
antibody
engineering,
targeting
additional
inhibitory
checkpoints,
including
LAG-3,
TIM-3,
TIGIT,
CD47,
B7
family
members
becoming
important
part
research
discovery,
as
structurally
functionally
optimized
agonists
co-stimulatory
molecules
T
cells.
Exemplified
bispecific
cell
engagers,
newly
emerging
bi-specific
multi-specific
antibodies
can
provide
considerable
benefits.
Next-generation
also
include
epigenetic
drugs
cytokine-based
therapeutics.
Cell
therapies,
vaccines,
oncolytic
viruses
not
covered
review.
This
comprehensive
review
might
aid
development
fastest
possible
adoption
effective
immuno-oncology
modalities
for
benefit
patients.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Jan. 26, 2024
Background
Pancreatic
cancer
remains
an
extremely
malignant
digestive
tract
tumor,
posing
a
significant
global
public
health
burden.
Patients
with
pancreatic
cancer,
once
metastasis
occurs,
lose
all
hope
of
cure,
and
prognosis
is
poor.
It
important
to
investigate
liver
in
depth,
not
just
because
it
the
most
common
form
but
also
crucial
for
treatment
planning
assessment.
This
study
aims
delve
into
mechanisms
metastasis,
goal
providing
scientific
groundwork
development
future
methods
drugs.
Methods
We
explored
using
single-cell
sequencing
data
(GSE155698
GSE154778)
bulk
(GSE71729,
GSE19279,
TCGA-PAAD).
Initially,
Seurat
package
was
employed
processing
obtain
expression
matrices
primary
lesions
metastatic
lesions.
Subsequently,
high-dimensional
weighted
gene
co-expression
network
analysis
(hdWGCNA)
used
identify
genes
associated
metastasis.
Machine
learning
algorithms
COX
regression
models
were
further
screen
related
patient
prognosis.
Informed
by
both
biological
understanding
outcomes
algorithms,
we
meticulously
identified
ultimate
set
metastasis-related
(LRG).
In
LRG
genes,
various
databases
utilized
validate
their
association
order
analyze
effects
these
agents
on
tumor
microenvironment,
conducted
in-depth
analysis,
including
changes
signaling
pathways
(GSVA),
cell
differentiation
(pseudo-temporal
analysis),
communication
networks
(cell
downstream
transcription
factors
(transcription
factor
activity
prediction).
Additionally,
drug
sensitivity
metabolic
performed
reveal
gemcitabine
resistance
pathways.
Finally,
functional
experiments
silencing
PANC-1
Bx-PC-3
cells
its
influence
proliferation
invasiveness
cells.
Results
Through
series
algorithmic
filters,
PAK2
as
key
promoting
GSVA
elucidated
activation
TGF-beta
pathway
promote
occurrence
Pseudo-temporal
revealed
correlation
between
lower
status
Cell
that
overexpression
promotes
microenvironment.
Transcription
prediction
displayed
regulated
PAK2.
Drug
impact
CCK8
showed
led
decrease
proliferative
capacity
scratch
demonstrated
low
decreased
invasion
capability
Flow
cytometry
reveals
significantly
inhibited
apoptosis
lines.
Molecules
inhibition
PAK2,
there
corresponding
molecules
EMT.
Conclusion
facilitated
angiogenic
potential
epithelial-mesenchymal
transition
process
activating
pathway.
Simultaneously,
level
cells,
consequently
enhancing
malignancy.
fostered
augments
chemoresistance,
modulates
energy
metabolism
summary,
emerged
pivotal
orchestrating
Intervening
may
offer
promising
therapeutic
strategy
preventing
improving
Diagnostics,
Journal Year:
2024,
Volume and Issue:
14(2), P. 174 - 174
Published: Jan. 12, 2024
Pancreatic
cancer
is
a
highly
aggressive
and
difficult-to-detect
with
poor
prognosis.
Late
diagnosis
common
due
to
lack
of
early
symptoms,
specific
markers,
the
challenging
location
pancreas.
Imaging
technologies
have
improved
diagnosis,
but
there
still
room
for
improvement
in
standardizing
guidelines.
Biopsies
histopathological
analysis
are
tumor
heterogeneity.
Artificial
Intelligence
(AI)
revolutionizes
healthcare
by
improving
treatment,
patient
care.
AI
algorithms
can
analyze
medical
images
precision,
aiding
disease
detection.
also
plays
role
personalized
medicine
analyzing
data
tailor
treatment
plans.
It
streamlines
administrative
tasks,
such
as
coding
documentation,
provides
assistance
through
chatbots.
However,
challenges
include
privacy,
security,
ethical
considerations.
This
review
article
focuses
on
potential
transforming
pancreatic
care,
offering
diagnostics,
treatments,
operational
efficiency,
leading
better
outcomes.
Signal Transduction and Targeted Therapy,
Journal Year:
2025,
Volume and Issue:
10(1)
Published: Feb. 11, 2025
Abstract
Accumulated
evidence
has
implicated
the
diverse
and
substantial
influence
of
lactate
on
cellular
differentiation
fate
regulation
in
physiological
pathological
settings,
particularly
intricate
conditions
such
as
cancer.
Specifically,
been
demonstrated
to
be
pivotal
molding
tumor
microenvironment
(TME)
through
its
effects
different
cell
populations.
Within
cells,
impacts
signaling
pathways,
augments
shuttle
process,
boosts
resistance
oxidative
stress,
contributes
lactylation.
In
various
populations,
interplay
between
immune
cells
governs
processes
differentiation,
response,
surveillance,
treatment
effectiveness.
Furthermore,
communication
stromal/endothelial
supports
basal
membrane
(BM)
remodeling,
epithelial-mesenchymal
transitions
(EMT),
metabolic
reprogramming,
angiogenesis,
drug
resistance.
Focusing
production
transport,
specifically
dehydrogenase
(LDH)
monocarboxylate
transporters
(MCT),
shown
promise
Inhibitors
targeting
LDH
MCT
act
both
suppressors
enhancers
immunotherapy,
leading
a
synergistic
therapeutic
effect
when
combined
with
immunotherapy.
The
review
underscores
importance
progression
provides
valuable
perspectives
potential
approaches
that
target
vulnerability
metabolism,
highlighting
Heel
Achilles
for
cancer
treatment.