Department of Oral and Maxillofacial Surgery, Peking University School and Hospital of Stomatology, Beijing, 100081, China.
Department of Central Laboratory, Peking University School and Hospital of Stomatology, Beijing, 100081, China.
Cell Death Dis. 2023 Mar 9;14(3):187. doi: 10.1038/s41419-023-05710-6.
Cancer stem cells (CSCs) cause tumor metastasis and immune evasion by as-yet-unknown molecular mechanisms. In the present study, we identify a long noncoding RNA (lncRNA), termed PVT1, which is highly expressed in CSCs and correlated closely with lymph node metastasis of head and neck squamous cell carcinoma (HNSCC). PVT1 inhibition eliminates CSCs, prevents metastasis, and stimulates anti-tumor immunity, while inhibiting HNSCC growth. Moreover, PVT1 inhibition promotes the infiltration of CD8 T cells into the tumor microenvironment, thereby enhancing immunotherapy by PD1 blockade. Mechanistically, PVT1 inhibition stimulates the DNA damage response, which induces CD8 T cell-recruiting chemokines, while preventing CSCs and metastasis via regulating the miR-375/YAP1 axis. In conclusion, targeting PVT1 might potentiate the elimination of CSCs via immune checkpoint blockade, prevent metastasis, and inhibit HNSCC growth.
癌症干细胞 (CSCs) 通过目前尚不清楚的分子机制导致肿瘤转移和免疫逃逸。在本研究中,我们鉴定了一种长非编码 RNA (lncRNA),称为 PVT1,它在 CSCs 中高度表达,并与头颈部鳞状细胞癌 (HNSCC) 的淋巴结转移密切相关。PVT1 抑制消除了 CSCs,防止了转移,并刺激了抗肿瘤免疫,同时抑制了 HNSCC 的生长。此外,PVT1 抑制促进了 CD8 T 细胞浸润到肿瘤微环境中,从而通过 PD1 阻断增强了免疫治疗。在机制上,PVT1 抑制刺激了 DNA 损伤反应,从而诱导了 CD8 T 细胞募集趋化因子,同时通过调节 miR-375/YAP1 轴来防止 CSCs 和转移。总之,靶向 PVT1 可能通过免疫检查点阻断增强 CSCs 的消除,防止转移并抑制 HNSCC 的生长。