H-Ras and K-Ras Oncoproteins Induce Different Tumor Spectra When Driven by the Same Regulatory Sequences.

Abstract

Genetic studies in mice have provided evidence that H-Ras and K-Ras proteins are bioequivalent. However, human tumors display marked differences in the association of RAS oncogenes with tumor type. Thus, to further assess the bioequivalence of oncogenic H-Ras and K-Ras, we replaced the coding region of the murine K-Ras locus with H-Rasoncogene sequences. Germline expression of H-Rasor K-Rasfrom the K-Ras locus resulted in embryonic lethality. However, expression of these genes in adult mice led to different tumor phenotypes. Whereas H-Raselicited papillomas and hematopoietic tumors, K-Rasinduced lung tumors and gastric lesions. Pulmonary expression of H-Rascreated a senescence-like state caused by excessive MAPK signaling. Likewise, H-Rasbut not K-Rasinduced senescence in mouse embryonic fibroblasts. Label-free quantitative analysis revealed that minor differences in H-Rasexpression levels led to drastically different biological outputs, suggesting that subtle differences in MAPK signaling confer nonequivalent functions that influence tumor spectra induced by RAS oncoproteins. Cancer Res; 77(3); 707-18. ©2016 AACR.