EZH2-mediated upregulation of ROS1 oncogene promotes oral cancer metastasis

摘要

Current anti-epidermal growth factor receptor (EGFR) therapy for oral cancer does not provide satisfactory efficacy due to drug resistance or reduced EGFR level. As an alternative candidate target for therapy, here we identified an oncogene, ROS1, as an important driver for oral squamous cell carcinoma (OSCC) metastasis. Among tumors from 188 oral cancer patients, upregulated ROS1 expression strongly correlated with metastasis to lung and lymph nodes. Mechanistic studies uncover that the activated ROS1 results from highly expressed ROS1 gene instead of gene rearrangement, a phenomenon distinct from other cancers. Our data further reveal a novel mechanism that reduced histone methyltransferase EZH2 leads to a lower trimethylation of histone H3 lysine 27 suppressive modification, relaxes chromatin, and promotes the accessibility of the transcription factor STATI to the enhancer and the intron regions of R0S1 target genes, CXCL1 and GLH1 for upregulating their expressions. Down-regulation of R0S1 in highly invasive OSCC cells, nevertheless, reduces cell proliferation and inhibits metastasis to lung in the tail-vein injection and the oral cavity xenograft models. Our findings highlight R0S1 as a candidate biomarker and therapeutic target for OSCC. Finally, we demonstrate that co-targeting of R0S1 and EGFR could potentially offer an effective oral cancer therapy.