Open Access

Effects of LDOC1 on colorectal cancer cells via downregulation of the Wnt/β-catenin signaling pathway

  • Authors:
    • Jiayi Jiang
    • You Li
    • Zheng Jiang
  • View Affiliations

  • Published online on: April 17, 2019     https://doi.org/10.3892/or.2019.7126
  • Pages: 3281-3291
  • Copyright: © Jiang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

Colorectal cancer (CRC) is one of the most common tumor types of the digestive tract. Its incidence and mortality rates are among the highest of all gastrointestinal tumor types. The expression of leucine zipper downregulated in cancer 1 (LDOC1) is decreased in numerous cancer types. In the present study, the aim was to investigate the role of LDOC1 and determine the potential molecular mechanisms of its action in CRC. The expression of LDOC1 in CRC tissues and adjacent normal tissues was detected by reverse transcription‑quantitative polymerase chain reaction and immunohistochemistry. LDOC1 expression in four CRC cell lines, compared with normal colorectal tissue, was determined by reverse transcription‑ polymerase chain reaction (RT‑PCR), and two cell lines with relatively low expression were screened. Human LDOC1 cDNA was inserted into a lentiviral vector, and transfected into HCT‑116 and Caco2 cell lines. The transfection efficiency was identified by RT‑PCR and western blot analysis. Cell proliferation was detected by Cell Counting Kit‑8 and colony formation assays. Cell cycle and apoptosis were detected by flow cytometry assay. Migration and invasion were assessed using Transwell and Matrigel assays, respectively. Additionally, whether LDOC1 regulates the Wnt/β‑catenin pathway was investigated by western blot analysis, and the expression and localization of β‑catenin in CRC cells were demonstrated by cellular immunofluorescence. LDOC1 expression was downregulated in CRC tissues and cells. LDOC1 overexpression inhibited cell proliferation, migration and invasion, but promoted cells apoptosis. Furthermore, LDOC1 downregulated the Wnt/β‑catenin pathway in CRC. In conclusion, LDOC1 is a tumor suppressor in CRC and it inhibits cell proliferation and promotes cell apoptosis. Additionally, it inhibits CRC cell metastasis by downregulating the Wnt/β‑catenin signaling pathway.
View Figures
View References

Related Articles

Journal Cover

June 2019
Volume 41 Issue 6

Print ISSN: 1021-335X
Online ISSN:1791-2431

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
APA
Jiang, J., Li, Y., & Jiang, Z. (2019). Effects of LDOC1 on colorectal cancer cells via downregulation of the Wnt/β-catenin signaling pathway . Oncology Reports, 41, 3281-3291. https://doi.org/10.3892/or.2019.7126
MLA
Jiang, J., Li, Y., Jiang, Z."Effects of LDOC1 on colorectal cancer cells via downregulation of the Wnt/β-catenin signaling pathway ". Oncology Reports 41.6 (2019): 3281-3291.
Chicago
Jiang, J., Li, Y., Jiang, Z."Effects of LDOC1 on colorectal cancer cells via downregulation of the Wnt/β-catenin signaling pathway ". Oncology Reports 41, no. 6 (2019): 3281-3291. https://doi.org/10.3892/or.2019.7126