Lee Jeong-Won, Choi Chel Hun, Choi Jung-Joo, Park Young-Ae, Kim Seung-Jun, Hwang Seung Yong, Kim Woo Young, Kim Tae-Joong, Lee Je-Ho, Kim Byoung-Gie, Bae Duk-Soo
Department of Obstetrics and Gynecology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Clin Cancer Res. 2008 May 1;14(9):2535-42. doi: 10.1158/1078-0432.CCR-07-1231.
MicroRNAs (miRNA) are small noncoding RNAs that are 18 to 25 nucleotides in length; they regulate the stability or translational efficiency of target mRNAs. Emerging evidence suggests that miRNAs might be involved in the pathogenesis of a variety of human cancers.
In this study, we profiled miRNA expression in 10 early stage invasive squamous cell carcinomas (ISCC) and 10 normal cervical squamous epithelial specimens using TaqMan real-time quantitative PCR array methods. In order to evaluate the role of miR-199a, one of the most significantly overexpressed in ISCCs, we transfected cervical cancer cells (SiHa and ME-180) with anti-miR-199a oligonucleotides and assessed the cell viability.
We found 70 genes (68 up-regulated, 2 down-regulated) with significantly different expression in the ISCCs compared with normal samples (P < 0.05). When we analyzed the expression of the 10 most significant miRNAs in 31 ISCCs, increased miR-127 expression was significantly associated with lymph node metastasis (P = 0.006). Transfection of anti-miR-199a oligonucleotides to cervical cancer cells suppressed cell growth in vitro, which was potentiated with the anticancer agent cisplatin.
Our results show that miRNA deregulation may play an important role in the malignant transformation of cervical squamous cells. In addition, they may offer new candidate targets to be exploited for both prognostic and therapeutic strategies in patients with cervical cancer.
微小RNA(miRNA)是长度为18至25个核苷酸的小型非编码RNA;它们调节靶mRNA的稳定性或翻译效率。新出现的证据表明,miRNA可能参与多种人类癌症的发病机制。
在本研究中,我们使用TaqMan实时定量PCR阵列方法分析了10例早期浸润性鳞状细胞癌(ISCC)和10例正常宫颈鳞状上皮标本中的miRNA表达。为了评估ISCC中表达最显著上调的miR-199a的作用,我们用抗miR-199a寡核苷酸转染宫颈癌细胞(SiHa和ME-180)并评估细胞活力。
我们发现与正常样本相比,ISCC中有70个基因(68个上调,2个下调)表达存在显著差异(P < 0.05)。当我们分析31例ISCC中10个最显著的miRNA的表达时,miR-127表达增加与淋巴结转移显著相关(P = 0.006)。将抗miR-199a寡核苷酸转染到宫颈癌细胞中可抑制体外细胞生长,抗癌药物顺铂可增强这种抑制作用。
我们的结果表明,miRNA失调可能在宫颈鳞状细胞的恶性转化中起重要作用。此外,它们可能为宫颈癌患者的预后和治疗策略提供新的可利用候选靶点。