TY - JOUR
T1 - The chimeric aptamer axl-miR-214sponge inhibits breast cancer and melanoma dissemination
AU - Quirico, Lorena
AU - Rizzolio, Sabrina
AU - Bertone, Sofia
AU - Cirillo, Priscila D.R.
AU - Savino, Aurora
AU - Vitale, Nicoletta
AU - Catuogno, Silvia
AU - Esposito, Carla L.
AU - Stadler, Michael B.
AU - Defilippi, Paola
AU - de Franciscis, Vittorio
AU - Orso, Francesca
AU - Taverna, Daniela
N1 - Publisher Copyright:
© 2025 The Author(s)
PY - 2025
Y1 - 2025
N2 - MicroRNAs (miRNAs) are often deregulated in cancer. We previously showed that inhibition of the pro-metastatic miR-214 strongly impairs tumor dissemination. We recently developed a chimeric aptamer, axl-miR-214sponge, including an oligonucleotide sequence able to inhibit miR-214 (miR-214sponge) linked to GL21.T (axl), an aptamer that binds specifically to axl, an oncogenic tyrosine kinase receptor abundantly expressed on various malignant melanoma and breast cancer cells. When axl-positive but not axl-negative cancer cells were treated with axl-miR-214sponge, reduced migration, invasion, and transendothelial migration were observed. In parallel, augmented levels of two miR-214 direct targets, TFAP2C and ITGA3, were seen. Instead, expression of ALCAM, a target of the anti-metastatic miR-148b and downstream effector of miR-214, was found to be decreased. More important, when mice carrying xenotransplants derived from triple-negative breast cancer or melanoma cells were treated in loco or systemically with the axl-miR-214sponge conjugates, reduced cancer dissemination was seen, together with increased cell death in primary tumor masses. No toxicity was noted in animals. In summary, our data suggest that axl-miR-214sponge is specific, effective, and safe in blocking axl-positive cancer cell spreading. Thus, it represents a promising targeted therapy tool to fight metastasis.
AB - MicroRNAs (miRNAs) are often deregulated in cancer. We previously showed that inhibition of the pro-metastatic miR-214 strongly impairs tumor dissemination. We recently developed a chimeric aptamer, axl-miR-214sponge, including an oligonucleotide sequence able to inhibit miR-214 (miR-214sponge) linked to GL21.T (axl), an aptamer that binds specifically to axl, an oncogenic tyrosine kinase receptor abundantly expressed on various malignant melanoma and breast cancer cells. When axl-positive but not axl-negative cancer cells were treated with axl-miR-214sponge, reduced migration, invasion, and transendothelial migration were observed. In parallel, augmented levels of two miR-214 direct targets, TFAP2C and ITGA3, were seen. Instead, expression of ALCAM, a target of the anti-metastatic miR-148b and downstream effector of miR-214, was found to be decreased. More important, when mice carrying xenotransplants derived from triple-negative breast cancer or melanoma cells were treated in loco or systemically with the axl-miR-214sponge conjugates, reduced cancer dissemination was seen, together with increased cell death in primary tumor masses. No toxicity was noted in animals. In summary, our data suggest that axl-miR-214sponge is specific, effective, and safe in blocking axl-positive cancer cell spreading. Thus, it represents a promising targeted therapy tool to fight metastasis.
KW - aptamer
KW - axl
KW - breast cancer
KW - melanoma
KW - metastasis
KW - miR-214
KW - miRNA
KW - sponge
KW - targeted therapy
UR - https://www.scopus.com/pages/publications/105013136956
U2 - 10.1016/j.ymthe.2025.07.039
DO - 10.1016/j.ymthe.2025.07.039
M3 - Article
SN - 1525-0016
JO - Molecular Therapy
JF - Molecular Therapy
ER -