Oncotarget

Research Papers:

Activation of RAS family members confers resistance to ROS1 targeting drugs

Marilisa Cargnelutti, Simona Corso, Margherita Pergolizzi, Laurence Mévellec, Dara L. Aisner, Rafal Dziadziuszko, Marileila Varella-Garcia, Paolo M. Comoglio, Robert C. Doebele, Jorge Vialard and Silvia Giordano _

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Oncotarget. 2015; 6:5182-5194. https://doi.org/10.18632/oncotarget.3311

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Abstract

Marilisa Cargnelutti1, Simona Corso1,2, Margherita Pergolizzi1, Laurence Mévellec3, Dara L. Aisner4, Rafal Dziadziuszko5, Marileila Varella-Garcia4,6, Paolo M. Comoglio1,2, Robert C. Doebele6, Jorge Vialard7 and Silvia Giordano1,2

1 Candiolo Cancer Institute - FPO, IRCCS, Torino, Italy

2 Department of Oncology, University of Torino, Italy

3 Janssen Research & Development, Janssen-Cilag, Val-de-Reuil, France

4 Department of Pathology, University of Colorado School of Medicine, Aurora, CO, USA

5 Medical University of Gdansk, Poland

6 Department of Medicine, Division of Medical Oncology University of Colorado School of Medicine, Aurora, CO, USA

7 Janssen Research & Development, a division of Janssen Pharmaceutica NV, Beerse, Belgium

Correspondence:

Simona Corso, email:

Silvia Giordano, email:

Keywords: drug resistance, RAS, ROS1, lung cancer, targeted therapy

Received: November 11, 2014 Accepted: December 29, 2014 Published: December 31, 2014

Abstract

The ROS1 tyrosine kinase is activated in lung cancer as a consequence of chromosomal rearrangement. Although high response rates and disease control have been observed in lung cancer patients bearing rearranged ROS1 tumors (ROS1+) treated with the kinase inhibitor crizotinib, many of these patients eventually relapse.

To identify mechanisms of resistance to ROS1 inhibitors we generated resistant cells from HCC78 lung cancer cells bearing the SLC34A2-ROS1 rearrangement. We found that activation of the RAS pathway in the HCC78 cell model, due to either KRAS/NRAS mutations or to KRAS amplification, rendered the cells resistant to ROS1 inhibition. These cells were cross-resistant to different ROS1 inhibitors, but sensitive to inhibitors of the RAS signaling pathway. Interestingly, we identified focal KRAS amplification in a biopsy of a tumor from a patient that had become resistant to crizotinib treatment.

Altogether our data suggest that the activation of members of the RAS family can confer resistance to ROS1 inhibitors. This has important clinical implications as: (i) RAS genetic alterations in ROS1+ primary tumors are likely negative predictors of efficacy for targeted drugs and (ii) this kind of resistance is unlikely to be overcome by the use of more specific or more potent ROS1 targeting drugs.


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