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10.1038/s41419-018-0548-3

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suck abstract from ncbi


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pmid29725063
      Cell+Death+Dis 2018 ; 9 (5 ): 517
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  • Actin like-6A promotes glioma progression through stabilization of transcriptional regulators YAP/TAZ #MMPMID29725063
  • Ji J ; Xu R ; Zhang X ; Han M ; Xu Y ; Wei Y ; Ding K ; Wang S ; Bin Huang ; Chen A ; Di Zhang ; Jiang Z ; Xu S ; Zhang Q ; Li W ; Ni S ; Wang J ; Li X
  • Cell Death Dis 2018[May]; 9 (5 ): 517 PMID29725063 show ga
  • Increased Actin-like 6A (ACTL6A) expression has been implicated in the development of diverse cancers and recently associated with the Hippo signaling pathway, which is known to regulate biological properties, including proliferation, tissue regeneration, stem cell biology, as well as tumorigenesis. Here we first show that ACTL6A is upregulated in human gliomas and its expression is associated with glioma patient survival. ACTL6A promotes malignant behaviors of glioma cells in vitro and in orthotopic xenograft model. In co-immunoprecipitation assays, we discover that ACTL6A physically associated with YAP/TAZ and furthermore disrupts the interaction between YAP and ?-TrCP E3 ubiquitin ligase, which promotes YAP protein degradation. Moreover, effects of ACTL6A on glioma cells proliferation, migration, and invasion could be mediated by YAP/TAZ. These data indicate that ACTL6A may contribute to cancer progression by stabilizing YAP/TAZ and therefore provide a novel therapeutic target for the treatment of human gliomas.
  • |*Gene Expression Regulation, Neoplastic [MESH]
  • |Actins/antagonists & inhibitors/*genetics/metabolism [MESH]
  • |Adaptor Proteins, Signal Transducing/*genetics/metabolism [MESH]
  • |Aged [MESH]
  • |Animals [MESH]
  • |Brain Neoplasms/*genetics/metabolism/mortality/pathology [MESH]
  • |Cell Line, Tumor [MESH]
  • |Cell Movement [MESH]
  • |Cell Proliferation [MESH]
  • |Chromosomal Proteins, Non-Histone/antagonists & inhibitors/*genetics/metabolism [MESH]
  • |DNA-Binding Proteins/antagonists & inhibitors/*genetics/metabolism [MESH]
  • |Disease Progression [MESH]
  • |Female [MESH]
  • |Glioblastoma/*genetics/metabolism/mortality/pathology [MESH]
  • |Humans [MESH]
  • |Intracellular Signaling Peptides and Proteins/*genetics/metabolism [MESH]
  • |Male [MESH]
  • |Mice [MESH]
  • |Mice, Nude [MESH]
  • |Middle Aged [MESH]
  • |Neoplasm Invasiveness [MESH]
  • |Phosphoproteins/*genetics/metabolism [MESH]
  • |Protein Binding [MESH]
  • |Protein Stability [MESH]
  • |RNA, Small Interfering/genetics/metabolism [MESH]
  • |Signal Transduction [MESH]
  • |Survival Analysis [MESH]
  • |Trans-Activators [MESH]
  • |Transcription Factors [MESH]
  • |Transcriptional Coactivator with PDZ-Binding Motif Proteins [MESH]
  • |Tumor Burden [MESH]
  • |Xenograft Model Antitumor Assays [MESH]
  • |YAP-Signaling Proteins [MESH]


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