Shackney S E, Shankey T V
Allegheny University of the Health Sciences, Department of Human Oncology, Allegheny Campus, Pittsburgh, Pennsylvania 15212, USA.
Cytometry. 1997 Sep 1;29(1):1-27.
Human solid tumors develop multiple genetic evolutionary abnormalities as they evolve. Studies that have focused primarily on early colorectal cancer have suggested that genetic instability is a prominent feature of preinvasive disease. At least two separate mechanisms for the generation of genetic instability have been identified. The first, which involves widespread microsatellite instability in near-diploid cells, affects less than one-fifth of colon cancers. The second form of genetic instability is characterized by the development of p53 gene abnormalities that result in gross aneuploidy and multiple structural chromosomal changes. p53/aneuploidy affects most colon cancers, breast cancers, and many other solid tumors. This genetic evolutionary change commonly occurs at the interface between severe dysplasia and invasive disease. Specific post-aneuploid sequences of genetic changes that are relevant to tumor progression often involve the accumulation of multiple gain-of-function abnormalities in individual cells. The co-occurrence of Her-2/neu overexpression and EGF receptor overexpression in the same aneuploid cells defines an adeno/squamous genetic evolutionary sequence that is common to ductal breast cancers, non-small cell lung cancers, and other solid tumors. Later steps in this sequence include ras and c-myc overexpression. The neuroendocrine genetic evolutionary sequence is a separate branch of the p53/aneuploidy sequence with distinctive features that include loss of Rb and raf1 overexpression. Her-2/neu overexpression is not characteristic of this sequence; c-myc amplification/overexpression is common to both p53-associated sequences. The neuroendocrine sequence is found in small cell carcinoma of the lung and in minor proportions of other solid tumors, including breast cancer. Multiparameter cell-based methods are especially well suited for elucidation in human solid tumors of the genetic evolutionary sequences that could provide a rational scientific basis for determining prognosis and for optimizing therapy in individual cancer patients.
人类实体瘤在演变过程中会出现多种基因进化异常。主要聚焦于早期结直肠癌的研究表明,基因不稳定是侵袭前疾病的一个突出特征。已确定至少有两种产生基因不稳定的独立机制。第一种机制涉及近二倍体细胞中广泛的微卫星不稳定,影响不到五分之一的结肠癌。第二种基因不稳定形式的特征是p53基因异常的出现,导致严重非整倍体和多种染色体结构变化。p53/非整倍体影响大多数结肠癌、乳腺癌和许多其他实体瘤。这种基因进化变化通常发生在重度发育异常与侵袭性疾病的交界处。与肿瘤进展相关的特定非整倍体后基因变化序列通常涉及单个细胞中多个功能获得性异常的积累。在同一非整倍体细胞中同时出现Her-2/neu过表达和表皮生长因子受体过表达,定义了一种腺/鳞状基因进化序列,这在乳腺导管癌、非小细胞肺癌和其他实体瘤中很常见。该序列的后续步骤包括ras和c-myc过表达。神经内分泌基因进化序列是p53/非整倍体序列的一个独立分支,具有独特特征,包括Rb缺失和raf1过表达。Her-2/neu过表达不是该序列的特征;c-myc扩增/过表达在两个与p53相关的序列中都很常见。神经内分泌序列见于肺小细胞癌以及其他实体瘤(包括乳腺癌)的小部分病例中。基于多参数细胞的方法特别适合于阐明人类实体瘤中的基因进化序列,这些序列可为确定个体癌症患者的预后和优化治疗提供合理的科学依据。