MicroRNA-493 is a prognostic factor in triple-negative breast cancer

被引:26
作者
Yao, Ling [1 ]
Liu, Yirong [1 ]
Cao, Zhigang [1 ]
Li, Junjing [2 ]
Huang, Yanni [1 ]
Hu, Xin [1 ]
Shao, Zhiming [1 ]
机构
[1] Fudan Univ, Shanghai Canc Ctr, Dept Breast Surg, Key Lab Breast Canc Shanghai, Shanghai, Peoples R China
[2] Fujian Med Univ, Dept Breast Surg, Affiliated Union Hosp, Fuzhou, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
breast cancer; DFS; microRNA; 493; prognostic factor; triple-negative; TRANSCRIPTOME ANALYSIS; CELL MOTILITY; STATISTICS; EXPRESSION; REVEALS; METASTASIS; SIGNATURE; SURVIVAL; MIR-27A; GROWTH;
D O I
10.1111/cas.13644
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer is one of the most common malignant diseases in women. Triple-negative breast cancer (TNBC) shows higher aggressiveness and recurrence rates than other subtypes, and there are no effective targets or tailored treatments for TNBC patients. Thus, finding effective prognostic markers for TNBC could help clinicians in their ability to care for their patients. We used tissue microarrays (TMAs) to detect microRNA-493 (miR-493) expression in breast cancer samples. A miRCURY LNA detection probe specific for miR-493 was used in insitu hybridization assays. Staining results were reviewed by two independent pathologists and classified as high or low expression of miR-493. Kaplan-Meier survival plots and multivariate Cox analysis were carried out to clarify the relationship between miR-493 and survival. In the Kaplan-Meier analysis, patients with high miR-493 expression had better disease-free survival than patients with low miR-493 expression. After adjusting for common clinicopathological factors in breast cancer, the expression level of miR-493 was still a significant prognostic factor in breast cancer. Further subtype analysis revealed that miR-493 expression levels were only significantly prognostic in TNBC patients. These results were validated in the Molecular Taxonomy of Breast Cancer International Consortium database for overall survival. We proved the prognostic role of miR-493 in TNBC by using one of the largest breast cancer TMAs available and validated it in a large public RNA sequencing database.
引用
收藏
页码:2294 / 2301
页数:8
相关论文
共 42 条
[1]   High expression of microRNA-454 is associated with poor prognosis in triple-negative breast cancer [J].
Cao, Zhi-Gang ;
Li, Jun-Jing ;
Yao, Ling ;
Huang, Yan-Ni ;
Liu, Yi-Rong ;
Hu, Xin ;
Song, Chuan-Gui ;
Shao, Zhi-Ming .
ONCOTARGET, 2016, 7 (40) :64900-64909
[2]   Positive expression of miR-361-5p indicates better prognosis for breast cancer patients [J].
Cao, Zhi-Gang ;
Huang, Yan-Ni ;
Yao, Ling ;
Liu, Yi-Rong ;
Hu, Xin ;
Hou, Yi-Feng ;
Shao, Zhi-Min .
JOURNAL OF THORACIC DISEASE, 2016, 8 (07) :1772-1779
[3]   MicroRNA-205 signaling regulates mammary stem cell fate and tumorigenesis [J].
Chao, Chi-Hong ;
Chang, Chao-Ching ;
Wu, Meng-Ju ;
Ko, How-Wen ;
Wang, Da ;
Hung, Mien-Chie ;
Yang, Jer-Yen ;
Chang, Chun-Ju .
JOURNAL OF CLINICAL INVESTIGATION, 2014, 124 (07) :3093-3106
[4]   Tumor Grafting Induces Changes of Gut Microbiota in Athymic Nude Mice in the Presence and Absence of Medicinal Gynostemma Saponins [J].
Chen, Lei ;
Tai, William C. S. ;
Brar, Manreetpal S. ;
Leung, Frederick C. C. ;
Hsiao, W. L. Wendy .
PLOS ONE, 2015, 10 (05)
[5]   Downregulation of miR-493 promoted melanoma proliferation by suppressing IRS4 expression [J].
Cui, Aili ;
Jin, Zhehu ;
Gao, Zhonggao ;
Jin, Mingji ;
Zhu, Lianhua ;
Li, Lianhua ;
Jin, Chenglong ;
An, Yinghua .
TUMOR BIOLOGY, 2017, 39 (05)
[6]   The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups [J].
Curtis, Christina ;
Shah, Sohrab P. ;
Chin, Suet-Feung ;
Turashvili, Gulisa ;
Rueda, Oscar M. ;
Dunning, Mark J. ;
Speed, Doug ;
Lynch, Andy G. ;
Samarajiwa, Shamith ;
Yuan, Yinyin ;
Graef, Stefan ;
Ha, Gavin ;
Haffari, Gholamreza ;
Bashashati, Ali ;
Russell, Roslin ;
McKinney, Steven ;
Langerod, Anita ;
Green, Andrew ;
Provenzano, Elena ;
Wishart, Gordon ;
Pinder, Sarah ;
Watson, Peter ;
Markowetz, Florian ;
Murphy, Leigh ;
Ellis, Ian ;
Purushotham, Arnie ;
Borresen-Dale, Anne-Lise ;
Brenton, James D. ;
Tavare, Simon ;
Caldas, Carlos ;
Aparicio, Samuel .
NATURE, 2012, 486 (7403) :346-352
[7]  
de la Mare Jo-Anne, 2014, Recent Pat Anticancer Drug Discov, V9, P153
[8]   Breast Cancer Statistics, 2013 [J].
DeSantis, Carol ;
Ma, Jiemin ;
Bryan, Leah ;
Jemal, Ahmedin .
CA-A CANCER JOURNAL FOR CLINICIANS, 2014, 64 (01) :52-62
[9]   Breast cancer statistics, 2011 [J].
DeSantis, Carol ;
Siegel, Rebecca ;
Bandi, Priti ;
Jemal, Ahmedin .
CA-A CANCER JOURNAL FOR CLINICIANS, 2011, 61 (06) :409-418
[10]   Breast Cancer Statistics, 2015: Convergence of Incidence Rates Between Black and White Women [J].
DeSantis, Carol E. ;
Fedewa, Stacey A. ;
Sauer, Ann Goding ;
Kramer, Joan L. ;
Smith, Robert A. ;
Jemal, Ahmedin .
CA-A CANCER JOURNAL FOR CLINICIANS, 2016, 66 (01) :31-42