Single-walled carbon nanotube: One specific inhibitor of cancer stem cells in osteosarcoma upon downregulation of the TGFβ1 signaling

Biomaterials. 2017 Dec:149:29-40. doi: 10.1016/j.biomaterials.2017.09.032. Epub 2017 Sep 26.

Abstract

Cancer stem cells (CSCs) are believed to have a critical role in tumorigenesis, metastasis, therapeutic resistance or recurrence. Therefore, strategies designed to specifically target and eliminate CSCs have become one of the most promising and desirable ways for tumor treatment. Osteosarcoma stem cells (OSCs), the CSCs in osteosarcoma (OS), are critically associated with OS progression. Here, we show that single-walled carbon nanotubes (SWCNTs), including unmodified SWCNT (SWCNT-Raw) and SWCNT-COOH, have the ability to specifically inhibit the process of TGFβ1-induced OS cells dedifferentiation, prevent the stem cell phenotypes acquisition in OS cells and reduce the OSC viability under conditions which mimic the OS microenvironment. Concurrently, SWCNT treatment significantly down-regulates the expression of OSC markers in OS, and markedly reduces the tumor microvessel density and tumor growth. Furthermore, we found that SWCNT could suppress the TGFβ1-induced activation of TGFβ type I receptor and downstream signaling, which are key for the OSC formation and maintenance. Our results reveal an unexpected function of SWCNT in negative modulation of OSCs, and provide significant implications for the potential CSCs-targeted therapeutic applications of SWCNT.

Keywords: Cancer stem cell; Dedifferentiation; Osteosarcoma; Osteosarcoma stem cell; Single-walled carbon nanotube; TGFβ1 signaling.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Apoptosis
  • Bone Neoplasms / blood supply
  • Bone Neoplasms / drug therapy*
  • Bone Neoplasms / metabolism
  • Bone Neoplasms / pathology
  • Cell Dedifferentiation
  • Cell Line, Tumor
  • Cell Proliferation
  • Down-Regulation
  • Female
  • Humans
  • Mice, Inbred BALB C
  • Nanotubes, Carbon / chemistry*
  • Neoplastic Stem Cells / drug effects*
  • Neoplastic Stem Cells / metabolism
  • Neoplastic Stem Cells / pathology
  • Osteosarcoma / blood supply
  • Osteosarcoma / drug therapy*
  • Osteosarcoma / metabolism
  • Osteosarcoma / pathology
  • Particle Size
  • Signal Transduction
  • Transforming Growth Factor beta1 / metabolism*
  • Tumor Microenvironment

Substances

  • Antineoplastic Agents
  • Nanotubes, Carbon
  • TGFB1 protein, human
  • Transforming Growth Factor beta1