Wang Mingxi, Zhang Qiang, Wang Junbin, Zhai Yunzhi
Department of Oncology, The First Affiliated Hospital of Bengbu Medical College, Anhui Province, China.
J Cancer Res Ther. 2015 Aug;11 Suppl 1:C107-11. doi: 10.4103/0973-1482.163859.
Non-small cell lung cancer (NSCLC) is the most common type of human lung cancer, with highly aggressive, lethal malignancy and microRNAs have already been proven to be associated with NSCLC tumorigenesis. In this study, we sought to determine the expression, the clinical value and its role in NSCLC tumor progression.
Clinical NSCLC tissues and common cell lines were collected. Real-time PCR was performed to quantify the miR-498 expression. In addition, the association of miR-498 expression with clinical pathological factors and prognosis was statistically analyzed. Furthermore, cell proliferation was measured after miR-498 was overexpressed transiently in cells.
We found that miR-498 was significantly decreased in NSCLC tumors as well as cell lines, when compared with their separated controls. Decreased miR-498 expression was associated with sex, tumor type and tumor size. Functionally, ectopic expression of miR-498 in A549 and H661 cells inhibited cell proliferation.
Our data indicated that miR-498 is downregulated and correlated with tumor progression, which might be a putitive therapeutic target in NSCLC treatment.
非小细胞肺癌(NSCLC)是人类肺癌最常见的类型,具有高度侵袭性、致死性恶性特征,且微小RNA已被证实与NSCLC的肿瘤发生有关。在本研究中,我们试图确定miR-498在NSCLC中的表达、临床价值及其在肿瘤进展中的作用。
收集临床NSCLC组织和常见细胞系。采用实时定量PCR检测miR-498的表达。此外,对miR-498表达与临床病理因素及预后的相关性进行统计学分析。进一步地,在细胞中瞬时过表达miR-498后检测细胞增殖情况。
我们发现,与各自的对照相比,miR-498在NSCLC肿瘤组织及细胞系中显著降低。miR-498表达降低与性别、肿瘤类型和肿瘤大小有关。在功能上,miR-498在A549和H661细胞中的异位表达抑制了细胞增殖。
我们的数据表明,miR-498表达下调且与肿瘤进展相关,这可能是NSCLC治疗中一个潜在的治疗靶点。