- Author:
Ju Young PARK
1
;
Jeong Eun LEE
;
Jong Bae PARK
;
Heon YOO
;
Seung Hoon LEE
;
Jong Heon KIM
Author Information
- Publication Type:Review
- Keywords: Non-coding RNA; lncRNA; Tumorigenesis; Glioma
- MeSH: Adenocarcinoma; Carcinogenesis*; Gene Expression; Genes, Homeobox; Glioma*; Homeostasis; Humans; Lung; Prostatic Neoplasms; RNA; RNA, Long Noncoding*; RNA, Untranslated; Transcutaneous Electric Nerve Stimulation
- From:Brain Tumor Research and Treatment 2014;2(1):1-6
- CountryRepublic of Korea
- Language:English
- Abstract: More than 98% of eukaryotic transcriptomes are composed of non-coding RNAs with no functional protein-coding capacity. Those transcripts also include tens of thousands of long non-coding RNAs (lncRNAs) which are emerging as key elements of cellular homeostasis, essentially tumorigenesis steps. However, we are only beginning to understand the nature and extent of the involvement of lncRNAs on tumorigeneis. Here, we highlight recent progresses that have identified a myriad of molecular functions on tumorigenesis for several lncRNAs including metastasis-associated lung adenocarcinoma transcript 1 (MALAT1), prostate cancer associated non-coding RNA 1 (PRNCR1), prostate cancer gene expression marker 1 (PCGEM1), H19, and homeobox transcript antisense intergenic RNA (HOTAIR), and several new lncRNAs for glioma development. Potential therapeutic approaches for the lncRNAs in various human diseases are also discussed.