Ware J L
Department of Pathology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298.
Am J Pathol. 1994 Nov;145(5):983-93.
This review examines selected areas of contemporary prostate cancer research in terms of the impact of prostatic cellular and histopathological heterogeneity. Prostate tumor progression is accompanied by dysregulation of multiple growth factor networks as well as disruption of normal patterns of cell-cell interactions. Molecular and cytogenetic studies demonstrate that prostate cancer results from the accumulation of several different genetic defects. No single event predominates, but modifications in tumor suppressor genes or functional elimination of the suppressor gene product are more common than activation of known oncogenes. Intratumor heterogeneity is also detectable at the genetic level. This further complicates efforts to correlate modifications at specific loci with progression or outcome. The development of new in vitro and in vivo systems for the study of human prostate cancer should increase our understanding of this complex disease. In each approach, knowledge of the histopathology of the normal and neoplastic prostate is essential.
本综述从前列腺细胞和组织病理学异质性的影响方面,审视当代前列腺癌研究的某些选定领域。前列腺肿瘤进展伴随着多种生长因子网络的失调以及正常细胞间相互作用模式的破坏。分子和细胞遗传学研究表明,前列腺癌是由几种不同的基因缺陷积累所致。没有单一事件占主导,但肿瘤抑制基因的修饰或抑制基因产物的功能消除比已知癌基因的激活更为常见。肿瘤内异质性在基因水平也可检测到。这使得将特定基因座的修饰与进展或结果相关联的努力更加复杂。用于研究人类前列腺癌的新的体外和体内系统的开发,应能增进我们对这种复杂疾病的理解。在每种方法中,了解正常和肿瘤性前列腺的组织病理学至关重要。