Levy A
University Research Centre for Neuroendocrinology, Bristol Royal Infirmary, Marlborough Street, BS2 8HW, Bristol, UK.
Trends Endocrinol Metab. 2001 Sep;12(7):301-7. doi: 10.1016/s1043-2760(01)00434-9.
It is believed and hoped that clonality assignment of tumours predicts long-term behaviour, narrows the search for the putative pathogenic event or events, identifies the extent of involvement of surrounding and distant tissues and assesses the completeness of surgical clearance. It should define optimal therapeutic strategies, such as gene therapy, and the most fruitful directions for research. Because the histological characteristics that are central to establishing prognosis in most neoplasms are of limited value in endocrine tumours, the benefits of interpretation of clonality are potentially even more valuable and far-reaching in these tissues. So, can clonality be accurately defined and, if it can, can the distinction between a polyclonal expansion of cells that are simply 'obeying orders' and the presumed progeny of a single anarchic mutant be usefully made? This review comes to the conclusion that the answer is 'probably not'.
人们相信并希望肿瘤的克隆性分析能够预测其长期行为,缩小对假定致病事件的搜索范围,确定周围和远处组织的受累程度,并评估手术切除的完整性。它应该能够确定最佳治疗策略,如基因治疗,以及最有成效的研究方向。由于在大多数肿瘤中对判断预后至关重要的组织学特征在内分泌肿瘤中的价值有限,因此在这些组织中解释克隆性的益处可能更有价值且影响深远。那么,克隆性能够被准确界定吗?如果可以,能否有效区分仅仅是“服从指令”的细胞多克隆扩增与单个无节制突变体的假定后代呢?这篇综述得出的结论是答案“可能是否定的”。