Neoplasma. 2017;64(6):847-855. doi: 10.4149/neo_2017_606.
Urinary bladder cancer (UBC) is one of the most common urogenital malignancies. Cancer stem-like cells (CSCs) play a vital role in tumor development and recurrence. Long noncoding RNAs (lncRNAs) are reported to influence cancer progression via transcriptional, posttranscriptional or epigenetic regulation. Dysregulation of several lncRNAs has been implicated in UBC. In our study, we found that an uncharacterized lncRNA, ASAP1-IT1, was overexpressed in UBC tissues compared with adjacent non-malignant tissues. High ASAP1-IT1 expression levels in UBC specimens were correlated with advanced tumor stage, higher clinical stage, poor pathological differentiation and bad overall survival. We further found that depletion of ASAP1-IT1 in T24 cells by RNA interference reduced the stemness of bladder cancer, whereas forced overexpression of ASAP1-IT1 in J82 cells enhanced cancer cell stemness by sphere assay, ALDEFLUOR and flow cytometry assay on CD44+ population. Our data suggest that ASAP1-IT1 plays an oncogenic role in bladder cancer and can be used as a potential prognostic and therapeutic target.
膀胱癌(UBC)是最常见的泌尿生殖系统恶性肿瘤之一。癌症干细胞样细胞(CSCs)在肿瘤的发展和复发中起着至关重要的作用。长链非编码 RNA(lncRNA)据报道通过转录、转录后或表观遗传调控影响癌症的进展。几种 lncRNA 的失调与 UBC 有关。在我们的研究中,我们发现一种未被描述的 lncRNA,ASAP1-IT1,在膀胱癌组织中的表达高于相邻的非恶性组织。UBC 标本中 ASAP1-IT1 的高表达水平与肿瘤晚期、较高的临床分期、较差的病理分化和较差的总生存期相关。我们进一步发现,RNA 干扰使 T24 细胞中的 ASAP1-IT1 耗竭,降低了膀胱癌的干细胞特性,而通过球体试验、ALDEFLUOR 和 CD44+群体的流式细胞术试验,强制过表达 J82 细胞中的 ASAP1-IT1 增强了癌细胞的干性。我们的数据表明,ASAP1-IT1 在膀胱癌中发挥致癌作用,可以作为潜在的预后和治疗靶点。