Single-cell RNA sequencing of solid pseudopapillary neoplasms of the pancreas in children

被引:2
作者
Meng, Lingdu [1 ]
Zhan, Yong [1 ]
Wei, Meng [1 ,2 ]
Yang, Ran [1 ]
Wang, Junfeng [1 ]
Weng, Shuting [1 ]
Chen, Lian [3 ]
Zheng, Shan [1 ,4 ]
Dong, Kuiran [1 ]
Dong, Rui [1 ,4 ]
机构
[1] Fudan Univ, Childrens Hosp, Dept Pediat Surg, Shanghai Key Lab Birth Defect, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Childrens Hosp, Sch Med, Dept Hematol, Shanghai, Peoples R China
[3] Fudan Univ, Childrens Hosp, Dept Pathol, Shanghai, Peoples R China
[4] Fudan Univ, Childrens Hosp, Dept Pediat Surg, Shanghai Key Lab Birth Defect, 399 Wan Yuan Rd, Shanghai 201102, Peoples R China
基金
中国国家自然科学基金;
关键词
epithelial-to-mesenchymal transition; MYC-associated pathway; single-cell RNA sequencing; solid pseudopapillary neoplasm of the pancreas; Wnt/beta-catenin pathway; CYSTIC NEOPLASM; GENE-EXPRESSION; BETA-CATENIN; TUMOR; PAPILLARY; MALIGNANCY; PATHWAYS; INVASION; TFE3;
D O I
10.1111/cas.15744
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Solid pseudopapillary neoplasm (SPN) of the pancreas is a rare pancreatic tumor in children. Its origin remains elusive, along with its pathogenesis. Heterogeneity within SPN has not been previously described. In addition, low malignant but recurrent cases have occasionally been reported. To comprehensively unravel these profiles, single-cell RNA sequencing was performed using surgical specimens. We identified the cell types and suggested the origin of pancreatic endocrine progenitors. The Wnt/beta-catenin pathway may be involved in tumorigenesis, while the epithelial-to-mesenchymal transition may be responsible for SPN recurrence. Furthermore, NOV, DCN were nominated as primary and S100A10, MGP as recurrent SPN marker genes, respectively. Our results provide insight into the pathogenesis of SPN.
引用
收藏
页码:1986 / 2000
页数:15
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