Gifu University, Yanagido, Japan.
Cancer Lett. 2011 Jan 28;300(2):197-204. doi: 10.1016/j.canlet.2010.10.006. Epub 2010 Nov 9.
MiR-34a was identified as one of the down-regulated micro-RNAs (miRs) in human colorectal cancer 5-fluorouracil (5-FU)-resistant DLD-1 cells compared with those in the parental DLD-1 cells. Exposure to 5-FU at 30 μM activated phosphoinositide 3-kinase (PI3K)/Akt signaling markedly from 12h up to 48 h in the 5-FU-resistant cells compared with that in the parental cells and resulted in an overt difference in growth at those times. Furthermore, the expression of miR-34a in the 5-FU-resistant cells was sustained at a low-level, whereas it was up-regulated in the parental cells after the 5-FU treatment. Sirt1, which is one of the target genes for miR-34a and related to drug-resistance, was strikingly up-regulated in the 5-FU-resistant cells. The ectopic expression of miR-34a in the 5-FU-resistant cells inhibited growth, as in the parental cells, and attenuated the resistance to 5-FU through the down-regulation of Sirt1 and E2F3. Moreover, the silencing of Sirt1 significantly canceled the resistance to 5-FU in the 5-FU-resistant cells. These findings suggest that miR-34a targeting the Sirt1 and E2F3 genes could negatively regulate, at least in part, the resistance to 5-FU in human colorectal cancer DLD-1 cells.
miR-34a 被鉴定为人类结直肠癌细胞 5-氟尿嘧啶(5-FU)耐药株 DLD-1 细胞中下调的 micro-RNAs(miRs)之一,与亲本 DLD-1 细胞相比。与亲本细胞相比,在 5-FU 耐药细胞中,30 μM 的 5-FU 在 12 小时至 48 小时内显著激活磷酸肌醇 3-激酶(PI3K)/Akt 信号通路,导致在这些时间点生长出现明显差异。此外,miR-34a 在耐药细胞中的表达保持在低水平,而在 5-FU 处理后亲本细胞中的表达上调。Sirt1 是 miR-34a 的靶基因之一,与耐药性有关,在 5-FU 耐药细胞中显著上调。在 5-FU 耐药细胞中过表达 miR-34a 抑制生长,如同在亲本细胞中一样,通过下调 Sirt1 和 E2F3 减弱对 5-FU 的耐药性。此外,Sirt1 的沉默显著取消了 5-FU 耐药细胞对 5-FU 的耐药性。这些发现表明,miR-34a 靶向 Sirt1 和 E2F3 基因至少部分负调控人结直肠癌细胞 DLD-1 对 5-FU 的耐药性。