Department of General Surgery, The First Affiliated Hospital of Nanjing University of Traditional Chinese Medicine, Nanjing, China.
J Surg Oncol. 2012 Sep 1;106(3):260-6. doi: 10.1002/jso.22153. Epub 2011 Nov 21.
The aim of this study is to investigate clinical significance of miR-155 expression in breast cancer.
TaqMan real-time RT-PCR was performed to detect miR-155 expression in breast cancer tissues. The correlation of miR-155 expression with clinicopathological factors and prognosis of breast cancer patients was analyzed. Then, the prognostic value of miR-155 expression was analyzed by univariate and multivariate analyses. Moreover, the effect of miR-155 expression on phenotypes of breast cancer cell was determined by antisense technology.
The relative expression of miR-155 was significantly higher in breast cancer tissues than in corresponding nontumor tissues. High miR-155 expression was correlated with higher tumor grade, advanced tumor stage and lymph node metastasis (P = 0.012, 0.001, and 0.003, respectively). Kaplan-Meier survival analysis indicated that the disease-free and overall survival rates of high miR-155 group were significantly lower than those of low miR-155 group (P = 0.038 and 0.029, respectively). Multivariate analysis showed that high miR-155 expression was a poor prognostic factor (P = 0.009). Furthermore, antisense targeting miR-155 could inhibit growth, induce cell arrest in G(0) /G(1) phase, enhance apoptosis, and increase radiosensitivity in breast cancer cells.
MiR-155 expression might be an independent prognostic factor and a therapeutic target for human breast cancer.
本研究旨在探讨 miR-155 在乳腺癌中的表达的临床意义。
采用 TaqMan 实时 RT-PCR 检测乳腺癌组织中 miR-155 的表达。分析 miR-155 表达与乳腺癌患者临床病理因素及预后的相关性。然后,通过单因素和多因素分析评估 miR-155 表达的预后价值。此外,通过反义技术确定 miR-155 表达对乳腺癌细胞表型的影响。
miR-155 的相对表达在乳腺癌组织中明显高于相应的非肿瘤组织。高 miR-155 表达与肿瘤分级高、肿瘤分期晚和淋巴结转移有关(P=0.012、0.001 和 0.003)。Kaplan-Meier 生存分析表明,高 miR-155 组的无病生存率和总生存率明显低于低 miR-155 组(P=0.038 和 0.029)。多因素分析表明,高 miR-155 表达是预后不良的因素(P=0.009)。此外,反义靶向 miR-155 可抑制乳腺癌细胞的生长,诱导细胞停滞在 G0/G1 期,增强细胞凋亡,增加细胞对放射的敏感性。
miR-155 的表达可能是人类乳腺癌的一个独立的预后因素和治疗靶点。