Combined inhibition of RNA polymerase I and mTORC1/2 synergize to combat oral squamous cell carcinoma

We provide a graphical abstract to summarize the antitumor mechanisms of CX5461 and INK128 individually and in combination in OSCC. The RNA polymerase I inhibitor CX5461 remarkably suppresses rRNA transcription and induces nucleolar disruption and oxidative stress, which leads to DNA damage. The mTORC1/2 inhibitor INK128 primarily suppresses cell proliferation and cell cycle progression. The antioxidant NAC significantly prevents CX5461-induced ROS generation, DNA damage, and apoptosis. INK128 treatment compromises the NHEJ-DNA repair pathway to reinforce CX5461-induced DNA damage. The combined administration of CX5461 and INK128 acts synergistically to trigger OSCC cell apoptosis. OSCC tumor cells, with a reduced 45S rDNA copy number, are highly sensitive to treatments with CX5461 and coadministration of CX5461 and INK128. [Display omitted] •CX5461 and INK128 synergistically suppress oral squamous cell carcinoma.•Primary oral tumors frequently exhibit a partial loss of 45S rDNA copy number.•Fewer rDNA copies can improve sensitivity to CX5461 and the combined treatment.•CX5461 and INK128 are more cytotoxic towards oral cancer cells than normal cells.•INK128 impairs the NHEJ repair pathway to reinforce the antitumor effect of CX5461. Oral squamous cell carcinoma (OSCC) is the major cause of morbidity and mortality in head and neck cancer patients worldwide. This malignant disease is challenging to treat because of the lack of effective curative strategies and the high incidence of recurrence. This study aimed to investigate the efficacy of a single and dual approach targeting ribosome biogenesis and protein translation to treat OSCC associated with the copy number variation (CNV) of ribosomal DNA (rDNA). Here, we found that primary OSCC tumors frequently exhibited a partial loss of 45S rDNA copy number and demonstrated a high susceptibility to CX5461 (a selective inhibitor of RNA polymerase I) and the coadministration of CX5461 and INK128 (a potent inhibitor of mTORC1/2). Combined treatment displayed the promising synergistic effects that induced cell apoptosis and reactive oxygen species (ROS) generation, and inhibited cell growth and proliferation. Moreover, INK128 compromised NHEJ-DNA repair pathway to reinforce the antitumor activity of CX5461. In vivo, the cotreatment synergistically suppressed tumor growth, triggered apoptosis and strikingly extended the survival time of tumor-bearing mice. Additionally, treatment with the individual compounds and coa