A validated tumorgraft model reveals activity of dovitinib against renal cell carcinoma

Sharanya Sivanand, Samuel Peña-Llopis, Hong Zhao, Blanka Kucejova, Patrick Spence, Andrea Pavia-Jimenez, Toshinari Yamasaki, David J. McBride, Jessica Gillen, Nicholas C. Wolff, Lorraine Morlock, Yair Lotan, Ganesh Raj, Arthur I Sagalowsky, Vitaly Margulis, Jeffrey A Cadeddu, Mark T. Ross, David R. Bentley, Wareef Kabbani, Xian-Jin XiePayal Kapur, Noelle S Williams, James B Brugarolas

Research output: Contribution to journalArticlepeer-review

148 Scopus citations


Most anticancer drugs entering clinical trials fail to achieve approval from the U.S. Food and Drug Administration. Drug development is hampered by the lack of preclinical models with therapeutic predictive value. Herein, we report the development and validation of a tumorgraft model of renal cell carcinoma (RCC) and its application to the evaluation of an experimental drug. Tumor samples from 94 patients were implanted in the kidneys of mice without additives or disaggregation. Tumors from 35 of these patients formed tumorgrafts, and 16 stable lines were established. Samples from metastatic sites engrafted at higher frequency than those from primary tumors, and stable engraftment of primary tumors in mice correlated with decreased patient survival. Tumorgrafts retained the histology, gene expression, DNA copy number alterations, and more than 90% of the protein-coding gene mutations of the corresponding tumors. As determined by the induction of hypercalcemia in tumorgraft-bearing mice, tumorgrafts retained the ability to induce paraneoplastic syndromes. In studies simulating drug exposures in patients, RCC tumorgraft growth was inhibited by sunitinib and sirolimus (the active metabolite of temsirolimus in humans), but not by erlotinib, which was used as a control. Dovitinib, a drug in clinical development, showed greater activity than sunitinib and sirolimus. The routine incorporation of models recapitulating the molecular genetics and drug sensitivities of human tumors into preclinical programs has the potential to improve oncology drug development.

Original languageEnglish (US)
Article number137ra75
JournalScience translational medicine
Issue number137
StatePublished - Jun 6 2012

ASJC Scopus subject areas

  • Medicine(all)


Dive into the research topics of 'A validated tumorgraft model reveals activity of dovitinib against renal cell carcinoma'. Together they form a unique fingerprint.

Cite this