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Article

Inhibition of DACH1 activity by short hairpin RNA represses cell proliferation and tumor invasion in pancreatic cancer

  • Authors:
    • Xiao-Na Bu
    • Chan Qiu
    • Chuan Wang
    • Zheng Jiang
  • View Affiliations / Copyright

    Affiliations: Department of Gastroenterology, The First Affiliated Hospital, Chongqing Medical University, Chongqing 400016, P.R. China, Department of Gastroenterology, The Third People's Hospital of Chongqing, Chongqing 400014, P.R. China
  • Pages: 745-754
    |
    Published online on: June 2, 2016
       https://doi.org/10.3892/or.2016.4843
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Abstract

Cancer of the pancreas is one of the most lethal diseases worldwide. Better understanding of the molecular mechanisms involved in tumorigenesis is of great consequence to elevate the survival rate. Human Dachshund homologue 1 (DACH1) plays a controversial role in human malignancy progression with its expression being altered in a variety of cancers. Nevertheless, its functional roles and molecular mechanisms in pancreatic cancer remain unknown. The expression of DACH1 in pancreatic cancer cell lines and the ductal epithelial cells were evaluated both at mRNA and protein levels. Three pairs of siRNA targeting the DACH1 gene were designed and synthesized, double-stranded short hairpin RNA (shRNA) were annealed and inserted into pGenesil-1 vector, which was confirmed by enzymatic digestion and sequencing analyses. The successfully constructed recombinant plasmids were transfected into Capan-1 cells and our data indicated that knockdown of DACH1 gene expression showed strong correlation with repressing tumorigenesis. The proliferation of Capan-1 cells was significantly repressed as evaluated by CCK-8 and colony formation assays. Flow cymetry revealed that cell apoptosis was promoted in interference plasmid group compared with control groups (P<0.05), whereas cell cycle had no significant differences among the groups (P>0.05). Transwell assay validated the abilities of migration and invasion as being significantly reduced in pshRNA-DACH1 group. Furthermore, our study suggested that DACH1 expression regulates the pancreatic cancer cell apoptosis through interacting with Bcl-2 signaling axis, whereas it controls cell migration and invasion via epithelial-mesenchymal transition (EMT) process.
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Copy and paste a formatted citation
Spandidos Publications style
Bu X, Qiu C, Wang C and Jiang Z: Inhibition of DACH1 activity by short hairpin RNA represses cell proliferation and tumor invasion in pancreatic cancer. Oncol Rep 36: 745-754, 2016.
APA
Bu, X., Qiu, C., Wang, C., & Jiang, Z. (2016). Inhibition of DACH1 activity by short hairpin RNA represses cell proliferation and tumor invasion in pancreatic cancer. Oncology Reports, 36, 745-754. https://doi.org/10.3892/or.2016.4843
MLA
Bu, X., Qiu, C., Wang, C., Jiang, Z."Inhibition of DACH1 activity by short hairpin RNA represses cell proliferation and tumor invasion in pancreatic cancer". Oncology Reports 36.2 (2016): 745-754.
Chicago
Bu, X., Qiu, C., Wang, C., Jiang, Z."Inhibition of DACH1 activity by short hairpin RNA represses cell proliferation and tumor invasion in pancreatic cancer". Oncology Reports 36, no. 2 (2016): 745-754. https://doi.org/10.3892/or.2016.4843
Copy and paste a formatted citation
x
Spandidos Publications style
Bu X, Qiu C, Wang C and Jiang Z: Inhibition of DACH1 activity by short hairpin RNA represses cell proliferation and tumor invasion in pancreatic cancer. Oncol Rep 36: 745-754, 2016.
APA
Bu, X., Qiu, C., Wang, C., & Jiang, Z. (2016). Inhibition of DACH1 activity by short hairpin RNA represses cell proliferation and tumor invasion in pancreatic cancer. Oncology Reports, 36, 745-754. https://doi.org/10.3892/or.2016.4843
MLA
Bu, X., Qiu, C., Wang, C., Jiang, Z."Inhibition of DACH1 activity by short hairpin RNA represses cell proliferation and tumor invasion in pancreatic cancer". Oncology Reports 36.2 (2016): 745-754.
Chicago
Bu, X., Qiu, C., Wang, C., Jiang, Z."Inhibition of DACH1 activity by short hairpin RNA represses cell proliferation and tumor invasion in pancreatic cancer". Oncology Reports 36, no. 2 (2016): 745-754. https://doi.org/10.3892/or.2016.4843
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