miR-221/222: promising biomarkers for breast cancer

被引:111
|
作者
Chen, Wei-Xian [1 ,3 ]
Hu, Qing [2 ,3 ]
Qiu, Man-Tang [1 ]
Zhong, Shan-Liang [4 ]
Xu, Jin-Jin [4 ]
Tang, Jin-Hai [3 ]
Zhao, Jian-Hua [4 ]
机构
[1] Nanjing Med Univ, Clin Coll 4, Nanjing, Jiangsu, Peoples R China
[2] Xuzhou Med Coll, Grad Sch, Xuzhou, Peoples R China
[3] Nanjing Med Univ, Canc Hosp, Canc Inst Jiangsu Prov, Dept Gen Surg, Nanjing, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Canc Hosp, Canc Inst Jiangsu Prov, Ctr Clin Lab, Nanjing, Jiangsu, Peoples R China
关键词
MicroRNA; miR-221; miR-222; miR-221/222; Breast cancer; ESTROGEN-RECEPTOR-ALPHA; EPITHELIAL-MESENCHYMAL TRANSITIONS; TAMOXIFEN RESISTANCE; MICRORNA EXPRESSION; TELOMERE MAINTENANCE; ER-ALPHA; TARGET; CARCINOMA; PROTEIN; CELLS;
D O I
10.1007/s13277-013-0750-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are small noncoding RNAs of 19-25 nt that can regulate gene expression at a posttranscriptional level. Increasing evidence indicates that miRNAs participate in almost every step of cellular processes and are often aberrantly expressed in human cancer. miR-221 and miR-222 are two highly homologous miRNAs that always act as a gene cluster (miR-221/222) in cellular regulation and have extensively been studied in cancer network. Here, we review the role of miR-221/222 in breast cancer (BCa) development and progression: regulating proliferative signaling pathways, altering telomere and telomerase activity, avoiding cell death from tumor suppressors, autophagy and apoptosis, monitoring angiogenesis, supporting epithelial-mesenchymal transition, and even controlling cell-specific function within microenvironment. We consider that miR-221/222 act as promising biomarkers for BCa and they would offer a new way in molecular targeting cancer treatment.
引用
收藏
页码:1361 / 1370
页数:10
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