Pro-metastatic splicing of Ron proto-oncogene mRNA can be reversed: Therapeutic potential of bifunctional oligonucleotides and indole derivatives

• Published in: RNA biology Vol. 7; no. 4; pp. 495 - 503
• Main Authors: Ghigna, Claudia, De Toledo, Marion, Bonomi, Serena, Valacca, Cristina, Gallo, Stefania, Apicella, Maria, Eperon, Ian, Tazi, Jamal, Biamonti, Giuseppe
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 01.07.2010
• Subjects: Binding; Biochemistry, Molecular Biology; Biology; Bioscience; Calcium; Cancer; Cell; Cell Line, Tumor; Cycle; HeLa Cells; Humans; Indoles - pharmacology; Landes; Life Sciences; Neoplasm Metastasis - genetics; Neoplasm Metastasis - therapy; Oligonucleotides - pharmacology; Organogenesis; Proteins; Receptor Protein-Tyrosine Kinases - genetics; RNA Splicing - drug effects
• ISSN: 1547-6286; 1555-8584
• DOI: 10.4161/rna.7.4.12744

Alternative splicing is a key molecular mechanism for increasing the complexity of the human transcriptome. Nearly all human genes are regulated by alternative splicing and the deregulation of this process has a causative role in various human diseases, including cancer. The discovery that alternatively spliced isoforms of several genes are expressed selectively in tumor cells opened the exciting possibility that pharmacological treatment of aberrant splicing could lead to new anti-cancer therapeutic approaches. An alternatively spliced isoform of a scatter factor receptor and proto-oncogene, Ron, accumulates during tumor progression of epithelial tissues and is able to confer an invasive phenotype to the expressing cells. This isoform, called ΔRon, originates from skipping of exon 11, and this specific splicing event is controlled by the expression level of the splicing factor and proto-oncogene SF2/ASF. Over-expression of SF2/ASF, which occurs frequently in various human tumors, induces the production of ΔRon and activates the epithelial to mesenchymal transition (EMT), leading to increased cell motility. In this paper, we have used targeted oligonucleotide enhancers of splicing (TOES) to recruit positive splicing factors to Ron exon 11 and thereby stimulate its inclusion. As an alternative approach, we have used selected indole derivatives that target ASF/SF2 splicing activity. Both treatments correct aberrant ΔRon splicing, restoring the incorporation of Ron exon 11. Notably, indole derivatives are also able to affect the invasive phenotype of the cells. Thus, these treatments may have therapeutic applications for anti-cancer purposes.