High antigen-presenting CAF levels correlate with reduced glycosaminoglycan biosynthesis-heparan sulfate/heparin metabolism in immune cells and poor prognosis in esophageal squamous cell carcinoma: Insights from bulk and single-cell transcriptome profiling
Siliang Wang,
No information about this author
Van Kelly,
No information about this author
Mei Zhen
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et al.
International Journal of Biological Macromolecules,
Journal Year:
2025,
Volume and Issue:
unknown, P. 140418 - 140418
Published: Jan. 1, 2025
Language: Английский
Paeonol enhances a recombinant EGFR-targeted fusion protein-drug conjugate induced antitumor efficacy in esophageal cancer
Biochemical Pharmacology,
Journal Year:
2025,
Volume and Issue:
236, P. 116856 - 116856
Published: March 5, 2025
Language: Английский
Unlocking the Therapeutic Potential of Natural Polyphenols in Esophageal Cancer
Current Treatment Options in Oncology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 22, 2025
Language: Английский
Synthesis of Amphiphilic Amino Poly-Amido-Saccharide and Poly(lactic) Acid Block Copolymers and Fabrication of Paclitaxel-Loaded Mucoadhesive Nanoparticles
Robert C. Sabatelle,
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Abraham D. Geller,
No information about this author
Siyuan Li
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et al.
Bioconjugate Chemistry,
Journal Year:
2024,
Volume and Issue:
35(9), P. 1429 - 1440
Published: Aug. 19, 2024
Drug
delivery
to
the
esophagus
through
systemic
administration
remains
challenging,
as
minimal
drug
reaches
desired
target.
Local
offers
potential
for
improved
efficacy
while
minimizing
off-target
toxicities
but
necessitates
bioadhesive
properties
mucosal
delivery.
Herein,
we
describe
synthesis
of
two
new
mucoadhesive
amphiphilic
copolymers
prepared
by
sequential
ring-opening
copolymerization
or
postpolymerization
click
conjugation.
Both
strategies
yield
block
containing
a
hydrophilic
amine-functionalized
poly-amido-saccharide
and
either
hydrophobic
alkyl
derivatized
poly(lactic
acid),
respectively.
The
latter
resulting
readily
self-assemble
into
spherical,
≈200
nm
diameter,
positively
charged
nanoparticles.
NPs
entrap
ultrahigh
levels
paclitaxel
via
encapsulation
free
conjugated
biodegradable,
biocompatible
poly(1,2-glycerol
carbonate).
Paclitaxel-loaded
rapidly
enter
cells,
release
paclitaxel,
are
cytotoxic
esophageal
OE33
OE19
tumor
cells
in
vitro,
and,
importantly,
demonstrate
mucoadhesion
compared
conventional
poly(ethylene
glycol)-poly(lactic
acid)
nanoparticles
ex
vivo
tissue.
Language: Английский