Cargando…
A genome-wide miRNA screen revealed miR-603 as a MGMT-regulating miRNA in glioblastomas
MGMT expression is a critical determinant for therapeutic resistance to DNA alkylating agents. We previously demonstrated that MGMT expression is post-transcriptionally regulated by miR-181d and other miRNAs. Here, we performed a genome-wide screen to identify MGMT regulating miRNAs. Candidate miRNA...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147303/ https://www.ncbi.nlm.nih.gov/pubmed/24994119 |
_version_ | 1782332420638375936 |
---|---|
author | Kushwaha, Deepa Ramakrishnan, Valya Ng, Kimberly Steed, Tyler Nguyen, Thien Futalan, Diahnn Akers, Johnny C. Sarkaria, Jann Jiang, Tao Chowdhury, Dipanjan Carter, Bob S. Chen, Clark C. |
author_facet | Kushwaha, Deepa Ramakrishnan, Valya Ng, Kimberly Steed, Tyler Nguyen, Thien Futalan, Diahnn Akers, Johnny C. Sarkaria, Jann Jiang, Tao Chowdhury, Dipanjan Carter, Bob S. Chen, Clark C. |
author_sort | Kushwaha, Deepa |
collection | PubMed |
description | MGMT expression is a critical determinant for therapeutic resistance to DNA alkylating agents. We previously demonstrated that MGMT expression is post-transcriptionally regulated by miR-181d and other miRNAs. Here, we performed a genome-wide screen to identify MGMT regulating miRNAs. Candidate miRNAs were further tested for inverse correlation with MGMT expression in clinical specimens. We identified 15 candidate miRNAs and characterized the top candidate, miR-603. Transfection of miR-603 suppressed MGMT mRNA/protein expression in vitro and in vivo; this effect was reversed by transfection with antimiR-603. miR-603 affinity-precipitated with MGMT mRNA and suppressed luciferase activity in an MGMT-3'UTR-luciferase assay, suggesting direct interaction between miR-603 and MGMT 3'UTR. miR-603 transfection enhanced the temozolomide (TMZ) sensitivity of MGMT-expressing glioblastoma cell lines. Importantly, miR-603 mediated MGMT suppression and TMZ resistance were reversed by expression of an MGMT cDNA. In a collection of 74 clinical glioblastoma specimens, both miR-603 and miR-181d levels inversely correlated with MGMT expression. Moreover, a combined index of the two miRNAs better reflected MGMT expression than each individually. These results suggest that MGMT is co-regulated by independent miRNAs. Characterization of these miRNAs should contribute toward strategies for enhancing the efficacy of DNA alkylating agents. |
format | Online Article Text |
id | pubmed-4147303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-41473032014-08-29 A genome-wide miRNA screen revealed miR-603 as a MGMT-regulating miRNA in glioblastomas Kushwaha, Deepa Ramakrishnan, Valya Ng, Kimberly Steed, Tyler Nguyen, Thien Futalan, Diahnn Akers, Johnny C. Sarkaria, Jann Jiang, Tao Chowdhury, Dipanjan Carter, Bob S. Chen, Clark C. Oncotarget Priority Research Paper MGMT expression is a critical determinant for therapeutic resistance to DNA alkylating agents. We previously demonstrated that MGMT expression is post-transcriptionally regulated by miR-181d and other miRNAs. Here, we performed a genome-wide screen to identify MGMT regulating miRNAs. Candidate miRNAs were further tested for inverse correlation with MGMT expression in clinical specimens. We identified 15 candidate miRNAs and characterized the top candidate, miR-603. Transfection of miR-603 suppressed MGMT mRNA/protein expression in vitro and in vivo; this effect was reversed by transfection with antimiR-603. miR-603 affinity-precipitated with MGMT mRNA and suppressed luciferase activity in an MGMT-3'UTR-luciferase assay, suggesting direct interaction between miR-603 and MGMT 3'UTR. miR-603 transfection enhanced the temozolomide (TMZ) sensitivity of MGMT-expressing glioblastoma cell lines. Importantly, miR-603 mediated MGMT suppression and TMZ resistance were reversed by expression of an MGMT cDNA. In a collection of 74 clinical glioblastoma specimens, both miR-603 and miR-181d levels inversely correlated with MGMT expression. Moreover, a combined index of the two miRNAs better reflected MGMT expression than each individually. These results suggest that MGMT is co-regulated by independent miRNAs. Characterization of these miRNAs should contribute toward strategies for enhancing the efficacy of DNA alkylating agents. Impact Journals LLC 2014-05-14 /pmc/articles/PMC4147303/ /pubmed/24994119 Text en Copyright: © 2014 Kushwaha et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Priority Research Paper Kushwaha, Deepa Ramakrishnan, Valya Ng, Kimberly Steed, Tyler Nguyen, Thien Futalan, Diahnn Akers, Johnny C. Sarkaria, Jann Jiang, Tao Chowdhury, Dipanjan Carter, Bob S. Chen, Clark C. A genome-wide miRNA screen revealed miR-603 as a MGMT-regulating miRNA in glioblastomas |
title | A genome-wide miRNA screen revealed miR-603 as a MGMT-regulating miRNA in glioblastomas |
title_full | A genome-wide miRNA screen revealed miR-603 as a MGMT-regulating miRNA in glioblastomas |
title_fullStr | A genome-wide miRNA screen revealed miR-603 as a MGMT-regulating miRNA in glioblastomas |
title_full_unstemmed | A genome-wide miRNA screen revealed miR-603 as a MGMT-regulating miRNA in glioblastomas |
title_short | A genome-wide miRNA screen revealed miR-603 as a MGMT-regulating miRNA in glioblastomas |
title_sort | genome-wide mirna screen revealed mir-603 as a mgmt-regulating mirna in glioblastomas |
topic | Priority Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147303/ https://www.ncbi.nlm.nih.gov/pubmed/24994119 |
work_keys_str_mv | AT kushwahadeepa agenomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT ramakrishnanvalya agenomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT ngkimberly agenomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT steedtyler agenomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT nguyenthien agenomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT futalandiahnn agenomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT akersjohnnyc agenomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT sarkariajann agenomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT jiangtao agenomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT chowdhurydipanjan agenomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT carterbobs agenomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT chenclarkc agenomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT kushwahadeepa genomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT ramakrishnanvalya genomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT ngkimberly genomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT steedtyler genomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT nguyenthien genomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT futalandiahnn genomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT akersjohnnyc genomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT sarkariajann genomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT jiangtao genomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT chowdhurydipanjan genomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT carterbobs genomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas AT chenclarkc genomewidemirnascreenrevealedmir603asamgmtregulatingmirnainglioblastomas |