Institute for Chemical Carcinogenesis, State Key Laboratory of Respiratory Disease, Guangzhou Medical University, 195 Dongfengxi Road, Guangzhou 510182, People's Republic of China.
Carcinogenesis. 2012 Jan;33(1):131-9. doi: 10.1093/carcin/bgr226. Epub 2011 Oct 19.
Aberrant expression of microRNA (miRNA) has been previously demonstrated to play an important role in a wide range of cancer types and further elucidation of its role in the mechanisms underlying tumorigenesis, anticarcinogenesis and potential chemotherapeutics is warranted. We chose the anti-benzo[a]pyrene-7,8-diol-9,10-epoxide-transformed human bronchial epithelial cell line 16HBE-T to study miRNAs involved in anticarcinogenesis. In resveratrol-treated cells, we found that miR-622 was upregulated, whereas it was downregulated in 16HBE-T cells, suggesting that miR-622 potentially acts as a tumor suppressor. Increasing the level of miR-622 by transient transfection-induced inhibition of proliferation and G(0) arrest in 16HBE-T cells and the lung cancer cell line H460 as demonstrated by cell viability and cell cycle analysis. MiR-622 dramatically suppressed the ability of 16HBE-T cells to form colonies in vitro and to develop tumors in nude mice. According to bioinformatics analysis, K-Ras messenger RNA was predicted as a putative miR-622 target; this was confirmed by western blot and luciferase reporter assays. Cell growth retardation was inhibited upon knockdown of K-Ras and an increase in the level of miR-622 in 16HBE-T cells. Furthermore, miR-622 inhibitor partially impaired the growth of 16HBE-T cells as demonstrated by luciferase reporter activity and K-Ras protein expression in 16HBE-T cells. In summary, miR-622 functions as a tumor suppressor by targeting K-Ras and impacting the anticancer effect of resveratrol. Therefore, miR-622 is potentially useful as a clinical therapy. MiR-622 impacts the K-Ras signal pathway and the potentially anticarcinogenic or chemotherapeutic properties warrant further investigation.
异常表达的 microRNA(miRNA)已被证明在多种癌症类型中发挥重要作用,进一步阐明其在肿瘤发生、抗癌和潜在化疗机制中的作用是必要的。我们选择抗苯并[a]芘-7,8-二醇-9,10-环氧化物转化的人支气管上皮细胞系 16HBE-T 来研究参与抗癌作用的 miRNAs。在白藜芦醇处理的细胞中,我们发现 miR-622 上调,而在 16HBE-T 细胞中下调,表明 miR-622 可能作为肿瘤抑制因子发挥作用。通过瞬时转染抑制细胞增殖和 G0 期阻滞,增加 16HBE-T 细胞和肺癌细胞系 H460 中的 miR-622 水平,如细胞活力和细胞周期分析所示。miR-622 显著抑制 16HBE-T 细胞在体外形成集落和在裸鼠中形成肿瘤的能力。根据生物信息学分析,K-Ras 信使 RNA 被预测为 miR-622 的潜在靶标;这通过 Western blot 和荧光素酶报告基因检测得到证实。在 16HBE-T 细胞中敲低 K-Ras 和增加 miR-622 水平会抑制细胞生长。此外,miR-622 抑制剂部分削弱了 16HBE-T 细胞的生长,如荧光素酶报告基因活性和 16HBE-T 细胞中 K-Ras 蛋白表达所示。总之,miR-622 通过靶向 K-Ras 发挥肿瘤抑制作用,并影响白藜芦醇的抗癌作用。因此,miR-622 作为一种潜在的临床治疗方法具有一定的应用价值。miR-622 影响 K-Ras 信号通路,其潜在的抗癌或化疗特性值得进一步研究。