Long Non-Coding RNAs, Cell Cycle, and Human Breast Cancer

The long non-coding RNAs (lncRNAs) constitute an important class of the human transcriptome. The discovery of lncRNAs provided one of many unexpected results of the post-genomic era and uncovered a huge number of previously ignored transcriptional events. In recent years, lncRNAs are known to be linked with human diseases, with particular focus on cancer. Growing evidence has indicated that dysregulation of lncRNAs in breast cancer (BC) is strongly associated with the occurrence, development, and progress. Increasing numbers of lncRNAs have been found to interact with cell cycle progression and tumorigenesis in BC. The lncRNAs can exert their effect as a tumor suppressor or oncogene and regulate tumor development through direct or indirect regulation of cancer-related modulators and signaling pathways. What is more, lncRNAs are excellent candidates for promising therapeutic targets in BC due to the features of high tissue and cell-type specific expression. However, the underlying mechanisms of lncRNAs in BC still remain largely undefined. Here, we concisely summarize and sort out the current understanding of research progress in relationships of the roles for lncRNA in regulating the cell cycle. We also summarize the evidence for aberrant lncRNA expression in BC, and the potential for lncRNA to improve BC therapy is also discussed. Together, lncRNAs can be considered as exciting therapeutic candidates whose expression can be altered to impede BC progression.

Automated summary

Long non-coding RNAs (lncRNAs) are an important category of the human transcriptome that were unexpectedly discovered in the post-genomic era, revealing previously ignored transcriptional events. They have been found to be strongly associated with the occurrence, development, and progress of breast cancer (BC), acting as tumor suppressors or oncogenes through regulation of cancer-related modulators and signaling pathways. Additionally, lncRNAs show high tissue and cell-type specific expression, making them potential therapeutic targets for BC treatment. However, the exact mechanisms of lncRNAs in BC remain largely undefined.