Ozen H
Hacettepe University, Department of Urology, Ankara, Turkey.
Curr Opin Oncol. 1996 May;8(3):259-63.
For many years it has been apparent that transitional cell carcinomas are a heterogeneous group of neoplasms with two clinical forms that exhibit distinctly different prognoses. Approximately 20% of the tumors are invasive at presentation, which is associated with poor prognoses. The remaining carcinomas are superficial, and an excellent outcome can be expected in the majority of patients treated with local therapies. However, 20% of the latter will progress to muscle invasive disease during the follow-up. The problem is to identify those who will progress and to distinguish those tumors likely to respond to therapy. Genetic changes that identify the subgroups of these tumors may be the key issue. During the past decade, studies of human cancer have begun to yield molecular information on the identity of multiple genetic changes that underline development and progression. Attention was focused initially on oncogenes and more recently on tumor-suppressor genes.
多年来显而易见的是,移行细胞癌是一组异质性肿瘤,有两种临床形式,其预后明显不同。大约20%的肿瘤在初诊时即为浸润性,这与预后不良相关。其余的癌为表浅性,大多数接受局部治疗的患者可望获得良好结局。然而,后者中有20%在随访期间会进展为肌层浸润性疾病。问题在于识别那些将会进展的患者,并区分那些可能对治疗有反应的肿瘤。确定这些肿瘤亚组的基因变化可能是关键问题。在过去十年中,对人类癌症的研究已开始产生有关多种基因变化特征的分子信息,这些变化是肿瘤发生和进展的基础。最初注意力集中在癌基因上,最近则集中在肿瘤抑制基因上。