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Long noncoding RNAs in regulation of human breast cancer: Table 1
Author(s) -
Guangxue Wang,
Cuicui Liu,
Shengqiong Deng,
Qian Zhao,
Tieyan Li,
Shanshan Qiao,
Lei Shen,
Yue Zhang,
Jinhui Lü,
Lingyu Meng,
Chunli Liang,
Zuoren Yu
Publication year - 2015
Publication title -
briefings in functional genomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.22
H-Index - 67
eISSN - 2041-2647
pISSN - 2041-2649
DOI - 10.1093/bfgp/elv049
Subject(s) - biology , long non coding rna , breast cancer , human genome , gene , rna , genome , cancer , computational biology , genetics , suppressor , regulation of gene expression , non coding rna , microrna , function (biology)
Less than 2% of the human genome DNA is composed of protein-coding genes, although the majority of the human genome is transcribed, indicating the transcripts mostly are noncoding RNAs. Those noncoding RNAs with length between 200 nt and 200 kb are categorized as long noncoding RNA (lncRNA). Around 30 000 lncRNAs have been predicted or identified, although little is known regarding the regulatory function for a vast majority of these sequences. Emerging evidence demonstrated that lncRNAs play crucial roles in regulation of many cancer types, including breast cancer, serving as oncogenes or tumor suppressors. Aberrant and differential expression of lncRNA in breast cancer has been frequently reported. Their regulation of breast cancer is still the beginning to be elucidated. This review collected those experimentally validated lncRNAs in human breast cancer, summarizing their biological function as well as the regulatory mechanism. In addition, the potential of lncRNAs as biomarkers for better diagnosis or therapeutic targets for cancer treatment was discussed.

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