Crende O, García-Gallastegui P, Luzuriaga J, Badiola I, de la Hoz C, Unda F, Ibarretxe G, Pineda J R
Department of Cell Biology and Histology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain.
Achucarro Basque Center for Neuroscience Fundazioa, 48940 Leioa, Spain.
Biology (Basel). 2020 Nov 27;9(12):426. doi: 10.3390/biology9120426.
The conversion of healthy stem cells into cancer stem cells (CSCs) is believed to underlie tumor relapse after surgical removal and fuel tumor growth and invasiveness. CSCs often arise from the malignant transformation of resident multipotent stem cells, which are present in most human tissues. Some organs, such as the gut and the brain, can give rise to very aggressive types of cancers, contrary to the dental pulp, which is a tissue with a very remarkable resistance to oncogenesis. In this review, we focus on the similarities and differences between gut, brain and dental pulp stem cells and their related CSCs, placing a particular emphasis on both their shared and distinctive cell markers, including the expression of pluripotency core factors. We discuss some of their similarities and differences with regard to oncogenic signaling, telomerase activity and their intrinsic propensity to degenerate to CSCs. We also explore the characteristics of the events and mutations leading to malignant transformation in each case. Importantly, healthy dental pulp stem cells (DPSCs) share a great deal of features with many of the so far reported CSC phenotypes found in malignant neoplasms. However, there exist literally no reports about the contribution of DPSCs to malignant tumors. This raises the question about the particularities of the dental pulp and what specific barriers to malignancy might be present in the case of this tissue. These notable differences warrant further research to decipher the singular properties of DPSCs that make them resistant to transformation, and to unravel new therapeutic targets to treat deadly tumors.
健康干细胞向癌症干细胞(CSCs)的转化被认为是手术切除后肿瘤复发的基础,并推动肿瘤生长和侵袭。CSCs通常源于大多数人体组织中存在的常驻多能干细胞的恶性转化。一些器官,如肠道和大脑,会引发极具侵袭性的癌症类型,而牙髓则是一种对肿瘤发生具有显著抗性的组织。在本综述中,我们重点关注肠道、大脑和牙髓干细胞及其相关CSCs之间的异同,特别强调它们共有的和独特的细胞标志物,包括多能性核心因子的表达。我们讨论它们在致癌信号传导、端粒酶活性以及它们向CSCs退化的内在倾向方面的一些异同。我们还探讨了每种情况下导致恶性转化的事件和突变的特征。重要的是,健康的牙髓干细胞(DPSCs)与迄今在恶性肿瘤中报道的许多CSC表型具有大量共同特征。然而,实际上尚无关于DPSCs对恶性肿瘤贡献的报道。这就引出了关于牙髓特殊性以及该组织可能存在哪些特定恶性肿瘤屏障的问题。这些显著差异值得进一步研究,以破译使DPSCs具有抗转化能力的独特特性,并揭示治疗致命肿瘤的新治疗靶点。