Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.23/841
Título: A transcriptomic signature mediated by HOXA9 promotes human glioblastoma initiation, aggressiveness and resistance to temozolomide
Autor: Pojo, M
Gonçalves, CS
Xavier-Magalhães, A
Oliveira, AI
Gonçalves, T
Correia, S
Rodrigues, AJ
Costa, S
Pinto, L
Pinto, AA
Lopes, JM
Reis, RM
Rocha, M
Sousa, N
Costa, BM
Palavras-chave: Glioblastoma
Data: 2015
Citação: Oncotarget. 2015 Feb 20. [Epub ahead of print]
Resumo: Glioblastoma is the most malignant brain tumor, exhibiting remarkable resistance to treatment. Here we investigated the oncogenic potential of HOXA9 in gliomagenesis, the molecular and cellular mechanisms by which HOXA9 renders glioblastoma more aggressive, and how HOXA9 affects response to chemotherapy and survival. The prognostic value of HOXA9 in glioblastoma patients was validated in two large datasets from TCGA and Rembrandt, where high HOXA9 levels were associated with shorter survival. Transcriptomic analyses identified novel HOXA9-target genes with key roles in cancer-related processes, including cell proliferation, DNA repair, and stem cell maintenance. Functional studies with HOXA9-overexpressing and HOXA9-silenced glioblastoma cell models revealed that HOXA9 promotes cell viability, stemness and invasion, and inhibits apoptosis. Additionally, HOXA9 promoted the malignant transformation of human immortalized astrocytes in an orthotopic in vivo model, and caused tumor-associated death. HOXA9 also mediated resistance to temozolomide treatment in vitro and in vivo via upregulation of BCL2. Importantly, the pharmacological inhibition of BCL2 with the BH3 mimetic ABT-737 reverted temozolomide resistance in HOXA9-positive cells. These data establish HOXA9 as a driver of glioma initiation, aggressiveness and resistance to therapy. In the future, the combination of BH3 mimetics with temozolomide should be further explored as an alternative treatment for glioblastoma.
Peer review: yes
URI: http://hdl.handle.net/10400.23/841
Aparece nas colecções:HB - NCIR - Artigos

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