Downregulation of SMARCB1/INI1 expression in pediatric chordomas correlates with upregulation of miR-671-5p and miR-193a-5p expressions

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 expressio...

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Veröffentlicht in:Brain tumor pathology 2017-10, Vol.34 (4), p.155-159
Hauptverfasser: Malgulwar, Prit Benny, Pathak, Pankaj, Singh, Manmohan, Kale, Shashank Sharad, Suri, Vaishali, Sarkar, Chitra, Sharma, Mehar Chand
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Sprache:eng
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Zusammenfassung: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.
ISSN:1433-7398
1861-387X
DOI:10.1007/s10014-017-0295-7