Advances in medical diagnosis, treatment, and care (AMDTC) book series,
Journal Year:
2024,
Volume and Issue:
unknown, P. 1 - 28
Published: Dec. 17, 2024
The
clinical
translation
of
spatial
transcriptomics
represents
cancer
diagnosis
and
therapy
based
on
the
role
heterogeneity
cancer-associated
fibroblasts
(CAFs)
within
tumor
microenvironment
(TME).
Recent
developments
in
have
enabled
a
detailed
characterization
organization
cellular
interactions
tumors.
data
integration,
multi-omics
approaches,
along
with
developing
standardized
protocols
is
essential
for
effective
translation.
experimental
selection
regimes
factorial
designs
reveals
novel
insights
into
biomarkers
prognostic
value
CAFs.
incorporation
optogenetics
advancements
bio-engineered
gene
circuits,
therapeutics
tissue
engineering
further
underscores
potential
to
refine
patient
stratification
improve
treatment
responsiveness.
By
integrating
workflows,
this
work
aims
advance
personalized
therapies
biology.
Advances in Anatomic Pathology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 17, 2025
Follicular
lymphoma
(FL)
is
a
mature
B
cell
neoplasm
classically
characterized
by
cells
harboring
the
t(14;18)
IGH::BCL2
leading
to
overexpression
of
BCL2
in
most
cases.
Conventional
FL
occurs
lymph
nodes
and
typically
shows
follicular
B-cell
proliferation
expressing
at
least
one
germinal
center
marker.
Two
early
lesions
closely
related
conventional
are
recognized
as
variants,
namely
situ
neoplasia
(ISFN),
duodenal-type
(DTFL).
lacking
rearrangement
(
-R
negative)
accounts
for
around
10%
15%
FLs
constitutes
heterogeneous
group
FLs.
Most
these
alternative
forms
considered
distinct
entities
separate
from
2022
International
Consensus
Classification.
This
review
aims
summarize
key
pathologic
diagnostic
features
its
well
further
emphasize
increasing
role
molecular
studies
work-up.
Hematology,
Journal Year:
2025,
Volume and Issue:
30(1)
Published: Feb. 18, 2025
The
tumor
microenvironment
(TME)
represents
a
heterogeneous,
complicated
ecosystem
characterized
by
intricate
interactions
between
cells
and
immune
cells.
During
the
past
decade,
especially
T
were
found
to
play
an
important
role
in
progression
of
many
related
checkpoints
drugs
created.
In
recent
years,
more
scientists
revealed
critical
B-cells
within
TME,
particularly
various
populations
non-malignant
B
Some
studies
indicated
that
may
exert
'double-edged
sword'
solid
tumors.
However,
there
has
been
comparatively
less
focus
on
hematologic
malignancies.
this
review,
we
development
summarized
its
functions
antitumor
immunity
with
emphasis
elucidating
roles
potential
mechanisms
diseases
including
classical
Hodgkin's
lymphoma,
non-Hodgkin's
B-cell
T-cell
leukemia
multiple
myeloma.
British Journal of Haematology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 3, 2025
Summary
The
peripheral
blood
lymphocyte‐to‐monocyte
ratio
(LMR)
has
been
shown
to
predict
outcomes
in
follicular
lymphoma
(FL).
Among
1018
patients
from
the
RELEVANCE
trial
(for
previously
untreated,
high
tumour
burden
FL),
median
LMR
was
2.5
(range,
0.3–93.5)
and
an
cut‐off
of
2
mostly
associated
with
survival
end‐points.
Patients
≤2
(
n
=
372;
37%)
were
older
had
higher
risk
disease.
An
a
shorter
progression‐free
(PFS)
(hazard
[HR]
1.39,
p
0.002)
overall
(OS)
(HR
1.44,
0.049).
association
PFS
significant
rituximab
plus
chemotherapy
arm
0.01)
inconclusive
lenalidomide
0.08).
Within
three
Follicular
Lymphoma
International
Prognostic
Index
categories,
retained
its
only
low‐risk
group
0.03).
also
progression
disease
within
24
months
treatment
initiation
(univariable
odds
(OR)
1.84,
<
0.001;
multivariable
OR
1.58,
0.02).
In
conclusion,
is
easily
accessible
parameter
informative
FL
need
treatment,
being
especially
helpful
otherwise
patients.
Whether
incorporation
immunomodulators
such
as
will
reduce
negative
prognostic
value
needs
be
further
investigated.
Cancer Cell International,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: March 18, 2025
The
development
of
immunotherapy
has
enriched
the
treatment
hepatocellular
carcinoma
(HCC),
but
efficacy
is
not
as
expected,
which
may
be
due
to
immune
evasion.
Immune
evasion
related
microenvironment
HCC,
there
little
research
on
it.
We
employed
unsupervised
clustering
analysis
categorize
patients
from
TCGA
based
182
evasion-related
genes
(IEGs).
utilized
single-sample
gene
set
enrichment
(ssGSEA)
and
CIBERSORT
calculate
differences
in
cell
infiltration
between
clusters.
cells
immune-related
pathways
were
assessed
using
GSEA.
constructed
an
escape
prognosis
signature
(IEPS)
univariate
Cox
LASSO
algorithms
evaluated
predictive
performance
IEPS
with
receiver
operating
characteristic
(ROC)
curves
survival
curves.
Additionally,
we
established
a
nomogram
for
clinical
application
IEPS.
IHC
validated
expression
Carbamoyl
phosphate
synthetase
2,
Aspartate
transcarbamylase,
Dihydroorotase
(CAD)
Phosphatidylinositol
Glycan
Anchor
Biosynthesis
Class
U
(PIGU)
HCC.
transfected
liver
cancer
lines
siRNA
overexpression
plasmids,
confirmed
relationship
CAD,
PIGU,
potential
downstream
TGF-β1
HCC
qRT-PCR
Western
blot.
Finally,
tumor
response
CAD
animal
model.
Unsupervised
IEGs
divided
into
two
groups.
There
significant
characteristics
groups
patients.
Scoring
revealed
that
higher
scores
associated
poorer
overall
(OS).
Validation
was
performed
ICGC
database.
TIME
indicated
high-IEPS
group
immunosuppressive
state,
possibly
increase
Treg
infiltration.
Compared
normal
cells,
expressed
levels
PIGU.
Cellular
experimental
results
showed
positive
correlation
PIGU
expression.
Animal
experiments
demonstrated
significantly
promoted
progression,
strong
prognostic
value
patients,
provide
perspectives
new
biomarkers
therapeutic
targets
Cancers,
Journal Year:
2025,
Volume and Issue:
17(7), P. 1219 - 1219
Published: April 4, 2025
Follicular
lymphoma
(FL)
is
a
heterogeneous
and
incurable
disease.
One
of
the
hallmark
features
FL
cells
introduction
N-glycosylation
(N-gly)
amino
acid
sequence
motifs
into
immunoglobulin
variable
(IgV)
region
through
ongoing
somatic
hypermutation
(SHM)
in
early
stages
development.
These
N-gly
motifs,
containing
oligomannoses,
are
rarely
found
healthy
B
but
evidently
play
crucial
role
clonal
evolution
survival
hostile
environment
germinal
centers.
The
random
nature
SHM
occasionally
results
loss
productive
(Ig)
genes
or
elimination
genes.
Such
events
typically
lead
to
deletion,
as
demonstrated
by
longitudinal
analysis
samples.
However,
rare
N-gly-negative
subclones
demonstrate
prolonged
with
evidence
SHM,
giving
rise
new
before
eventual
deletion.
This
observation
suggests
presence
specific
mechanisms
supporting
their
proliferation.
perspective
examines
current
literature
explores
whether
detailed
transcriptomic
functional
comparison
characterized
different
statuses,
particular
focus
on
subclones,
will
comprehensive
understanding
both
N-gly-dependent
independent
pro-survival
proliferative
transcriptional
signatures.
Specifically,
it
aims
deepen
our
pathobiology
identify
novel
therapeutic
targets
for
better
disease
management.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 5, 2024
Leveraging
endogenous
tumor-resident
T-cells
for
immunotherapy
using
bispecific
antibodies
(BsAb)
targeting
CD20
and
CD3
has
emerged
as
a
promising
therapeutic
strategy
patients
with
B-cell
non-Hodgkin
lymphomas.
However,
features
associated
treatment
response
or
resistance
are
unknown.
To
this
end,
we
analyzed
data
from
treated
epcoritamab-containing
regimens
in
the
EPCORE
NHL-2
trial
(NCT04663347).
We
observed
downregulation
of
expression
on
B-cells
following
initiation
both
progressing
achieving
durable
complete
responses
(CR),
suggesting
that
does
not
universally
predict
to
BsAb-based
therapy.
Single-cell
immune
profiling
tumor
biopsies
obtained
one
cycle
therapy
revealed
substantial
clonal
expansion
cytotoxic
CD4+
CD8+
CR,
an
follicular
helper
regulatory
whose
disease
progressed.
These
results
identify
distinct
T-cell
profiles
BsAb
Cancer Medicine,
Journal Year:
2024,
Volume and Issue:
13(17)
Published: Sept. 1, 2024
Abstract
Objective
Previous
results
about
prognostic
value
of
CD4+
T
cells
in
follicular
lymphoma
(FL)
remain
controversial.
Methods
Immunohistochemistry
was
used
to
examine
expression
positive
CD4
103
patients
with
FL
1‐3A.
Early
failure
described
as
failing
achieve
event‐free
survival
(EFS)
at
12
or
24
months.
Results
There
were
49
(47.6%)
male
and
54
(52.4%)
females,
a
median
age
years.
Compared
<20%
cells,
≥20%
exhibited
significant
lower
risk
early
(2‐year
EFS
rate:
56.7%
vs
73.5%,
p
=
0.047).
When
stratified
based
on
cell
combined
FLIPI,
the
(
0.002)
OS
0.007)
significantly
different.
Conclusions
This
study
demonstrated
that
higher
predicts
lymphoma,
combination
analysis
FLIPI
could
better
predict
disease
relapse
outcome.