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Aberrant Expression Profile of Long Noncoding RNA in Human Sinonasal Squamous Cell Carcinoma by Microarray Analysis
Ling-Zhao Meng1, Ju-Gao Fang2, Jing-Wu Sun1
1Department of Otolaryngology-Head and Neck Surgery, Beijing Anzhen Hospital, Capital Medical University, Beijing 100029, China.
Biomed Research International
|January 4, 2017
Summary
This study identified novel long noncoding RNAs (lncRNAs) in sinonasal squamous cell carcinoma (SSCC), offering new insights into cancer development and potential therapeutic targets.
Area of Science:
- Oncology
- Genomics
- Molecular Biology
Background:
- Sinonasal squamous cell carcinoma (SSCC) is a rare malignancy.
- The molecular mechanisms underlying SSCC development are not fully understood.
- Long noncoding RNAs (lncRNAs) are increasingly recognized for their roles in cancer.
Purpose of the Study:
- To identify aberrantly expressed lncRNAs in SSCC.
- To explore the potential functions of these lncRNAs in SSCC pathogenesis.
- To establish a foundation for understanding SSCC molecular mechanisms.
Main Methods:
- Microarray analysis of lncRNA and mRNA expression in SSCC tissues and adjacent noncancerous tissues from 6 patients.
- Gene Ontology (GO) and pathway analysis to determine gene functions.
- Quantitative real-time polymerase chain reaction (qRT-PCR) to validate key lncRNAs in 22 additional patients.
Main Results:
- Identification of 3146 differentially expressed lncRNAs and 2208 differentially expressed mRNAs in SSCC.
- GO and pathway analyses revealed SSCC-associated biological processes and cancer pathways.
- lncRNA-mRNA and gene signal networks highlighted potential key molecules in SSCC pathogenesis.
- qRT-PCR validated the differential expression of 5 selected lncRNAs.
Conclusions:
- This is the first study to screen and analyze the lncRNA expression profile in SSCC.
- The identified lncRNAs may play crucial roles in SSCC development.
- Findings provide novel insights into SSCC pathogenesis and potential diagnostic/therapeutic targets.
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In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA (lncRNA)...
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MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...

