Antitumor effect of sunitinib against skeletal metastatic renal cell carcinoma through inhibition of osteoclast function

Int J Cancer. 2012 Feb 1;130(3):677-84. doi: 10.1002/ijc.26034. Epub 2011 Jun 10.

Abstract

We investigated the inhibitory effect of sunitinib, a newly approved multitargeted tyrosine kinase inhibitor, against the progression of renal cell cancer (RCC) bone metastases in vivo. In vitro cell proliferation was determined using the MTS assay. To investigate the inhibitory effects of sunitinib in vivo, we established luciferase-labeled ACHN(Luc) cells derived from papillary RCC. Mice in which ACHN(Luc) cells had been transplanted into the left ventricle to establish bone metastases were treated orally with 40 mg/kg/day sunitinib or vehicle control for 3 weeks. Growth of the cancer cells was monitored using an in vivo imaging system. In addition, 16 patients with metastatic RCC were treated with sunitinib, and serum and urine levels of amino-terminal telopeptide (NTx) were measured as markers of bone resorption. Sunitinib did not inhibit the growth of RCC cells in vitro at clinically or experimentally achievable serum levels (100 nM-1 μM). To investigate the inhibitory effect of sunitinib in vivo, we established luciferase-labeled human RCC cells (ACHN(Luc) ). Sunitinib prevented the growth of ACHN(Luc) RCC cells in the bone metastatic mouse model. The number of osteoclasts in sunitinib-treated mice was significantly less than that in control mice. Serum and urine levels of NTx in patients with metastatic RCC declined significantly during the first 4 weeks of sunitinib treatment (p = 0.027). Sunitinib is a potent anticancer agent for RCC bone metastases, at least for papillary RCC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use*
  • Bone Neoplasms / drug therapy*
  • Bone Neoplasms / secondary*
  • Carcinoma, Renal Cell / pathology*
  • Cell Proliferation / drug effects
  • Collagen Type I / blood
  • Collagen Type I / urine
  • Disease Models, Animal
  • Female
  • Humans
  • Indoles / pharmacology
  • Indoles / therapeutic use*
  • Kidney Neoplasms / pathology*
  • Macrophage Colony-Stimulating Factor / blood
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Middle Aged
  • Osteoclasts / drug effects*
  • Peptides / blood
  • Peptides / urine
  • Pyrroles / pharmacology
  • Pyrroles / therapeutic use*
  • Sunitinib
  • Vascular Endothelial Growth Factor A / blood

Substances

  • Antineoplastic Agents
  • Collagen Type I
  • Indoles
  • Peptides
  • Pyrroles
  • Vascular Endothelial Growth Factor A
  • collagen type I trimeric cross-linked peptide
  • Macrophage Colony-Stimulating Factor
  • Sunitinib