Targeting antisense mitochondrial noncoding RNAs induces bladder cancer cell death and inhibition of tumor growth through reduction of survival and invasion factors
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2020Metadata
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Borgna Christie, Vincenzo
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Targeting antisense mitochondrial noncoding RNAs induces bladder cancer cell death and inhibition of tumor growth through reduction of survival and invasion factors
Author
- Borgna Christie, Vincenzo;
- Lobos González, Lorena;
- Guevara, Francisca;
- Landerer, Eduardo;
- Bendek, Maximiliano;
- Ávila, Rodolfo;
- Silva, Verónica;
- Villota, Claudio;
- Araya, Mariela;
- Rivas, Alexis;
- López, Constanza;
- Socias, Teresa;
- Castillo, Jorge;
- Alarcón Navarrete, Luis;
- Burzio, Luis O.;
- Burzio, Verónica A.;
- Villegas, Jaime;
Abstract
Knockdown of the antisense noncoding mitochondrial RNAs (ASncmtRNAs) induces apoptotic death of several human tumor cell lines, but not normal cells, supporting a selective therapy against different types of cancer. In this work, we evaluated the effects of knockdown of ASncmtRNAs on bladder cancer (BCa). We transfected the BCa cell lines UMUC-3, RT4 and T24 with the specific antisense oligonucleotide Andes-1537S, targeted to the human ASncmtRNAs. Knockdown induced a strong inhibition of cell proliferation and increase in cell death in all three cell lines. As observed in UMUC-3 cells, the treatment triggered apoptosis, evidenced by loss of mitochondrial membrane potential and Annexin V staining, along with activation of procaspase-3 and downregulation of the anti-apoptotic factors survivin and Bcl-xL. Treatment also inhibited cell invasion and spheroid formation together with inhibition of N-cadherin and MMP 11. In vivo treatment of subcutaneous xenograft UMUC-3 tumors in NOD/SCID mice with Andes-1537S induced inhibition of tumor growth as compared to saline control. Similarly, treatment of a high-grade bladder cancer PDX with Andes-1537S resulted in a strong inhibition of tumor growth. Our results suggest that ASncmtRNAs could be potent targets for bladder cancer as adjuvant therapy.
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Comisión Nacional de Investigación Científica y Tecnológica (CONICYT) Fondecyt-1140345 Fondef-D04I1338 Basal AFB 170004
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Journal of Cancer 2020, Vol. 11
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