| Literature DB >> 28825187 |
Prit Benny Malgulwar1, Pankaj Pathak1, Manmohan Singh2, Shashank Sharad Kale2, Vaishali Suri1, Chitra Sarkar1, Mehar Chand Sharma3.
Abstract
Loss of SMARCB1/INI1 expression is considered to be a hallmark for childhood chordomas (CCs). Although mutation/loss of 22q has strongly established the loss of SMARCB1/INI1 in cancers, the cause in CCs remains elusive. Recent studies suggest role of miRNAs in regulation of SMARCB1/INI1 expressions. We examined 5 reported/target predicted miRNAs to SMARCB1/INI1 in SMARCB1/INI1 immunonegative and immunopositive cases, and found upregulation of miR-671-5p and miR-193a-5p in SMARCB1/INI1-immunonegative cases. Notably, these two miRNAs were significantly predicted to target TGF-β signaling, suggestive of dysregulation of developmental and osteoblast regulation pathway in CCs. Overall, we suggest miR-671-5p- and miR-193a-5p-mediated epigenetic mode of SMARCB1/INI1 loss and downregulated TGF-β pathway in CCs.Entities:
Keywords: Childhood tumours; Chordomas; SMARCB1/INI1 loss; TGF-beta-pathway; miR-193a-5p; miR-671-5p
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Year: 2017 PMID: 28825187 DOI: 10.1007/s10014-017-0295-7
Source DB: PubMed Journal: Brain Tumor Pathol ISSN: 1433-7398 Impact factor: 3.298