Detail

Description

Expression Detail
Experiment ID:
EXP00177
Reference:
  • Title: Keratinization-associated miR-7 and miR-21 regulate tumor suppressor reversion-inducing cysteine-rich protein with kazal motifs (RECK) in oral cancer.
  • Author: Jung HM, Phillips BL, Patel RS, Cohen DM, Jakymiw A, Kong WW, Cheng JQ, Chan EK
  • Journal: The Journal of biological chemistry.2012 Aug 24;287(35):29261-72.doi:10.1074/jbc.M112.366518.
  • Abstract: MicroRNAs (miRNAs) are small non-coding RNAs that posttranscriptionally regulate gene expression during many biological processes. Recently, the aberrant expressions of miRNAs have become a major focus in cancer research. The purpose of this study was to identify deregulated miRNAs in oral cancer and further focus on specific miRNAs that were related to patient survival. Here, we report that miRNA expression profiling provided more precise information when oral squamous cell carcinomas were subcategorized on the basis of clinicopathological parameters (tumor primary site, histological subtype, tumor stage, and HPV16 status). An innovative radar chart analysis method was developed to depict subcategories of cancers taking into consideration the expression patterns of multiple miRNAs combined with the clinicopathological parameters. Keratinization of tumors and the high expression of miR-21 were the major factors related to the poor prognosis of patients. Interestingly, a majority of the keratinized tumors expressed high levels of miR-21. Further investigations demonstrated the regulation of the tumor suppressor gene reversion-inducing cysteine-rich protein with kazal motifs (RECK) by two keratinization-associated miRNAs, miR-7 and miR-21. Transfection of miR-7 and miR-21-mimics reduced the expression of RECK through direct miRNA-mediated regulation, and these miRNAs were inversely correlated with RECK in CAL 27 orthotopic xenograft tumors. Furthermore, a similar inverse correlation was demonstrated in CAL 27 cells treated in vitro by different external stimuli such as trypsinization, cell density, and serum concentration. Taken together, our data show that keratinization is associated with poor prognosis of oral cancer patients and keratinization-associated miRNAs mediate deregulation of RECK which may contribute to the aggressiveness of tumors.
  • PMID: 22761427
Expression Profile:
  • Description:Differential expression of microRNAs between oral squamous cell carcinoma and healthy control tongues
  • Organism:Homo sapiens
  • Source:GEO
  • Source ID:GSE28100
  • Platform: GPL10850
  • Number of samples:20
  • Overall design:Human tissues of oral squamous cell carcinoma and healthy normal tongues were used for microRNA microarray profile to identify aberrantly expressed microRNAs in oral squamous cell carcinomas.
  • Instrument:Agilent-021827 Human miRNA Microarray (V3) (miRBase release 12.0 miRNA ID version)
Design and Sample:
  • Cancer Type:oral squamous cell carcinoma
  • Cancer SubType:N/A
  • Cell Line:N/A
  • Experimental Design:cancer vs normal
  • Case Sample:oral squamous cell carcinoma
  • Control Sample:healthy control tongue
  • Num of Case:17
  • Num of Control:3
  • Quantification Software:Limma
  • Num of miRNAs:851
Identification:
  • Num of Up:37
  • Num of Down:20
Time Info:
  • Create Time2016-03-14
  • Update Time:2021-05-27

Differentially Expressed miRNAs List

Status:
miRNA ID Cancer Type Design logFC AveExpr T value P value adj Pvalue Status Plot