Bai Yuchen, Boath Jarryd, White Gabrielle R, Kariyawasam Uluvitike G I U, Farah Camile S, Darido Charbel
Peter MacCallum Cancer Centre, 305 Grattan St., Melbourne, VIC 3000, Australia.
Australian Centre for Oral Oncology Research & Education, Perth, WA 6009, Australia.
Cancers (Basel). 2021 Oct 13;13(20):5123. doi: 10.3390/cancers13205123.
The oral epithelium is one of the fastest repairing and continuously renewing tissues. Stem cell activation within the basal layer of the oral epithelium fuels the rapid proliferation of multipotent progenitors. Stem cells first undergo asymmetric cell division that requires tightly controlled and orchestrated differentiation networks to maintain the pool of stem cells while producing progenitors fated for differentiation. Rapidly expanding progenitors subsequently commit to advanced differentiation programs towards terminal differentiation, a process that regulates the structural integrity and homeostasis of the oral epithelium. Therefore, the balance between differentiation and terminal differentiation of stem cells and their progeny ensures progenitors commitment to terminal differentiation and prevents epithelial transformation and oral squamous cell carcinoma (OSCC). A recent comprehensive molecular characterization of OSCC revealed that a disruption of terminal differentiation factors is indeed a common OSCC event and is superior to oncogenic activation. Here, we discuss the role of differentiation and terminal differentiation in maintaining oral epithelial homeostasis and define terminal differentiation as a critical tumour suppressive mechanism. We further highlight factors with crucial terminal differentiation functions and detail the underlying consequences of their loss. Switching on terminal differentiation in differentiated progenitors is likely to represent an extremely promising novel avenue that may improve therapeutic interventions against OSCC.
口腔上皮是修复速度最快且不断更新的组织之一。口腔上皮基底层内的干细胞激活推动了多能祖细胞的快速增殖。干细胞首先经历不对称细胞分裂,这需要严格控制和精心编排的分化网络,以维持干细胞池,同时产生注定要分化的祖细胞。快速扩增的祖细胞随后进入晚期分化程序,朝着终末分化发展,这一过程调节着口腔上皮的结构完整性和稳态。因此,干细胞及其后代的分化和终末分化之间的平衡确保了祖细胞向终末分化的定向发展,并防止上皮转化和口腔鳞状细胞癌(OSCC)的发生。最近对OSCC的全面分子特征分析表明,终末分化因子的破坏确实是OSCC的常见事件,且比致癌激活更为常见。在此,我们讨论分化和终末分化在维持口腔上皮稳态中的作用,并将终末分化定义为一种关键的肿瘤抑制机制。我们进一步强调具有关键终末分化功能的因子,并详细阐述其缺失的潜在后果。在已分化的祖细胞中开启终末分化可能是一条极具前景的新途径,有望改善针对OSCC的治疗干预措施。