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A gene expression signature of epithelial tubulogenesis and a role for ASPM in pancreatic tumor progression.
Wang, Wei-Yu; Hsu, Chung-Chi; Wang, Ting-Yun; Li, Chi-Rong; Hou, Ya-Chin; Chu, Jui-Mei; Lee, Chung-Ta; Liu, Ming-Sheng; Su, Jimmy J-M; Jian, Kuan-Ying; Huang, Shenq-Shyang; Jiang, Shih-Sheng; Shan, Yan-Shen; Lin, Pin-Wen; Shen, Yin-Ying; Lee, Michael T-L; Chan, Tze-Sian; Chang, Chun-Chao; Chen, Chung-Hsing; Chang, I-Shou; Lee, Yen-Ling; Chen, Li-Tzong; Tsai, Kelvin K.
Afiliação
  • Wang WY; Laboratory for Tumor Epigenetics and Stemness, National Institute of Cancer Research and Translational Center for Glandular Malignancies, National Health Research Institutes, Tainan, Taiwan; Department of Pathology, National Cheng-Kung University Hospital and College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Gastroenterology ; 145(5): 1110-20, 2013 Nov.
Article em En | MEDLINE | ID: mdl-23896173
ABSTRACT
BACKGROUND &

AIMS:

Many patients with pancreatic ductal adenocarcinoma (PDAC) develop recurrent or metastatic diseases after surgery, so it is important to identify those most likely to benefit from aggressive therapy. Disruption of tissue microarchitecture is an early step in pancreatic tumorigenesis and a parameter used in pathology grading of glandular tumors. We investigated whether changes in gene expression during pancreatic epithelial morphogenesis were associated with outcomes of patients with PDAC after surgery.

METHODS:

We generated architectures of human pancreatic duct epithelial cells in a 3-dimensional basement membrane matrix. We identified gene expression profiles of the cells during different stages of tubular morphogenesis (tubulogenesis) and of PANC-1 cells during spheroid formation. Differential expression of genes was confirmed by immunoblot analysis. We compared the gene expression profile associated with pancreatic epithelial tubulogenesis with that of PDAC samples from 27 patients, as well as with their outcomes after surgery.

RESULTS:

We identified a gene expression profile associated with tubulogenesis that resembled the profile of human pancreatic tissue with differentiated morphology and exocrine function. Patients with PDACs with this profile fared well after surgery. Based on this profile, we established a 6-28 gene tubulogenesis-specific signature that accurately determined the prognosis of independent cohorts of patients with PDAC (total n = 128; accuracy = 81.2%-95.0%). One gene, ASPM, was down-regulated during tubulogenesis but up-regulated in human PDAC cell lines and tumor samples; up-regulation correlated with patient outcomes (Cox regression P = .0028). Bioinformatic, genetic, biochemical, functional, and clinical correlative studies showed that ASPM promotes aggressiveness of PDAC by maintaining Wnt-ß-catenin signaling and stem cell features of PDAC cells.

CONCLUSIONS:

We identified a gene expression profile associated with pancreatic epithelial tubulogenesis and a tissue architecture-specific signature of PDAC cells that is associated with patient outcomes after surgery.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ductos Pancreáticos / Neoplasias Pancreáticas / Regulação Neoplásica da Expressão Gênica / Diferenciação Celular / Progressão da Doença / Carcinoma Ductal Pancreático / Transcriptoma / Proteínas do Tecido Nervoso Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ductos Pancreáticos / Neoplasias Pancreáticas / Regulação Neoplásica da Expressão Gênica / Diferenciação Celular / Progressão da Doença / Carcinoma Ductal Pancreático / Transcriptoma / Proteínas do Tecido Nervoso Idioma: En Ano de publicação: 2013 Tipo de documento: Article