Sun Huiyan, Meng Yu, Yao Lei, Du Songtao, Li Yayun, Zhou Qian, Liu Yihuang, Dian Yating, Sun Yuming, Wang Xiaomin, Liang Xiao-Wei, Deng Guangtong, Chen Xiang, Zeng Furong
Department of Dermatology Xiangya Hospital Central South University Changsha China.
National Engineering Research Center of Personalized Diagnostic and Therapeutic Technology Changsha China.
MedComm (2020). 2024 Aug 12;5(8):e684. doi: 10.1002/mco2.684. eCollection 2024 Aug.
Metastasis is a major contributing factor that affects the prognosis of melanoma patients. Nevertheless, the underlying molecular mechanisms involved in melanoma metastasis are not yet entirely understood. Here, we identified ubiquitin-specific protease 22 (USP22) as a pro-oncogenic protein in melanoma through screening the survival profiles of 52 ubiquitin-specific proteases (USPs). USP22 demonstrates a strong association with poor clinical outcomes and is significantly overexpressed in melanoma. Ablation of USP22 expression remarkably attenuates melanoma migration, invasion, and epithelial-mesenchymal transition in vitro and suppresses melanoma metastasis in vivo. Mechanistically, USP22 controls melanoma metastasis through the SIRT1/PTEN/PI3K pathway. In addition, we conducted an United States Food and Drug Administration-approved drug library screening and identified topotecan as a clinically applicable USP22-targeting molecule by promoting proteasomal degradation of USP22. Finally, we found that both pharmacological and genetic silence of USP22 sensitize RSL3-induced ferroptosis through suppressing the PI3K/Akt/mTOR pathway and its downstream SCD, and ferroptosis inhibitor could partly rescued the decreased lung metastasis by topotecan in vivo. Overall, our findings reveal a prometastatic role of USP22 and identify topotecan as a potent USP22-targeting drug to limit melanoma metastasis.
转移是影响黑色素瘤患者预后的主要因素。然而,黑色素瘤转移所涉及的潜在分子机制尚未完全明确。在此,我们通过筛选52种泛素特异性蛋白酶(USP)的生存谱,确定泛素特异性蛋白酶22(USP22)为黑色素瘤中的一种促癌蛋白。USP22与不良临床结局密切相关,且在黑色素瘤中显著过表达。敲除USP22表达可显著减弱黑色素瘤在体外的迁移、侵袭及上皮-间质转化,并在体内抑制黑色素瘤转移。机制上,USP22通过SIRT1/PTEN/PI3K通路控制黑色素瘤转移。此外,我们进行了美国食品药品监督管理局批准的药物库筛选,并通过促进USP22的蛋白酶体降解确定拓扑替康为一种临床适用的靶向USP22的分子。最后,我们发现USP22的药理学沉默和基因沉默均通过抑制PI3K/Akt/mTOR通路及其下游的SCD使RSL3诱导的铁死亡敏感化,并且铁死亡抑制剂可部分挽救拓扑替康在体内导致的肺转移减少。总体而言,我们的研究结果揭示了USP22的促转移作用,并确定拓扑替康为一种有效的靶向USP22的药物以限制黑色素瘤转移。