Chakraborty Amit Kumar, Raut Rajnikant Dilip, Iqbal Kisa, Choudhury Chumki, Alhousami Thabet, Chogle Sami, Acosta Alexa S, Fagman Lana, Deabold Kelly, Takada Marilia, Sahay Bikash, Kumar Vikas, Bais Manish V
Department of Translational Dental Medicine, Boston University Henry M. Goldman School of Dental Medicine, Boston, USA.
Department of Endodontics, Henry M. Goldman School of Dental Medicine, Boston University, Boston, USA.
Int J Oral Sci. 2025 Apr 17;17(1):31. doi: 10.1038/s41368-025-00363-x.
Oral squamous cell carcinoma (OSCC) progresses from preneoplastic precursors via genetic and epigenetic alterations. Previous studies have focused on the treatment of terminally developed OSCC. However, the role of epigenetic regulators as therapeutic targets during the transition from preneoplastic precursors to OSCC has not been well studied. Our study identified lysine-specific demethylase 1 (LSD1) as a crucial promoter of OSCC, demonstrating that its knockout or pharmacological inhibition in mice reversed OSCC preneoplasia. LSD1 inhibition by SP2509 disrupted cell cycle, reduced immunosuppression, and enhanced CD4+ and CD8+ T-cell infiltration. In a feline model of spontaneous OSCC, a clinical LSD1 inhibitor (Seclidemstat or SP2577) was found to be safe and effectively inhibit the STAT3 network. Mechanistic studies revealed that LSD1 drives OSCC progression through STAT3 signaling, which is regulated by phosphorylation of the cell cycle mediator CDK7 and immunosuppressive CTLA4. Notably, LSD1 inhibition reduced the phosphorylation of CDK7 at Tyr170 and eIF4B at Ser422, offering insights into a novel mechanism by which LSD1 regulates the preneoplastic-to-OSCC transition. This study provides a deeper understanding of OSCC progression and highlights LSD1 as a potential therapeutic target for controlling OSCC progression from preneoplastic lesions.
口腔鳞状细胞癌(OSCC)通过基因和表观遗传改变从癌前病变前体发展而来。以往的研究主要集中在终末期OSCC的治疗上。然而,表观遗传调节因子在从癌前病变前体向OSCC转变过程中作为治疗靶点的作用尚未得到充分研究。我们的研究确定赖氨酸特异性去甲基化酶1(LSD1)是OSCC的关键促进因子,表明在小鼠中敲除或药物抑制LSD1可逆转OSCC癌前病变。SP2509对LSD1的抑制作用扰乱了细胞周期,降低了免疫抑制作用,并增强了CD4+和CD8+T细胞浸润。在自发OSCC的猫模型中,发现一种临床LSD1抑制剂(Seclidemstat或SP2577)安全且能有效抑制STAT3网络。机制研究表明,LSD1通过STAT3信号通路驱动OSCC进展,该信号通路受细胞周期调节因子CDK7和免疫抑制性CTLA4磷酸化的调控。值得注意的是,抑制LSD1可降低Tyr170位点的CDK7和Ser422位点的eIF4B的磷酸化水平,为LSD1调节癌前病变向OSCC转变的新机制提供了见解。本研究对OSCC进展有了更深入的了解,并突出了LSD1作为控制OSCC从癌前病变进展的潜在治疗靶点。