题名 | NFATc4 Regulates Sox9 Gene Expression in Acinar Cell Plasticity and Pancreatic Cancer Initiation |
作者 | |
发表日期 | 2016-12-31 |
发表期刊 | STEM CELLS INTERNATIONAL 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
其他关键词 | EPIDERMAL-GROWTH-FACTOR ; DUCTAL ADENOCARCINOMA ; FACTOR RECEPTOR ; ONCOGENIC KRAS ; EGF RECEPTOR ; DIFFERENTIATION ; OVEREXPRESSION ; PROGRESSION ; REGENERATION ; ACTIVATION |
摘要 | Acinar transdifferentiation toward a duct-like phenotype constitutes the defining response of acinar cells to external stress signals and is considered to be the initial step in pancreatic carcinogenesis. Despite the requirement for oncogenic Kras in pancreatic cancer (PDAC) development, oncogenic Kras is not sufficient to drive pancreatic carcinogenesis beyond the level of premalignancy. Instead, secondary events, such as inflammation-induced signaling activation of the epidermal growth factor (EGFR) or induction of Sox9 expression, are required for tumor formation. Herein, we aimed to dissect the mechanism that links EGFR signaling to Sox9 gene expression during acinar-to-ductal metaplasia in pancreatic tissue adaptation and PDAC initiation. We show that the inflammatory transcription factor NFATc4 is highly induced and localizes in the nucleus in response to inflammation-induced EGFR signaling. Moreover, we demonstrate that NFATc4 drives acinar-to-ductal conversion and PDAC initiation through direct transcriptional induction of Sox9. Therefore, strategies designed to disrupt NFATc4 induction might be beneficial in the prevention or therapy of PDAC. |
资助项目 | German Cancer Research Foundation [109423]; Wilhelm Sander Foundation [2013.037.1]; Center of Regenerative Medicine at the Mayo Clinic, Jacksonville; National Cancer InstituteUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Cancer Institute (NCI) [R01 CA140182]; National Cancer Institute Pancreas SPORE grant [P50 CA102701]; NATIONAL CANCER INSTITUTEUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Cancer Institute (NCI) [P50CA102701] Funding Source: NIH RePORTER |
出版者 | HINDAWI LTD |
出版地 | LONDON |
ISSN | 1687-966X |
EISSN | 1687-9678 |
卷号 | 2016页码:5272498 |
DOI | 10.1155/2016/5272498 |
页数 | 11 |
WOS类目 | Cell & Tissue Engineering |
WOS研究方向 | Cell Biology |
WOS记录号 | WOS:000371083800001 |
收录类别 | SCIE ; PUBMED ; SCOPUS |
URL | 查看原文 |
PubMed ID | 26697077 |
PMC记录号 | PMC4677249 |
SCOPUSEID | 2-s2.0-84949967577 |
通讯作者地址 | [Koenig, Alexander]Department of Gastroenterology and Gastrointestinal Oncology,University Medical Center Göttingen,Robert-Koch Street 40,Göttingen,37075,Germany |
Scopus学科分类 | Molecular Biology;Cell Biology |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/8102 |
专题 | 药学院(分析测试中心) 药学院(分析测试中心)_生物制药系_生物制药工程 |
通讯作者 | Koenig, Alexander |
作者单位 | 1.Department of Gastroenterology and Gastrointestinal Oncology,University Medical Center Göttingen,Robert-Koch Street 40,Göttingen,37075,Germany; 2.Schulze Center for Novel Therapeutics,Division of Oncology Research,Mayo Clinic,200 1st Street SW No. W4,Rochester,55905,United States; 3.School of Pharmaceutical Sciences and Key Laboratory of Biotechnology and Pharmaceutical Engineering,Wenzhou Medical University,Wenzhou, Zhejiang,China; 4.Department of Cancer Biology,Mayo Clinic Cancer Center,4500 San Pablo Road,Jacksonville,32224,United States |
推荐引用方式 GB/T 7714 | Hessmann, Elisabeth,Zhang, Jin-San,Chen, Nai-Ming,et al. NFATc4 Regulates Sox9 Gene Expression in Acinar Cell Plasticity and Pancreatic Cancer Initiation[J]. STEM CELLS INTERNATIONAL,2016,2016:5272498. |
APA | Hessmann, Elisabeth., Zhang, Jin-San., Chen, Nai-Ming., Hasselluhn, Marie., Liou, Geou-Yarh., ... & Koenig, Alexander. (2016). NFATc4 Regulates Sox9 Gene Expression in Acinar Cell Plasticity and Pancreatic Cancer Initiation. STEM CELLS INTERNATIONAL, 2016, 5272498. |
MLA | Hessmann, Elisabeth,et al."NFATc4 Regulates Sox9 Gene Expression in Acinar Cell Plasticity and Pancreatic Cancer Initiation".STEM CELLS INTERNATIONAL 2016(2016):5272498. |
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