Wnt5A regulates the expression of ROR2 tyrosine kinase receptor in ovarian cancer cells.

Abstract

Wnt5A and receptor tyrosine kinase-like orphan receptor 2 (ROR2) proteins both regulate developmental processes, cell movement, and cell polarity. The purpose of this study was to evaluate a possible regulatory role of Wnt5A on ROR2 expression in human ovarian cancer cell lines. Moreover, the expression of Wnt5A and ROR2 mRNA and protein levels were assessed in human epithelial serous ovarian cancer (HSOC) specimens. ROR2 was strongly decreased in cells treated with siRNA against Wnt5A compared with scramble-treated or lipofectamine-treated cells (P < 0.001). There was 34% decreased cell invasion (P < 0.01) in Wnt5A knock-down cells compared with lipofectamine-treated and scramble-treated cells; however, cell invasion remained unchanged upon addition of anti-ROR2 antibody to the culture media of these cells. In contrast, addition of anti-ROR2 antibody to the culture media for lipofectamine-treated and scramble-treated cells led to 32% decreased cell invasion (P < 0.01). Normal ovarian specimens were negative, and variable immunostaining was observed in HSOC for Wnt5A and ROR2 immunostaining. Furthermore, there was a positive correlation between Wnt5A and ROR2 expression in high-grade SOC samples at the mRNA level (P < 0.05; r = 0.38). This is the first report to show the regulatory role of Wnt5A on ROR2 expression in ovarian cancer.

• Authors: Ghamartaj Hossein, Somayeh Arabzadeh, Zahra Salehi-Dulabi, Zeinab Dehghani-Ghobadi, Yassaman Heidarian, Maryam Talebi-Juybari
• Journal: Biochemistry and cell biology = Biochimie et biologie cellulaire (Biochem Cell Biol) Vol. 95 Issue 6 Pg. 609-615 (12 2017) ISSN: 1208-6002 [Electronic] Canada
• PMID: 28538104 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Retracted Publication)

Chemical References

• Lipids
• Lipofectamine
• RNA, Small Interfering
• WNT5A protein, human
• Wnt-5a Protein
• Receptor Tyrosine Kinase-like Orphan Receptors

Topics

• Cell Line, Tumor
• Female
• Humans
• Lipids (pharmacology)
• Neoplasms, Cystic, Mucinous, and Serous (metabolism, pathology)
• Ovarian Neoplasms (metabolism, pathology)
• RNA, Small Interfering (pharmacology)
• Receptor Tyrosine Kinase-like Orphan Receptors (antagonists & inhibitors, genetics, metabolism)
• Wnt-5a Protein (antagonists & inhibitors, metabolism)