Targeting antisense mitochondrial noncoding RNAs induces bladder cancer cell death and inhibition of tumor growth through reduction of survival and invasion factors

被引:16
作者
Borgna, Vincenzo [1 ,2 ,3 ]
Lobos-Gonzalez, Lorena [4 ]
Guevara, Francisca [1 ,5 ]
Landerer, Eduardo [6 ]
Bendek, Maximiliano [1 ]
Avila, Rodolfo [1 ]
Silva, Veronica [1 ]
Villota, Claudio [7 ]
Araya, Mariela [1 ,8 ]
Rivas, Alexis [1 ]
Lopez, Constanza [1 ]
Socias, Teresa [1 ]
Castillo, Jorge [9 ]
Alarcon, Luis [3 ]
Burzio, Luis O. [1 ,5 ,8 ]
Burzio, Veronica A. [1 ,5 ,8 ]
Villegas, Jaime [1 ,5 ,8 ,10 ]
机构
[1] Fdn Ciencia & Vida, Santiago, Chile
[2] Univ Santiago, Fac Med, Santiago, Chile
[3] Hosp Barros Luco, Serv Urol, Santiago, Chile
[4] Univ Desarrollo, Fac Med, Clin Alemana, Ctr Med Regenerat, Concepcion, Chile
[5] Andes Biotechnol SpA, Santiago, Chile
[6] Univ San Sebastian, Fac Med, Concepcion, Chile
[7] Univ Bernardo OHiggins, Fac Salud, Escuela Nutr & Dietet, Santiago, Chile
[8] Univ Andres Bello, Fac Ciencias Vida, Santiago, Chile
[9] Hosp Barros Luco, Serv Anat Patol, Santiago, Chile
[10] Univ Andres Bello, Ctr Med Vet, Camino Lo Pinto S-N, Santiago, Chile
来源
JOURNAL OF CANCER | 2020年 / 11卷 / 07期
关键词
bladder cancer; antisense therapy; noncoding RNA; apoptosis; MESENCHYMAL TRANSITION; XENOGRAFT MODEL; EXPRESSION; APOPTOSIS; BETA; PROSTATE; CADHERIN; NCRNAS; SWITCH;
D O I
10.7150/jca.38880
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:1780 / 1791
页数:12
相关论文
共 51 条
[1]   Survivin - The inconvenient IAP [J].
Altieri, Dario C. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2015, 39 :91-96
[2]   EMT: 2016 [J].
Angela Nieto, M. ;
Huang, Ruby Yun-Ju ;
Jackson, Rebecca A. ;
Thiery, Jean Paul .
CELL, 2016, 166 (01) :21-45
[3]  
[Anonymous], J CLIN ONCOL S
[4]   E/N-cadherin switch mediates cancer progression via TGF-β-induced epithelial-to-mesenchymal transition in extrahepatic cholangiocarcinoma [J].
Araki, K. ;
Shimura, T. ;
Suzuki, H. ;
Tsutsumi, S. ;
Wada, W. ;
Yajima, T. ;
Kobayahi, T. ;
Kubo, N. ;
Kuwano, H. .
BRITISH JOURNAL OF CANCER, 2011, 105 (12) :1885-1893
[5]   Sleeping beauty: awakening urothelium from its slumber [J].
Balsara, Zarine R. ;
Li, Xue .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2017, 312 (04) :F732-F743
[6]   Mitochondrial ASncmtRNA-1 and ASncmtRNA-2 as potent targets to inhibit tumor growth and metastasis in the RenCa murine renal adenocarcinoma model [J].
Borgna, Vincenzo ;
Villegas, Jaime ;
Burzio, Veronica A. ;
Belmar, Sebastian ;
Araya, Mariela ;
Jeldes, Emanuel ;
Lobos-Gonzalez, Lorena ;
Silva, Veronica ;
Villota, Claudio ;
Oliveira-Cruz, Luciana ;
Lopez, Constanza ;
Socias, Teresa ;
Castillo, Octavio ;
Burzio, Luis O. .
ONCOTARGET, 2017, 8 (27) :43692-43708
[7]   Mutant p53 gain of function: reduction of tumor malignancy of human cancer cell lines through abrogation of mutant p53 expression [J].
Bossi, G ;
Lapi, E ;
Strano, S ;
Rinaldo, C ;
Blandino, G ;
Sacchi, A .
ONCOGENE, 2006, 25 (02) :304-309
[8]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[9]   Expression of a family of noncoding mitochondrial RNAs distinguishes normal from cancer cells [J].
Burzio, Veronica A. ;
Villota, Claudio ;
Villegas, Jaime ;
Landerer, Eduardo ;
Boccardo, Enrique ;
Villa, Luisa L. ;
Martinez, Ronny ;
Lopez, Constanza ;
Gaete, Fancy ;
Toro, Viviana ;
Rodriguez, Ximena ;
Burzio, Luis O. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (23) :9430-9434
[10]   An Integrative Approach to Precision Cancer Medicine Using Patient-Derived Xenografts [J].
Cho, Sung-Yup ;
Kang, Wonyoung ;
Han, Jee Yun ;
Min, Seoyeon ;
Kang, Jinjoo ;
Lee, Ahra ;
Kwon, Jee Young ;
Lee, Charles ;
Park, Hansoo .
MOLECULES AND CELLS, 2016, 39 (02) :77-86