Literature DB >> 25731618

Wnt2 protein plays a role in the progression of pancreatic cancer promoted by pancreatic stellate cells.

Yong Xu1, Hua Li, Chongbiao Huang, Tiansuo Zhao, Huan Zhang, Chen Zheng, He Ren, Jihui Hao.   

Abstract

This study aimed to investigate the expression of Wnt2 protein in pancreatic cancer tissues and pancreatic stellate cells (PSCs), and determine its effect on the biological functions of pancreatic cancer cells. Immunohistochemistry was used to study the expression pattern of Wnt2 in pancreatic cancer tissues. The relationship between Wnt2 protein expression level and patient prognosis was analyzed. PSCs were isolated and cultured. The expression of Wnt2 in activated PSCs was investigated using Western blot and immunofluorescence. We also analyzed the effect of Wnt2 recombinant protein and stellate cell culture supernatant on the Wnt/β-catenin signaling pathway, as well as the effect of Wnt2 recombinant protein on the biological functions of pancreatic cancer cells. The expression of Wnt2 in interstitial cells of pancreatic cancer was correlated with the prognosis of pancreatic cancer. Wnt2 protein was expressed in activated PSCs. Both stellate cell culture supernatant and Wnt2 recombinant protein could activate the classic Wnt/β-catenin signaling pathway. Wnt2 protein enhanced the migration, invasion, and metastasis of pancreatic cancer cells. These results suggested that Wnt2 protein secreted by PSCs promoted the progression of pancreatic cancer by activating the classic Wnt/β-catenin signaling pathway.

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Year:  2015        PMID: 25731618     DOI: 10.1007/s12032-015-0513-2

Source DB:  PubMed          Journal:  Med Oncol        ISSN: 1357-0560            Impact factor:   3.064


  17 in total

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Review 5.  WNT Ligand Dependencies in Pancreatic Cancer.

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Journal:  Front Cell Dev Biol       Date:  2021-04-28

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9.  Wnt2 contributes to the progression of gastric cancer by promoting cell migration and invasion.

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Review 10.  Extracellular Influences: Molecular Subclasses and the Microenvironment in Pancreatic Cancer.

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