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Investigational New Drugs

, Volume 31, Issue 5, pp 1136–1141 | Cite as

Genotype-dependent cooperation of ionizing radiation with BRAF inhibition in BRAF V600E-mutated carcinomas

  • Tina Dasgupta
  • Daphne A. Haas-Kogan
  • Xiaodong Yang
  • Aleksandra Olow
  • Daniel X. Yang
  • Ashley Gragg
  • Lisa A. Orloff
  • Sue S. YomEmail author
PRECLINICAL STUDIES

Summary

Background A substantial proportion of solid tumors carry the BRAF V600E mutation, which causes activation of the MEK/MAPK pathway and is a poor prognostic indicator. Patients with locally advanced human cancers are often treated with external beam radiation therapy. Given the association of Raf overactivation with radioresistance, we hypothesized that, in BRAF V600E-mutated carcinomas, there would be combinatorial activity between radiation and PLX4720, a specific BRAF V600E-inhibitor. Methods Two BRAF V600E-mutated cancer cell lines and one BRAF-V600E wildtype (WT) cancer cell line were obtained. We performed cell viability assays and clonogenic assays using combinations of radiation and PLX4720. We assessed MEK and MAPK phosphorylation at different PLX4720 concentrations with western blotting, and cell cycle progression was evaluated by flow cytometry. Results Our results show combinatorial, additive activity between radiation and PLX4720 in BRAF V600E-mutated cell lines, but not in the BRAF WT line. In BRAF V600E-mutated cells, there was a PLX4720 concentration-dependent decrease in MEK and MAPK phosphorylation. In cells with BRAF V600E mutations, PLX4720 caused cell cycle arrest at G1, and, when combined with radiation, caused a combined G1 and G2 cell cycle arrest; this pattern of cell cycle effects was not seen in the BRAF WT cell line. Conclusions These data suggest additive, combinatorial activity between radiation and PLX4720 in cancers carrying BRAF V600E mutations. Our data has potential for translation into the multimodality treatment of BRAF V600E-mutated cancers.

Keywords

BRAF V600E PLX4720 PLX4032 vemurafenib Radiosensitization 

Notes

Acknowledgments

We thank Plexxikon, Inc. for providing PLX4720, and Dr. Brian L. West for this thoughtful advice and assistance during this study.

Author disclosures and conflict of interest

None. The authors report no conflict of interest.

Ethical standards

The submitted manuscript complies with the current laws of the country, the United States of America, in which the experiments and analysis were performed.

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Copyright information

© Springer Science+Business Media New York 2013

Authors and Affiliations

  • Tina Dasgupta
    • 1
  • Daphne A. Haas-Kogan
    • 1
  • Xiaodong Yang
    • 1
  • Aleksandra Olow
    • 1
  • Daniel X. Yang
    • 1
  • Ashley Gragg
    • 1
  • Lisa A. Orloff
    • 2
  • Sue S. Yom
    • 1
    • 2
    Email author
  1. 1.Department of Radiation OncologyUniversity of California, San FranciscoSan FranciscoUSA
  2. 2.Department of Otolaryngology - Head and Neck SurgeryUniversity of California, San FranciscoSan FranciscoUSA

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