MiR-221/-222 differentiate prognostic groups in advanced breast cancers and influence cell invasion

被引:56
作者
Falkenberg, N. [1 ]
Anastasov, N. [2 ]
Rappl, K. [1 ]
Braselmann, H. [3 ]
Auer, G. [4 ]
Walch, A. [1 ,5 ]
Huber, M. [1 ]
Hoefig, I. [2 ]
Schmitt, M. [6 ,7 ]
Hoefler, H. [1 ,8 ]
Atkinson, M. J. [2 ]
Aubele, M. [1 ]
机构
[1] German Res Ctr Environm Hlth, Helmholtz Zentrum Munchen, Inst Pathol, D-85764 Neuherberg, Germany
[2] German Res Ctr Environm Hlth, Helmholtz Zentrum Munchen, Inst Radiat Biol, D-85764 Neuherberg, Germany
[3] German Res Ctr Environm Hlth, Helmholtz Zentrum Munchen, Res Unit Radiat Cytogenet, D-85764 Neuherberg, Germany
[4] Karolinska Hosp & Inst, Dept Pathol & Oncol, S-17176 Stockholm, Sweden
[5] German Res Ctr Environm Hlth, Helmholtz Zentrum Munchen, Res Unit Analyt Pathol, D-85764 Neuherberg, Germany
[6] Dept Obstet & Gynecol, Clin Res Unit, D-81675 Munich, Germany
[7] Tech Univ Munich, D-80290 Munich, Germany
[8] Tech Univ Munich, Inst Pathol, D-81675 Munich, Germany
关键词
therapy; prognosticator; prognosis; metastasis; malignancy; miR-221; miR-222; urokinase-type plasminogen activator system; uPAR; ESTROGEN-RECEPTOR-ALPHA; UROKINASE PLASMINOGEN-ACTIVATOR; TAMOXIFEN RESISTANCE; MESSENGER-RNA; EXPRESSION; MICRORNAS; METASTASIS; MIR-222; HER2; STABILIZATION;
D O I
10.1038/bjc.2013.625
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: MiR-221/-222 are frequently overexpressed in breast cancer and are associated with increased malignancy. The specific modification of microRNAs (miRNAs) expression could be a promising strategy in breast cancer therapy, leading to the suppression of tumourigenic processes in tumour cells. Methods: MiR-221/-222 expressions were analysed in 86 breast cancer tissues by quantitative RT-PCR and tested for correlation with immunohistochemistry data and clinical follow-up. In vitro assays were conducted using human breast cancer cell lines with lentiviral overexpression of miR-221/-222. Results: In tumour tissues, miR-221/-222 were associated with the occurrence of distant metastases. In particular, high levels of miR-221 were revealed to have a high prognostic impact for the identification of significantly different groups with advanced tumours. MiR-221/-222 overexpression strongly increased cell proliferation and invasion in vitro. Following miR-221/-222 overexpression an increased uPAR expression and cell invasion were observed. Conclusion: This study demonstrates a significant role for highly expressed miR-221/-222 in advanced breast cancers allowing for the identification of significantly different prognostic groups, particularly for HER2-positive and lymph-node-positive breast cancers. Considering that miR-221/-222 are strongly involved in cell invasion, these miRNAs may be promising markers for breast cancer prognosis and therapy.
引用
收藏
页码:2714 / 2723
页数:10
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