SCCOHT tumors acquire chemoresistance and protection by interacting mesenchymal stroma/stem cells within the tumor microenvironment

Int J Oncol. 2016 Dec;49(6):2453-2463. doi: 10.3892/ijo.2016.3735. Epub 2016 Oct 14.

Abstract

Chemotherapeutic drug testing of SCCOHT-1 and BIN-67 tumor cells revealed synergistic growth-inhibition of >95% in vitro with a combination of foretinib and FK228. Application of this drug combination in vivo in NODscid mice-induced SCCOHT-1GFP tumors was associated with ~6-fold reduction in tumor mass within 10 days, whereby synergistic effects of the two compounds remained undetectable compared to previous results with foretinib treatment alone. Histopathologic evaluation revealed a reduced vascularization and a lower amount of proliferating cells in the treated tumors. Surprisingly, a simultaneous significant accumulation of extracellular matrix structures with positive elastin-van Gieson staining was observed following foretinib/FK228 exposure. Expression analysis of treated animal tumors exhibited various changes including increased mouse transcript levels of elastin, laminin, and fibronectin. In parallel, markers for mesenchymal stroma/stem cells (MSC) including CD73 and CD90 were detectable in all mouse tumors suggesting a possible involvement of these cells in extracellular matrix restructure. Indeed, incubation of MSC with FK228 or foretinib/FK228 demonstrated morphologic alterations and enhanced expression of laminin and fibronectin. Moreover, a co-culture of MSC with lentiviral-labeled SCCOHT-1GFP cells contributed to protection of the tumor cells against FK228-mediated cytotoxicity. Furthermore, explant cultures of SCCOHT-1GFP-induced tumors acquired an increased resistance to FK228 and a combination of foretinib/FK228 in contrast to foretinib alone. Together, these data suggested that FK228-mediated extracellular matrix protein expression by MSC contributes to increased protection and enhanced resistance of SCCOHT tumors which could represent a more general mechanism of MSC during drug-induced alterations of a tumor microenvironment.

MeSH terms

  • 5'-Nucleotidase / metabolism
  • Anilides / pharmacology*
  • Animals
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology*
  • Cell Line, Tumor
  • Depsipeptides / pharmacology*
  • Drug Resistance, Neoplasm
  • Elastin / metabolism
  • Extracellular Matrix / physiology
  • Female
  • Fibronectins / metabolism
  • Humans
  • Laminin / metabolism
  • Mesenchymal Stem Cells / pathology*
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Ovarian Neoplasms / drug therapy*
  • Quinolines / pharmacology*
  • Thy-1 Antigens / metabolism
  • Tumor Microenvironment / physiology*
  • Xenograft Model Antitumor Assays

Substances

  • Anilides
  • Antineoplastic Agents
  • Depsipeptides
  • Fibronectins
  • GSK 1363089
  • Laminin
  • Quinolines
  • Thy-1 Antigens
  • Elastin
  • romidepsin
  • 5'-Nucleotidase