Abstract

Mutation-specific effects of cancer driver genes influence drug responses and the success of clinical trials. We reasoned that these effects could unbalance the distribution of each mutation across different cancer types, as a result, the cancer preference can be used to distinguish the effects of the causal mutation. Here, we developed a network-based framework to systematically measure cancer diversity for each driver mutation. We found that half of the driver genes harbor cancer type-specific and pancancer mutations simultaneously, suggesting that the pervasive functional heterogeneity of the mutations from even the same driver gene. We further demonstrated that the specificity of the mutations could influence patient drug responses. Moreover, we observed that diversity was generally increased in advanced tumors. Finally, we scanned potentially novel cancer driver genes based on the diversity spectrum. Diversity spectrum analysis provides a new approach to define driver mutations and optimize off-label clinical trials.

Highlights

  • Mutation-specific effects of cancer driver genes influence drug responses and the success of clinical trials

  • A multicenter clinical study[10] on the efficacy of the HER kinase inhibitor neratinib showed that the responses of patients were determined by both cancer types and mutations, which is consistent with the conclusion of a previous clinical study[14] in which the BRAF inhibitor vemurafenib was tested on patients from different cancer types but harboring BRAF V600 mutation

  • To maximally keep with the conventions of clinical genomic literature and minimize the influence of biased curation in the existing cancer genomics databases, we applied a rule-based approach to identify driver mutations (Supplementary Data 1) in well-characterized cancer driver genes, which has been widely used in many clinical cancer studies[21,22]

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Summary

Introduction

Mutation-specific effects of cancer driver genes influence drug responses and the success of clinical trials. To demonstrate the potential value of the cancer diversity spectrum for clinical and biological problems, we leveraged this information to predict patient drug responses and identify new cancer driver genes.

Results
Conclusion
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