Abnormal miRNA-30e Expression is Associated with Breast Cancer Progression

被引:28
|
作者
Lin, Ziying [1 ]
Li, Jian-Wen [2 ]
Wang, Yahong [1 ]
Chen, Ting [1 ]
Ren, Nina [1 ]
Yang, Lawei [1 ]
Xu, Wenya [1 ]
He, Huijuan [1 ]
Jiang, Yun [1 ]
Chen, Xiaodong [2 ]
Liu, Tie [3 ]
Liu, Gang [1 ]
机构
[1] Guangdong Med Univ, Clin Res Ctr, Zhanjiang 524001, Guangdong, Peoples R China
[2] Guangdong Med Univ, Dept Vasc Thyroid & Breast Surg, Affiliated Hosp, Zhanjiang 524001, Guangdong, Peoples R China
[3] Xi An Jiao Tong Univ, Sch Med, Immunol & Tumor Res Inst, Affiliated Hosp 1, Xian 710061, Shanxi, Peoples R China
关键词
miRNA; Breast cancer; RT-PCR; miR-30e; CIRCULATING MICRORNAS; SELF-RENEWAL; SIGNATURES; GROWTH; PLASMA; BIOMARKERS; MARKERS;
D O I
10.7754/Clin.Lab.2015.150607
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: microRNAs (miRNAs) are involved in the regulation of various cellular processes, such as differentiation, proliferation, metabolism, and apoptosis, and they have been implicated in several diseases, including cancers. Methods: To assess the role of miRNA in the progression of breast cancer, we performed TaqMan-based miRNA profiling for plasma from patients with breast cancer (n = 53), unrelated diseases (n = 40), or matched healthy controls (n = 40), and for breast tumors or adjacent non-tumors (n = 41). Results: We selected 18 miRNAs with predicted roles in breast cancer and demonstrated that let-7i (p = 0.019), let 7a (p = 0.02), and miR-650 (p = 0.008) were significantly up-regulated in plasma; miR-21 (p < 0.001) is up-regulated in breast cancer tissue, and miR-30e was down-regulated in both plasma (p < 0.001) and breast cancer tissues (p = 0.004). Plasma miR-30e expression was shown to be statistically associated with age (p = 0.0402) and clinical stage (p = 0.007). However, receiver-operating characteristic curve analyses suggested that miR-30e expression cannot significantly differentiate breast cancer from healthy tissue or plasma. Consistent with a potential role for miR-30e in breast cancer, three predicted targets of miR-30e (RAB11A, BNIP3L, and RAB32) are up-regulated in breast cancer tissue. Conclusions: These findings suggest that reduced miR-30e correlates with the clinical stage of breast cancer. It is worthwhile to further explore that the potential role of miR-30e as a tumor suppressor in breast cancer, as well as its potential therapeutic utility.
引用
收藏
页码:121 / 128
页数:8
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