
Faculty, Staff and Student Publications
Publication Date
2-3-2023
Journal
Scientific Reports
Abstract
One of the major obstacles to treating pancreatic ductal adenocarcinoma (PDAC) is its immunoresistant microenvironment. The functional importance and molecular mechanisms of Schwann cells in PDAC remains largely elusive. We characterized the gene signature of tumor-associated nonmyelinating Schwann cells (TASc) in PDAC and indicated that the abundance of TASc was correlated with immune suppressive tumor microenvironment and the unfavorable outcome of patients with PDAC. Depletion of pancreatic-specific TASc promoted the tumorigenesis of PDAC tumors. TASc-expressed long noncoding RNA (lncRNA) plasmacytoma variant translocation 1 (
Keywords
Humans, Carcinoma, Pancreatic Ductal, Cell Line, Tumor, Cell Proliferation, Gene Expression Regulation, Neoplastic, Kynurenine, Pancreatic Neoplasms, RNA, Long Noncoding, Tumor Microenvironment
DOI
10.1126/sciadv.add6995
PMID
36724291
PMCID
PMC9891701
PubMedCentral® Posted Date
February 2023
PubMedCentral® Full Text Version
Post-print
Published Open-Access
yes
Included in
Bioinformatics Commons, Biomedical Informatics Commons, Medical Sciences Commons, Oncology Commons
Comments
Supplementary Material
PMID: 36724291