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Hedgehog Signaling Regulates Epithelial-Mesenchymal Transition in Pancreatic Cancer Stem-Like Cells

Hedgehog (Hh) signaling is crucially involved in tumorigenesis. This study aimed to assess the role of Hh signaling in the regulation of epithelial-mesenchymal transition (EMT), stemness properties and chemoresistance of human pancreatic Panc-1 cancer stem cells (CSCs). Panc-1 cells were transfected...

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Autores principales: Wang, Feng, Ma, Ling, Zhang, Zhengkui, Liu, Xiaoran, Gao, Hongqiao, Zhuang, Yan, Yang, Pei, Kornmann, Marko, Tian, Xiaodong, Yang, Yinmo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749361/
https://www.ncbi.nlm.nih.gov/pubmed/26918054
http://dx.doi.org/10.7150/jca.13305
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author Wang, Feng
Ma, Ling
Zhang, Zhengkui
Liu, Xiaoran
Gao, Hongqiao
Zhuang, Yan
Yang, Pei
Kornmann, Marko
Tian, Xiaodong
Yang, Yinmo
author_facet Wang, Feng
Ma, Ling
Zhang, Zhengkui
Liu, Xiaoran
Gao, Hongqiao
Zhuang, Yan
Yang, Pei
Kornmann, Marko
Tian, Xiaodong
Yang, Yinmo
author_sort Wang, Feng
collection PubMed
description Hedgehog (Hh) signaling is crucially involved in tumorigenesis. This study aimed to assess the role of Hh signaling in the regulation of epithelial-mesenchymal transition (EMT), stemness properties and chemoresistance of human pancreatic Panc-1 cancer stem cells (CSCs). Panc-1 cells were transfected with recombinant lentiviral vectors to silence SMO and serum-free floating-culture system was used to isolate Panc-1 tumorspheres. The expression of CSC and EMT markers was detected by flow cytometry, real-time RT-PCR and Western blot analysis. Malignant behaviors of Panc-1 CSC were evaluated by tumorigenicity assays and nude mouse lung metastasis model. We found that tumorspheres derived from pancreatic cancer cell line Panc-1 possessed self-renewal, differentiation and stemness properties. Hh pathway and EMT were active in Panc-1 tumorspheres. Inhibition of Hh signaling by SMO knockdown inhibited self-renewal, EMT, invasion, chemoresistance, pulmonary metastasis, tumorigenesis of pancreatic CSCs. In conclusion, Hh signaling contributes to the maintenance of stem-like properties and chemoresistance of pancreatic CSC and promotes the tumorigenesis and metastasis of pancreatic cancer. Hh pathway is a potential molecular target for the development of therapeutic strategies for pancreatic CSCs.
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spelling pubmed-47493612016-02-25 Hedgehog Signaling Regulates Epithelial-Mesenchymal Transition in Pancreatic Cancer Stem-Like Cells Wang, Feng Ma, Ling Zhang, Zhengkui Liu, Xiaoran Gao, Hongqiao Zhuang, Yan Yang, Pei Kornmann, Marko Tian, Xiaodong Yang, Yinmo J Cancer Research Paper Hedgehog (Hh) signaling is crucially involved in tumorigenesis. This study aimed to assess the role of Hh signaling in the regulation of epithelial-mesenchymal transition (EMT), stemness properties and chemoresistance of human pancreatic Panc-1 cancer stem cells (CSCs). Panc-1 cells were transfected with recombinant lentiviral vectors to silence SMO and serum-free floating-culture system was used to isolate Panc-1 tumorspheres. The expression of CSC and EMT markers was detected by flow cytometry, real-time RT-PCR and Western blot analysis. Malignant behaviors of Panc-1 CSC were evaluated by tumorigenicity assays and nude mouse lung metastasis model. We found that tumorspheres derived from pancreatic cancer cell line Panc-1 possessed self-renewal, differentiation and stemness properties. Hh pathway and EMT were active in Panc-1 tumorspheres. Inhibition of Hh signaling by SMO knockdown inhibited self-renewal, EMT, invasion, chemoresistance, pulmonary metastasis, tumorigenesis of pancreatic CSCs. In conclusion, Hh signaling contributes to the maintenance of stem-like properties and chemoresistance of pancreatic CSC and promotes the tumorigenesis and metastasis of pancreatic cancer. Hh pathway is a potential molecular target for the development of therapeutic strategies for pancreatic CSCs. Ivyspring International Publisher 2016-01-20 /pmc/articles/PMC4749361/ /pubmed/26918054 http://dx.doi.org/10.7150/jca.13305 Text en © Ivyspring International Publisher. Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. See http://ivyspring.com/terms for terms and conditions.
spellingShingle Research Paper
Wang, Feng
Ma, Ling
Zhang, Zhengkui
Liu, Xiaoran
Gao, Hongqiao
Zhuang, Yan
Yang, Pei
Kornmann, Marko
Tian, Xiaodong
Yang, Yinmo
Hedgehog Signaling Regulates Epithelial-Mesenchymal Transition in Pancreatic Cancer Stem-Like Cells
title Hedgehog Signaling Regulates Epithelial-Mesenchymal Transition in Pancreatic Cancer Stem-Like Cells
title_full Hedgehog Signaling Regulates Epithelial-Mesenchymal Transition in Pancreatic Cancer Stem-Like Cells
title_fullStr Hedgehog Signaling Regulates Epithelial-Mesenchymal Transition in Pancreatic Cancer Stem-Like Cells
title_full_unstemmed Hedgehog Signaling Regulates Epithelial-Mesenchymal Transition in Pancreatic Cancer Stem-Like Cells
title_short Hedgehog Signaling Regulates Epithelial-Mesenchymal Transition in Pancreatic Cancer Stem-Like Cells
title_sort hedgehog signaling regulates epithelial-mesenchymal transition in pancreatic cancer stem-like cells
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749361/
https://www.ncbi.nlm.nih.gov/pubmed/26918054
http://dx.doi.org/10.7150/jca.13305
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