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Nestin depletion induces melanoma matrix metalloproteinases and invasion.

Laboratory investigation; a journal of technical methods and pathology | 2014

Matrix metalloproteinases (MMPs) are key biological mediators of processes as diverse as wound healing, embryogenesis, and cancer progression. Although MMPs may be induced through multiple signaling pathways, the precise mechanisms for their regulation in cancer are incompletely understood. Because cytoskeletal changes are known to accompany MMP expression, we sought to examine the potential role of the poorly understood cytoskeletal protein, nestin, in modulating melanoma MMPs. Nestin knockdown (KD) upregulated the expression of specific MMPs and MMP-dependent invasion both through extracellular matrix barriers in vitro and in peritumoral connective tissue of xenografts in vivo. The development of three-dimensional melanospheres that in vitro partially recapitulate noninvasive tumorigenic melanoma growth was inhibited by nestin KD, although ECM invasion by aberrant melanospheres that did form was enhanced. Mechanistically, nestin KD-dependent melanoma invasion was associated with intracellular redistribution of phosphorylated focal adhesion kinase and increased melanoma cell responsiveness to transforming growth factor-beta, both implicated in pathways of melanoma invasion. The results suggest that the heretofore poorly understood intermediate filament, nestin, may serve as a novel mediator of MMPs critical to melanoma virulence.

Pubmed ID: 25365206 RIS Download

Associated grants

  • Agency: NCI NIH HHS, United States
    Id: R01 CA113796
  • Agency: NIAMS NIH HHS, United States
    Id: T32 AR007098
  • Agency: NHLBI NIH HHS, United States
    Id: T32 HL007627
  • Agency: NCI NIH HHS, United States
    Id: 5P50CA093683-09
  • Agency: NCI NIH HHS, United States
    Id: P50 CA093683
  • Agency: RRD VA, United States
    Id: I01 RX000989
  • Agency: NHLBI NIH HHS, United States
    Id: 5T32HL7627-29
  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR000170
  • Agency: NCI NIH HHS, United States
    Id: R01 CA138231
  • Agency: NIAMS NIH HHS, United States
    Id: T32AR007098-38
  • Agency: NIAMS NIH HHS, United States
    Id: 2T32AR7098-37
  • Agency: NCI NIH HHS, United States
    Id: R01 CA158467

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