Decreased expression of key tumour suppressor microRNAs is associated with lymph node metastases in triple negative breast cancer

被引:79
作者
Avery-Kiejda, Kelly A. [1 ,2 ]
Braye, Stephen G. [3 ]
Mathe, Andrea [1 ,2 ]
Forbes, John F. [4 ,5 ]
Scott, Rodney J. [1 ,2 ,3 ]
机构
[1] Hunter Med Res Inst, Ctr Informat Based Med, New Lambton Heights, NSW 2305, Australia
[2] Univ Newcastle, Fac Hlth, Sch Biomed Sci & Pharm, Callaghan, NSW 2308, Australia
[3] John Hunter Hosp, Hunter Area Pathol Serv, New Lambton Heights, NSW 2305, Australia
[4] Calvary Mater Newcastle Hosp, Australian New Zealand Breast Canc Trials Grp, Dept Surg Oncol, Waratah, NSW 2298, Australia
[5] Univ Newcastle, Fac Hlth, Sch Med & Publ Hlth, Callaghan, NSW 2308, Australia
来源
BMC CANCER | 2014年 / 14卷
关键词
miRNA; Breast cancer; Triple negative; Metastases; Tumour suppressor; DOWN-REGULATION; MESENCHYMAL TRANSITION; MESSENGER-RNA; PATTERNS; TARGETS; CELLS; DICER; SIGNATURES; PROGNOSIS; PATHWAY;
D O I
10.1186/1471-2407-14-51
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Breast cancer is the most common malignancy that develops in women, responsible for the highest cancer-associated death rates. Triple negative breast cancers represent an important subtype that have an aggressive clinical phenotype, are associated with a higher likelihood of metastasis and are not responsive to current targeted therapies. miRNAs have emerged as an attractive candidate for molecular biomarkers and treatment targets in breast cancer, but their role in the progression of triple negative breast cancer remains largely unexplored. Methods: This study has investigated miRNA expression profiles in 31 primary triple negative breast cancer cases and in 13 matched lymph node metastases compared with 23 matched normal breast tissues to determine miRNAs associated with the initiation of this disease subtype and those associated with its metastasis. Results: 71 miRNAs were differentially expressed in triple negative breast cancer, the majority of which have previously been associated with breast cancer, including members of the miR-200 family and the miR-17-92 oncogenic cluster, suggesting that the majority of miRNAs involved in the initiation of triple negative breast cancer are not subtype specific. However, the repertoire of miRNAs expressed in lymph node negative and lymph node positive triple negative breast cancers were largely distinct from one another. In particular, miRNA profiles associated with lymph node negative disease tended to be up-regulated, while those associated with lymph node positive disease were down-regulated and largely overlapped with the profiles of their matched lymph node metastases. From this, 27 miRNAs were identified that are associated with metastatic capability in the triple negative breast cancer subtype. Conclusions: These results provide novel insight into the repertoire of miRNAs that contribute to the initiation of and progression to lymph node metastasis in triple negative breast cancer and have important implications for the treatment of this breast cancer subtype.
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页数:14
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