Pancreatic-duodenal homeobox 1 (Pdx1) expression distinguishes between duodenal and pancreatic gastrinomas

Author(s):  
V. Fendrich ◽  
R. Ramerth ◽  
J. Waldmann ◽  
P. Langer ◽  
D. K. Bartsch ◽  
...  
Keyword(s):  
PLoS ONE ◽  
2010 ◽  
Vol 5 (9) ◽  
pp. e12958 ◽  
Author(s):  
Jessica A. Hill ◽  
Marta Szabat ◽  
Corinne A. Hoesli ◽  
Blair K. Gage ◽  
Yu Hsuan C. Yang ◽  
...  

2009 ◽  
Vol 16 (2) ◽  
pp. 613-622 ◽  
Author(s):  
Volker Fendrich ◽  
Ricarda Ramerth ◽  
Jens Waldmann ◽  
Katja Maschuw ◽  
Peter Langer ◽  
...  

Some 80–90% of gastrinomas are located in the gastrinoma triangle, which includes the duodenum, the pancreatic head, and the hepatoduodenal ligament. The natural history of the tumors depends on their origin. Duodenal gastrinomas are much less aggressive than pancreatic primaries and infrequently develop liver metastases. The reason therefore is unclear. The transcription factor pancreatic-duodenal homeobox 1 (Pdx1) is important in differentiation and development of the pancreas and duodenum. In embryonic development, Sonic hedgehog (Shh) expression establishes a sharp molecular boundary, which allows for the proper patterning of the duodenal and pancreatic epithelium. Pancreatic polypeptide (PP) is expressed in pancreatic islets and is known to be expressed in pancreatic endocrine tumors. This study aims to clarify the expression pattern of Pdx1, Shh, and PP in duodenal and pancreatic gastrinomas. Tissue from 15 patients with duodenal and from 11 patients with pancreatic gastrinomas that underwent surgery between 1987 and 2007 at our institution because of a gastrinoma were evaluated by immunohistochemistry (IHC). Furthermore, tissue from lymph node metastases from two patients with a so far undetected primary gastrinoma was analyzed. IHC revealed strong Pdx1 expression in pancreatic gastrinomas, but not in duodenal gastrinomas. By contrast, there was no Shh expression detectable in pancreatic gastrinomas, but found in all duodenal gastrinomas. This pattern was also true for associated metastases. Shh expression combined with absence of Pdx1 expression in lymph node metastases from patients with an unknown location of the primary suggests a so far undetected duodenal gastrinoma. We show for the first time that only pancreatic, but not duodenal gastrinomas express Pdx1. Moreover, only duodenal gastrinomas express Shh, suggesting a different genetic background of these two tumors. Whereas the expression of Pdx1 in pancreatic gastrinomas might suggest their endocrine origin from islets, duodenal gastrinomas develop from a Pdx1 negative cell cluster. The expression pattern of Pdx1, Shh, and PP in resected metastases can help to locate an otherwise undetected primary gastrinoma.


2011 ◽  
Vol 25 (16) ◽  
pp. 1680-1685 ◽  
Author(s):  
Y.-P. Yang ◽  
F. Thorel ◽  
D. F. Boyer ◽  
P. L. Herrera ◽  
C. V. E. Wright

2011 ◽  
Vol 19 (5) ◽  
pp. 444-449 ◽  
Author(s):  
Jason Y. Park ◽  
Seung-Mo Hong ◽  
David S. Klimstra ◽  
Michael G. Goggins ◽  
Anirban Maitra ◽  
...  

Author(s):  
Han Yan ◽  
Zhenzhen Chen ◽  
Haizeng Zhang ◽  
Weili Yang ◽  
Xiangyang Liu ◽  
...  

AbstractFAM3A is a recently identified mitochondrial protein that stimulates pancreatic-duodenal homeobox 1 (PDX1) and insulin expressions by promoting ATP release in islet β cells. In this study, the role of intracellular ATP in FAM3A-induced PDX1 expression in pancreatic β cells was further examined. Acute FAM3A inhibition using siRNA transfection in mouse pancreatic islets significantly reduced PDX1 expression, impaired insulin secretion, and caused glucose intolerance in normal mice. In vitro, FAM3A overexpression elevated both intracellular and extracellular ATP contents and promoted PDX1 expression and insulin secretion. FAM3A-induced increase in cellular calcium (Ca2+) levels, PDX1 expression, and insulin secretion, while these were significantly repressed by inhibitors of P2 receptors or the L-type Ca2+ channels. FAM3A-induced PDX1 expression was abolished by a calmodulin inhibitor. Likewise, FAM3A-induced β-cell proliferation was also inhibited by a P2 receptor inhibitor and an L-type Ca2+ channels inhibitor. Both intracellular and extracellular ATP contributed to FAM3A-induced PDX1 expression, insulin secretion, and proliferation of pancreatic β cells.


2019 ◽  
Vol 15 (7) ◽  
pp. 1472-1487 ◽  
Author(s):  
Chen Liang ◽  
Fang Hao ◽  
Xinlei Yao ◽  
Ye Qiu ◽  
Lei Liu ◽  
...  
Keyword(s):  
Β Cells ◽  

2009 ◽  
Vol 21 (9) ◽  
pp. 17
Author(s):  
R. Simmons

The abnormal intrauterine milieu of intrauterine growth retardation (IUGR) permanently alters gene expression and function of pancreatic b -cells leading to the development of diabetes in adulthood. Expression of the pancreatic homeobox transcription factor Pdx1 is permanently reduced in IUGR and epigenetic modifications are responsible for this decrease. Exendin-4 (Ex-4), a long-acting glucagon-like peptide 1 (GLP-1) analog, given on days 1-6 of life increases Pdx1 expression and prevents the development of diabetes in the IUGR rat. Here we show that Ex-4 increases USF-1 and PCAF association at the proximal promoter of Pdx1, thereby increasing histone acetyl transferase (HAT) activity leading to a permanent increase in histone H3 acetylation and H3K4 methylation. Normalization of these histone modifications precludes DNA methylation thereby preventing silencing of Pdx1 in islets of IUGR animals. These studies demonstrate a novel mechanism whereby a short treatment course of Ex-4 in the newborn period prevents diabetes in adulthood by restoring Pdx1 promoter chromatin structure thus preserving Pdx1 transcription.


2014 ◽  
Vol 21 (2) ◽  
pp. 306
Author(s):  
Yuan Yuan ◽  
Kate Hartland ◽  
Zarko Boskovic ◽  
Yikai Wang ◽  
Deepika Walpita ◽  
...  

2013 ◽  
Vol 20 (12) ◽  
pp. 1513-1522 ◽  
Author(s):  
Yuan Yuan ◽  
Kate Hartland ◽  
Zarko Boskovic ◽  
Yikai Wang ◽  
Deepika Walpita ◽  
...  

2012 ◽  
Vol 343 (2) ◽  
pp. 141-145 ◽  
Author(s):  
Haiying Yu ◽  
Zhonghua Sun ◽  
Junsheng Cui ◽  
Guohua Song ◽  
Fuqing Wang ◽  
...  

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