Fully accessible fitness landscape of oncogene-negative lung adenocarcinoma

Author:

Yousefi Maryam1,Andrejka Laura1,Szamecz Márton2ORCID,Winslow Monte M.134,Petrov Dmitri A.35,Boross Gábor5

Affiliation:

1. Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305

2. Eötvös Loránd University, Faculty of Informatics, Budapest 1053, Hungary

3. Cancer Biology Program, Stanford University School of Medicine, Stanford, CA 94305

4. Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305

5. Department of Biology, Stanford University, Stanford, CA 94305

Abstract

Cancer genomes are almost invariably complex with genomic alterations cooperating during each step of carcinogenesis. In cancers that lack a single dominant oncogene mutation, cooperation between the inactivation of multiple tumor suppressor genes can drive tumor initiation and growth. Here, we shed light on how the sequential acquisition of genomic alterations generates oncogene-negative lung tumors. We couple tumor barcoding with combinatorial and multiplexed somatic genome editing to characterize the fitness landscapes of three tumor suppressor genes NF1, RASA1, and PTEN, the inactivation of which jointly drives oncogene-negative lung adenocarcinoma initiation and growth. The fitness landscape was surprisingly accessible, with each additional mutation leading to growth advantage. Furthermore, the fitness landscapes remained fully accessible across backgrounds with the inactivation of additional tumor suppressor genes. These results suggest that while predicting cancer evolution will be challenging, acquiring the multiple alterations that drive the growth of oncogene-negative tumors can be facilitated by the lack of constraints on mutational order.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference44 articles.

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