Skip to main content
Oncotarget logoLink to Oncotarget
. 2019 Sep 24;10(54):5669. doi: 10.18632/oncotarget.27216

Correction: The heparan sulfate mimetic PG545 interferes with Wnt/β-catenin signaling and significantly suppresses pancreatic tumorigenesis alone and in combination with gemcitabine

Deok-Beom Jung 1,*, Miyong Yun 1,*, Eun-Ok Kim 1,2, Jaekwang Kim 1, Bonglee Kim 1, Ji Hoon Jung 1, Enfeng Wang 3, Debabrata Mukopadhyay 3, Edward Hammond 4, Keith Dredge 4, Viji Shridhar 5,**,, Sung-Hoon Kim 1,**,
PMCID: PMC6771454  PMID: 31608142

This article has been corrected: The IHC pictures of ‘Control #1 group’ and ‘PG545 #2 group’ have been removed from Figure 6. In addition, the ‘Cyclin D1 in Control 1 group’ is mistakenly similar to the IHC picture of ‘PCNA in Gem group’ already presented in Figure 5F. The corrected Figure 6 is shown below. The authors declare that these corrections do not change the results or conclusions of this paper.

Original article: Oncotarget. 2015; 6:4992-5004. 4992-5004. https://doi.org/10.18632/oncotarget.3214

Figure 6. PG545 inhibits β-catenin signaling in AsPC-1 orthotopic xenograft mouse model.

Figure 6

(A) Immunohistochemical analysis of β-catenin and β-catenin-regulated proteins, Cyclin D1, MMP-7 and VEGF in pancreatic tumor tissues from mice. Quantitation of staining was performed using 10 fields per analyte. **P & 0.01, ***P & 0.001. (B) Frozen tumor tissues were homogenized on ice and the extracts were subjected to Western blotting. (C) β-catenin and (D) Cyclin D1 levels were quantified by Image J software and plotted relative to the control group in Fig. 6B. **P & 0.01, ***P & 0.001 vs. control.


Articles from Oncotarget are provided here courtesy of Impact Journals, LLC

RESOURCES