Oncogenic KRAS mutation confers chemoresistance by upregulating SIRT1 in non-small cell lung cancer.

Kirsten rat sarcoma viral oncogene homologue (KRAS) is a frequent oncogenic driver of solid tumors, including non-small cell lung cancer (NSCLC). The treatment and outcomes of KRAS-mutant cancers have not been dramatically revolutionized by direct KRAS-targeted therapies because of the lack of deep binding pockets for specific small molecule inhibitors. Here, we demonstrated that the mRNA and protein levels of the class III histone deacetylase SIRT1 were upregulated by the KRAS Mut -Raf-MEK-c-Myc axis in KRAS Mut lung cancer cells and in lung tumors of a mouse model with spontaneous Kras G12D expression. KRAS Mut -induced SIRT1 bound to KRAS Mut and stably deacetylated KRAS Mut at lysine 104, which increased KRAS Mut activity. SIRT1 knockdown (K/D) or the SIRT1 H363Y mutation increased KRAS Mut acetylation, which decreased KRAS Mut activity and sensitized tumors to the anticancer effects of cisplatin and erlotinib. Furthermore, in Kras G12D/+ ;Sirt1 co/co mice, treatment with cisplatin and erlotinib robustly reduced the tumor burden and increased survival rates compared with those in spontaneous LSL-Kras G12D/+ ;Sirt1 +/+ mice and mice in each single-drug treatment group. Then, we identified p300 as a KRAS Mut acetyltransferase that reinforced KRAS Mut lysine 104 acetylation and robustly decreased KRAS Mut activity. KRAS Mut lysine 104 acetylation by p300 and deacetylation by SIRT1 were confirmed by LC‒MS/MS. Consistent with this finding, the SIRT1 inhibitor EX527 suppressed KRAS Mut activity, which synergistically abolished cell proliferation and colony formation, as well as the tumor burden in KRAS Mut mice, when combined with cisplatin or erlotinib. Our data reveal a novel pathway critical for the regulation of KRAS Mut lung cancer progression and provide important evidence for the potential application of SIRT1 inhibitors and p300 activators for the combination treatment of KRAS Mut lung cancer patients.