Alcantara Llaguno Sheila R, Parada Luis F
Brain Tumor Center and Cancer Biology & Genetics Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Br J Cancer. 2016 Dec 6;115(12):1445-1450. doi: 10.1038/bjc.2016.354. Epub 2016 Nov 10.
The cellular origin of gliomas remains a topic of controversy in cancer research. Advances in neurobiology, molecular genetics, and functional genomics have ushered new insights through exploiting the development of more sophisticated tools to address this question. Diverse distinct cell populations in the adult brain have been reported to give rise to gliomas, although how these studies relate physiologically to mechanisms of spontaneous tumour formation via accumulation of tumour-initiating mutations within a single cell are less well developed. Recent studies in animal models indicate that the lineage of the tumour-initiating cell may contribute to the biological and genomic phenotype of glioblastoma. These results suggest that the cell of origin may not only serve as a source of diversity for these tumours, but may also provide new avenues for improved diagnostics and therapeutic targeting that may prolong the lives of patients.
神经胶质瘤的细胞起源仍是癌症研究中一个有争议的话题。神经生物学、分子遗传学和功能基因组学的进展,通过开发更精密的工具来解决这个问题,带来了新的见解。据报道,成人大脑中不同的细胞群会引发神经胶质瘤,尽管这些研究在生理上与通过单个细胞内肿瘤起始突变的积累而形成自发肿瘤的机制之间的关系尚不明确。动物模型的最新研究表明,肿瘤起始细胞的谱系可能有助于胶质母细胞瘤的生物学和基因组表型。这些结果表明,起源细胞不仅可能是这些肿瘤多样性的来源,还可能为改进诊断和治疗靶点提供新途径,从而延长患者的生命。