Sevinc Elif Demirdogen, Cecener Gulsah, Ak Secil, Tunca Berrin, Egeli Unal, Gokgoz Sehsuvar, Tolunay Sahsine, Tasdelen Ismet
Department of Medical Biology, Faculty of Medicine, University of Uludag, Bursa, Turkey.
Department of Medical Biology, Faculty of Medicine, University of Uludag, Bursa, Turkey.
Gene. 2016 Sep 30;590(2):278-84. doi: 10.1016/j.gene.2016.05.033. Epub 2016 May 25.
The dysregulation of miRNA expression has frequently been observed in breast cancer. Therefore, we investigated the expression profile of miRNAs that may be associated with expression of the FHIT gene in breast cancer and assessed their clinicopathological significance. The expression levels of miR-143, miR-663a, miR-668, miR-922 and FHIT were analyzed in normal and malignant breast tissues from 65 patients with breast cancer. We studied the correlation between the expression of miR-143, miR-663a, miR-668, miR-922 and FHIT and the clinicopathological features presented by the patients. The expression levels of the miRNAs and FHIT were downregulated in breast cancer tissue. The expression levels of miR-143, miR-663a and miR-668 were significantly reduced in FHIT downregulated tumors. miR-668 expression was also significantly altered relative to FHIT down- and up- regulated tumor tissues. Reduced miR-663a expression was statistically associated with high-grade ER/PR (+) status, benign reactive hyperplasia, lymph-node metastasis, in-situ component >25% and Ki 67>15% compared with non-tumor tissues. Additionally, reduced miR-668 expression was significantly different between tumors with and without lymph-node metastasis. miR-668 may play an important role in breast cancer development and progression by regulating the expression of FHIT. Furthermore, miR-668 and miR-663a may be potential prognostic biomarkers for breast cancer.
在乳腺癌中经常观察到miRNA表达失调。因此,我们研究了可能与乳腺癌中FHIT基因表达相关的miRNA表达谱,并评估了它们的临床病理意义。分析了65例乳腺癌患者正常和恶性乳腺组织中miR-143、miR-663a、miR-668、miR-922和FHIT的表达水平。我们研究了miR-143、miR-663a、miR-668、miR-922和FHIT的表达与患者临床病理特征之间的相关性。miRNA和FHIT的表达水平在乳腺癌组织中下调。在FHIT下调的肿瘤中,miR-143、miR-663a和miR-668的表达水平显著降低。相对于FHIT下调和上调的肿瘤组织,miR-668的表达也有显著改变。与非肿瘤组织相比,miR-663a表达降低与高级别ER/PR(+)状态、良性反应性增生、淋巴结转移、原位成分>25%和Ki 67>15%在统计学上相关。此外,有淋巴结转移和无淋巴结转移的肿瘤之间miR-668表达降低有显著差异。miR-668可能通过调节FHIT的表达在乳腺癌的发生和发展中发挥重要作用。此外,miR-668和miR-663a可能是乳腺癌潜在的预后生物标志物。