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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

机译:靶向反义线粒体非编码RNA诱导膀胱癌细胞死亡,通过降低存活和侵袭因子来抑制肿瘤生长

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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.? The author(s).
机译:反义非沉积线粒体RNA(ASNCMTRNA)的敲低诱导几种人肿瘤细胞系的凋亡死亡,但不是正常细胞,支持针对不同类型的癌症的选择性治疗。在这项工作中,我们评估了Asnctnas敲低对膀胱癌(BCA)的影响。我们将BCA细胞系UMUC-3,RT4和T24与靶向人Asnctnas的特异性反义寡核苷酸和1537s转染。敲低诱导对所有三种细胞系中细胞增殖的强烈抑制和细胞死亡增加。如在UMUC-3细胞中所观察到的,治疗触发凋亡,通过损失线粒体膜电位和膜蛋白V染色证明,以及促进酶-3的激活和抗凋亡因子Survivin和Bcl-XL的下调。治疗还抑制了细胞侵袭和球形形成,抑制N-Cadherin和MMP 11.在NOD / SCID小鼠中,与盐水对照诱导肿瘤生长抑制肿瘤生长中皮下异叶癌肿瘤的体内治疗。类似地,使用Andes-1537S的高级膀胱癌PDX的处理导致肿瘤生长的强烈抑制。我们的研究结果表明,Asncmtrnas可能是膀胱癌作为辅助治疗的有效目标。作者。
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